Rolland MO - Search Results

1

[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.

2

[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.

3

An intestinal obstruction in an eight-month-old child suffering from mevalonic aciduria.

Nimubona L, Laloum D, Rolland MO, Read MH, Guillois B, Duhamel JF. Nimubona L, et al. Among authors: rolland mo. Acta Paediatr. 2002;91(6):714-6. doi: 10.1080/080352502760069179. Acta Paediatr. 2002. PMID: 12162608

4

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

5

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.

6

[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder].

Pierron S, Giudicelli H, Moreigne M, Khalfi A, Touati G, Caruba C, Rolland MO, Acquaviva C. Pierron S, et al. Among authors: rolland mo. Arch Pediatr. 2010 Jan;17(1):10-3. doi: 10.1016/j.arcped.2009.09.022. Epub 2009 Nov 22. Arch Pediatr. 2010. PMID: 19932602 French.

7

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

8

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

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

Metabolic studies in twin brothers with 2-methylacetoacetyl-CoA thiolase deficiency.

Fontaine M, Briand G, Ser N, Armelin I, Rolland MO, Degand P, Vamecq J. Fontaine M, et al. Among authors: rolland mo. Clin Chim Acta. 1996 Nov 15;255(1):67-83. doi: 10.1016/0009-8981(96)06391-7. Clin Chim Acta. 1996. PMID: 8930414

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