E. Balaban, G. Buchanan, M. Graham, and E. Frenkel, 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

J. Lipton, E. Atsidaftos, I. Zyskind, and A. Vlachos, 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

V. Gupta, S. Tripathi, V. Tilak, and B. Bhatia, 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

S. Memon, S. Shaikh, and M. Nizamani, Etiological spectrum of pancytopenia based on bone marrow examination in children, J. Coll. Physicians Surg. Pak, 2008.

N. Giri, E. Kang, and J. Tisdale, 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

S. Ellis and J. Lipton, 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

J. Flygare and S. Karlsson, Diamond-Blackfan anemia: erythropoiesis lost in translation, Blood, vol.109, issue.8, pp.3152-3154, 2007.
DOI : 10.1182/blood-2006-09-001222

G. Gerrits, C. Van-oostrom, G. De-vaan, and J. Bakkeren, Transient erythroblastopenia of childhood, European Journal of Pediatrics, vol.7, issue.4, pp.266-270, 1984.
DOI : 10.1007/BF00540249

I. Cherrick, G. Karayalcin, and P. Lanzkowsky, Transient erythroblastopenia of childhood. Prospective study of fifty patients, Am. J. Pediatr. Hematol. Oncol, 1994.

L. Penchansky and J. Jordan, 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

A. Prassouli, V. Papadakis, and A. Tsakris, 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

D. Geetha, J. Zachary, H. Baldado, J. Kronz, and E. Kraus, 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

G. Skeppner, A. Kreuger, and G. Elinder, 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

J. Shaw and R. Meeder, 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

D. Van, O. Broeckaert-van, V. Desmet, and R. Verwilghen, Gaucher-like cells and congenital dyserythropoietic anaemia, type II (HEMPAS), Br. J. Haematol, 1973.

M. Block, 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

P. Sharma, N. Khurana, and T. Singh, 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

E. Zaino, M. Rossi, T. Pham, and H. Azar, Gaucher's cells in thalassemia, Blood, vol.38, issue.4, pp.457-462, 1971.

T. Miyata, J. Takeda, and Y. Iida, 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

G. Socie, J. Mary, and G. De, 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

W. Wanachiwanawin, U. Siripanyaphinyo, N. Piyawattanasakul, and T. Kinoshita, 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

M. Perlman, J. Schwab, J. Nachman, and C. Rubin, 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

I. Kuku, E. Kaya, S. Yologlu, R. Gokdeniz, and A. Baydin, 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

K. Finberg, M. Heeney, and D. Campagna, 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

F. Guillem, S. Lawson, C. Kannengiesser, M. Westerman, C. Beaumont et al., 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

M. Melis, M. Cau, and R. Congiu, 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

R. Hill, J. Pettit, M. Tattersall, N. Kiley, and S. Lewis, Iron Deficiency and Dyserythropoiesis, British Journal of Haematology, vol.6, issue.4, pp.507-512, 1972.
DOI : 10.1038/204582a0

G. Weiss and L. Goodnough, Anemia of Chronic Disease, New England Journal of Medicine, vol.352, issue.10, pp.1011-1023, 2005.
DOI : 10.1056/NEJMra041809

M. Voulgarelis, S. Kokori, J. Ioannidis, A. Tzioufas, D. Kyriaki et al., 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

C. Mavragani, E. Vlachaki, and M. Voulgarelis, 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

A. Hara, T. Wada, and S. Kitajima, 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

P. Das, D. Wherrett, and Y. Dror, 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

S. Fukaya, S. Yasuda, and T. Hashimoto, 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

R. Bass, V. Pullarkat, D. Feinstein, A. Kaul, C. Winberg et al., Pathology of Autoimmune Myelofibrosis, American Journal of Clinical Pathology, vol.116, issue.2, pp.211-216, 2001.
DOI : 10.1309/6Q99-VRNL-7BTP-W1G8

M. Munoz, I. Villar, and J. Garcia-erce, An update on iron physiology, World Journal of Gastroenterology, vol.15, issue.37, pp.4617-4626, 2009.
DOI : 10.3748/wjg.15.4617

E. Nemeth, E. Valore, M. Territo, G. Schiller, A. Lichtenstein et al., 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

E. Nemeth, S. Rivera, and V. Gabayan, 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

M. Voulgarelis, S. Giannouli, A. Tasidou, D. Anagnostou, P. Ziakas et al., 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

S. Yetgin, S. Ozen, U. Saatci, A. Bakkaloglu, N. Besbas et al., 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

B. Kirel, S. Yetgin, U. Saatci, S. Ozen, A. Bakkaloglu et al., Anaemia in juvenile chronic arthritis, Clinical Rheumatology, vol.66, issue.4, pp.236-241, 1996.
DOI : 10.1007/BF02229700

Y. Oka, J. Kameoka, and Y. Hirabayashi, 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

J. Lee, J. Chang, Y. Cho, and W. Han, 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

T. Tanvetyanon and J. Leighton, 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

S. Wickramasinghe, Diagnosis of megaloblastic anaemias, Blood Reviews, vol.20, issue.6, pp.299-318, 2006.
DOI : 10.1016/j.blre.2006.02.002

L. Boxer and D. Dale, Neutropenia: Causes and consequences, Seminars in Hematology, vol.39, issue.2, 2002.
DOI : 10.1053/shem.2002.31911

D. Dale, A. Bolyard, and B. Schwinzer, The Severe Chronic Neutropenia International Registry: 10-Year Follow-up Report. Support. Cancer Ther, Jul, vol.13, issue.4, pp.220-231, 2006.

P. Aggett, N. Cavanagh, D. Matthew, J. Pincott, J. Sutcliffe et al., 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

Y. Dror, P. Durie, and H. Ginzberg, 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

H. Ginzberg, J. Shin, and L. Ellis, 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

D. Mack, G. Forstner, M. Wilschanski, M. Freedman, and P. Durie, 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

O. Smith, I. Hann, J. Chessells, B. Reeves, and P. Milla, 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

G. Boocock, J. Morrison, and M. Popovic, 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

E. Maserati, B. Pressato, and R. Valli, 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

S. Toiviainen-salo, M. Mayranpaa, and P. Durie, 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

R. Kostmann, Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria, Acta Paediatr. Feb, vol.45, pp.1-78, 1956.

M. Horwitz, Z. Duan, B. Korkmaz, H. Lee, M. Mealiffe et al., Neutrophil elastase in cyclic and severe congenital neutropenia, Blood, vol.109, issue.5, pp.1817-1824, 2007.
DOI : 10.1182/blood-2006-08-019166

D. Dale, R. Person, and A. Bolyard, Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia, Blood, vol.96, issue.7, pp.2317-2322, 2000.

C. Klein, M. Grudzien, and G. Appaswamy, HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease), Nature Genetics, vol.191, issue.1, 2007.
DOI : 10.1038/ng1940

J. Skokowa, M. Germeshausen, C. Zeidler, and K. Welte, Severe congenital neutropenia: inheritance and pathophysiology, Current Opinion in Hematology, vol.14, issue.1, pp.22-28, 2007.
DOI : 10.1097/00062752-200701000-00006

H. Hasle, C. Niemeyer, and J. Chessells, A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases, Leukemia, vol.17, issue.2, 2003.
DOI : 10.1038/sj.leu.2402765

P. Rosenberg, B. Alter, and A. Bolyard, 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

C. Haurie, D. Dale, and M. Mackey, Cyclical neutropenia and other periodic hematological disorders: a review of mechanisms and mathematical models, Blood, vol.92, issue.8, pp.2629-2640, 1998.

M. Horwitz, K. Benson, R. Person, A. Aprikyan, and D. Dale, 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

D. Dale, T. Cottle, and C. Fier, 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

J. Donadieu, T. Leblanc, and M. Bader, 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.

M. Freedman, M. Bonilla, and C. Fier, 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.

H. Birgens and H. Karle, 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

P. Quesenberry, Cyclic hematopoiesis: disorders of primitive hematopoietic stem cells, Exp. Hematol, vol.11, issue.8, pp.687-700, 1983.

F. Laporte, S. Hamdi, F. Oksman, and F. Huguet, 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

H. Papadaki, H. Michelakaki, J. Bux, and G. Eliopoulos, 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

H. Shimizu, K. Sawada, N. Katano, K. Sasaki, S. Kawai et al., Intramedullary Neutrophil Phagocytosis by Histiocytes in Autoimmune Neutropenia of Infancy, Acta Haematologica, vol.84, issue.4, pp.201-203, 1990.
DOI : 10.1159/000205065

M. Akhtari, E. Waller, and D. Jaye, 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

H. Papadaki, A. Eliopoulos, and T. Kosteas, 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

H. Papadaki, A. Chatzivassili, K. Stefanaki, V. Koumaki, P. Kanavaros et al., 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

M. Ballmaier, M. Germeshausen, and H. Schulze, 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

M. Ballmaier, M. Germeshausen, S. Krukemeier, and K. Welte, 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

M. Ballmaier and M. Germeshausen, 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

M. Rose, K. Nicol, M. Skeens, T. Gross, and B. Kerlin, 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

J. Hall, J. Levin, J. Kuhn, E. Ottenheimer, K. Van-berkum et al., THROMBOCYTOPENIA WITH ABSENT RADIUS (TAR), Medicine, vol.48, issue.6, 1969.
DOI : 10.1097/00005792-196948060-00001

L. Bonsi, C. Marchionni, and F. Alviano, 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

V. Hedberg and J. Lipton, Thrombocytopenia with Absent Radii, Journal of Pediatric Hematology/Oncology, vol.10, issue.1, pp.51-64, 1988.
DOI : 10.1097/00043426-198821000-00010

D. Cines and V. Blanchette, Immune Thrombocytopenic Purpura, New England Journal of Medicine, vol.346, issue.13, pp.995-1008, 2002.
DOI : 10.1056/NEJMra010501

S. Jubelirer and R. Harpold, 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

M. Muhury, A. Mathai, S. Rai, R. Naik, M. Pai et al., Megakaryocytic alterations in thrombocytopenia: a bone marrow aspiration study, Indian J. Pathol. Microbiol, vol.52, issue.4, pp.490-494, 2009.

D. Kuter, G. Mufti, B. Bain, R. Hasserjian, W. Davis et al., 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

R. Hoffman, E. Bruno, and J. Elwell, Acquired amegakaryocytic thrombocytopenic purpura: a syndrome of diverse etiologies, Blood, vol.60, issue.5, pp.1173-1178, 1982.

C. Zent, J. Ratajczak, M. Ratajczak, J. Anastasi, P. Hoffman et al., 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

M. Levitus, M. Rooimans, and J. Steltenpool, 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

J. Dorsman, M. Levitus, and D. Rockx, Identification of the Fanconi anemia complementation group I gene, FANCI, Cell Oncol, vol.29, issue.3, pp.211-218, 2007.

I. Dokal and T. Vulliamy, 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

P. Giampietro, P. Verlander, J. Davis, and A. Auerbach, 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

D. Kutler, B. Singh, and J. Satagopan, 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

A. Cioc, J. Wagner, M. Macmillan, T. Defor, and B. Hirsch, 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

B. Alter, 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

P. Jacobs and C. Karabus, 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

A. Zhu, D. Andrea, A. Sahani, D. Hasserjian, and R. , 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.

S. Knight, T. Vulliamy, A. Copplestone, E. Gluckman, P. Mason et al., 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

R. Calado and N. Young, 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

A. Tichelli, A. Gratwohl, C. Nissen, E. Signer, G. Stebler et al., Morphology in patients with severe aplastic anemia treated with antilymphocyte globulin, Blood Jul, vol.1580, issue.2, pp.337-345, 1992.

S. Rosenfeld, D. Follmann, O. Nunez, and N. Young, Antithymocyte Globulin and Cyclosporine for Severe Aplastic Anemia, JAMA, vol.289, issue.9, pp.1130-1135, 2003.
DOI : 10.1001/jama.289.9.1130

J. Maciejewski, A. Risitano, E. Sloand, O. Nunez, and N. Young, 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

M. De-planque, A. Bacigalupo, and A. Wursch, 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

R. Milosevic, G. Jankovic, N. Antonijevic, V. Jovanovic, D. Babic et al., Histopathologic characteristics of bone marrow in patients with aplastic anemia (abstract)], Srp. Arh. Celok. Lek, vol.128, pp.5-6200, 2000.

V. Te and H. Haak, 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.

I. Baumann, C. Niemeyer, J. Bennet, and K. Shannon, Childhood myelodysplastic syndrome WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, pp.104-107

I. Lorand-metze, D. Meira, C. Lima, J. Vassallo, and K. Metze, The differential diagnosis between aplastic anemia and hypocellular myelodysplasia in patients with pancytopenia, Haematologica, vol.84, issue.6, pp.564-565, 1999.

I. Fohlmeister, R. Fischer, B. Modder, M. Rister, and H. Schaefer, 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

A. Orazi, M. Albitar, N. Heerema, S. Haskins, and R. Neiman, 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

W. Matsui, R. Brodsky, B. Smith, M. Borowitz, and R. Jones, 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

H. Hasle, L. Wadsworth, B. Massing, M. Mcbride, and K. Schultz, 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

S. Passmore, J. Chessells, H. Kempski, I. Hann, P. Brownbill et al., 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

G. Kardos, I. Baumann, and S. Passmore, 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

R. Brunning, A. Orazi, and U. Germing, Myelodysplastic syndromes/neoplasms, overview WHO classification of tumours of haematopoietic and lymphoid tissues, p.75, 2010.

J. Stary, I. Baumann, U. Creutzig, J. Harbott, K. Michalova et al., 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

S. Polychronopoulou, J. Panagiotou, L. Kossiva, A. Mavrou, D. Anagnostou et al., 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

A. Orazi, 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

X. Zhao, N. Sun, M. Witt, M. Keller, and Y. Niihara, Changing Pattern of AIDS, American Journal of Clinical Pathology, vol.121, issue.3, pp.393-401, 2004.
DOI : 10.1309/K8FU6KW125UTJE7B

D. Meira, I. Lorand-metze, A. Toro, M. Silva, and M. Vilela, 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

B. Bain, 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