Rolland MO - Search Results

1

Clinical approach to inherited peroxisomal disorders: a series of 27 patients.

Baumgartner MR, Poll-The BT, Verhoeven NM, Jakobs C, Espeel M, Roels F, Rabier D, Levade T, Rolland MO, Martinez M, Wanders RJ, Saudubray JM. Baumgartner MR, et al. Among authors: rolland mo. Ann Neurol. 1998 Nov;44(5):720-30. doi: 10.1002/ana.410440505. Ann Neurol. 1998. PMID: 9818927

2

Evaluation of the presence of premature atherosclerosis in adults with heterozygosity for cystathionine-beta-synthase deficiency.

de Valk HW, van Eeden MK, Banga JD, van der Griend R, de Groot E, Haas FJ, Meuwissen OJ, Duran M, Smeitink JA, Poll-The BT, de Klerk JB, Wittebol-Post D, Rolland MO. de Valk HW, et al. Among authors: rolland mo. Stroke. 1996 Jun;27(6):1134-6. Stroke. 1996. PMID: 8650730 No abstract available.

3

Resistance to erucic acid as a selectable marker for peroxisomal activity: isolation of revertants of an infantile Refsum disease cell line.

Bachir Bioukar E, Straehli F, Ng KH, Rolland MO, Hashimoto T, Carreau JP, Deschatrette J. Bachir Bioukar E, et al. Among authors: rolland mo. J Inherit Metab Dis. 1994;17(1):41-59. doi: 10.1007/BF00735394. J Inherit Metab Dis. 1994. PMID: 7519689

4

Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblasts.

Cartier N, Lopez J, Moullier P, Rocchiccioli F, Rolland MO, Jorge P, Mosser J, Mandel JL, Bougnères PF, Danos O, et al. Cartier N, et al. Among authors: rolland mo. Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1674-8. doi: 10.1073/pnas.92.5.1674. Proc Natl Acad Sci U S A. 1995. PMID: 7878038 Free PMC article.

5

Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionine beta-synthase mutations.

Sperandeo MP, Candito M, Sebastio G, Rolland MO, Turc-Carel C, Giudicelli H, Dellamonica P, Andria G. Sperandeo MP, et al. Among authors: rolland mo. J Inherit Metab Dis. 1996;19(3):351-6. doi: 10.1007/BF01799266. J Inherit Metab Dis. 1996. PMID: 8803779

6

[Delayed diagnosis of homocystinuria by major deficiency in cystathionine beta synthase].

Tur MD, De Maistre E, Franck P, Rolland MO, Fremont S, Lecompte T, Vidailhet M. Tur MD, et al. Among authors: rolland mo. Rev Med Interne. 2004 Feb;25(2):150-3. doi: 10.1016/j.revmed.2003.10.012. Rev Med Interne. 2004. PMID: 14744647 French.

7

Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantation.

Aubourg P, Blanche S, Jambaqué I, Rocchiccioli F, Kalifa G, Naud-Saudreau C, Rolland MO, Debré M, Chaussain JL, Griscelli C, et al. Aubourg P, et al. Among authors: rolland mo. N Engl J Med. 1990 Jun 28;322(26):1860-6. doi: 10.1056/NEJM199006283222607. N Engl J Med. 1990. PMID: 2348839 Free article. No abstract available.

8

Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear family.

Nadal N, Rolland MO, Tranchant C, Reutenauer L, Gyapay G, Warter JM, Mandel JL, Koenig M. Nadal N, et al. Among authors: rolland mo. Hum Mol Genet. 1995 Oct;4(10):1963-6. doi: 10.1093/hmg/4.10.1963. Hum Mol Genet. 1995. PMID: 8595422

9

NTBC treatment in tyrosinaemia type I: long-term outcome in French patients.

Masurel-Paulet A, Poggi-Bach J, Rolland MO, Bernard O, Guffon N, Dobbelaere D, Sarles J, de Baulny HO, Touati G. Masurel-Paulet A, et al. Among authors: rolland mo. J Inherit Metab Dis. 2008 Feb;31(1):81-7. doi: 10.1007/s10545-008-0793-1. Epub 2008 Jan 25. J Inherit Metab Dis. 2008. PMID: 18214711

10

[Severe hyperhomocysteinemia revealing homocystinuria in two young adults with mild phenotype].

Ducros V, Rousset J, Garambois K, Boujet C, Rolland MO, Valenti K, Bouillet L, Jaillard A, Favier A. Ducros V, et al. Among authors: rolland mo. Rev Med Interne. 2006 Feb;27(2):140-3. doi: 10.1016/j.revmed.2005.09.018. Epub 2005 Nov 7. Rev Med Interne. 2006. PMID: 16298022 French.

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