Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'ALPHA-THALASSEMIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 411 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Ballas, SK
      Effect of alpha-globin genotype on the pathophysiology of sickle cell disease

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    2. Nagel, RL; Steinberg, MH
      Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    3. Blackwell, JM
      Genetics and genomics in infectious disease susceptibility

      TRENDS IN MOLECULAR MEDICINE
    4. 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
    5. 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
    6. Castellvi-Bel, S; Mila, M
      Genes responsible for nonspecific mental retardation

      MOLECULAR GENETICS AND METABOLISM
    7. 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
    8. 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
    9. Feroze, M; Aravindan, KP
      Sickle cell disease in Wayanad, Kerala: Gene frequencies and disease characteristics

      NATIONAL MEDICAL JOURNAL OF INDIA
    10. 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
    11. Chen, CP
      Severe terminal transverse limb reduction defects in homozygous Southeast-Asian alpha-thalassaemia-1

      CLINICAL DYSMORPHOLOGY
    12. 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
    13. 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
    14. Cadet, E; Warin, R; Perez, AS; Rochette, J; Capron, D
      The rusty genotypes

      M S-MEDECINE SCIENCES
    15. 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
    16. Zhao, YZ; Xu, XM
      alpha 2(CD31) (AGG -> AAG,) (Arg -> Lys) causing non-deletional alpha-thalassemia in a Chinese family with HbH disease

      HAEMATOLOGICA
    17. Ma, ESK; Chan, AYY; Ha, SY; Lau, YL; Chan, LC
      Thalassemia screening based on red cell indices in the Chinese

      HAEMATOLOGICA
    18. 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
    19. Villegas, A; Ropero, P; Gonzalez, FA; Anguita, E; Espinos, D
      The thalassemia syndromes: Molecular characterization in the spanish population

      HEMOGLOBIN
    20. Adekile, AD
      Sickle cell disease in Kuwait

      HEMOGLOBIN
    21. 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
    22. 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
    23. 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
    24. Sarnaik, SA; Ballas, SK
      Molecular characteristics of pediatric patients with sickle cell anemia and stroke

      AMERICAN JOURNAL OF HEMATOLOGY
    25. Adekile, AD; Kutlar, F; Haider, MZ; Kutlar, A
      Frequency of the 677 C -> T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients

      AMERICAN JOURNAL OF HEMATOLOGY
    26. Padmanabhan, A; Thomas, S; Sheth, H; Venugopalan, P
      High prevalence of microcytic anaemia in Omani children: a prospective study

      ANNALS OF TROPICAL PAEDIATRICS
    27. Yu, J; Russell, JE
      Structural and functional analysis of an mRNP complex that mediates the high stability of human beta-globin mRNA

      MOLECULAR AND CELLULAR BIOLOGY
    28. Tuzmen, S; Schechter, AN
      Genetic diseases of hemoglobin: diagnostic methods for elucidating beta-thalassemia mutations

      BLOOD REVIEWS
    29. Zhou, X; Ha, SY; Chan, GCF; Luk, CW; Chan, V; Hawkins, B; Lam, YH; Liang, RHS; Lau, YL
      Successful mismatched sibling cord blood transplant in Hb Bart's disease

      BONE MARROW TRANSPLANTATION
    30. Smetanina, NS; Kazanetz, EG; Tokarev, YN
      Correlation between genotype and clinical features of beta-thalassemia.

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    31. Kleanthous, M; Kyriacou, K; Kyrri, A; Kalogerou, E; Vassiliades, PH; Drousiotou, A; Kallikas, I; Ioannou, P; Angastiniotis, M
      Alpha-thalassaemia prenatal diagnosis by two PCR-based methods

      PRENATAL DIAGNOSIS
    32. Badenas, C; Castellvi-Bel, S; Volpini, V; Jimenez, D; Sanchez, A; Estivill, X; Mila, M
      Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21

      AMERICAN JOURNAL OF MEDICAL GENETICS
    33. Waye, JS; Chui, DHK
      The alpha-globin gene cluster: genetics and disorders

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    34. Leung, KFS; Au, WY; Chan, AYY; Chan, LC; Waye, JS; Chui, DHK; Ma, SK
      Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family

      CLINICAL AND LABORATORY HAEMATOLOGY
    35. Borges, E; Wenning, MRSC; Kimura, EM; Gervasio, SA; Costa, FF; Sonati, MF
      High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia

      BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH
    36. Fibach, E
      Cell culture and animal models to screen for promising fetal hemoglobin-stimulating compounds

      SEMINARS IN HEMATOLOGY
    37. Tongsong, T; Wanapirak, C; Sirivatanapa, P; Sa-nguansermsri, T; Sirichotiyakul, S; Piyamongkol, W; Chanprapaph, P; Steger, HF; Sekararithi, R; Tuggapichitti, A
      Prenatal eradication of Hb Bart's hydrops fetalis

      JOURNAL OF REPRODUCTIVE MEDICINE
    38. Chan, LC; Ma, SK; Chan, AYY; Ha, SY; Waye, JS; Lau, YL; Chui, DHK
      Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?

      JOURNAL OF CLINICAL PATHOLOGY
    39. Sun, CF; Lee, CH; Cheng, SW; Lin, MH; Wu, TL; Tsao, KC; Chiu, DTY; Liou, JD; Chu, DC
      Real-time quantitative PCR analysis for alpha-thalassemia-1 of Southeast Asian type deletion in Taiwan

      CLINICAL GENETICS
    40. Siriratmanawong, N; Fucharoen, G; Sanchaisuriya, K; Ratanasiri, T; Fucharoen, S
      Simultaneous PCR detection of beta-thalassemia and alpha-thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome

      CLINICAL BIOCHEMISTRY
    41. Chan, V; Yip, B; Lam, YH; Tse, HY; Wong, HS; Chan, TK
      Quantitative polmerase chain reaction for the rapid prenatal diagnosis of homozygous alpha-thalassaemia (Hb Barts hydrops fetalis)

      BRITISH JOURNAL OF HAEMATOLOGY
    42. Lorey, F; Charoenkwan, P; Witkowska, HE; Lafferty, J; Patterson, M; Eng, B; Waye, JS; Finklestein, JZ; Chui, DHK
      Hb H hydrops foetalis syndrome: a case report and review of literature

      BRITISH JOURNAL OF HAEMATOLOGY
    43. Chang, YPC; Littera, R; Garau, R; Smith, KD; Dover, GJ; Iannelli, S; Cacace, E; Contu, L
      The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermedia

      BRITISH JOURNAL OF HAEMATOLOGY
    44. Adekile, AD; Gupta, R; Yacoub, F; Sinan, T; Al-Bloushi, M; Haider, MZ
      Avascular necrosis of the hip in children with sickle cell disease and high Hb F: Magnetic resonance imaging findings and influence of alpha-thalassemia trait

      ACTA HAEMATOLOGICA
    45. Cao, A; Moi, P
      Genetic modifying factors in beta-thalassemia

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    46. Reddy, PL; Bowie, LJ; Jiang, HS
      Blood pressure changes after intravenous administration of cell-free hemoglobin A and hemoglobin H in the rat

      NITRIC OXIDE-BIOLOGY AND CHEMISTRY
    47. Traeger-Synodinos, J; Papassotiriou, I; Metaxotou-Mavrommati, A; Vrettou, C; Stamoulakatou, A; Kanavakis, E
      Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb Heraklion, alpha 1cd37(C2)Pro > 0): Comparison to other alpha-thalassemic hemoglobinopathies

      BLOOD CELLS MOLECULES AND DISEASES
    48. Singer, ST; Styles, L; Bojanowski, J; Quirolo, K; Foote, D; Vichinsky, EP
      Changing outcome of homozygous alpha-thalassemia: Cautious optimism

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    49. Lorey, F
      Asian immigration and public health in California: Thalassemia in newbornsin California

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    50. Rees, DC
      Hemoglobin F and hemoglobin E/beta-thalassemia

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    51. Ballif, BC; Kashork, CD; Shaffer, LG
      FISHing for mechanisms of cytogenetically defined terminal deletions usingchromosome-specific subtelomeric probes

      EUROPEAN JOURNAL OF HUMAN GENETICS
    52. Berube, NG; Smeenk, CA; Picketts, DJ
      Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

      HUMAN MOLECULAR GENETICS
    53. Kayser, M; Brauer, S; Weiss, G; Underhill, PA; Roewer, L; Schiefenhovel, W; Stoneking, M
      Melanesian origin of Polynesian Y chromosomes

      CURRENT BIOLOGY
    54. Lam, YH; Tang, MHY
      Limb reduction defects as the sonographic manifestation of hemoglobin Bart's disease at 10 weeks of gestation

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    55. Mirabile, E; Samperi, P; Di Cataldo, A; Poli, A; La Spina, M; Schiliro, G
      Phenotype-genotype correlation in Sicilian patients with Hb H

      EUROPEAN JOURNAL OF HAEMATOLOGY
    56. Neonato, MG; Guilloud-Bataille, M; Beauvais, P; Begue, P; Belloy, M; Benkerrou, M; Ducrocq, R; Maier-Redelsperger, M; de Montalembert, M; Quinet, B; Elion, J; Feingold, J; Girot, R
      Acute clinical events in 299 homozygous sickle cell patients living in France

      EUROPEAN JOURNAL OF HAEMATOLOGY
    57. Pfeifer, D; Poulat, F; Holinski-Feder, E; Kooy, F; Scherer, G
      The SOX8 gene is located within 700 kb of the tip of chromosome 16p and isdeleted in a patient with ATR-16 syndrome

      GENOMICS
    58. Ballas, SK
      Acute chest syndrome in sickle cell anemia

      JOURNAL OF INTENSIVE CARE MEDICINE
    59. Lacombe, D
      Developmental gene diseases

      M S-MEDECINE SCIENCES
    60. Villegas, A; Anguita, E; Noguera, N; Gonzalez, FA; Ropero, P; Sanchez, J; Milani, AC; Espinos, D; Bowden, D; Higgs, D
      A new polymorphism (G -> A) in the psi zeta 1 globin gene

      HAEMATOLOGICA
    61. Noguera, NI; Gonzalez, FA; Ropero, P; Anguita, E; Milani, AC; Villegas, A
      Homozygous Constant Spring: the first case described in the West

      HAEMATOLOGICA
    62. Villegas, A; Ropero, P; Gonzalez, FA; Anguita, E; Sanchez, J; Quevedo, E; San Juan, I
      Is the alpha--(cal) mutation prevalent in central Spain?

      HAEMATOLOGICA
    63. Quadri, MI; Islam, SA
      Hemoglobin H disease in the eastern region of Saudi Arabia

      SAUDI MEDICAL JOURNAL
    64. Ballas, SK; Marcolina, MJ
      Determinants of red cell survival and erythropoietic activity in patients with sickle cell anemia in the steady state

      HEMOGLOBIN
    65. Waye, JS; Walker, L; Chui, DHK; Lafferty, J; Kirby, M
      Homozygous Hb Sallanches [alpha 104(G11)Cys -> Tyr] in a Pakistani child with Hb H disease

      HEMOGLOBIN
    66. Vrettou, C; Kanavakis, E; Traeger-Synodinos, J; Metaxotou-Mavrommati, A; Basiakos, I; Maragoudaki, E; Stamoulakatou, A; Papassotiriou, I; Kattamis, C
      Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels

      HEMOGLOBIN
    67. Cuellar-Ambrosi, F; Mondragon, MC; Figueroa, M; Prehu, C; Galacteros, F; Ruiz-Linares, A
      Sickle cell anemia and beta-globin gene cluster haplotypes in Colombia

      HEMOGLOBIN
    68. Khan, SN; Riazuddin, S; Galanello, R
      Identification of three rare beta-thalassemia mutations in the Pakistani population

      HEMOGLOBIN
    69. Khan, SN; Butt, FI; Riazuddin, S; Galanello, R
      Hb Sallanches [alpha 104(G11)Cys -> Tyr]: a rare alpha 2-globin chain variant found in the homozygous state in three members of a Pakistani family

      HEMOGLOBIN
    70. Oron-Karni, V; Filon, D; Shifrin, Y; Fried, E; Pogrebijsky, G; Oppenheim, A; Rund, D
      Diversity of alpha-globin mutations and clinical presentation of alpha-thalassemia in Israel

      AMERICAN JOURNAL OF HEMATOLOGY
    71. Arends, A; Alvarez, M; Velazquez, D; Bravo, M; Salazar, R; Guevara, JM; Castillo, O
      Determination of beta-globin gene cluster haplotypes and prevalence of alpha-thalassemia in sickle cell anemia patients in Venezuela

      AMERICAN JOURNAL OF HEMATOLOGY
    72. Daar, S; Hussain, HM; Gravell, D; Nagel, RL; Krishnamoorthy, R
      Genetic epidemiology of HbS in omen: Multicentric origin for the beta(S) gene

      AMERICAN JOURNAL OF HEMATOLOGY
    73. Al-Jam'a, AH; Al-Dabbous, IA; Chirala, SK; Al-Majid, H; Al-Ali, J
      Splenic function in sickle cell anemia patients in Qatif, Saudi Arabia

      AMERICAN JOURNAL OF HEMATOLOGY
    74. Eng, B; Patterson, M; Borys, S; Chui, DHK; Waye, JS
      PCR-based diagnosis of the Filipino (__(FIL)) and Thai (__(THAI)) alpha-thalassemia-1 deletions

      AMERICAN JOURNAL OF HEMATOLOGY
    75. Fujiwara, H; Nakazato, Y; Okazaki, S; Ninaki, O
      Stability and telomere structure of chromosomal fragments in two differentmosaic strains of the silkworm, Bombyx mori.

      ZOOLOGICAL SCIENCE
    76. van de Moesdijk, D; van Weel-Sipman, MH
      An infant with severe combined immunodeficiency syndrome, an alpha-thalassemia trait and renal Fanconi syndrome

      BONE MARROW TRANSPLANTATION
    77. Quadri, MI; Islam, SIAM; Nasserullah, Z
      The effect of alpha-thalassemia on cord blood red cell indices and interaction with sickle cell gene

      ANNALS OF SAUDI MEDICINE
    78. Lam, YH; Tang, MHY
      Prenatal diagnosis of haemoglobin Bart's disease by cordocentesis at 12-14weeks-experience with the first 59 cases

      PRENATAL DIAGNOSIS
    79. Stevenson, RE
      Splitting and lumping in the nosology of XLMR

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. Gibbons, RJ; Higgs, DR
      Molecular-clinical spectrum of the ATR-X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. Chu, DC; Lee, CH; Lo, MD; Cheng, SW; Chen, DP; Wu, TL; Tsao, KC; Chiu, DTY; Sun, CF
      Non-radioactive Southern hybridization for early diagnosis of alpha-thalassemia with Southeast Asian-type deletion in Taiwan

      AMERICAN JOURNAL OF MEDICAL GENETICS
    82. Goldwurm, S; Biondi, A
      Case of congenital hypotransferrinemia suggests that tissue hypoxia duringfetal development may cause hypospadias

      AMERICAN JOURNAL OF MEDICAL GENETICS
    83. Goldwurm, S; Biondi, A
      Case of congenital hypotransferrinemia suggests that tissue hypoxia duringfetal development may cause hypospadias - Response

      AMERICAN JOURNAL OF MEDICAL GENETICS
    84. Stevenson, RE; Abidi, F; Schwartz, CE; Lubs, HA; Holmes, LB
      Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    85. Wada, T; Kubota, T; Fukushima, Y; Saitoh, S
      Molecular genetic study of Japanese patients with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    86. Wyandt, HE; Lebo, RV; Fenerci, EY; Sadhu, DN; Milunsky, JM
      Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    87. Villard, L; Fontes, M; Ades, LC; Gecz, J
      Identification of a mutation in the XNP/ATR-X gene in a family reported asSmith-Fineman-Myers syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    88. Elchalal, U; Ezra, Y; Levi, Y; Bar-Oz, B; Yanai, N; Intrator, O; Nadjari, M
      Sonographically thick placenta: a marker for increased perinatal risk - a prospective cross-sectional study

      PLACENTA
    89. Wenning, MRSC; Kimura, EM; Costa, FF; Saad, STO; Gervasio, S; de Jorge, SB; Borges, E; Silva, NM; Sonati, MF
      alpha-globin genes: thalassemic and structural alterations in a Brazilian population

      BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH
    90. Krauss, JS
      The proportion of hybrid heterodimers in homozygous or doubly heterozygousbeta chain variant hemoglobinopathies associated with alpha chain hemoglobin variants

      ANNALS OF CLINICAL AND LABORATORY SCIENCE
    91. Mockenhaupt, FP; Rong, B; Gunther, M; Beck, S; Till, H; Kohne, E; Thompson, WNA; Bienzle, U
      Anaemia in pregnant Ghanaian women: importance of malaria, iron deficiency, and haemoglobinopathies

      TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE
    92. Chen, FE; Ooi, C; Ha, SY; Cheung, BMY; Todd, D; Liang, R; Chan, TK; Chan, V
      Genetic and clinical features of hemoglobin H disease in Chinese patients

      NEW ENGLAND JOURNAL OF MEDICINE
    93. Knight, SJL; Flint, J
      Perfect endings: a review of subtelomeric probes and their use in clinicaldiagnosis

      JOURNAL OF MEDICAL GENETICS
    94. Cardoso, C; Lutz, Y; Mignon, C; Compe, E; Depetris, D; Mattei, MG; Fontes, M; Colleaux, L
      ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein

      JOURNAL OF MEDICAL GENETICS
    95. Hutagalung, R; Wilairatana, P; Looareesuwan, S; Brittenham, GM; Gordeuk, VR
      Influence of hemoglobin E trait on the antimalarial effect of artemisinin derivatives

      JOURNAL OF INFECTIOUS DISEASES
    96. Mouele, R; Bodo, JM; Mpele, DMB; Feingold, J; Galacteros, F
      beta-globin gene haplotypes and alpha-thalassemia analysis in Babinga pygmies from Congo-Brazzaville

      HUMAN BIOLOGY
    97. Balgir, RS
      The burden of haemoglobinopathies in India and the challenges ahead

      CURRENT SCIENCE
    98. Kanavakis, E; Papassotiriou, I; Karagiorga, M; Vrettou, C; Metaxotou-Mavrommati, A; Stamoulakatou, A; Kattamis, C; Traeger-Synodinos, J
      Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience

      BRITISH JOURNAL OF HAEMATOLOGY
    99. Pootrakul, P; Sirankapracha, P; Hemsorach, S; Moungsub, W; Kumbunlue, R; Piangitjagum, A; Wasi, P; Ma, L; Schrier, SL
      A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia

      BLOOD
    100. Chong, SS; Boehm, CD; Higgs, DR; Cutting, GR
      Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia

      BLOOD


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/06/20 alle ore 11:15:39