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Page 1
Leigh's disease due to a new mutation in the PDHX gene.
Schiff M, Miné M, Brivet M, Marsac C, Elmaleh-Bergés M, Evrard P, Ogier de Baulny H. Schiff M, et al. Ann Neurol. 2006 Apr;59(4):709-14. doi: 10.1002/ana.20818. Ann Neurol. 2006. PMID: 16566017
Early-onset hyperargininaemia: a severe disorder?
Schiff M, Benoist JF, Cardoso ML, Elmaleh-Bergès M, Forey P, Santiago J, Ogier de Baulny H. Schiff M, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S175-8. doi: 10.1007/s10545-009-1137-5. Epub 2009 Apr 20. J Inherit Metab Dis. 2009. PMID: 19381865
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. 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
[Should a metabolic work-up be performed in autism?].
Schiff M, Delorme R, Benoist JF, Ogier de Baulny H. Schiff M, et al. Arch Pediatr. 2010 Jun;17(6):802-3. doi: 10.1016/S0929-693X(10)70119-6. Arch Pediatr. 2010. PMID: 20654901 French. No abstract available.
[Sjögren-Larsson syndrome: 2 case reports].
Galoin-Bertail C, Ogier de Baulny H, Wanders R, Schiff M, Bellavoine V, Mlika A, Benoist G, Baruteau J. Galoin-Bertail C, et al. Among authors: schiff m. Arch Pediatr. 2012 Feb;19(2):135-41. doi: 10.1016/j.arcped.2011.11.004. Epub 2011 Dec 20. Arch Pediatr. 2012. PMID: 22192722 French.
706 results