Chazot G - Search Results

1

[Hereditary motor and sensory neuropathy of Charcot-Marie-Tooth disease].

Sturtz F, Gonnaud PM, Besse JL, Chazot G, Vandenberghe A. Sturtz F, et al. Among authors: chazot g. Arch Pediatr. 1995 Jan;2(1):70-8. doi: 10.1016/0929-693x(96)89813-7. Arch Pediatr. 1995. PMID: 7735430 Review. French.

2

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: chazot g. Eur Neurol. 1996;36(4):224-8. doi: 10.1159/000117254. Eur Neurol. 1996. PMID: 8814426

3

New mutations in the X-linked form of Charcot-Marie-Tooth disease.

Latour P, Fabreguette A, Ressot C, Blanquet-Grossard F, Antoine JC, Calvas P, Chapon F, Corbillon E, Ollagnon E, Sturtz F, Boucherat M, Chazot G, Dautigny A, Pham-Dinh D, Vandenberghe A. Latour P, et al. Among authors: chazot g. Eur Neurol. 1997;37(1):38-42. doi: 10.1159/000117403. Eur Neurol. 1997. PMID: 9018031 Review.

4

Clinical and electrophysiological phenotype of a homozygously duplicated Charcot-Marie-Tooth (type 1A) disease.

Sturtz FG, Latour P, Mocquard Y, Cruz S, Fenoll B, LeFur JM, Mabin D, Chazot G, Vandenberghe A. Sturtz FG, et al. Among authors: chazot g. Eur Neurol. 1997;38(1):26-30. doi: 10.1159/000112898. Eur Neurol. 1997. PMID: 9252795

5

Charcot-Marie-Tooth disease from first description to genetic localization of mutations.

Sturtz FG, Chazot G, Vandenberghe AJ. Sturtz FG, et al. Among authors: chazot g. J Hist Neurosci. 1992 Jan;1(1):47-58. doi: 10.1080/09647049209525514. J Hist Neurosci. 1992. PMID: 11618415

6

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. Among authors: chazot g. 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.

7

Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO gene.

Blanquet-Grossard F, Pham-Dinh D, Dautigny A, Latour P, Bonnebouche C, Corbillon E, Chazot G, Vandenberghe A. Blanquet-Grossard F, et al. Among authors: chazot g. Clin Genet. 1995 Dec;48(6):281-3. doi: 10.1111/j.1399-0004.1995.tb04109.x. Clin Genet. 1995. PMID: 8835320

8

DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations.

Gonnaud PM, Sturtz F, Fourbil Y, Bonnebouche C, Tranchant C, Warter JM, Chazot G, Bady B, Vial C, Brechard AS, et al. Gonnaud PM, et al. Among authors: chazot g. Acta Neurol Scand. 1995 Oct;92(4):313-8. doi: 10.1111/j.1600-0404.1995.tb00135.x. Acta Neurol Scand. 1995. PMID: 8848937

9

Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French population.

Latour P, Lévy N, Paret M, Chapon F, Chazot G, Clavelou P, Couratier P, Dumas R, Ollagnon E, Pouget J, Setiey A, Vallat JM, Boucherat M, Fontes M, Vandenberghe A. Latour P, et al. Among authors: chazot g. Neurogenetics. 1997 Sep;1(2):117-23. doi: 10.1007/s100480050017. Neurogenetics. 1997. PMID: 10732813

10

Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplication.

Latour P, Boutrand L, Levy N, Bernard R, Boyer A, Claustrat F, Chazot G, Boucherat M, Vandenberghe A. Latour P, et al. Among authors: chazot g. Clin Chem. 2001 May;47(5):829-37. Clin Chem. 2001. PMID: 11325885

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