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La ricerca find articoli where soggetti phrase all words 'BETA-THALASSEMIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 967 riferimenti
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    1. Radu, P; Atsmon, J
      Gilbert's syndrome - Clinical and pharmacological implications

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    2. Lappin, S; Cahlik, J; Gold, B
      Robot printing of reverse dot blot arrays for human mutation detection

      JOURNAL OF MOLECULAR DIAGNOSTICS
    3. 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
    4. Ballas, SK
      Effect of alpha-globin genotype on the pathophysiology of sickle cell disease

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    5. Stuart, MJ; Setty, BNY
      Hemostatic alterations in sickle cell disease: Relationships to disease pathophysiology

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    6. Weatherall, DJ
      Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias

      NATURE REVIEWS GENETICS
    7. 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
    8. 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
    9. 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
    10. 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
    11. 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
    12. Farquharson, MJ; Bagshaw, AP
      Monitoring body iron burden using X-ray fluorescence (XRF)

      RADIATION PHYSICS AND CHEMISTRY
    13. 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
    14. Holzgreve, W; Hahn, S
      Fetal cells in maternal circulation. What is the relationship to obstetricultrasound?

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    15. 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
    16. Makis, AC; Chaliasos, N; Hatzimichael, EC; Bourantas, KL
      Recombinant human erythropoietin therapy in a transfusion-dependent beta-thalassemia major patient

      ANNALS OF HEMATOLOGY
    17. 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
    18. 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
    19. 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
    20. Kurtman, C; Ozbilgin, MK; Andrieu, MN; Celebioglu, B
      Paratracheal extramedullary hematopoiesis

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    21. 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
    22. 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
    23. 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
    24. 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
    25. 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
    26. Kattamis, C; Kattamis, AC
      Oxidative stress disturbances in erythrocytes of beta-thalassemia

      PEDIATRIC HEMATOLOGY AND ONCOLOGY
    27. Cadet, E; Warin, R; Perez, AS; Rochette, J; Capron, D
      The rusty genotypes

      M S-MEDECINE SCIENCES
    28. 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
    29. Tiosano, D; Hochberg, Z
      Endocrine complications of thalassemia

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    30. 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
    31. 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
    32. 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
    33. 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
    34. 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
    35. Ma, ESK; Chan, AYY; Au, WY; Yeung, YM; Chan, LC
      Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia

      HAEMATOLOGICA
    36. 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
    37. Villegas, A; Ropero, P; Gonzalez, FA; Anguita, E; Espinos, D
      The thalassemia syndromes: Molecular characterization in the spanish population

      HEMOGLOBIN
    38. 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
    39. Efremov, GD
      Forty-four years (1955-1999) devoted to hemoglobin research: Titus H. J. Huisman (1923-1999) - In memoriam

      HEMOGLOBIN
    40. Adekile, AD
      Sickle cell disease in Kuwait

      HEMOGLOBIN
    41. 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
    42. 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
    43. 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
    44. 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
    45. Sadiq, MF; Eigel, A; Horst, J
      Spectrum of beta-thalassemia in Jordan: Identification of two novel mutations

      AMERICAN JOURNAL OF HEMATOLOGY
    46. Mazzone, A; Vezzoli, M; Ottini, E
      Masked deficit of B-12 and folic acid in thalassemia

      AMERICAN JOURNAL OF HEMATOLOGY
    47. Sanchaisuriya, K; Fucharoen, G; Sae-ung, N; Siriratmanawong, N; Surapot, S; Fucharoen, S
      Molecular characterization of hemoglobin C in Thailand

      AMERICAN JOURNAL OF HEMATOLOGY
    48. Aliberti, B; Patrikiou, A; Terentiou, A; Frangatou, S; Papadimitriou, A
      Spinal cord compression due to extramedullary haematopoiesis in two patients with thalassaemia: complete regression with blood transfusion therapy

      JOURNAL OF NEUROLOGY
    49. Cavallo, L; Acquafredda, A; Zecchino, C; De Sanctis, V; Cisternino, M; Nicoletti, MC; Galati, M; Massolo, F
      Recombinant growth hormone treatment in short patients with thalassemia major: Results after 24 and 36 months

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    50. Filosa, A; Di Maio, S; Esposito, G; De Martinis, F; De Terlizzi, F
      Persistence of delayed adrenarche in boys with Thalassemia

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    51. Chatterjee, R; Katz, M
      Evaluation of gonadotrophin insufficiency in thalassemic boys with pubertal failure: Spontaneous versus provocative test

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    52. Nobili, B; Perrotta, S; Matarese, SMR; Conte, ML; del Giudice, EM
      Evaluation of body iron status in Italian carriers of beta-thalassemia trait

      NUTRITION RESEARCH
    53. Banerjee, S; Owen, C; Chopra, S
      Sickle cell hepatopathy

      HEPATOLOGY
    54. De Simone, M; Verrotti, A; Iughetti, L; Palumbo, M; Di Bartolomeo, P; Olioso, P; Rosato, T
      Final height of thalassemic patients who underwent bone marrow transplantation during childhood

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

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    56. De Rycke, M; Van de Velde, H; Sermon, K; Lissens, W; De Vos, A; Vandervorst, M; Vanderfaeillie, A; Van Steirteghem, A; Liebaers, I
      Preimplantation genetic diagnosis for sickle-cell anemia and for beta-thalassemia

      PRENATAL DIAGNOSIS
    57. Hoffbrand, AV
      Diagnosing myocardial iron overload

      EUROPEAN HEART JOURNAL
    58. Anderson, LJ; Holden, S; Davis, B; Prescott, E; Charrier, CC; Bunce, NH; Firmin, DN; Wonke, B; Porter, J; Walker, JM; Pennell, DJ
      Cardiovascular T2-star (T2*) magnetic resonance for the early diagnosis ofmyocardial iron overload

      EUROPEAN HEART JOURNAL
    59. Sarkar, PK; Bhattacharya, DK; Sarkar, D
      Splenectomy and splenic slice grafting in the management of thalassemia

      PEDIATRIC SURGERY INTERNATIONAL
    60. Reich, DE; Lander, ES
      On the allelic spectrum of human disease

      TRENDS IN GENETICS
    61. Peters, WHM
      Heterozygosity for a polymorphism in the promoter region of the UGT1A1 gene - Reply

      JOURNAL OF HEPATOLOGY
    62. Ito, N; Sawa, H; Nagane, M; Noguchi, A; Hara, M; Saito, I
      Inhibitory effects of sodium butyrate on proliferation and invasiveness ofhuman glioma cells

      NEUROSURGERY
    63. Waye, JS; Chui, DHK
      The alpha-globin gene cluster: genetics and disorders

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    64. Yuregir, GT; Kilinc, M; Ekerbicer, H; Bilaloglu, N; Tekin, N
      Screening of hemoglobinopathies in Kahramanmaras province (Turkey) situated in a high prevalence area

      JOURNAL OF TROPICAL PEDIATRICS
    65. 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
    66. Mentzer, WC; Kan, YW
      Prospects for research in hematologic disorders - Sickle cell disease and thalassemia

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    67. Beutler, E; Felitti, V; Gelbart, T; Ho, N
      Genetics of iron storage and hemochromatosis

      DRUG METABOLISM AND DISPOSITION
    68. Di Iorio, BR; Aucella, F; Stallone, C; Aversano, AT; Rubino, R; Bellizzi, V
      The use of recombinant human erythropoietin in hemoglobinopathy and uremia

      DIALYSIS & TRANSPLANTATION
    69. Modell, B; Khan, M; Darlison, M; King, A; Layton, M; Old, J; Petrou, M; Varnavides, L
      A national register for surveillance of inherited disorders: beta thalassaemia in the United Kingdom

      BULLETIN OF THE WORLD HEALTH ORGANIZATION
    70. Lecchi, L; Rebulla, P; Ratti, I; Magri, M; Garcea, F; Marangoni, F; Bertele, T; Giordano, R; Sirchia, G
      Outcomes of a program to evaluate mother and baby 6 months after umbilicalcord blood donation

      TRANSFUSION
    71. Zakynthinos, E; Vassilakopoulos, T; Kaltsas, P; Malagari, E; Daniil, Z; Roussos, C; Zakynthinos, SG
      Pulmonary hypertension, interstitial lung fibrosis, and lung iron deposition in thalassaemia major

      THORAX
    72. Perrimond, H
      beta-thalassemia: clinical manifestations.

      BULLETIN DE LA SOCIETE DE PATHOLOGIE EXOTIQUE
    73. Thuret, I
      Treatment of thalassemia major.

      BULLETIN DE LA SOCIETE DE PATHOLOGIE EXOTIQUE
    74. Brittenham, GM; Sheth, S; Allen, CJ; Farrell, DE
      Noninvasive methods for quantitative assessment of transfusional iron overload in sickle cell disease

      SEMINARS IN HEMATOLOGY
    75. Bartfay, WJ; Bartfay, E
      Selenium and glutathione peroxidase with beta-thalassemia major

      NURSING RESEARCH
    76. Steinberg, MH; Rodgers, GP
      Pharmacologic modulation of fetal hemoglobin

      MEDICINE
    77. Filosa, A; Esposito, V; Meoli, I; Stefanelli, F; Cassandro, R
      Evidence of a restrictive spirometric pattern in older thalassemic patients

      RESPIRATION
    78. Ogus, C; Ozdemir, T; Kabaalioglu, A
      Right hilar mass in a patient with beta-thalassemia major

      RESPIRATION
    79. Junca, J
      A diagnostic algorithm for ferropenia

      MEDICINA CLINICA
    80. Kontoghiorghes, GJ
      Clinical use, therapeutic aspects and future potential of deferiprone in thalassemia and other conditions of iron and other metal toxicity

      DRUGS OF TODAY
    81. Bruno, D; Wigfall, DR; Zimmerman, SA; Rosoff, PM; Wiener, JS
      Genitourinary complications of sickle cell disease

      JOURNAL OF UROLOGY
    82. Link, G; Konijn, AM; Breuer, W; Cabantchik, ZI; Hershko, C
      Exploring the "iron shuttle" hypothesis in chelation therapy: Effects of combined deferoxamine and deferiprone treatment in hypertransfused rats withlabeled iron stores and in iron-loaded rat heart cells in culture

      JOURNAL OF LABORATORY AND CLINICAL MEDICINE
    83. Wenk, J; Foitzik, A; Achterberg, V; Sabiwalsky, A; Dissemond, J; Meewes, C; Reitz, A; Brenneisen, P; Wlaschek, M; Meyer-Ingold, W; Scharffetter-Kochanek, K
      Selective pick-up of increased iron by deferoxamine-coupled cellulose abrogates the iron-driven induction of matrix-degrading metalloproteinase 1 andlipid peroxidation in human dermal fibroblasts in vitro: A new dressing concept

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    84. 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
    85. Pandya, K; Donze, D; Townes, TM
      Novel transactivation domain in erythroid Kruppel-like Factor (EKLF)

      JOURNAL OF BIOLOGICAL CHEMISTRY
    86. Lao, TT; Ho, LE
      alpha-thalassaemia trait and gestational diabetes mellitus in Hong Kong

      DIABETOLOGIA
    87. 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
    88. Barone, R; Bertrand, G; Simporo, J; Malaguarnera, M; Musumeci, S
      Plasma chitotriosidase activity in beta-thalassemia major: a comparative study between Sicilian and Sardinian patients

      CLINICA CHIMICA ACTA
    89. Chakraborty, D; Bhattacharyya, M
      Antioxidant defense status of red blood cells of patients with beta-thalassemia and E beta-thalassemia

      CLINICA CHIMICA ACTA
    90. Porter, JB
      Practical management of iron overload

      BRITISH JOURNAL OF HAEMATOLOGY
    91. 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
    92. Giribaldi, G; Ulliers, D; Mannu, F; Arese, P; Turrini, F
      Growth of Plasmodium falciparum induces stage-dependent haemichrome formation, oxidative aggregation of band 3, membrane deposition of complement andantibodies, and phagocytosis of parasitized erythrocytes

      BRITISH JOURNAL OF HAEMATOLOGY
    93. Voskaridou, E; Kyrtsonis, MC; Terpos, E; Skordili, M; Theodoropoulos, I; Bergele, A; Diamanti, E; Kalovidouris, A; Loutradi, A; Loukopoulos, D
      Bone resorption is increased in young adults with thalassaemia major

      BRITISH JOURNAL OF HAEMATOLOGY
    94. Coghill, E; Eccleston, S; Fox, V; Cerruti, L; Brown, C; Cunningham, J; Jane, S; Perkins, A
      Erythroid Kruppel-like factor (EKLF) coordinates erythroid cell proliferation and hemoglobinization in cell lines derived from EKLF null mice

      BLOOD
    95. Dalle, B; Henri, A; Rouyer-Fessard, P; Bettan, M; Scherman, D; Beuzard, Y; Payen, E
      Dimeric erythropoietin fusion protein with enhanced erythropoietic activity in vitro and in vivo

      BLOOD
    96. Aessopos, A; Farmakis, D; Karagiorga, M; Voskaridou, E; Loutradi, A; Hatziliami, A; Joussef, J; Rombos, J; Loukopoulos, D
      Cardiac involvement in thalassemia intermedia: a multicenter study

      BLOOD
    97. Barton, C; Pollitzer, M
      Haemoglobinopathy as a cause of nucleated red cells in the fetus and neonate

      ARCHIVES OF DISEASE IN CHILDHOOD
    98. Hansen, KM; Ji, HF; Wu, GH; Datar, R; Cote, R; Majumdar, A; Thundat, T
      Cantilever-based optical deflection assay for discrimination of DNA single-nucleotide mismatches

      ANALYTICAL CHEMISTRY
    99. Consolini, R; Calleri, A; Legitimo, A; Massei, F
      Immunological evaluation of patients with beta-thalassemia major

      ACTA HAEMATOLOGICA
    100. Corrons, JLVI
      Chronic non-spherocytic haemolytic anaemia due to congenital pyrimidine 5 ' nucleotidase deficiency: 25 years later

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY


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Documento generato il 27/01/21 alle ore 19:09:23