Vandenberghe A - Search Results

1

[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy].

Degos B, Echaniz-Laguna A, Latour P, Vandenberghe A, Anheim M, Talmant V, Tranchant C. Degos B, et al. Among authors: vandenberghe a. Rev Neurol (Paris). 2004 Dec;160(12):1203-6. doi: 10.1016/s0035-3787(04)71168-6. Rev Neurol (Paris). 2004. PMID: 15602369 French.

2

[Hereditary neuropathy with tendency to pressure palsies (HNPP) in a child: clinical and biological diagnosis. A case report].

Lesca G, Meunier S, Zine A, Jeannoël P, Latour P, Vandenberghe A. Lesca G, et al. Among authors: vandenberghe a. Arch Pediatr. 2000 Mar;7(3):271-3. doi: 10.1016/s0929-693x(00)88744-8. Arch Pediatr. 2000. PMID: 10761604 French.

3

Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A.

Rajabally Y, Vital A, Ferrer X, Vital C, Julien J, Latour P, Vandenberghe A, Lagueny A. Rajabally Y, et al. Among authors: vandenberghe a. J Peripher Nerv Syst. 2000 Sep;5(3):158-62. doi: 10.1046/j.1529-8027.2000.00014.x. J Peripher Nerv Syst. 2000. PMID: 11442172

4

Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene.

Stojkovic T, Latour P, Viet G, de Seze J, Hurtevent JF, Vandenberghe A, Vermersch P. Stojkovic T, et al. Among authors: vandenberghe a. Neuromuscul Disord. 2004 Apr;14(4):261-4. doi: 10.1016/j.nmd.2004.01.003. Neuromuscul Disord. 2004. PMID: 15019704

5

Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ gene.

Lagueny A, Latour P, Vital A, Le Masson G, Rouanet M, Ferrer X, Vital C, Vandenberghe A. Lagueny A, et al. Among authors: vandenberghe a. J Neurol Neurosurg Psychiatry. 2001 Feb;70(2):232-5. doi: 10.1136/jnnp.70.2.232. J Neurol Neurosurg Psychiatry. 2001. PMID: 11160475 Free PMC article.

6

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

7

Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination.

Lopes J, Ravisé N, Vandenberghe A, Palau F, Ionasescu V, Mayer M, Lévy N, Wood N, Tachi N, Bouche P, Latour P, Ruberg M, Brice A, LeGuern E. Lopes J, et al. Among authors: vandenberghe a. Hum Mol Genet. 1998 Jan;7(1):141-8. doi: 10.1093/hmg/7.1.141. Hum Mol Genet. 1998. PMID: 9384615

8

Prenatal detection of the 17p11.2 duplication in Charcot-Marie-Tooth disease type 1A: necessity of a multidisciplinary approach for heterogeneous disorders.

Bernard R, Boyer A, Nègre P, Malzac P, Latour P, Vandenberghe A, Philip N, Lévy N. Bernard R, et al. Among authors: vandenberghe a. Eur J Hum Genet. 2002 May;10(5):297-302. doi: 10.1038/sj.ejhg.5200804. Eur J Hum Genet. 2002. PMID: 12082504

9

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: vandenberghe a. Eur Neurol. 1997;38(1):26-30. doi: 10.1159/000112898. Eur Neurol. 1997. PMID: 9252795

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: vandenberghe a. Clin Chem. 2001 May;47(5):829-37. Clin Chem. 2001. PMID: 11325885

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