{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T00:39:01Z","timestamp":1791247141217,"version":"4.1.0"},"reference-count":51,"publisher":"MathDoc\/Centre Mersenne","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p id=\"spar0005\">Hematopoietic stem cell transplantation (HSCT) is the one and only curative therapy available for patient with severe sickle cell disease (SCD). Until today, several hundreds of patients have undergone geno-identical HSCT. More than 200 patients were transplanted in France. The first indication was cerebral vasculopathy. Among both malignant and non-malignant diseases treated with HSCT, the success rate obtained in SCD patients appears as the best one. From the year 2000, more than 95% of transplanted patients survived the HSCT procedure and more than 90% are completely cured and experience a very satisfying health condition post-transplantation. However, the current standard procedure includes a myeloablative conditioning regimen for warranting engraftment. Such regime is linked to severe long-term side effects such as hypofertility. Due to the excellent obtained results, we have to think about a possible widening of indications, a decrease of conditioning intensity and toxicity, and about HSCT from alternative stem cell sources, such as mismatch family donor, unrelated volunteer donor or unrelated cord blood.<\/jats:p>","DOI":"10.1016\/j.crvi.2012.09.004","type":"journal-article","created":{"date-parts":[[2012,10,12]],"date-time":"2012-10-12T17:44:35Z","timestamp":1350063875000},"page":"148-151","source":"Crossref","is-referenced-by-count":6,"title":["Hematopoietic stem cell transplantation in SCD"],"prefix":"10.5802","volume":"336","author":[{"given":"Jean-Hugues","family":"Dalle","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"3842","published-online":{"date-parts":[[2012,10,12]]},"reference":[{"issue":"3","key":"key2025102316363597118_1","first-page":"319","article-title":"Treatment of severe forms of sickle cell anemia with bone marrow allograft: French experience (15 cases). SFGM","volume":"35","author":"Bernaudin, F.","year":"1993","unstructured":"[1] Bernaudin, F.; Souillet, G.; Vannier, J.P. et al. Treatment of severe forms of sickle cell anemia with bone marrow allograft: French experience (15 cases). SFGM, Nouvelle Revue Fran\u00e7aise d\u2019H\u00e9matologie, Volume 35 (1993) no. 3, pp. 319-323","journal-title":"Nouvelle Revue Fran\u00e7aise d\u2019H\u00e9matologie"},{"issue":"1","key":"key2025102316363597118_2","first-page":"22","article-title":"Bone marrow transplantation for sickle cell disease. The United States experience","volume":"16","author":"Johnson, F.L.","year":"1994","unstructured":"[2] Johnson, F.L.; Mentzer, W.C.; Kalinyak, K.A. et al. Bone marrow transplantation for sickle cell disease. The United States experience, The American Journal of Pediatric Hematology\/Oncology, Volume 16 (1994) no. 1, pp. 22-26","journal-title":"The American Journal of Pediatric Hematology\/Oncology"},{"issue":"6","key":"key2025102316363597118_3","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1056\/NEJM199608083350601","article-title":"Bone marrow transplantation for sickle cell disease","volume":"335","author":"Walters, M.C.","year":"1996","unstructured":"[3] Walters, M.C.; Patience, M.; Leisenring, W. et al. Bone marrow transplantation for sickle cell disease, The New England Journal of Medicine, Volume 335 (1996) no. 6, pp. 369-376","journal-title":"The New England Journal of Medicine"},{"issue":"17","key":"key2025102316363597118_4","doi-asserted-by":"crossref","first-page":"3447","DOI":"10.1182\/blood-2009-07-233700","article-title":"Improved survival of children and adolescents with sickle cell disease","volume":"115","author":"Quinn, C.T.","year":"2010","unstructured":"[4] Quinn, C.T.; Rogers, Z.R.; McCavit, T.L. et al. Improved survival of children and adolescents with sickle cell disease, Blood, Volume 115 (2010) no. 17, pp. 3447-3452","journal-title":"Blood"},{"key":"key2025102316363597118_5","unstructured":"[5] Sant\u00e9 Had. Syndromes dr\u00e9panocytaires majeurs de l\u2019enfant et de l\u2019adolescent 2010. Available from: http:\/\/www.has-sante.fr\/portail\/upload\/docs\/application\/pdf\/2010-04\/ald_10_pnds_drepano_enfant_web.pdf."},{"issue":"10","key":"key2025102316363597118_6","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1056\/NEJMc1000134","article-title":"Stem cell transplantation for sickle cell disease","volume":"362","author":"Walters, M.C.","year":"2010","unstructured":"[6] Walters, M.C.; Sullivan, K.M. Stem cell transplantation for sickle cell disease, The New England Journal of Medicine, Volume 362 (2010) no. 10, pp. 955-956 (author reply 6)","journal-title":"The New England Journal of Medicine"},{"issue":"6","key":"key2025102316363597118_7","doi-asserted-by":"crossref","first-page":"e1552","DOI":"10.1542\/peds.2010-3686","article-title":"Management of children with sickle cell disease: a comprehensive review of the literature","volume":"128","author":"Kavanagh, P.L.","year":"2011","unstructured":"[7] Kavanagh, P.L.; Sprinz, P.G.; Vinci, S.R. et al. Management of children with sickle cell disease: a comprehensive review of the literature, Pediatrics, Volume 128 (2011) no. 6, p. e1552-e1574","journal-title":"Pediatrics"},{"issue":"1","key":"key2025102316363597118_8","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1038\/sj.bmt.1701291","article-title":"Haematopoietic stem cell transplantation for sickle cell anaemia: the first 50 patients transplanted in Belgium","volume":"22","author":"Vermylen, C.","year":"1998","unstructured":"[8] Vermylen, C.; Cornu, G.; Ferster, A. et al. Haematopoietic stem cell transplantation for sickle cell anaemia: the first 50 patients transplanted in Belgium, Bone Marrow Transplantation, Volume 22 (1998) no. 1, pp. 1-6","journal-title":"Bone Marrow Transplantation"},{"issue":"5","key":"key2025102316363597118_9","first-page":"633","article-title":"Stem cell transplantation in sickle cell disease: results, perspectives","volume":"15","author":"Bernaudin, F.","year":"2008","unstructured":"[9] Bernaudin, F. Stem cell transplantation in sickle cell disease: results, perspectives, Archives de P\u00e9diatrie\u00a0: Organe Officiel de la Societ\u00e9 Fran\u00e7aise de P\u00e9diatrie, Volume 15 (2008) no. 5, pp. 633-635","journal-title":"Archives de P\u00e9diatrie\u00a0: Organe Officiel de la Societ\u00e9 Fran\u00e7aise de P\u00e9diatrie"},{"issue":"16","key":"key2025102316363597118_10","doi-asserted-by":"crossref","first-page":"4491","DOI":"10.1182\/blood-2011-07-367490","article-title":"Is there still a place for myeloablative regimen to transplant young adults with sickle cell disease?","volume":"118","author":"Kuentz, M.","year":"2011","unstructured":"[10] Kuentz, M.; Robin, M.; Dhedin, N. et al. Is there still a place for myeloablative regimen to transplant young adults with sickle cell disease?, Blood, Volume 118 (2011) no. 16, pp. 4491-4492 (author reply 2\u20133)","journal-title":"Blood"},{"issue":"3","key":"key2025102316363597118_11","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1007\/s00247-005-1419-5","article-title":"Long-term follow-up of pediatric sickle cell disease patients with abnormal high velocities on transcranial Doppler","volume":"35","author":"Bernaudin, F.","year":"2005","unstructured":"[11] Bernaudin, F.; Verlhac, S.; Coic, L. et al. Long-term follow-up of pediatric sickle cell disease patients with abnormal high velocities on transcranial Doppler, Pediatric Radiology, Volume 35 (2005) no. 3, pp. 242-248","journal-title":"Pediatric Radiology"},{"key":"key2025102316363597118_12","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1186\/1477-7525-3-50","article-title":"Health-related quality of life in sickle cell patients: the PiSCES project","volume":"3","author":"McClish, D.K.","year":"2005","unstructured":"[12] McClish, D.K.; Penberthy, L.T.; Bovbjerg, V.E. et al. Health-related quality of life in sickle cell patients: the PiSCES project, Health and Quality of Life Outcomes, Volume 3 (2005), p. 50","journal-title":"Health and Quality of Life Outcomes"},{"issue":"3","key":"key2025102316363597118_13","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1111\/j.1365-2141.2005.05622.x","article-title":"Health-related quality of life in children with sickle cell disease: child and parent perception","volume":"130","author":"Panepinto, J.A.","year":"2005","unstructured":"[13] Panepinto, J.A.; O\u2019Mahar, K.M.; DeBaun, M.R. et al. Health-related quality of life in children with sickle cell disease: child and parent perception, British Journal of Haematology, Volume 130 (2005) no. 3, pp. 437-444","journal-title":"British Journal of Haematology"},{"issue":"11","key":"key2025102316363597118_14","doi-asserted-by":"crossref","first-page":"1264","DOI":"10.1164\/rccm.200601-125OC","article-title":"Abnormal pulmonary function in adults with sickle cell anemia","volume":"173","author":"Klings, E.S.","year":"2006","unstructured":"[14] Klings, E.S.; Wyszynski, D.F.; Nolan, V.G. et al. Abnormal pulmonary function in adults with sickle cell anemia, American Journal of Respiratory and Critical Care Medicine, Volume 173 (2006) no. 11, pp. 1264-1269","journal-title":"American Journal of Respiratory and Critical Care Medicine"},{"issue":"4","key":"key2025102316363597118_15","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1111\/j.1365-2214.2009.00967.x","article-title":"Emotional and behavioural problems in subgroups of children with chronic illness: results from a large-scale population study","volume":"35","author":"Hysing, M.","year":"2009","unstructured":"[15] Hysing, M.; Elgen, I.; Gillberg, C. et al. Emotional and behavioural problems in subgroups of children with chronic illness: results from a large-scale population study, Child: Care, Health and Development, Volume 35 (2009) no. 4, pp. 527-533","journal-title":"Child: Care, Health and Development"},{"issue":"6","key":"key2025102316363597118_16","doi-asserted-by":"crossref","first-page":"665","DOI":"10.1093\/jpepsy\/jsn095","article-title":"Sleep in children with chronic illness, and the relation to emotional and behavioral problems: a population-based study","volume":"34","author":"Hysing, M.","year":"2009","unstructured":"[16] Hysing, M.; Sivertsen, B.; Stormark, K.M. et al. Sleep in children with chronic illness, and the relation to emotional and behavioral problems: a population-based study, Journal of Pediatric Psychology, Volume 34 (2009) no. 6, pp. 665-670","journal-title":"Journal of Pediatric Psychology"},{"issue":"3","key":"key2025102316363597118_17","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1111\/j.1365-2214.2008.00916.x","article-title":"Chronic illnesses in Canadian children: what is the effect of illness on academic achievement, and anxiety and emotional disorders?","volume":"35","author":"Martinez, Y.J.","year":"2009","unstructured":"[17] Martinez, Y.J.; Ercikan, K. Chronic illnesses in Canadian children: what is the effect of illness on academic achievement, and anxiety and emotional disorders?, Child: Care, Health and Development, Volume 35 (2009) no. 3, pp. 391-401","journal-title":"Child: Care, Health and Development"},{"issue":"4 Suppl","key":"key2025102316363597118_18","doi-asserted-by":"crossref","first-page":"S550","DOI":"10.1016\/j.amepre.2010.01.004","article-title":"Sickle cell disease-related pediatric medical expenditures in the US","volume":"38","author":"Amendah, D.D.","year":"2010","unstructured":"[18] Amendah, D.D.; Mvundura, M.; Kavanagh, P.L. et al. Sickle cell disease-related pediatric medical expenditures in the US, American Journal of Preventive Medicine, Volume 38 (2010) no. 4 Suppl, p. S550-S556","journal-title":"American Journal of Preventive Medicine"},{"issue":"8","key":"key2025102316363597118_19","doi-asserted-by":"crossref","first-page":"1505","DOI":"10.1007\/s00467-010-1536-8","article-title":"Prevalence and clinical correlates of microalbuminuria in children with sickle cell disease","volume":"25","author":"Becton, L.J.","year":"2010","unstructured":"[19] Becton, L.J.; Kalpatthi, R.V.; Rackoff, E. et al. Prevalence and clinical correlates of microalbuminuria in children with sickle cell disease, Pediatric Nephrology (Berlin, Germany), Volume 25 (2010) no. 8, pp. 1505-1511","journal-title":"Pediatric Nephrology (Berlin, Germany)"},{"issue":"4","key":"key2025102316363597118_20","doi-asserted-by":"crossref","first-page":"1130","DOI":"10.1182\/blood-2010-06-293514","article-title":"Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohort","volume":"117","author":"Bernaudin, F.","year":"2011","unstructured":"[20] Bernaudin, F.; Verlhac, S.; Arnaud, C. et al. Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohort, Blood, Volume 117 (2011) no. 4, pp. 1130-1140 (quiz 436)","journal-title":"Blood"},{"issue":"16","key":"key2025102316363597118_21","doi-asserted-by":"crossref","first-page":"3684","DOI":"10.1182\/blood-2011-05-349621","article-title":"Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, gender and relative high systolic blood pressure","volume":"119","author":"Debaun, M.R.","year":"2012","unstructured":"[21] Debaun, M.R.; Sarnaik, S.A.; Rodeghier, M.J. et al. Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, gender and relative high systolic blood pressure, Blood, Volume 119 (2012) no. 16, pp. 3684-3690","journal-title":"Blood"},{"issue":"1","key":"key2025102316363597118_22","doi-asserted-by":"crossref","first-page":"106","DOI":"10.1111\/j.1365-2141.2011.08806.x","article-title":"Mortality and causes of death in children with sickle cell disease in the Netherlands, before the introduction of neonatal screening","volume":"155","author":"van der Plas, E.M.","year":"2011","unstructured":"[22] van der Plas, E.M.; van den Tweel, X.W.; Geskus, R.B. et al. Mortality and causes of death in children with sickle cell disease in the Netherlands, before the introduction of neonatal screening, British Journal of Haematology, Volume 155 (2011) no. 1, pp. 106-110","journal-title":"British Journal of Haematology"},{"issue":"3","key":"key2025102316363597118_23","doi-asserted-by":"crossref","first-page":"484","DOI":"10.1542\/peds.2010-1791","article-title":"Quality of care indicators for children with sickle cell disease","volume":"128","author":"Wang, C.J.","year":"2011","unstructured":"[23] Wang, C.J.; Kavanagh, P.L.; Little, A.A. et al. Quality of care indicators for children with sickle cell disease, Pediatrics, Volume 128 (2011) no. 3, pp. 484-493","journal-title":"Pediatrics"},{"issue":"5","key":"key2025102316363597118_24","doi-asserted-by":"crossref","first-page":"705","DOI":"10.1002\/pbc.23000","article-title":"Sickle cell disease and compromised cognition","volume":"56","author":"Wang, W.C.","year":"2011","unstructured":"[24] Wang, W.C. Sickle cell disease and compromised cognition, Pediatric Blood &amp; Cancer, Volume 56 (2011) no. 5, pp. 705-706","journal-title":"Pediatric Blood &amp; Cancer"},{"issue":"5","key":"key2025102316363597118_25","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1111\/j.1365-2141.2011.08999.x","article-title":"Acute splenic sequestration crisis in sickle cell disease: cohort study of 190 paediatric patients","volume":"156","author":"Brousse, V.","year":"2012","unstructured":"[25] Brousse, V.; Elie, C.; Benkerrou, M. et al. Acute splenic sequestration crisis in sickle cell disease: cohort study of 190 paediatric patients, British Journal of Haematology, Volume 156 (2012) no. 5, pp. 643-648","journal-title":"British Journal of Haematology"},{"issue":"20","key":"key2025102316363597118_26","doi-asserted-by":"crossref","first-page":"4587","DOI":"10.1182\/blood-2011-02-272682","article-title":"Silent cerebral infarcts: a review on a prevalent and progressive cause of neurological injury in sickle cell anemia","volume":"119","author":"Debaun, M.R.","year":"2012","unstructured":"[26] Debaun, M.R.; Armstrong, F.D.; McKinstry, R.C. et al. Silent cerebral infarcts: a review on a prevalent and progressive cause of neurological injury in sickle cell anemia, Blood, Volume 119 (2012) no. 20, pp. 4587-4596","journal-title":"Blood"},{"issue":"1","key":"key2025102316363597118_27","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1017\/S1355617711001469","article-title":"Nocturnal oxygen desaturation and disordered sleep as a potential factor in executive dysfunction in sickle cell anemia","volume":"18","author":"Hollocks, M.J.","year":"2012","unstructured":"[27] Hollocks, M.J.; Kok, T.B.; Kirkham, F.J. et al. Nocturnal oxygen desaturation and disordered sleep as a potential factor in executive dysfunction in sickle cell anemia, Journal of the International Neuropsychological Society: JINS, Volume 18 (2012) no. 1, pp. 168-173","journal-title":"Journal of the International Neuropsychological Society: JINS"},{"issue":"1","key":"key2025102316363597118_28","first-page":"27","article-title":"Availability of related donors for bone marrow transplantation in sickle cell anemia","volume":"16","author":"Mentzer, W.C.","year":"1994","unstructured":"[28] Mentzer, W.C.; Heller, S.; Pearle, P.R. et al. Availability of related donors for bone marrow transplantation in sickle cell anemia, The American Journal of Pediatric Hematology\/Oncology, Volume 16 (1994) no. 1, pp. 27-29","journal-title":"The American Journal of Pediatric Hematology\/Oncology"},{"issue":"2","key":"key2025102316363597118_29","first-page":"100","article-title":"Barriers to bone marrow transplantation for sickle cell anemia","volume":"2","author":"Walters, M.C.","year":"1996","unstructured":"[29] Walters, M.C.; Patience, M.; Leisenring, W. et al. Barriers to bone marrow transplantation for sickle cell anemia, Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 2 (1996) no. 2, pp. 100-104","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"6","key":"key2025102316363597118_30","doi-asserted-by":"crossref","first-page":"2137","DOI":"10.1182\/blood-2002-07-2090","article-title":"Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease","volume":"101","author":"Locatelli, F.","year":"2003","unstructured":"[30] Locatelli, F.; Rocha, V.; Reed, W. et al. Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease, Blood, Volume 101 (2003) no. 6, pp. 2137-2143","journal-title":"Blood"},{"issue":"7","key":"key2025102316363597118_31","doi-asserted-by":"crossref","first-page":"2749","DOI":"10.1182\/blood-2007-03-079665","article-title":"Long-term results of related myeloablative stem cell transplantation to cure sickle cell disease","volume":"110","author":"Bernaudin, F.","year":"2007","unstructured":"[31] Bernaudin, F.; Socie, G.; Kuentz, M. et al. Long-term results of related myeloablative stem cell transplantation to cure sickle cell disease, Blood, Volume 110 (2007) no. 7, pp. 2749-2756","journal-title":"Blood"},{"issue":"5","key":"key2025102316363597118_32","doi-asserted-by":"crossref","first-page":"479","DOI":"10.1111\/j.1365-2141.2007.06592.x","article-title":"Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research","volume":"137","author":"Panepinto, J.A.","year":"2007","unstructured":"[32] Panepinto, J.A.; Walters, M.C.; Carreras, J. et al. Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research, British Journal of Haematology, Volume 137 (2007) no. 5, pp. 479-485","journal-title":"British Journal of Haematology"},{"issue":"7","key":"key2025102316363597118_33","doi-asserted-by":"crossref","first-page":"547","DOI":"10.1038\/sj.bmt.1703887","article-title":"Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies","volume":"31","author":"Krishnamurti, L.","year":"2003","unstructured":"[33] Krishnamurti, L.; Abel, S.; Maiers, M. et al. Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies, Bone Marrow Transplantation, Volume 31 (2003) no. 7, pp. 547-550","journal-title":"Bone Marrow Transplantation"},{"issue":"9","key":"key2025102316363597118_34","doi-asserted-by":"crossref","first-page":"1375","DOI":"10.1016\/j.bbmt.2011.01.012","article-title":"Umbilical cord blood transplantation for children with thalassemia and sickle cell disease","volume":"17","author":"Ruggeri, A.","year":"2011","unstructured":"[34] Ruggeri, A.; Eapen, M.; Scaravadou, A. et al. Umbilical cord blood transplantation for children with thalassemia and sickle cell disease, Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 17 (2011) no. 9, pp. 1375-1382","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"8","key":"key2025102316363597118_35","doi-asserted-by":"crossref","first-page":"1265","DOI":"10.1016\/j.bbmt.2012.01.019","article-title":"Unrelated donor cord blood transplantation for children with severe sickle cell disease: results of one cohort from the phase ii study from the blood and marrow transplant clinical trials network (BMT CTN)","volume":"18","author":"Kamani, N.R.","year":"2012","unstructured":"[35] Kamani, N.R.; Walters, M.C.; Carter, S. Unrelated donor cord blood transplantation for children with severe sickle cell disease: results of one cohort from the phase ii study from the blood and marrow transplant clinical trials network (BMT CTN), Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 18 (2012) no. 8, pp. 1265-1272","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"Suppl.\u00a02","key":"key2025102316363597118_36","doi-asserted-by":"crossref","first-page":"e15","DOI":"10.4081\/pr.2011.s2.e15","article-title":"Non-myeloablative, HLA-haplo-identical bone marrow transplantation with high dose, post-transplantation cyclophosphamide","volume":"3","author":"Munchel, A.","year":"2011","unstructured":"[36] Munchel, A.; Kesserwan, C.; Symons, H.J. et al. Non-myeloablative, HLA-haplo-identical bone marrow transplantation with high dose, post-transplantation cyclophosphamide, Pediatric Reports, Volume 3 (2011) no. Suppl.\u00a02, p. e15","journal-title":"Pediatric Reports"},{"issue":"3","key":"key2025102316363597118_37","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1016\/j.beha.2011.05.001","article-title":"Treatment of hematological malignancies with non-myeloablative, HLA-haplo-identical bone marrow transplantation and high dose, post-transplantation cyclophosphamide","volume":"24","author":"Munchel, A.T.","year":"2011","unstructured":"[37] Munchel, A.T.; Kasamon, Y.L.; Fuchs, E.J. Treatment of hematological malignancies with non-myeloablative, HLA-haplo-identical bone marrow transplantation and high dose, post-transplantation cyclophosphamide, Best Practice &amp; Research Clinical Haematology, Volume 24 (2011) no. 3, pp. 359-368","journal-title":"Best Practice &amp; Research Clinical Haematology"},{"issue":"9","key":"key2025102316363597118_38","doi-asserted-by":"crossref","first-page":"1282","DOI":"10.3324\/haematol.2009.006924","article-title":"Is mobilized peripheral blood comparable with bone marrow as a source of hematopoietic stem cells for allogeneic transplantation from HLA-identical sibling donors? A case-control study","volume":"94","author":"Gallardo, D.","year":"2009","unstructured":"[38] Gallardo, D.; de la Camara, R.; Nieto, J.B. et al. Is mobilized peripheral blood comparable with bone marrow as a source of hematopoietic stem cells for allogeneic transplantation from HLA-identical sibling donors? A case-control study, Haematologica, Volume 94 (2009) no. 9, pp. 1282-1288","journal-title":"Haematologica"},{"issue":"Suppl.\u00a01","key":"key2025102316363597118_39","first-page":"118","article-title":"Bone marrow transplantation (BMT) in 14 children with severe sickle cell disease (SCD): the French experience. GEGMO","volume":"12","author":"Bernaudin, F.","year":"1993","unstructured":"[39] Bernaudin, F.; Souillet, G.; Vannier, J.P. et al. Bone marrow transplantation (BMT) in 14 children with severe sickle cell disease (SCD): the French experience. GEGMO, Bone Marrow Transplantation, Volume 12 (1993) no. Suppl.\u00a01, pp. 118-121","journal-title":"Bone Marrow Transplantation"},{"issue":"6","key":"key2025102316363597118_40","first-page":"1918","article-title":"Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell disease","volume":"95","author":"Walters, M.C.","year":"2000","unstructured":"[40] Walters, M.C.; Storb, R.; Patience, M. et al. Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell disease, Blood, Volume 95 (2000) no. 6, pp. 1918-1924","journal-title":"Blood"},{"issue":"4","key":"key2025102316363597118_41","doi-asserted-by":"crossref","first-page":"879","DOI":"10.1182\/blood.V85.4.879.bloodjournal854879","article-title":"Neurologic complications after allogeneic marrow transplantation for sickle cell anemia","volume":"85","author":"Walters, M.C.","year":"1995","unstructured":"[41] Walters, M.C.; Sullivan, K.M.; Bernaudin, F. et al. Neurologic complications after allogeneic marrow transplantation for sickle cell anemia, Blood, Volume 85 (1995) no. 4, pp. 879-884","journal-title":"Blood"},{"issue":"14","key":"key2025102316363597118_42","first-page":"1565","article-title":"Hematopoietic stem cell graft: cure for sickle cell anemia?","volume":"54","author":"Bernaudin, F.","year":"2004","unstructured":"[42] Bernaudin, F. Hematopoietic stem cell graft: cure for sickle cell anemia?, La Revue du Praticien, Volume 54 (2004) no. 14, pp. 1565-1567","journal-title":"La Revue du Praticien"},{"issue":"7","key":"key2025102316363597118_43","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1097\/MPH.0b013e31806451ac","article-title":"Children with sickle cell disease: growth and gonadal function after hematopoietic stem cell transplantation","volume":"29","author":"Brachet, C.","year":"2007","unstructured":"[43] Brachet, C.; Heinrichs, C.; Tenoutasse, S. et al. Children with sickle cell disease: growth and gonadal function after hematopoietic stem cell transplantation, Journal of Pediatric Hematology\/Oncology, Volume 29 (2007) no. 7, pp. 445-450","journal-title":"Journal of Pediatric Hematology\/Oncology"},{"issue":"4","key":"key2025102316363597118_44","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1111\/j.1365-2141.2006.06486.x","article-title":"Effect of myeloablative bone marrow transplantation on growth in children with sickle cell anaemia: results of the multicenter study of haematopoietic cell transplantation for sickle cell anaemia","volume":"136","author":"Eggleston, B.","year":"2007","unstructured":"[44] Eggleston, B.; Patience, M.; Edwards, S. et al. Effect of myeloablative bone marrow transplantation on growth in children with sickle cell anaemia: results of the multicenter study of haematopoietic cell transplantation for sickle cell anaemia, British Journal of Haematology, Volume 136 (2007) no. 4, pp. 673-676","journal-title":"British Journal of Haematology"},{"issue":"2","key":"key2025102316363597118_45","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1016\/j.bbmt.2009.10.005","article-title":"Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease","volume":"16","author":"Walters, M.C.","year":"2010","unstructured":"[45] Walters, M.C.; Hardy, K.; Edwards, S. et al. Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease, Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 16 (2010) no. 2, pp. 263-272","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"3","key":"key2025102316363597118_46","doi-asserted-by":"crossref","first-page":"164","DOI":"10.1097\/GCO.0b013e328353bb57","article-title":"How does bone marrow transplantation affect ovarian function and fertility?","volume":"24","author":"Jadoul, P.","year":"2012","unstructured":"[46] Jadoul, P.; Donnez, J. How does bone marrow transplantation affect ovarian function and fertility?, Current Opinion in Obstetrics &amp; Gynecology, Volume 24 (2012) no. 3, pp. 164-171","journal-title":"Current Opinion in Obstetrics &amp; Gynecology"},{"key":"key2025102316363597118_47","author":"Matthes, S.","year":"2012","unstructured":"[47] Matthes, S.; Lawitchka, A.; Fritsch, G. et al. 8th meeting of the EBMT Paediatric Diseases Working Party and 3rd meeting of the EBMT; Prague (2012)","journal-title":"8th meeting of the EBMT Paediatric Diseases Working Party and 3rd meeting of the EBMT; Prague"},{"issue":"8","key":"key2025102316363597118_48","doi-asserted-by":"crossref","first-page":"519","DOI":"10.1016\/S1083-8791(03)00192-7","article-title":"Results of minimally toxic non-myeloablative transplantation in patients with sickle cell anemia and beta-thalassemia","volume":"9","author":"Iannone, R.","year":"2003","unstructured":"[48] Iannone, R.; Casella, J.F.; Fuchs, E.J. et al. Results of minimally toxic non-myeloablative transplantation in patients with sickle cell anemia and beta-thalassemia, Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 9 (2003) no. 8, pp. 519-528","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"12","key":"key2025102316363597118_49","doi-asserted-by":"crossref","first-page":"1422","DOI":"10.1016\/j.bbmt.2007.08.050","article-title":"Fludarabine-based non-myeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics","volume":"13","author":"Horwitz, M.E.","year":"2007","unstructured":"[49] Horwitz, M.E.; Spasojevic, I.; Morris, A. et al. Fludarabine-based non-myeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics, Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 13 (2007) no. 12, pp. 1422-1426","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"11","key":"key2025102316363597118_50","doi-asserted-by":"crossref","first-page":"1270","DOI":"10.1016\/j.bbmt.2008.08.016","article-title":"Stable long-term donor engraftment following reduced intensity hematopoietic cell transplantation for sickle cell disease","volume":"14","author":"Krishnamurti, L.","year":"2008","unstructured":"[50] Krishnamurti, L.; Kharbanda, S.; Biernacki, M.A. et al. Stable long-term donor engraftment following reduced intensity hematopoietic cell transplantation for sickle cell disease, Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation, Volume 14 (2008) no. 11, pp. 1270-1278","journal-title":"Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation"},{"issue":"24","key":"key2025102316363597118_51","doi-asserted-by":"crossref","first-page":"2309","DOI":"10.1056\/NEJMoa0904971","article-title":"Allogeneic hematopoietic stem cell transplantation for sickle cell disease","volume":"361","author":"Hsieh, M.M.","year":"2009","unstructured":"[51] Hsieh, M.M.; Kang, E.M.; Fitzhugh, C.D. et al. Allogeneic hematopoietic stem cell transplantation for sickle cell disease, The New England Journal of Medicine, Volume 361 (2009) no. 24, pp. 2309-2317","journal-title":"The New England Journal of Medicine"}],"container-title":["Comptes Rendus. Biologies"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/comptes-rendus.academie-sciences.fr\/biologies\/item\/10.1016\/j.crvi.2012.09.004.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,23]],"date-time":"2025-10-23T14:49:36Z","timestamp":1761230976000},"score":1,"resource":{"primary":{"URL":"https:\/\/comptes-rendus.academie-sciences.fr\/biologies\/articles\/10.1016\/j.crvi.2012.09.004\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,10,12]]},"references-count":51,"journal-issue":{"issue":"3","published-online":{"date-parts":[[2013]]}},"alternative-id":["10.1016\/j.crvi.2012.09.004"],"URL":"https:\/\/doi.org\/10.1016\/j.crvi.2012.09.004","relation":{},"ISSN":["1631-0691","1768-3238"],"issn-type":[{"value":"1631-0691","type":"print"},{"value":"1768-3238","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,10,12]]}}}