Diamond-Blackfan syndrome in adult patients, The American Journal of Medicine, vol.78, issue.3, pp.533-538, 1985. ,
DOI : 10.1016/0002-9343(85)90352-3
Improving clinical care and elucidating the pathophysiology of Diamond Blackfan anemia: An update from the Diamond Blackfan Anemia Registry, Pediatric Blood & Cancer, vol.94, issue.5, pp.558-564, 2006. ,
DOI : 10.1002/pbc.20642
A study of clinico-haematological profiles of pancytopenia in children, Tropical Doctor, vol.125, issue.4, pp.241-243, 2008. ,
DOI : 10.1258/td.2008.070422
Etiological spectrum of pancytopenia based on bone marrow examination in children, J. Coll. Physicians Surg. Pak, 2008. ,
Clinical and laboratory evidence for a trilineage haematopoietic defect in patients with refractory Diamond-Blackfan anaemia, British Journal of Haematology, vol.51, issue.1, pp.167-175, 2000. ,
DOI : 10.1016/S0301-472X(98)00068-X
Chapter 8 Diamond Blackfan Anemia: A Disorder of Red Blood Cell Development, Curr. Top. Dev. Biol, vol.82, pp.217-241, 2008. ,
DOI : 10.1016/S0070-2153(07)00008-7
Diamond-Blackfan anemia: erythropoiesis lost in translation, Blood, vol.109, issue.8, pp.3152-3154, 2007. ,
DOI : 10.1182/blood-2006-09-001222
Transient erythroblastopenia of childhood, European Journal of Pediatrics, vol.7, issue.4, pp.266-270, 1984. ,
DOI : 10.1007/BF00540249
Transient erythroblastopenia of childhood. Prospective study of fifty patients, Am. J. Pediatr. Hematol. Oncol, 1994. ,
Transient Erythroblastopenia of Childhood Associated With Human Herpesvirus Type 6, Variant B, American Journal of Clinical Pathology, vol.108, issue.2, pp.127-132, 1997. ,
DOI : 10.1093/ajcp/108.2.127
Classic Transient Erythroblastopenia of Childhood With Human Parvovirus B19 Genome Detection in the Blood and Bone Marrow, Journal of Pediatric Hematology/Oncology, vol.27, issue.6, pp.333-336, 2005. ,
DOI : 10.1097/01.mph.0000169249.72858.8c
Pure red cell aplasia caused by Parvovirus B19 infection in solid organ transplant recipients: a case report and review of literature, Clinical Transplantation, vol.14, issue.6, pp.586-591, 2000. ,
DOI : 10.1034/j.1399-0012.2000.140612.x
Transient Erythroblastopenia of Childhood: Prospective Study of 10 Patients With Special Reference to Viral Infections, Journal of Pediatric Hematology/Oncology, vol.24, issue.4, pp.294-298, 2002. ,
DOI : 10.1097/00043426-200205000-00015
Transient Erythroblastopenia of Childhood in Siblings: Case Report and Review of the Literature, Journal of Pediatric Hematology/Oncology, vol.29, issue.9, pp.659-660, 2007. ,
DOI : 10.1097/MPH.0b013e31814684e9
Gaucher-like cells and congenital dyserythropoietic anaemia, type II (HEMPAS), Br. J. Haematol, 1973. ,
HISTOPATHOLOGIC STUDIES IN BETA-THALASSEMIA MINOR AND INTERMEDIA, Annals of the New York Academy of Sciences, vol.217, issue.1 Second Confer, pp.126-147, 1969. ,
DOI : 10.1016/0002-9343(53)90024-2
Pseudo-Gaucher cells in Hb E disease and thalassemia intermedia, Hematology, vol.128, issue.5, pp.457-459, 2007. ,
DOI : 10.1111/j.1600-0714.1993.tb01084.x
Gaucher's cells in thalassemia, Blood, vol.38, issue.4, pp.457-462, 1971. ,
The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis, Science, vol.259, issue.5099, pp.1318-1320, 1993. ,
DOI : 10.1126/science.7680492
Paroxysmal nocturnal haemoglobinuria: long-term follow-up and prognostic factors, The Lancet, vol.348, issue.9027, pp.573-577, 1996. ,
DOI : 10.1016/S0140-6736(95)12360-1
A cohort study of the nature of paroxysmal nocturnal hemoglobinuria clones and PIG-A mutations in patients with aplastic anemia, European Journal of Haematology, vol.86, issue.6, pp.502-509, 2006. ,
DOI : 10.1111/j.1365-2141.1999.01320.x
Thrombocytopenia in Children With Severe Iron Deficiency, Journal of Pediatric Hematology/Oncology, vol.24, issue.5, pp.380-384, 2002. ,
DOI : 10.1097/00043426-200206000-00011
Platelet counts in adults with iron deficiency anemia, Platelets, vol.132, issue.6, pp.401-405, 2009. ,
DOI : 10.1016/S0887-8994(96)00290-1
Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA), Nature Genetics, vol.14, issue.5, pp.569-571, 2008. ,
DOI : 10.1373/clinchem.2006.079186
Two nonsense mutations in the TMPRSS6 gene in a patient with microcytic anemia and iron deficiency, Blood, vol.112, issue.5, pp.2089-2091, 2008. ,
DOI : 10.1182/blood-2008-05-154740
A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron, Haematologica, vol.93, issue.10, pp.1473-1479, 2008. ,
DOI : 10.3324/haematol.13342
Iron Deficiency and Dyserythropoiesis, British Journal of Haematology, vol.6, issue.4, pp.507-512, 1972. ,
DOI : 10.1038/204582a0
Anemia of Chronic Disease, New England Journal of Medicine, vol.352, issue.10, pp.1011-1023, 2005. ,
DOI : 10.1056/NEJMra041809
Anaemia in systemic lupus erythematosus: aetiological profile and the role of erythropoietin, Annals of the Rheumatic Diseases, vol.59, issue.3, pp.217-222, 2000. ,
DOI : 10.1136/ard.59.3.217
Pure red cell aplasia in a Sj??gren's syndrome/lupus erythematosus overlap patient, American Journal of Hematology, vol.87, issue.4, pp.259-262, 2003. ,
DOI : 10.1002/ajh.10302
Combined pure red cell aplasia and autoimmune hemolytic anemia in systemic lupus erythematosus with anti-erythropoietin autoantibodies, American Journal of Hematology, vol.68, issue.9, pp.750-752, 2008. ,
DOI : 10.1002/ajh.21241
Remission of aplastic anemia induced by treatment for Graves disease in a pediatric patient, Pediatric Blood & Cancer, vol.118, issue.2, pp.210-212, 2007. ,
DOI : 10.1002/pbc.20640
Clinical features of haemophagocytic syndrome in patients with systemic autoimmune diseases: analysis of 30 cases, Rheumatology, vol.47, issue.11, pp.1686-1691, 2008. ,
DOI : 10.1093/rheumatology/ken342
Pathology of Autoimmune Myelofibrosis, American Journal of Clinical Pathology, vol.116, issue.2, pp.211-216, 2001. ,
DOI : 10.1309/6Q99-VRNL-7BTP-W1G8
An update on iron physiology, World Journal of Gastroenterology, vol.15, issue.37, pp.4617-4626, 2009. ,
DOI : 10.3748/wjg.15.4617
Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein, Blood, vol.101, issue.7, pp.2461-2463, 2003. ,
DOI : 10.1182/blood-2002-10-3235
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin, Journal of Clinical Investigation, vol.113, issue.9, pp.1271-1276, 2004. ,
DOI : 10.1172/JCI200420945
Bone marrow histological findings in systemic lupus erythematosus with hematologic abnormalities: A clinicopathological study, American Journal of Hematology, vol.97, issue.8, pp.590-597, 2006. ,
DOI : 10.1002/ajh.20593
Myelodysplastic features in juvenile rheumatoid arthritis, American Journal of Hematology, vol.88, issue.2, pp.166-169, 1997. ,
DOI : 10.1002/(SICI)1096-8652(199702)54:2<166::AID-AJH13>3.0.CO;2-D
Anaemia in juvenile chronic arthritis, Clinical Rheumatology, vol.66, issue.4, pp.236-241, 1996. ,
DOI : 10.1007/BF02229700
Reversible Bone Marrow Dysplasia in Patients with Systemic Lupus Erythematosus, Internal Medicine, vol.47, issue.8, pp.737-742, 2008. ,
DOI : 10.2169/internalmedicine.47.0607
A Case of Reactive Plasmacytosis Mimicking Multiple Myeloma in A Patient with Primary Sj??gren's Syndrome, Journal of Korean Medical Science, vol.20, issue.3, pp.506-508, 2005. ,
DOI : 10.3346/jkms.2005.20.3.506
Severe anemia and marrow plasmacytosis as presentation of Sj??gren's syndrome, American Journal of Hematology, vol.81, issue.3, p.233, 2002. ,
DOI : 10.1002/ajh.10038
Diagnosis of megaloblastic anaemias, Blood Reviews, vol.20, issue.6, pp.299-318, 2006. ,
DOI : 10.1016/j.blre.2006.02.002
Neutropenia: Causes and consequences, Seminars in Hematology, vol.39, issue.2, 2002. ,
DOI : 10.1053/shem.2002.31911
The Severe Chronic Neutropenia International Registry: 10-Year Follow-up Report. Support. Cancer Ther, Jul, vol.13, issue.4, pp.220-231, 2006. ,
Shwachman's syndrome. A review of 21 cases., Archives of Disease in Childhood, vol.55, issue.5, pp.331-347, 1980. ,
DOI : 10.1136/adc.55.5.331
Clonal evolution in marrows of patients with Shwachman-Diamond syndrome, Experimental Hematology, vol.30, issue.7, pp.659-669, 2002. ,
DOI : 10.1016/S0301-472X(02)00815-9
Shwachman syndrome: Phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar, The Journal of Pediatrics, vol.135, issue.1, 1999. ,
DOI : 10.1016/S0022-3476(99)70332-X
Shwachman syndrome: Exocrine pancreatic dysfunction and variable phenotypic expression, Gastroenterology, vol.111, issue.6, pp.1593-1602, 1996. ,
DOI : 10.1016/S0016-5085(96)70022-7
Haematological abnormalities in Shwachman-Diamond syndrome, British Journal of Haematology, vol.94, issue.2, 1996. ,
DOI : 10.1046/j.1365-2141.1996.d01-1788.x
Mutations in SBDS are associated with Shwachman???Diamond syndrome, Nature Genetics, vol.16, issue.1, pp.97-101, 2003. ,
DOI : 10.1093/NAR/25.24.4876
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies, British Journal of Haematology, vol.19, issue.2, pp.190-197, 2009. ,
DOI : 10.1111/j.1365-2141.2009.07611.x
Shwachman???Diamond syndrome is associated with low-turnover osteoporosis, Bone, vol.41, issue.6, pp.965-972, 2007. ,
DOI : 10.1016/j.bone.2007.08.035
Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria, Acta Paediatr. Feb, vol.45, pp.1-78, 1956. ,
Neutrophil elastase in cyclic and severe congenital neutropenia, Blood, vol.109, issue.5, pp.1817-1824, 2007. ,
DOI : 10.1182/blood-2006-08-019166
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia, Blood, vol.96, issue.7, pp.2317-2322, 2000. ,
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease), Nature Genetics, vol.191, issue.1, 2007. ,
DOI : 10.1038/ng1940
Severe congenital neutropenia: inheritance and pathophysiology, Current Opinion in Hematology, vol.14, issue.1, pp.22-28, 2007. ,
DOI : 10.1097/00062752-200701000-00006
A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases, Leukemia, vol.17, issue.2, 2003. ,
DOI : 10.1038/sj.leu.2402765
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy, Blood, vol.107, issue.12, pp.4628-4635, 2006. ,
DOI : 10.1182/blood-2005-11-4370
Cyclical neutropenia and other periodic hematological disorders: a review of mechanisms and mathematical models, Blood, vol.92, issue.8, pp.2629-2640, 1998. ,
Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis, Nature Genetics, vol.23, issue.4, pp.433-436, 1999. ,
DOI : 10.1038/70544
Severe chronic neutropenia: Treatment and follow-up of patients in the Severe Chronic Neutropenia International Registry, American Journal of Hematology, vol.4, issue.2, pp.82-93, 2003. ,
DOI : 10.1002/ajh.10255
Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group, Haematologica, vol.90, issue.1, pp.45-53, 2005. ,
Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy, Blood Jul, vol.1596, issue.2, pp.429-436, 2000. ,
Reversible adult-onset cyclic haematopoiesis with a cycle length of 100 days, British Journal of Haematology, vol.81, issue.2, pp.181-186, 1993. ,
DOI : 10.1097/00005792-198101000-00001
Cyclic hematopoiesis: disorders of primitive hematopoietic stem cells, Exp. Hematol, vol.11, issue.8, pp.687-700, 1983. ,
Auto-immune neutropenia associated with metformin in a patient with splenic marginal zone lymphoma, Pharmacy World & Science, vol.40, issue.4, 2008. ,
DOI : 10.1007/s11096-008-9218-3
Severe autoimmune neutropenia associated with bone marrow sea-blue histiocytosis, British Journal of Haematology, vol.118, issue.4, 2002. ,
DOI : 10.1046/j.1365-2141.2002.03658.x
Intramedullary Neutrophil Phagocytosis by Histiocytes in Autoimmune Neutropenia of Infancy, Acta Haematologica, vol.84, issue.4, pp.201-203, 1990. ,
DOI : 10.1159/000205065
Neutropenia in a Patient Treated With Ipilimumab (anti???CTLA-4 Antibody), Journal of Immunotherapy, vol.32, issue.3, pp.322-324, 2009. ,
DOI : 10.1097/CJI.0b013e31819aa40b
Impaired granulocytopoiesis in patients with chronic idiopathic neutropenia is associated with increased apoptosis of bone marrow myeloid progenitor cells, Blood, vol.101, issue.7, pp.2591-2600, 2003. ,
DOI : 10.1182/blood-2002-09-2898
Morphologically defined myeloid cell compartments, lymphocyte subpopulations, and histological findings of bone marrow in patients with nonimmune chronic idiopathic neutropenia of adults, Annals of Hematology, vol.79, issue.10, pp.563-570, 2000. ,
DOI : 10.1007/s002770000207
c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia, Blood, vol.97, issue.1, pp.139-146, 2001. ,
DOI : 10.1182/blood.V97.1.139
Thrombopoietin Is Essential for the Maintenance of Normal Hematopoiesis in Humans, Annals of the New York Academy of Sciences, vol.97, issue.Suppl 2, pp.17-25, 2003. ,
DOI : 10.1111/j.1749-6632.2003.tb03228.x
Advances in the understanding of congenital amegakaryocytic thrombocytopenia, British Journal of Haematology, vol.37, issue.1, pp.3-16, 2009. ,
DOI : 10.1111/j.1365-2141.2009.07706.x
Congenital amegakaryocytic thrombocytopenia: The diagnostic importance of combining pathology with molecular genetics, Pediatric Blood & Cancer, vol.11, issue.6, pp.1263-1265, 2008. ,
DOI : 10.1002/pbc.21453
THROMBOCYTOPENIA WITH ABSENT RADIUS (TAR), Medicine, vol.48, issue.6, 1969. ,
DOI : 10.1097/00005792-196948060-00001
Thrombocytopenia with absent radii (TAR) syndrome: from hemopoietic progenitor to mesenchymal stromal cell disease?, Experimental Hematology, vol.37, issue.1, pp.1-7, 2009. ,
DOI : 10.1016/j.exphem.2008.09.004
Thrombocytopenia with Absent Radii, Journal of Pediatric Hematology/Oncology, vol.10, issue.1, pp.51-64, 1988. ,
DOI : 10.1097/00043426-198821000-00010
Immune Thrombocytopenic Purpura, New England Journal of Medicine, vol.346, issue.13, pp.995-1008, 2002. ,
DOI : 10.1056/NEJMra010501
The Role of the Bone Marrow Examination in the Diagnosis of Immune Thrombocytopenic Purpura: Case Series and Literature Review, Clinical and Applied Thrombosis/Hemostasis, vol.104, issue.5, pp.73-76, 2002. ,
DOI : 10.1177/107602960200800110
Megakaryocytic alterations in thrombocytopenia: a bone marrow aspiration study, Indian J. Pathol. Microbiol, vol.52, issue.4, pp.490-494, 2009. ,
Evaluation of bone marrow reticulin formation in chronic immune thrombocytopenia patients treated with romiplostim, Blood, vol.114, issue.18, pp.3748-3756, 2009. ,
DOI : 10.1182/blood-2009-05-224766
Acquired amegakaryocytic thrombocytopenic purpura: a syndrome of diverse etiologies, Blood, vol.60, issue.5, pp.1173-1178, 1982. ,
Relationship between megakaryocyte mass and serum thrombopoietin levels as revealed by a case of cyclic amegakaryocytic thrombocytopenic purpura, British Journal of Haematology, vol.89, issue.2, pp.452-458, 1999. ,
DOI : 10.1038/369571a0
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes, Blood, vol.103, issue.7, pp.2498-2503, 2004. ,
DOI : 10.1182/blood-2003-08-2915
Identification of the Fanconi anemia complementation group I gene, FANCI, Cell Oncol, vol.29, issue.3, pp.211-218, 2007. ,
Inherited aplastic anaemias/bone marrow failure syndromes, Blood Reviews, vol.22, issue.3, pp.141-153, 2008. ,
DOI : 10.1016/j.blre.2007.11.003
Diagnosis of Fanconi anemia in patients without congenital malformations: An international Fanconi anemia registry study, American Journal of Medical Genetics, vol.84, issue.1, pp.58-61, 1997. ,
DOI : 10.1002/(SICI)1096-8628(19970110)68:1<58::AID-AJMG11>3.0.CO;2-N
A 20-year perspective on the International Fanconi Anemia Registry (IFAR), Blood, vol.101, issue.4, pp.1249-1256, 2003. ,
DOI : 10.1182/blood-2002-07-2170
Diagnosis of Myelodysplastic Syndrome Among a Cohort of 119 Patients With Fanconi Anemia, American Journal of Clinical Pathology, vol.133, issue.1, pp.92-100, 2010. ,
DOI : 10.1309/AJCP7W9VMJENZOVG
Diagnosis, Genetics, and Management of Inherited Bone Marrow Failure Syndromes, Hematology, vol.2007, issue.1, pp.29-39, 2007. ,
DOI : 10.1182/asheducation-2007.1.29
Fanconi's anemia. A family study with 20-year follow-up including associated breast pathology, Cancer, vol.40, issue.6, pp.1850-1853, 1984. ,
DOI : 10.1002/1097-0142(19841101)54:9<1850::AID-CNCR2820540914>3.0.CO;2-G
Case records of the Massachusetts General Hospital. Case 13-2006. A 50-year-old man with a painful bone mass and lesions in the liver, N. Engl. J. Med, vol.354, issue.17, pp.1828-1837, 2006. ,
Dyskeratosis Congenita (DC) Registry: identification of new features of DC, British Journal of Haematology, vol.5, issue.4, 1998. ,
DOI : 10.1001/archderm.121.11.1424
Telomere maintenance and human bone marrow failure, Blood, vol.111, issue.9, pp.4446-4455, 2008. ,
DOI : 10.1182/blood-2007-08-019729
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2343587
Morphology in patients with severe aplastic anemia treated with antilymphocyte globulin, Blood Jul, vol.1580, issue.2, pp.337-345, 1992. ,
Antithymocyte Globulin and Cyclosporine for Severe Aplastic Anemia, JAMA, vol.289, issue.9, pp.1130-1135, 2003. ,
DOI : 10.1001/jama.289.9.1130
Distinct clinical outcomes for cytogenetic abnormalities evolving from aplastic anemia, Blood, vol.99, issue.9, pp.3129-3135, 2002. ,
DOI : 10.1182/blood.V99.9.3129
Long-term follow-up of severe aplastic anaemia patients treated with antithymocyte globulin, British Journal of Haematology, vol.312, issue.5, pp.121-126, 1989. ,
DOI : 10.1016/0002-9343(81)90204-7
Histopathologic characteristics of bone marrow in patients with aplastic anemia (abstract)], Srp. Arh. Celok. Lek, vol.128, pp.5-6200, 2000. ,
Aplastic anaemia. Histological investigation of methacrylate embedded bone marrow biopsy specimens; correlation with survival after conventional treatment in 15 adult patients, Br. J. Haematol, vol.35, issue.1, pp.61-69, 1977. ,
Childhood myelodysplastic syndrome WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, pp.104-107 ,
The differential diagnosis between aplastic anemia and hypocellular myelodysplasia in patients with pancytopenia, Haematologica, vol.84, issue.6, pp.564-565, 1999. ,
Aplastic anaemia and the hypocellular myelodysplastic syndrome: histomorphological, diagnostic, and prognostic features., Journal of Clinical Pathology, vol.38, issue.11, pp.1218-1224, 1985. ,
DOI : 10.1136/jcp.38.11.1218
Hypoplastic Myelodysplastic Syndromes Can Be Distinguished From Acquired Aplastic Anemia by CD34 and PCNA Immunostaining of Bone Marrow Biopsy Specimens, American Journal of Clinical Pathology, vol.107, issue.3, pp.268-274, 1997. ,
DOI : 10.1093/ajcp/107.3.268
Quantitative analysis of bone marrow CD34 cells in aplastic anemia and hypoplastic myelodysplastic syndromes, Leukemia, vol.78, issue.3, pp.458-462, 2006. ,
DOI : 10.1016/S0145-2126(99)00194-0
A population-based study of childhood myelodysplastic syndrome in British Columbia, Canada, British Journal of Haematology, vol.87, issue.4, pp.1027-1032, 1999. ,
DOI : 10.1016/0925-5710(94)00339-G
Paediatric myelodysplastic syndromes and juvenile myelomonocytic leukaemia in the UK: a population-based study of incidence and survival, British Journal of Haematology, vol.82, issue.5, 2003. ,
DOI : 10.1046/j.1365-2141.2002.03369.x
Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7, Blood, vol.102, issue.6, pp.1997-2003, 2003. ,
DOI : 10.1182/blood-2002-11-3444
Myelodysplastic syndromes/neoplasms, overview WHO classification of tumours of haematopoietic and lymphoid tissues, p.75, 2010. ,
Getting the numbers straight in pediatric MDS: Distribution of subtypes after exclusion of down syndrome, Pediatric Blood & Cancer, vol.85, issue.2, pp.435-436, 2008. ,
DOI : 10.1002/pbc.21235
Clinical and morphological features of paediatric myelodysplastic syndromes: a review of 34 cases, Acta Paediatrica, vol.26, issue.Suppl 1, pp.1015-1023, 2004. ,
DOI : 10.1111/j.1651-2227.2004.tb02708.x
Histopathology in the Diagnosis and Classification of Acute Myeloid Leukemia, Myelodysplastic Syndromes, and Myelodysplastic/Myeloproliferative Diseases, Pathobiology, vol.74, issue.2, pp.97-114, 2007. ,
DOI : 10.1159/000101709
Changing Pattern of AIDS, American Journal of Clinical Pathology, vol.121, issue.3, pp.393-401, 2004. ,
DOI : 10.1309/K8FU6KW125UTJE7B
Bone Marrow Features in Children with HIV Infection and Peripheral Blood Cytopenias, Journal of Tropical Pediatrics, vol.51, issue.2, 2005. ,
DOI : 10.1093/tropej/fmh096
THE HAEMATOLOGICAL FEATURES OF HIV INFECTION, British Journal of Haematology, vol.99, issue.1, pp.1-8, 1997. ,
DOI : 10.1046/j.1365-2141.1997.2943111.x