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Moyamoya disease associated with hereditary spherocytosis.
Vo Van P, Sabouraud P, Mac G, Abely M, Bednarek N. Vo Van P, et al. Among authors: abely m. Pediatr Neurol. 2011 Jan;44(1):69-71. doi: 10.1016/j.pediatrneurol.2010.08.002. Pediatr Neurol. 2011. PMID: 21147392
Hereditary sensory neuropathy with spastic paraplegia.
Kherbaoui-Redouani L, Ploton D, Abely M, Bednarek N, Stourbe A, Sabouraud P, Motte J. Kherbaoui-Redouani L, et al. Among authors: abely m. Eur J Paediatr Neurol. 2004;8(2):95-9. doi: 10.1016/j.ejpn.2003.12.006. Eur J Paediatr Neurol. 2004. PMID: 15253057
Four family cases of acute renal failure. Diagnosis: Orellanus syndrome.
Talmud D, Wynckel A, Grossenbacher F, Saad S, Motte J, Abély M, Pietrement C. Talmud D, et al. Among authors: abely m. Pediatr Nephrol. 2011 Mar;26(3):385-8. doi: 10.1007/s00467-010-1545-7. Epub 2010 Jun 1. Pediatr Nephrol. 2011. PMID: 20514545 No abstract available.
53 results