Bost M - Search Results

1

Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France Network.

Sturtz FG, Chauvin F, Ollagnon-Roman E, Bost M, Latour P, Bonnebouche C, Gonnaud PM, Bady B, Chazot G, Vandenberghe A. Sturtz FG, et al. Among authors: bost m. Eur Neurol. 1996;36(4):224-8. doi: 10.1159/000117254. Eur Neurol. 1996. PMID: 8814426

2

New allele of probe D17S61 present in the Charcot-Marie-Tooth 1A duplication.

Bost M, Bonnebouche C, Gonnaud PM, Cochat P, Gilbert B, Dupont C, Chazot G, Vandenberghe A. Bost M, et al. Clin Genet. 1994 Nov;46(5):380-1. doi: 10.1111/j.1399-0004.1994.tb04184.x. Clin Genet. 1994. PMID: 7889651 No abstract available.

3

A RsaI RFLP at the human myelin protein zero (MPZ) locus.

Latour P, Bonnebouche C, Bost M, Diraison P, Chapon F, Boucherat M, Vandenberghe A. Latour P, et al. Among authors: bost m. Clin Genet. 1994 Oct;46(4):327-8. doi: 10.1111/j.1399-0004.1994.tb04172.x. Clin Genet. 1994. PMID: 7530611 No abstract available.

4

Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12.

Vandenberghe A, Latour P, Chauplannaz G, Chapon F, Pouget J, Dumas R, Laguenay A, Ollagnon E, Bost M, Duthel S, Chazot G, Boucherat M. Vandenberghe A, et al. Among authors: bost m. Clin Chem. 1996 Jul;42(7):1021-5. Clin Chem. 1996. PMID: 8674184

5

Peripheral blood markers of oxidative stress in Parkinson's disease.

Younes-Mhenni S, Frih-Ayed M, Kerkeni A, Bost M, Chazot G. Younes-Mhenni S, et al. Among authors: bost m. Eur Neurol. 2007;58(2):78-83. doi: 10.1159/000103641. Epub 2007 Jun 12. Eur Neurol. 2007. PMID: 17565220

6

Restriction polymorphisms of the ceruloplasmin gene on chromosome 3.

Bost M, Berkaw M, McBride OW, Chazot G, Arnaud P. Bost M, et al. Hum Genet. 1995 Aug;96(2):239-40. doi: 10.1007/BF00207390. Hum Genet. 1995. PMID: 7635481

7

CTG instability in myotonic dystrophy: molecular genetic analysis of families from south-eastern France with characteristics of intergenerational variation in CGT repeat numbers.

Duthel S, Bost M, Ollagnon E, Vial C, Petiot P, Chazot G, Vandenberghe A. Duthel S, et al. Among authors: bost m. Ann Genet. 1999;42(3):151-9. Ann Genet. 1999. PMID: 10526658 Clinical Trial.

8

Serum copper, zinc and selenium levels in Tunisian patients with Parkinson's disease.

Younes-Mhenni S, Aissi M, Mokni N, Boughammoura-Bouatay A, Chebel S, Frih-Ayed M, Kerkeni A, Bost M, Chazot G, Sfar MT, Sfar MH. Younes-Mhenni S, et al. Among authors: bost m. Tunis Med. 2013 Jun;91(6):402-5. Tunis Med. 2013. PMID: 23868039 Free article.

9

Genetic and molecular analysis of familial isolated growth hormone deficiency.

Ruiz-Pacheco R, Chatelain P, Sizonenko PC, Bost M, Garandau P, Sultan C. Ruiz-Pacheco R, et al. Among authors: bost m. Hum Genet. 1993 Oct 1;92(3):273-81. doi: 10.1007/BF00244472. Hum Genet. 1993. PMID: 8104861

10

Identification of a mutation, N543H, in exon 11 of the low-density lipoprotein receptor gene in a French family with familial hypercholesterolemia.

Tricot-Guerber F, Saint-Jore B, Valenti K, Foulon T, Bost M, Hadjian AJ. Tricot-Guerber F, et al. Among authors: bost m. Hum Mutat. 1995;6(1):87-8. doi: 10.1002/humu.1380060117. Hum Mutat. 1995. PMID: 7550239 No abstract available.

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