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Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources.
Souillet G, Guffon N, Maire I, Pujol M, Taylor P, Sevin F, Bleyzac N, Mulier C, Durin A, Kebaili K, Galambrun C, Bertrand Y, Froissart R, Dorche C, Gebuhrer L, Garin C, Berard J, Guibaud P. Souillet G, et al. Among authors: maire i. Bone Marrow Transplant. 2003 Jun;31(12):1105-17. doi: 10.1038/sj.bmt.1704105. Bone Marrow Transplant. 2003. PMID: 12796790
[Glycogenoses type 1b and 1c].
de Parscau L, Guibaud P, Maire I. de Parscau L, et al. Among authors: maire i. Pediatrie. 1988;43(8):661-5. Pediatrie. 1988. PMID: 3065719 Review. French.
Mutation analysis in 11 French patients with Fabry disease.
Guffon N, Froissart R, Chevalier-Porst F, Maire I. Guffon N, et al. Among authors: maire i. Hum Mutat. 1998;Suppl 1:S288-90. doi: 10.1002/humu.1380110190. Hum Mutat. 1998. PMID: 9452111 No abstract available.
Hunter syndrome: gene deletions and rearrangements.
Froissart R, Blond JL, Maire I, Guibaud P, Hopwood JJ, Mathieu M, Bozon D. Froissart R, et al. Among authors: maire i. Hum Mutat. 1993;2(2):138-40. doi: 10.1002/humu.1380020214. Hum Mutat. 1993. PMID: 8318991 No abstract available.
Mucopolysaccharidosis type II--genotype/phenotype aspects.
Froissart R, Moreira da Silva I, Guffon N, Bozon D, Maire I. Froissart R, et al. Among authors: maire i. Acta Paediatr Suppl. 2002;91(439):82-7. doi: 10.1111/j.1651-2227.2002.tb03116.x. Acta Paediatr Suppl. 2002. PMID: 12572848
Glycogen storage disease and inflammatory bowel disease.
de Parscau L, Maire I, Guibaud P, Gonthier R, Dumollard JM, Rousset H. de Parscau L, et al. Among authors: maire i. J Pediatr. 1989 Aug;115(2):337. doi: 10.1016/s0022-3476(89)80112-x. J Pediatr. 1989. PMID: 2754570 No abstract available.
144 results