Chazot G - Search Results

1

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP).

Le Guern E, Sturtz F, Gugenheim M, Gouider R, Bonnebouche C, Ravisé N, Gonnaud PM, Tardieu S, Bouche P, Chazot G, et al. Le Guern E, et al. Among authors: chazot g. Cytogenet Cell Genet. 1994;65(4):261-4. doi: 10.1159/000133643. Cytogenet Cell Genet. 1994. PMID: 7903071

2

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

3

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

4

[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.

5

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.

6

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

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

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

9

Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B.

Latour P, Blanquet F, Nelis E, Bonnebouche C, Chapon F, Diraison P, Ollagnon E, Dautigny A, Pham-Dinh D, Chazot G, et al. Latour P, et al. Among authors: chazot g. Hum Mutat. 1995;6(1):50-4. doi: 10.1002/humu.1380060110. Hum Mutat. 1995. PMID: 7550231

10

[Progressive lupus dementia. 2 cases with or without antiphospholipid antibodies].

Robin C, Gonnaud PM, Durieu I, Croisile B, Garassus P, Levrat R, Chazot G, Aimard G, Trillet M. Robin C, et al. Among authors: chazot g. Rev Neurol (Paris). 1995 Dec;151(12):699-707. Rev Neurol (Paris). 1995. PMID: 8787100 Review. French.

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