Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Radu, P; Atsmon, J
   Gilbert's syndrome - Clinical and pharmacological implications
   ISRAEL MEDICAL ASSOCIATION JOURNAL
   
   P. Radu e J. Atsmon, "Gilbert's syndrome - Clinical and pharmacological implications", ISR MED ASS, 3(8), 2001, pp. 593-598
2. Levine, AM; Berhane, K; Masri-Lavine, L; Sanchez, ML; Young, M; Augenbraun, M; Cohen, M; Anastos, K; Newman, M; Gange, SJ; Watts, H
   Prevalence and correlates of anemia in a large cohort of HIV-infected women: Women's interagency HIV study
   JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
   
   A.M. Levine et al., "Prevalence and correlates of anemia in a large cohort of HIV-infected women: Women's interagency HIV study", J ACQ IMM D, 26(1), 2001, pp. 28-35
3. Lappin, S; Cahlik, J; Gold, B
   Robot printing of reverse dot blot arrays for human mutation detection
   JOURNAL OF MOLECULAR DIAGNOSTICS
   
   S. Lappin et al., "Robot printing of reverse dot blot arrays for human mutation detection", J MOL DIAGN, 3(4), 2001, pp. 178-188
4. Tan, MQ; Qing, K; Zhou, SZ; Yoder, MC; Srivastava, A
   Adeno-associated virus 2-mediated transduction and erythroid lineage-restricted long-term expression of the human beta-globin gene in hematopoietic cells from homozygous beta-thalassemic mice
   MOLECULAR THERAPY
   
   M.Q. Tan et al., "Adeno-associated virus 2-mediated transduction and erythroid lineage-restricted long-term expression of the human beta-globin gene in hematopoietic cells from homozygous beta-thalassemic mice", MOL THER, 3(6), 2001, pp. 940-946
5. Ballas, SK
   Effect of alpha-globin genotype on the pathophysiology of sickle cell disease
   PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
   
   S.K. Ballas, "Effect of alpha-globin genotype on the pathophysiology of sickle cell disease", PEDIAT PATH, 20(2), 2001, pp. 107-121
6. Nagel, RL; Steinberg, MH
   Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia
   PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
   
   R.L. Nagel e M.H. Steinberg, "Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia", PEDIAT PATH, 20(2), 2001, pp. 123-136
7. Stuart, MJ; Setty, BNY
   Hemostatic alterations in sickle cell disease: Relationships to disease pathophysiology
   PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
   
   M.J. Stuart e B.N.Y. Setty, "Hemostatic alterations in sickle cell disease: Relationships to disease pathophysiology", PEDIAT PATH, 20(1), 2001, pp. 27-46
8. Blackwell, JM
   Genetics and genomics in infectious disease susceptibility
   TRENDS IN MOLECULAR MEDICINE
   
   J.M. Blackwell, "Genetics and genomics in infectious disease susceptibility", TRENDS MO M, 7(11), 2001, pp. 521-526
9. Weatherall, DJ
   Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias
   NATURE REVIEWS GENETICS
   
   D.J. Weatherall, "Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias", NAT REV GEN, 2(4), 2001, pp. 245-255
10. Daud, D; Harahap, A; Setianingsih, I; Nainggolan, I; Tranggana, S; Pakasi, R; Marzuki, S
    The Hemoglobin O mutation in Indonesia: distribution and phenotypic expression
    JOURNAL OF HUMAN GENETICS
    
    D. Daud et al., "The Hemoglobin O mutation in Indonesia: distribution and phenotypic expression", J HUM GENET, 46(9), 2001, pp. 499-505
11. Jaiswal, SPB; Chitnis, DS; Jain, AK; Inamdar, S; Porwal, A; Jain, SC
    Prevalence of hepatitis viruses among multi-transfused homogenous thalassaemia patients
    HEPATOLOGY RESEARCH
    
    S.P.B. Jaiswal et al., "Prevalence of hepatitis viruses among multi-transfused homogenous thalassaemia patients", HEPATOL RES, 19(3), 2001, pp. 247-253
12. Mockenhaupt, FP; May, J; Bergqvist, Y; Meyer, CG; Falusi, AG; Bienzle, U
    Evidence for a reduced effect of chloroquine against Plasmodium falciparumin alpha(+)-thalassaemic children
    TROPICAL MEDICINE & INTERNATIONAL HEALTH
    
    F.P. Mockenhaupt et al., "Evidence for a reduced effect of chloroquine against Plasmodium falciparumin alpha(+)-thalassaemic children", TR MED I H, 6(2), 2001, pp. 102-107
13. Rodgers, GP; Saunthararajah, Y
    Advances in experimental treatment of beta-thalassaemia
    EXPERT OPINION ON INVESTIGATIONAL DRUGS
    
    G.P. Rodgers e Y. Saunthararajah, "Advances in experimental treatment of beta-thalassaemia", EXPERT OP I, 10(5), 2001, pp. 925-934
14. Monge, L; Pinach, S; Caramellino, L; Bertero, MT; Dall'Omo, A; Carta, Q
    The possible role of autoimmunity in the pathogenesis of diabetes in beta-thalassemia major
    DIABETES & METABOLISM
    
    L. Monge et al., "The possible role of autoimmunity in the pathogenesis of diabetes in beta-thalassemia major", DIABETE MET, 27(2), 2001, pp. 149-154
15. Kanj, SS; Araj, GF; Taher, A; Reller, LB
    Campylobacter fetus pericarditis in a patient with beta-thalassemia: case report and review of the literature
    CLINICAL MICROBIOLOGY AND INFECTION
    
    S.S. Kanj et al., "Campylobacter fetus pericarditis in a patient with beta-thalassemia: case report and review of the literature", CL MICRO IN, 7(9), 2001, pp. 510-513
16. Ma, SK; Au, WY; Chan, AYY; Chan, LC
    Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta(0)-thalassemia in Chinese subjects
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    
    S.K. Ma et al., "Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta(0)-thalassemia in Chinese subjects", INT J MOL M, 8(2), 2001, pp. 171-175
17. Castellvi-Bel, S; Mila, M
    Genes responsible for nonspecific mental retardation
    MOLECULAR GENETICS AND METABOLISM
    
    S. Castellvi-Bel e M. Mila, "Genes responsible for nonspecific mental retardation", MOL GEN MET, 72(2), 2001, pp. 104-108
18. Lorey, F; Cunningham, G; Vichinsky, EP; Lubin, BH; Witkowska, HE; Matsunaga, A; Azimi, M; Sherwin, J; Eastman, J; Farina, F; Waye, JS; Chui, DHK
    Universal newborn screening for Hb H disease in California
    GENETIC TESTING
    
    F. Lorey et al., "Universal newborn screening for Hb H disease in California", GENET TEST, 5(2), 2001, pp. 93-100
19. Yang, YP; Corley, N; Garcia-Heras, J
    Reverse dot-blot hybridization as an improved tool for the molecular diagnosis of point mutations in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency
    MOLECULAR DIAGNOSIS
    
    Y.P. Yang et al., "Reverse dot-blot hybridization as an improved tool for the molecular diagnosis of point mutations in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency", MOL DIAGN, 6(3), 2001, pp. 193-199
20. Li, ZH; Liu, DP; Yin, WX; Guo, ZC; Liang, CC
    Targeted correction of the point mutations of beta-thalassemia and targeted mutagenesis of the nucleotide associated with HPFH by RNA/DNA oligonucleotides: Potential for beta-thalassemia gene therapy
    BLOOD CELLS MOLECULES AND DISEASES
    
    Z.H. Li et al., "Targeted correction of the point mutations of beta-thalassemia and targeted mutagenesis of the nucleotide associated with HPFH by RNA/DNA oligonucleotides: Potential for beta-thalassemia gene therapy", BL CELL M D, 27(2), 2001, pp. 530-538
21. Kapelushnik, J; Shalev, H; Schulman, H; Moser, A; Tamary, H
    Upper airway obstruction-related sleep apnea in a child with thalassemia intermedia
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    
    J. Kapelushnik et al., "Upper airway obstruction-related sleep apnea in a child with thalassemia intermedia", J PED H ONC, 23(8), 2001, pp. 525-526
22. Luporini, SM; Bendit, I; Manhani, R; Bracco, OL; Manzella, L; Giannella-Neto, D
    Growth hormone and insulin-like growth factor I axis and growth of children with different sickle cell anemia haplotypes
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    
    S.M. Luporini et al., "Growth hormone and insulin-like growth factor I axis and growth of children with different sickle cell anemia haplotypes", J PED H ONC, 23(6), 2001, pp. 357-363
23. Reed, W; Vichinsky, EP
    Transfusion therapy: A coming-of-age treatment for patients with sickle cell disease
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    
    W. Reed e E.P. Vichinsky, "Transfusion therapy: A coming-of-age treatment for patients with sickle cell disease", J PED H ONC, 23(4), 2001, pp. 197-202
24. Chan, PKS; Chik, KW; To, KF; Li, CK; Hui, M; Shing, MMK; Yuen, PMP; Tam, JS; Cheng, AF
    Clearance of TT virus after allogeneic bone marrow transplantation
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    
    P.K.S. Chan et al., "Clearance of TT virus after allogeneic bone marrow transplantation", J PED H ONC, 23(1), 2001, pp. 57-58
25. Tesoriere, L; D'Arpa, D; Butera, D; Allegra, M; Renda, D; Maggio, A; Bongiorno, A; Livrea, MA
    Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in beta-thalassemia intermedia patients
    FREE RADICAL RESEARCH
    
    L. Tesoriere et al., "Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in beta-thalassemia intermedia patients", FREE RAD RE, 34(5), 2001, pp. 529-540
26. Marcus, N; Garty, BZ
    Transient hypoparathyroidism due to amphotericin B-induced hypomagnesemia in a patient with beta-thalassemia
    ANNALS OF PHARMACOTHERAPY
    
    N. Marcus e B.Z. Garty, "Transient hypoparathyroidism due to amphotericin B-induced hypomagnesemia in a patient with beta-thalassemia", ANN PHARMAC, 35(9), 2001, pp. 1042-1044
27. Gemignani, F; Landi, S; DeMarini, DM; Kole, R
    Spontaneous and MNNG-induced reversion of an EGFP construct in HeLa cells:An assay for observing mutations in living cells by fluorescent microscopy
    HUMAN MUTATION
    
    F. Gemignani et al., "Spontaneous and MNNG-induced reversion of an EGFP construct in HeLa cells:An assay for observing mutations in living cells by fluorescent microscopy", HUM MUTAT, 18(6), 2001, pp. 526-534
28. Anionwu, EN
    Improving access and quality for ethnic minority women - Panel discussion
    WOMENS HEALTH ISSUES
    
    E.N. Anionwu, "Improving access and quality for ethnic minority women - Panel discussion", WOM HEAL IS, 11(4), 2001, pp. 366-370
29. Shiratsuchi, M; Muta, K; Minami, R; Motomura, S; Suehiro, Y; Abe, Y; Shiokawa, S; Umemura, T; Fukui, T; Nishimura, J; Nawata, H
    Aberrant BCR-ABL transcript with intronic insertion in a patient with Philadelphia chromosome-positive chronic myeloid leukemia: Implications for disease progression
    LEUKEMIA & LYMPHOMA
    
    M. Shiratsuchi et al., "Aberrant BCR-ABL transcript with intronic insertion in a patient with Philadelphia chromosome-positive chronic myeloid leukemia: Implications for disease progression", LEUK LYMPH, 41(3-4), 2001, pp. 411-415
30. Horsley, SW; Daniels, RJ; Anguita, E; Raynham, HA; Peden, JF; Villegas, A; Vickers, MA; Green, S; Waye, JS; Chui, DHK; Ayyub, H; MacCarthy, AB; Buckle, VJ; Gibbons, RJ; Kearney, L; Higgs, DR
    Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects
    EUROPEAN JOURNAL OF HUMAN GENETICS
    
    S.W. Horsley et al., "Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects", EUR J HUM G, 9(3), 2001, pp. 217-225
31. Feroze, M; Aravindan, KP
    Sickle cell disease in Wayanad, Kerala: Gene frequencies and disease characteristics
    NATIONAL MEDICAL JOURNAL OF INDIA
    
    M. Feroze e K.P. Aravindan, "Sickle cell disease in Wayanad, Kerala: Gene frequencies and disease characteristics", NAT MED J I, 14(5), 2001, pp. 267-270
32. Farquharson, MJ; Bagshaw, AP
    Monitoring body iron burden using X-ray fluorescence (XRF)
    RADIATION PHYSICS AND CHEMISTRY
    
    M.J. Farquharson e A.P. Bagshaw, "Monitoring body iron burden using X-ray fluorescence (XRF)", RADIAT PH C, 61(3-6), 2001, pp. 599-601
33. Ducrocq, R; Pascaud, O; Bevier, A; Finet, C; Benkerrou, M; Elion, J
    Strategy linking several analytical methods of neonatal screening for sickle cell disease
    JOURNAL OF MEDICAL SCREENING
    
    R. Ducrocq et al., "Strategy linking several analytical methods of neonatal screening for sickle cell disease", J MED SCREE, 8(1), 2001, pp. 8-14
34. Jensen, PD; Jensen, FT; Christensen, T; Heickendorff, L; Jensen, LG; Ellegaard, J
    Indirect evidence for the potential ability of magnetic resonance imaging to evaluate the myocardial iron content in patients with transfusional ironoverload
    MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE
    
    P.D. Jensen et al., "Indirect evidence for the potential ability of magnetic resonance imaging to evaluate the myocardial iron content in patients with transfusional ironoverload", MAGN RES MA, 12(2-3), 2001, pp. 153-166
35. Ferrali, M; Donati, D; Bambagioni, S; Fontani, M; Giorgi, G; Pietrangelo, A
    3-hydroxy-(4H)-benzopyran-4-ones as potential iron chelating agents in vivo
    BIOORGANIC & MEDICINAL CHEMISTRY
    
    M. Ferrali et al., "3-hydroxy-(4H)-benzopyran-4-ones as potential iron chelating agents in vivo", BIO MED CH, 9(11), 2001, pp. 3041-3047
36. Friebe, B; Kynast, RG; Zhang, P; Qi, LL; Dhar, M; Gill, BS
    Chromosome healing by addition of telomeric repeats in wheat occurs duringthe first mitotic divisions of the sporophyte and is a gradual process
    CHROMOSOME RESEARCH
    
    B. Friebe et al., "Chromosome healing by addition of telomeric repeats in wheat occurs duringthe first mitotic divisions of the sporophyte and is a gradual process", CHROMOS RES, 9(2), 2001, pp. 137-146
37. Chen, CP
    Severe terminal transverse limb reduction defects in homozygous Southeast-Asian alpha-thalassaemia-1
    CLINICAL DYSMORPHOLOGY
    
    C.P. Chen, "Severe terminal transverse limb reduction defects in homozygous Southeast-Asian alpha-thalassaemia-1", CLIN DYSMOR, 10(1), 2001, pp. 71-73
38. Kidd, RD; Baker, HM; Mathews, AJ; Brittain, T; Baker, EN
    Oligomerization and ligand binding in a homotetrameric hemoglobin: Two high-resolution crystal structures of hemoglobin Bart's (gamma(4)), a marker for alpha-thalassemia
    PROTEIN SCIENCE
    
    R.D. Kidd et al., "Oligomerization and ligand binding in a homotetrameric hemoglobin: Two high-resolution crystal structures of hemoglobin Bart's (gamma(4)), a marker for alpha-thalassemia", PROTEIN SCI, 10(9), 2001, pp. 1739-1749
39. Holzgreve, W; Hahn, S
    Fetal cells in maternal circulation. What is the relationship to obstetricultrasound?
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    
    W. Holzgreve e S. Hahn, "Fetal cells in maternal circulation. What is the relationship to obstetricultrasound?", ULTRASOUN O, 17(1), 2001, pp. 1-3
40. Lam, YH; Tang, MHY; Tse, HY
    Ductus venosus Doppler study in fetuses with homozygous alpha-thalassemia-1 at 12 to 13 weeks of gestation
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    
    Y.H. Lam et al., "Ductus venosus Doppler study in fetuses with homozygous alpha-thalassemia-1 at 12 to 13 weeks of gestation", ULTRASOUN O, 17(1), 2001, pp. 30-33
41. Christensen, DW; Kisling, R; Thompson, J; Kirby, MA
    Deferoxamine toxicity in hepatoma and primary rat cortical brain cultures
    HUMAN & EXPERIMENTAL TOXICOLOGY
    
    D.W. Christensen et al., "Deferoxamine toxicity in hepatoma and primary rat cortical brain cultures", HUM EXP TOX, 20(7), 2001, pp. 365-372
42. Zhou, XC; Huang, LQ; Li, SFY
    Microgravimetric DNA sensor based on quartz crystal microbalance: comparison of oligonucleotide immobilization methods and the application in geneticdiagnosis
    BIOSENSORS & BIOELECTRONICS
    
    X.C. Zhou et al., "Microgravimetric DNA sensor based on quartz crystal microbalance: comparison of oligonucleotide immobilization methods and the application in geneticdiagnosis", BIOSENS BIO, 16(1-2), 2001, pp. 85-95
43. Sougleri, M; Labropoulou-Karatza, C; Paraskevopoulou, P; Fragopanagou, H; Alexandrides, T
    Chronic hepatitis C virus infection without cirrhosis induces insulin resistance in patients with beta-thalassaemia major
    EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    
    M. Sougleri et al., "Chronic hepatitis C virus infection without cirrhosis induces insulin resistance in patients with beta-thalassaemia major", EUR J GASTR, 13(10), 2001, pp. 1195-1199
44. Signori, E; Bagni, C; Papa, S; Primerano, B; Rinaldi, M; Amaldi, F; Fazio, VM
    A somatic mutation in the 5 ' UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency
    ONCOGENE
    
    E. Signori et al., "A somatic mutation in the 5 ' UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency", ONCOGENE, 20(33), 2001, pp. 4596-4600
45. Bernhardt, PV; Chin, P; Richardson, DR
    Unprecedented oxidation of a biologically active aroylhydrazone chelator catalysed by iron(III): serendipitous identification of diacylhydrazine ligands with high iron chelation efficacy
    JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
    
    P.V. Bernhardt et al., "Unprecedented oxidation of a biologically active aroylhydrazone chelator catalysed by iron(III): serendipitous identification of diacylhydrazine ligands with high iron chelation efficacy", J BIOL I CH, 6(8), 2001, pp. 801-809
46. Makis, AC; Chaliasos, N; Hatzimichael, EC; Bourantas, KL
    Recombinant human erythropoietin therapy in a transfusion-dependent beta-thalassemia major patient
    ANNALS OF HEMATOLOGY
    
    A.C. Makis et al., "Recombinant human erythropoietin therapy in a transfusion-dependent beta-thalassemia major patient", ANN HEMATOL, 80(8), 2001, pp. 492-495
47. Ahmed, M; Stuhrmann, M; Bashawri, L; Kuhnau, W; El-Harith, EHA
    The beta-globin genotype E121Q/W15X (cd121GAA -> CAA/cd15TGG -> TGA) underlines Hb D/beta-(0) thalassaemia marked by domination of haemoglobin D
    ANNALS OF HEMATOLOGY
    
    M. Ahmed et al., "The beta-globin genotype E121Q/W15X (cd121GAA -> CAA/cd15TGG -> TGA) underlines Hb D/beta-(0) thalassaemia marked by domination of haemoglobin D", ANN HEMATOL, 80(11), 2001, pp. 629-633
48. Kyriakou, DS; Alexandrakis, MG; Kyriakou, ES; Liapi, D; Kourelis, TV; Passam, F; Papadakis, A
    Activated peripheral blood and endothelial cells in thalassemia patients
    ANNALS OF HEMATOLOGY
    
    D.S. Kyriakou et al., "Activated peripheral blood and endothelial cells in thalassemia patients", ANN HEMATOL, 80(10), 2001, pp. 577-583
49. Xiros, N; Economopoulos, T; Papageorgiou, E; Mantzios, G; Raptis, S
    Massive hemothorax due to intrathoracic extramedullary hematopoiesis in a patient with hereditary spherocytosis
    ANNALS OF HEMATOLOGY
    
    N. Xiros et al., "Massive hemothorax due to intrathoracic extramedullary hematopoiesis in a patient with hereditary spherocytosis", ANN HEMATOL, 80(1), 2001, pp. 38-40
50. Caprari, P; Caforio, MP; Cianciulli, P; Maffi, D; Pasquino, MT; Tarzia, A; Amadori, S; Salvati, AM
    6-phosphogluconate dehydrogenase deficiency in an Italian family
    ANNALS OF HEMATOLOGY
    
    P. Caprari et al., "6-phosphogluconate dehydrogenase deficiency in an Italian family", ANN HEMATOL, 80(1), 2001, pp. 41-44
51. Chourmouzi, D; Pistevou-Gompaki, K; Plataniotis, G; Skaragas, G; Papadopoulos, L; Drevelegas, A
    MRI findings of extramedullary haemopoiesis
    EUROPEAN RADIOLOGY
    
    D. Chourmouzi et al., "MRI findings of extramedullary haemopoiesis", EUR RADIOL, 11(9), 2001, pp. 1803-1806
52. Lasco, A; Morabito, N; Gaudio, A; Buemi, M; Wasniewska, M; Frisina, N
    Effects of hormonal replacement therapy on bone metabolism in young adultswith beta-thalassemia major
    OSTEOPOROSIS INTERNATIONAL
    
    A. Lasco et al., "Effects of hormonal replacement therapy on bone metabolism in young adultswith beta-thalassemia major", OSTEOPOR IN, 12(7), 2001, pp. 570-575
53. Altunbasak, S; Yildizdas, D; Anarat, A; Burgut, HR
    Renal tubular dysfunction in epileptic children on valproic acid therapy
    PEDIATRIC NEPHROLOGY
    
    S. Altunbasak et al., "Renal tubular dysfunction in epileptic children on valproic acid therapy", PED NEPHROL, 16(3), 2001, pp. 256-259
54. Morgan, HEG; Gautam, M; Geary, DF
    Maintenance intravenous iron therapy in pediatric hemodialysis patients
    PEDIATRIC NEPHROLOGY
    
    H.E.G. Morgan et al., "Maintenance intravenous iron therapy in pediatric hemodialysis patients", PED NEPHROL, 16(10), 2001, pp. 779-783
55. Kurtman, C; Ozbilgin, MK; Andrieu, MN; Celebioglu, B
    Paratracheal extramedullary hematopoiesis
    INTERNATIONAL JOURNAL OF HEMATOLOGY
    
    C. Kurtman et al., "Paratracheal extramedullary hematopoiesis", INT J HEMAT, 73(4), 2001, pp. 492-495
56. Tsomi, K; Karagiorga-Lagana, M; Karabatsos, F; Fragodimitri, C; van Vliet-Konstantinidou, C; Premetis, E; Stamoulakatou, A
    Arterial elastorrhexis in beta-thalassaemia intermedia, sickle cell thalassaemia and hereditary spherocytosis
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    K. Tsomi et al., "Arterial elastorrhexis in beta-thalassaemia intermedia, sickle cell thalassaemia and hereditary spherocytosis", EUR J HAEMA, 67(3), 2001, pp. 135-141
57. Laosombat, V; Wongchanchailert, M; Sattayasevana, B; Wiriyasateinkul, A; Fucharoen, S
    Clinical and hematological features of beta(+)-thalassemia (IVS-1 nt 5, G-C mutation) in Thai patients
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    V. Laosombat et al., "Clinical and hematological features of beta(+)-thalassemia (IVS-1 nt 5, G-C mutation) in Thai patients", EUR J HAEMA, 67(2), 2001, pp. 100-104
58. Taher, A; Sheikh-Taha, M; Koussa, M; Inati, A; Neeman, R; Mourad, F
    Comparison between deferoxamine and deferiprone (L1) in iron-loaded thalassemia patients
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    A. Taher et al., "Comparison between deferoxamine and deferiprone (L1) in iron-loaded thalassemia patients", EUR J HAEMA, 67(1), 2001, pp. 30-34
59. Fucharoen, S; Ayukarn, K; Sanchaisuriya, K; Fucharoen, G
    Atypical hemoglobin H disease in a Thai patient resulting from a combination of alpha-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    S. Fucharoen et al., "Atypical hemoglobin H disease in a Thai patient resulting from a combination of alpha-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity", EUR J HAEMA, 66(5), 2001, pp. 312-316
60. Giuliani, AL; Wiener, E; Lee, MJ; Brown, IN; Berti, G; Wickramasinghe, SN
    Changes in murine bone marrow macrophages and erythroid burst-forming cells following the intravenous injection of liposome-encapsulated dichloromethylene diphosphonate (Cl2MDP)
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    A.L. Giuliani et al., "Changes in murine bone marrow macrophages and erythroid burst-forming cells following the intravenous injection of liposome-encapsulated dichloromethylene diphosphonate (Cl2MDP)", EUR J HAEMA, 66(4), 2001, pp. 221-229
61. Laosombat, V; Wongchanchailert, M; Sattayasevana, B; Wiriyasateinkul, A; Fucharoen, S
    Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patients
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    V. Laosombat et al., "Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patients", EUR J HAEMA, 66(2), 2001, pp. 126-129
62. Tefferi, A; Jimenez, T; Gray, LA; Mesa, RA; Chen, MG
    Radiation therapy for symptomatic hepatomegaly in myelofibrosis with myeloid metaplasia
    EUROPEAN JOURNAL OF HAEMATOLOGY
    
    A. Tefferi et al., "Radiation therapy for symptomatic hepatomegaly in myelofibrosis with myeloid metaplasia", EUR J HAEMA, 66(1), 2001, pp. 37-42
63. Cin, S; Unal, E; Pamir, A; Kologlu, B; Cavdar, AO
    Blood zinc (plasma, red blood cell zinc) and insulin-like growth factor-1 in children from an 'impoverished" area in Ankara
    JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
    
    S. Cin et al., "Blood zinc (plasma, red blood cell zinc) and insulin-like growth factor-1 in children from an 'impoverished" area in Ankara", J TR EL EXP, 14(1), 2001, pp. 31-34
64. Samuni, AM; Afeworki, M; Stein, W; Yordanov, AT; DeGraff, W; Krishna, MC; Mitchell, JB; Brechbiel, MW
    Multifunctional antioxidant activity of HBED iron chelator
    FREE RADICAL BIOLOGY AND MEDICINE
    
    A.M. Samuni et al., "Multifunctional antioxidant activity of HBED iron chelator", FREE RAD B, 30(2), 2001, pp. 170-177
65. Yamashita, A; Ohnishi, T; Kashima, I; Taya, Y; Ohno, S
    Human SMG-1, a novel phosphatidylinositol 3-kinase-related protein kinase,associates with components of the mRNA surveillance complex and is involved in the regulation of nonsense-mediated mRNA decay
    GENES & DEVELOPMENT
    
    A. Yamashita et al., "Human SMG-1, a novel phosphatidylinositol 3-kinase-related protein kinase,associates with components of the mRNA surveillance complex and is involved in the regulation of nonsense-mediated mRNA decay", GENE DEV, 15(17), 2001, pp. 2215-2228
66. Rendtorff, ND; Frodin, M; Attie-Bitach, T; Vekemans, M; Tommerup, N
    Identification and characterization of an inner ear-expressed human melanoma inhibitory activity (MIA)-like gene (MIAL) with a frequent polymorphism that abolishes translation
    GENOMICS
    
    N.D. Rendtorff et al., "Identification and characterization of an inner ear-expressed human melanoma inhibitory activity (MIA)-like gene (MIAL) with a frequent polymorphism that abolishes translation", GENOMICS, 71(1), 2001, pp. 40-52
67. Tzetis, M; Kanavakis, E; Tsezou, A; Ladis, V; Pateraki, E; Georgakopoulou, T; Kavazarakis, E; Maragoudaki, E; Karpathios, T; Kitsiou-Tzeli, S
    Gilbert syndrome associated with beta-thalassemia
    PEDIATRIC HEMATOLOGY AND ONCOLOGY
    
    M. Tzetis et al., "Gilbert syndrome associated with beta-thalassemia", PED HEM ONC, 18(8), 2001, pp. 477-484
68. Kattamis, C; Kattamis, AC
    Oxidative stress disturbances in erythrocytes of beta-thalassemia
    PEDIATRIC HEMATOLOGY AND ONCOLOGY
    
    C. Kattamis e A.C. Kattamis, "Oxidative stress disturbances in erythrocytes of beta-thalassemia", PED HEM ONC, 18(2), 2001, pp. 85-88
69. Akpek, S; Canatan, D; Arac, M; Ilgit, ET
    Evaluation of osteoporosis in thalassemia by quantitative computed tomography: Is it reliable?
    PEDIATRIC HEMATOLOGY AND ONCOLOGY
    
    S. Akpek et al., "Evaluation of osteoporosis in thalassemia by quantitative computed tomography: Is it reliable?", PED HEM ONC, 18(2), 2001, pp. 111-116
70. Iyamu, EW; Fasold, H; Roa, D; Aguinaga, MD; Asakura, T; Turner, EA
    Hydroxyurea-induced oxidative damage of normal and sickle cell hemoglobinsin vitro: Amelioration by radical scavengers
    JOURNAL OF CLINICAL LABORATORY ANALYSIS
    
    E.W. Iyamu et al., "Hydroxyurea-induced oxidative damage of normal and sickle cell hemoglobinsin vitro: Amelioration by radical scavengers", J CL LAB AN, 15(1), 2001, pp. 1-7
71. Cadet, E; Warin, R; Perez, AS; Rochette, J; Capron, D
    The rusty genotypes
    M S-MEDECINE SCIENCES
    
    E. Cadet et al., "The rusty genotypes", M S-MED SCI, 17(6-7), 2001, pp. 753-759
72. Rey, J; Gagliano, R; Christides, C; Pillard, E; Magnan, F; Tourniaire, P; Arwidson, I; Raymond-Gelle, MC; Boulat, O; Arlaud, J
    Spinal cord compression due to extramedullary hematopoiesis foci in patients with thalassemia
    PRESSE MEDICALE
    
    J. Rey et al., "Spinal cord compression due to extramedullary hematopoiesis foci in patients with thalassemia", PRESSE MED, 30(27), 2001, pp. 1351-1353
73. Tiosano, D; Hochberg, Z
    Endocrine complications of thalassemia
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    
    D. Tiosano e Z. Hochberg, "Endocrine complications of thalassemia", J ENDOC INV, 24(9), 2001, pp. 716-723
74. Grosso, M; Rescigno, G; Zevino, C; Matarazzo, M; Poggi, V; Izzo, P
    A rare case of compound heterozygosity for delta(+)27 and Hb Neapolis (Dhonburi) associated to an atypical beta-thalassemia phenotype
    HAEMATOLOGICA
    
    M. Grosso et al., "A rare case of compound heterozygosity for delta(+)27 and Hb Neapolis (Dhonburi) associated to an atypical beta-thalassemia phenotype", HAEMATOLOG, 86(9), 2001, pp. 985-986
75. Politou, M; Kollia, P; Akel, S; Papassotiriou, Y; Stamoulakatou, A; Loukopoulos, D
    Valproic acid, trichostatin and their combination with hemin preferentially enhance gamma-globin gene expression in human erythroid liquid cultures
    HAEMATOLOGICA
    
    M. Politou et al., "Valproic acid, trichostatin and their combination with hemin preferentially enhance gamma-globin gene expression in human erythroid liquid cultures", HAEMATOLOG, 86(7), 2001, pp. 700-705
76. Garozzo, G; Distefano, R; Miceli, A; Bonomo, P
    Detection of ICAM-1, ICAM-2, ICAM-3, PECAM-1 and VCAM-1, evaluation of hypercoagulable state and platelet aggregation in hemoglobinopathy patients with erythroblasts
    HAEMATOLOGICA
    
    G. Garozzo et al., "Detection of ICAM-1, ICAM-2, ICAM-3, PECAM-1 and VCAM-1, evaluation of hypercoagulable state and platelet aggregation in hemoglobinopathy patients with erythroblasts", HAEMATOLOG, 86(7), 2001, pp. 778-779
77. Fucharoen, S; Sanchaisuriya, K; Fucharoen, G; Surapot, S
    Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients
    HAEMATOLOGICA
    
    S. Fucharoen et al., "Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients", HAEMATOLOG, 86(6), 2001, pp. 657-658
78. Ma, ESK; De Chow, EY; Chan, AYY; Chan, LC
    Interaction between (--(SEA)) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients
    HAEMATOLOGICA
    
    E.S.K. Ma et al., "Interaction between (--(SEA)) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients", HAEMATOLOG, 86(5), 2001, pp. 539-540
79. Zhao, YZ; Xu, XM
    alpha 2(CD31) (AGG -> AAG,) (Arg -> Lys) causing non-deletional alpha-thalassemia in a Chinese family with HbH disease
    HAEMATOLOGICA
    
    Y.Z. Zhao e X.M. Xu, "alpha 2(CD31) (AGG -> AAG,) (Arg -> Lys) causing non-deletional alpha-thalassemia in a Chinese family with HbH disease", HAEMATOLOG, 86(5), 2001, pp. 541-542
80. Traeger-Synodinos, J; Papassotiriou, I; Vrettou, C; Skarmoutsou, C; Stamoulakatou, A; Kanavakis, E
    Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional alpha-globin and beta-globin gene
    HAEMATOLOGICA
    
    J. Traeger-Synodinos et al., "Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional alpha-globin and beta-globin gene", HAEMATOLOG, 86(4), 2001, pp. 363-367
81. Ma, ESK; Chan, AYY; Au, WY; Yeung, YM; Chan, LC
    Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia
    HAEMATOLOGICA
    
    E.S.K. Ma et al., "Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia", HAEMATOLOG, 86(4), 2001, pp. 432-433
82. Laosombat, V; Wongchanchailert, M; Sattayasevana, B; Wiriyasateinkul, A; Fucharoen, S
    Clinical and hematologic features of beta(o)-thalassemia (frameshift 41/42mutation) in Thai patients
    HAEMATOLOGICA
    
    V. Laosombat et al., "Clinical and hematologic features of beta(o)-thalassemia (frameshift 41/42mutation) in Thai patients", HAEMATOLOG, 86(2), 2001, pp. 138-141
83. Ma, ESK; Chan, AYY; Ha, SY; Lau, YL; Chan, LC
    Thalassemia screening based on red cell indices in the Chinese
    HAEMATOLOGICA
    
    E.S.K. Ma et al., "Thalassemia screening based on red cell indices in the Chinese", HAEMATOLOG, 86(12), 2001, pp. 1310-1311
84. Harteveld, CL; Traeger-Synodinos, J; Ragusa, A; Fichera, M; Kanavakis, E; Kattamis, C; Giordano, P; Schiliro, G; Bernini, LF
    Different geographic origins of Hb constant spring [alpha(2) codon 142 TAA-> CAA]
    HAEMATOLOGICA
    
    C.L. Harteveld et al., "Different geographic origins of Hb constant spring [alpha(2) codon 142 TAA-> CAA]", HAEMATOLOG, 86(1), 2001, pp. 36-38
85. Sampietro, M; Tavazzi, D; di Montemuros, FM; Cerino, M; Zatelli, S; Lunghi, G; Orlandi, A; Fargion, S; Fiorelli, G; Cappellini, MD
    TT virus infection in adult beta-thalassemia major patients
    HAEMATOLOGICA
    
    M. Sampietro et al., "TT virus infection in adult beta-thalassemia major patients", HAEMATOLOG, 86(1), 2001, pp. 39-43
86. Li, ZQ; Liu, LP; Zhao, YZ; Zhong, XL; Xu, XM
    Two thalassemia intermedia patients with delta beta/beta-thalassemia and adeletional type alpha-thalassemia
    HAEMATOLOGICA
    
    Z.Q. Li et al., "Two thalassemia intermedia patients with delta beta/beta-thalassemia and adeletional type alpha-thalassemia", HAEMATOLOG, 86(1), 2001, pp. 108-108
87. Sifakis, S; Angelakis, E; Vardaki, E; Koumantaki, Y; Matalliotakis, I; Koumantakis, E
    Erythropoietin in the treatment of iron deficiency anemia during pregnancy
    GYNECOLOGIC AND OBSTETRIC INVESTIGATION
    
    S. Sifakis et al., "Erythropoietin in the treatment of iron deficiency anemia during pregnancy", GYNECOL OBS, 51(3), 2001, pp. 150-156
88. Yao, HX; Chen, ZB; Su, QH; Lin, X; Hu, ZH; Chen, LC
    Erythrocyte membrane protein abnormalities in beta-thalassemia of the Li nationality in Hainan
    CHINESE MEDICAL JOURNAL
    
    H.X. Yao et al., "Erythrocyte membrane protein abnormalities in beta-thalassemia of the Li nationality in Hainan", CHIN MED J, 114(5), 2001, pp. 486-488
89. Villegas, A; Ropero, P; Gonzalez, FA; Anguita, E; Espinos, D
    The thalassemia syndromes: Molecular characterization in the spanish population
    HEMOGLOBIN
    
    A. Villegas et al., "The thalassemia syndromes: Molecular characterization in the spanish population", HEMOGLOBIN, 25(3), 2001, pp. 273-283
90. Pistidda, P; Cherchi, L; Corda, M; Guiso, L; Pardini, S; Pirastru, M; Manca, L; Longinotti, M; Masala, B
    Hb Tigraye [beta 79(EF3)Asp -> His] in a Caucasian family from Sardinia
    HEMOGLOBIN
    
    P. Pistidda et al., "Hb Tigraye [beta 79(EF3)Asp -> His] in a Caucasian family from Sardinia", HEMOGLOBIN, 25(3), 2001, pp. 341-345
91. Efremov, GD
    Forty-four years (1955-1999) devoted to hemoglobin research: Titus H. J. Huisman (1923-1999) - In memoriam
    HEMOGLOBIN
    
    G.D. Efremov, "Forty-four years (1955-1999) devoted to hemoglobin research: Titus H. J. Huisman (1923-1999) - In memoriam", HEMOGLOBIN, 25(2), 2001, pp. 125-168
92. Adekile, AD
    Sickle cell disease in Kuwait
    HEMOGLOBIN
    
    A.D. Adekile, "Sickle cell disease in Kuwait", HEMOGLOBIN, 25(2), 2001, pp. 219-225
93. Papassotiriou, I; Traeger-Synodinos, J; Prome, D; Kister, J; Vrettou, C; Xaidara, A; Marden, M; Stamoulakatou, A; Wajcman, H; Kanavakis, E
    Hb Sitia [beta 128(H6)Ala -> Val]: An unstable variant with a substitutionin the alpha 1 beta 1 interface
    HEMOGLOBIN
    
    I. Papassotiriou et al., "Hb Sitia [beta 128(H6)Ala -> Val]: An unstable variant with a substitutionin the alpha 1 beta 1 interface", HEMOGLOBIN, 25(1), 2001, pp. 45-56
94. Wajcman, H; Lahary, A; Prome, D; Kister, J; Riou, J; Godart, C; Prehu, C; Traeger-Synodinos, J; Papassotiriou, I; Galacteros, F
    Hb Mont Saint Aignan [beta 128(H6)Ala -> Pro]: A new unstable variant leading to chronic microcytic anemia
    HEMOGLOBIN
    
    H. Wajcman et al., "Hb Mont Saint Aignan [beta 128(H6)Ala -> Pro]: A new unstable variant leading to chronic microcytic anemia", HEMOGLOBIN, 25(1), 2001, pp. 57-65
95. Qu, GZ; Elkins, S; Steinberg, MH
    Thalassemia intermedia and extramedullary hematopoiesis associated with compound heterozygosity for the 532 bp deletion of the beta-globin gene and gene deletion hereditary persistence of fetal hemoglobin
    HEMOGLOBIN
    
    G.Z. Qu et al., "Thalassemia intermedia and extramedullary hematopoiesis associated with compound heterozygosity for the 532 bp deletion of the beta-globin gene and gene deletion hereditary persistence of fetal hemoglobin", HEMOGLOBIN, 25(1), 2001, pp. 91-96
96. Kattamis, A; Dinopoulos, A; Ladis, V; Berdousi, H; Kattamis, C
    Variations of ferritin levels over a period of 15 years as a compliance chelation index in thalassemic patients
    AMERICAN JOURNAL OF HEMATOLOGY
    
    A. Kattamis et al., "Variations of ferritin levels over a period of 15 years as a compliance chelation index in thalassemic patients", AM J HEMAT, 68(4), 2001, pp. 221-224
97. Nadkarni, A; Gorakshakar, AC; Lu, CY; Krishnamoorthy, R; Ghosh, K; Colah, R; Mohanty, D
    Molecular pathogenesis and clinical variability of beta-thalassemia syndromes among Indians
    AMERICAN JOURNAL OF HEMATOLOGY
    
    A. Nadkarni et al., "Molecular pathogenesis and clinical variability of beta-thalassemia syndromes among Indians", AM J HEMAT, 68(2), 2001, pp. 75-80
98. Waye, JS; Eng, B; Patterson, M; Walker, L; Carcao, MD; Olivieri, NF; Chui, DHK
    Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases
    AMERICAN JOURNAL OF HEMATOLOGY
    
    J.S. Waye et al., "Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases", AM J HEMAT, 68(1), 2001, pp. 11-15
99. Sadiq, MF; Eigel, A; Horst, J
    Spectrum of beta-thalassemia in Jordan: Identification of two novel mutations
    AMERICAN JOURNAL OF HEMATOLOGY
    
    M.F. Sadiq et al., "Spectrum of beta-thalassemia in Jordan: Identification of two novel mutations", AM J HEMAT, 68(1), 2001, pp. 16-22
100. Divoky, V; Mrug, M; Thornley-Brown, D; Divoka, M; Prchal, JT
     Non-anemic homozygous beta degrees thalassemia in an african-american family: Association of high fetal hemoglobin levels with beta thalassemia alleles
     AMERICAN JOURNAL OF HEMATOLOGY
     
     V. Divoky et al., "Non-anemic homozygous beta degrees thalassemia in an african-american family: Association of high fetal hemoglobin levels with beta thalassemia alleles", AM J HEMAT, 68(1), 2001, pp. 43-50