Müh JP - Search Results

1

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.

Corcia P, Khoris J, Couratier P, Mayeux-Portas V, Bieth E, De Toffol B, Autret A, Müh JP, Andres C, Camu W. Corcia P, et al. Among authors: muh jp. Neurology. 2002 Nov 12;59(9):1464-6. doi: 10.1212/01.wnl.0000032500.73621.c5. Neurology. 2002. PMID: 12427909

2

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis.

Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Müh JP, Camu W, Andres C; French ALS Research Group. Amyotrophic Lateral Sclerosis. Corcia P, et al. Among authors: muh jp. Ann Neurol. 2002 Feb;51(2):243-6. doi: 10.1002/ana.10104. Ann Neurol. 2002. PMID: 11835381

3

Association study of the NF1 gene and autistic disorder.

Mbarek O, Marouillat S, Martineau J, Barthélémy C, Müh JP, Andres C. Mbarek O, et al. Among authors: muh jp. Am J Med Genet. 1999 Dec 15;88(6):729-32. Am J Med Genet. 1999. PMID: 10581497

4

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. Eur J Hum Genet. 2001 Jul;9(7):556-8. doi: 10.1038/sj.ejhg.5200660. Eur J Hum Genet. 2001. PMID: 11464249

5

Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor.

Vourc'h P, Moreau T, Arbion F, Marouillat-Védrine S, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. J Neurochem. 2003 May;85(4):889-97. doi: 10.1046/j.1471-4159.2003.01764.x. J Neurochem. 2003. PMID: 12716421 Free article.

6

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.

Vourc'h P, Dessay S, Mbarek O, Marouillat Védrine S, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. Brain Res Dev Brain Res. 2003 Sep 10;144(2):159-68. doi: 10.1016/s0165-3806(03)00167-6. Brain Res Dev Brain Res. 2003. PMID: 12935913

7

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.

Vourc'h P, Martin I, Marouillat S, Adrien JL, Barthélémy C, Moraine C, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. Neurosci Lett. 2003 Feb 27;338(2):115-8. doi: 10.1016/s0304-3940(02)01338-1. Neurosci Lett. 2003. PMID: 12566166

8

Monoamines (serotonin and catecholamines) and their derivatives in infantile autism: age-related changes and drug effects.

Martineau J, Barthélémy C, Jouve J, Muh JP, Lelord G. Martineau J, et al. Among authors: muh jp. Dev Med Child Neurol. 1992 Jul;34(7):593-603. doi: 10.1111/j.1469-8749.1992.tb11490.x. Dev Med Child Neurol. 1992. PMID: 1380929

9

Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder.

Vourc'h P, Petit E, Müh JP, Andres C, Bienvenu T, Beldjord C, Chelly J, Barthélémy C. Vourc'h P, et al. Among authors: muh jp. Am J Med Genet. 2002 Mar 1;108(2):164-7. doi: 10.1002/ajmg.10210. Am J Med Genet. 2002. PMID: 11857568 No abstract available.

10

Catecholaminergic metabolism and autism.

Martineau J, Hérault J, Petit E, Guérin P, Hameury L, Perrot A, Mallet J, Sauvage D, Lelord G, Müh JP. Martineau J, et al. Among authors: muh jp. Dev Med Child Neurol. 1994 Aug;36(8):688-97. doi: 10.1111/j.1469-8749.1994.tb11911.x. Dev Med Child Neurol. 1994. PMID: 7914177

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