Ollagnon E - Search Results

1

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene.

Ressot C, Latour P, Blanquet-Grossard F, Sturtz F, Duthel S, Battin J, Corbillon E, Ollagnon E, Serville F, Vandenberghe A, Dautigny A, Pham-Dinh D. Ressot C, et al. Among authors: ollagnon e. Hum Genet. 1996 Aug;98(2):172-5. doi: 10.1007/s004390050183. Hum Genet. 1996. PMID: 8698335

2

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: ollagnon e. Hum Mutat. 1995;6(1):50-4. doi: 10.1002/humu.1380060110. Hum Mutat. 1995. PMID: 7550231

3

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: ollagnon e. Clin Chem. 1996 Jul;42(7):1021-5. Clin Chem. 1996. PMID: 8674184

4

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: ollagnon e. Eur Neurol. 1997;37(1):38-42. doi: 10.1159/000117403. Eur Neurol. 1997. PMID: 9018031 Review.

5

NF2 gene in neurofibromatosis type 2 patients.

Zucman-Rossi J, Legoix P, Der Sarkissian H, Cheret G, Sor F, Bernardi A, Cazes L, Giraud S, Ollagnon E, Lenoir G, Thomas G. Zucman-Rossi J, et al. Among authors: ollagnon e. Hum Mol Genet. 1998 Dec;7(13):2095-101. doi: 10.1093/hmg/7.13.2095. Hum Mol Genet. 1998. PMID: 9817927

6

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: ollagnon e. Ann Genet. 1999;42(3):151-9. Ann Genet. 1999. PMID: 10526658 Clinical Trial.

7

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: ollagnon e. Neurogenetics. 1997 Sep;1(2):117-23. doi: 10.1007/s100480050017. Neurogenetics. 1997. PMID: 10732813

8

SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations.

Latour P, Gonnaud PM, Ollagnon E, Chan V, Perelman S, Stojkovic T, Stoll C, Vial C, Ziegler F, Vandenberghe A, Maire I. Latour P, et al. Among authors: ollagnon e. J Peripher Nerv Syst. 2006 Jun;11(2):148-55. doi: 10.1111/j.1085-9489.2006.00080.x. J Peripher Nerv Syst. 2006. PMID: 16787513

9

Characterisation of 16 polymorphic markers in the NF2 gene: application to hemizygosity detection.

Legoix P, Legrand MF, Ollagnon E, Lenoir G, Thomas G, Zucman-Rossi J. Legoix P, et al. Among authors: ollagnon e. Hum Mutat. 1999;13(4):290-3. doi: 10.1002/(SICI)1098-1004(1999)13:4<290::AID-HUMU5>3.0.CO;2-C. Hum Mutat. 1999. PMID: 10220142

10

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy.

Klebe S, Depienne C, Gerber S, Challe G, Anheim M, Charles P, Fedirko E, Lejeune E, Cottineau J, Brusco A, Dollfus H, Chinnery PF, Mancini C, Ferrer X, Sole G, Destée A, Mayer JM, Fontaine B, de Seze J, Clanet M, Ollagnon E, Busson P, Cazeneuve C, Stevanin G, Kaplan J, Rozet JM, Brice A, Durr A. Klebe S, et al. Among authors: ollagnon e. Brain. 2012 Oct;135(Pt 10):2980-93. doi: 10.1093/brain/aws240. Brain. 2012. PMID: 23065789 Free PMC article.

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