Ogier de Baulny H - Search Results

1

Morphological studies of skeletal muscle in lactic acidosis.

Romero NB, Lombès A, Touati G, Rigal O, Frachon P, Cheval MA, Giraud M, Possekel S, Fardeau M, Ogier de Baulny H. Romero NB, et al. Among authors: ogier de baulny h. J Inherit Metab Dis. 1996;19(4):528-34. doi: 10.1007/BF01799113. J Inherit Metab Dis. 1996. PMID: 8884576 Review.

2

Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newborn.

Lombes A, Romero NB, Touati G, Frachon P, Cheval MA, Giraud M, Simon D, Ogier de Baulny H. Lombes A, et al. Among authors: ogier de baulny h. J Inherit Metab Dis. 1996;19(3):286-95. doi: 10.1007/BF01799256. J Inherit Metab Dis. 1996. PMID: 8803770

3

In vivo functional investigations of lactic acid in patients with respiratory chain disorders.

Touati G, Rigal O, Lombès A, Frachon P, Giraud M, Ogier de Baulny H. Touati G, et al. Among authors: ogier de baulny h. Arch Dis Child. 1997 Jan;76(1):16-21. doi: 10.1136/adc.76.1.16. Arch Dis Child. 1997. PMID: 9059154 Free PMC article.

4

Neonatal cardiomyopathies and metabolic crises due to oxidative phosphorylation defects.

Schiff M, Ogier de Baulny H, Lombès A. Schiff M, et al. Among authors: ogier de baulny h. Semin Fetal Neonatal Med. 2011 Aug;16(4):216-21. doi: 10.1016/j.siny.2011.04.002. Epub 2011 May 24. Semin Fetal Neonatal Med. 2011. PMID: 21606011 Review.

5

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.

Barthélémy C, Ogier de Baulny H, Diaz J, Cheval MA, Frachon P, Romero N, Goutieres F, Fardeau M, Lombès A. Barthélémy C, et al. Among authors: ogier de baulny h. Ann Neurol. 2001 May;49(5):607-17. Ann Neurol. 2001. PMID: 11357951

6

Functional characterization of novel mutations in the human cytochrome b gene.

Legros F, Chatzoglou E, Frachon P, Ogier De Baulny H, Laforêt P, Jardel C, Godinot C, Lombès A. Legros F, et al. Among authors: ogier de baulny h. Eur J Hum Genet. 2001 Jul;9(7):510-8. doi: 10.1038/sj.ejhg.5200678. Eur J Hum Genet. 2001. PMID: 11464242

7

Progression despite replacement of a myopathic form of coenzyme Q10 defect.

Auré K, Benoist JF, Ogier de Baulny H, Romero NB, Rigal O, Lombès A. Auré K, et al. Among authors: ogier de baulny h. Neurology. 2004 Aug 24;63(4):727-9. doi: 10.1212/01.wnl.0000134607.76780.b2. Neurology. 2004. PMID: 15326254

8

Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children.

Possekel S, Lombes A, Ogier de Baulny H, Cheval MA, Fardeau M, Kadenbach B, Romero NB. Possekel S, et al. Among authors: ogier de baulny h. Histochem Cell Biol. 1995 Jan;103(1):59-68. doi: 10.1007/BF01464476. Histochem Cell Biol. 1995. PMID: 7736281 Clinical Trial.

9

SLC25A32 Mutations and Riboflavin-Responsive Exercise Intolerance.

Schiff M, Veauville-Merllié A, Su CH, Tzagoloff A, Rak M, Ogier de Baulny H, Boutron A, Smedts-Walters H, Romero NB, Rigal O, Rustin P, Vianey-Saban C, Acquaviva-Bourdain C. Schiff M, et al. Among authors: ogier de baulny h. N Engl J Med. 2016 Feb 25;374(8):795-7. doi: 10.1056/NEJMc1513610. N Engl J Med. 2016. PMID: 26933868 Free PMC article. No abstract available.

10

Should transcobalamin deficiency be treated aggressively?

Schiff M, Ogier de Baulny H, Bard G, Barlogis V, Hamel C, Moat SJ, Odent S, Shortland G, Touati G, Giraudier S. Schiff M, et al. Among authors: ogier de baulny h. J Inherit Metab Dis. 2010 Jun;33(3):223-9. doi: 10.1007/s10545-010-9074-x. Epub 2010 Mar 30. J Inherit Metab Dis. 2010. PMID: 20352340

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