Pham-Dinh D - Search Results

1

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. Clin Genet. 1995 Dec;48(6):281-3. doi: 10.1111/j.1399-0004.1995.tb04109.x. Clin Genet. 1995. PMID: 8835320

2

The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23.

Pham-Dinh D, Fourbil Y, Blanquet F, Mattéi MG, Roeckel N, Latour P, Chazot G, Vandenberghe A, Dautigny A. Pham-Dinh D, et al. Hum Mol Genet. 1993 Dec;2(12):2051-4. doi: 10.1093/hmg/2.12.2051. Hum Mol Genet. 1993. PMID: 7509228

3

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

4

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. Hum Genet. 1996 Aug;98(2):172-5. doi: 10.1007/s004390050183. Hum Genet. 1996. PMID: 8698335

5

Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po.

Blanquet-Grossard F, Pham-Dinh D, Dautigny A, Latour P, Bonnebouche C, Diraison P, Chapon F, Chazot G, Vandenberghe A. Blanquet-Grossard F, et al. Hum Mutat. 1996;8(2):185-6. doi: 10.1002/(SICI)1098-1004(1996)8:2<185::AID-HUMU13>3.0.CO;2-Z. Hum Mutat. 1996. PMID: 8844219 No abstract available.

6

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

7

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.

Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C. Nelis E, et al. Hum Genet. 1994 Dec;94(6):653-7. doi: 10.1007/BF00206959. Hum Genet. 1994. PMID: 7527371

8

Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene.

Pham-Dinh D, Boespflug-Tanguy O, Mimault C, Cavagna A, Giraud G, Leberre G, Lemarec B, Dautigny A. Pham-Dinh D, et al. Hum Mol Genet. 1993 Apr;2(4):465-7. doi: 10.1093/hmg/2.4.465. Hum Mol Genet. 1993. PMID: 7684945

9

Structure and polymorphism of the mouse myelin/oligodendrocyte glycoprotein gene.

Daubas P, Pham-Dinh D, Dautigny A. Daubas P, et al. Genomics. 1994 Sep 1;23(1):36-41. doi: 10.1006/geno.1994.1456. Genomics. 1994. PMID: 7829100

10

Characterization and expression of the cDNA coding for the human myelin/oligodendrocyte glycoprotein.

Pham-Dinh D, Allinquant B, Ruberg M, Della Gaspera B, Nussbaum JL, Dautigny A. Pham-Dinh D, et al. J Neurochem. 1994 Dec;63(6):2353-6. doi: 10.1046/j.1471-4159.1994.63062353.x. J Neurochem. 1994. PMID: 7964757

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