Pham-Dinh D - Search Results

1

Tumor-like enlargement of the optic chiasm in an infant with Alexander disease.

Mignot C, Desguerre I, Burglen L, Hertz-Pannier L, Renaldo F, Gadisseux JF, Gallet S, Pham-Dinh D, Boespflug-Tanguy O, Rodriguez D. Mignot C, et al. Among authors: pham dinh d. Brain Dev. 2009 Mar;31(3):244-7. doi: 10.1016/j.braindev.2008.05.005. Epub 2008 Jun 26. Brain Dev. 2009. PMID: 18584981

2

Alexander disease: putative mechanisms of an astrocytic encephalopathy.

Mignot C, Boespflug-Tanguy O, Gelot A, Dautigny A, Pham-Dinh D, Rodriguez D. Mignot C, et al. Cell Mol Life Sci. 2004 Feb;61(3):369-85. doi: 10.1007/s00018-003-3143-3. Cell Mol Life Sci. 2004. PMID: 14770299 Free PMC article. Review.

3

Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease.

Mignot C, Delarasse C, Escaich S, Della Gaspera B, Noé E, Colucci-Guyon E, Babinet C, Pekny M, Vicart P, Boespflug-Tanguy O, Dautigny A, Rodriguez D, Pham-Dinh D. Mignot C, et al. Among authors: pham dinh d. Exp Cell Res. 2007 Aug 1;313(13):2766-79. doi: 10.1016/j.yexcr.2007.04.035. Epub 2007 May 24. Exp Cell Res. 2007. PMID: 17604020

4

Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation.

Rodriguez D, Gauthier F, Bertini E, Bugiani M, Brenner M, N'guyen S, Goizet C, Gelot A, Surtees R, Pedespan JM, Hernandorena X, Troncoso M, Uziel G, Messing A, Ponsot G, Pham-Dinh D, Dautigny A, Boespflug-Tanguy O. Rodriguez D, et al. Am J Hum Genet. 2001 Nov;69(5):1134-40. doi: 10.1086/323799. Epub 2001 Sep 20. Am J Hum Genet. 2001. PMID: 11567214 Free PMC article.

5

Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases.

Rodriguez D, Gelot A, della Gaspera B, Robain O, Ponsot G, Sarliève LL, Ghandour S, Pompidou A, Dautigny A, Aubourg P, Pham-Dinh D. Rodriguez D, et al. Acta Neuropathol. 1999 May;97(5):469-80. doi: 10.1007/s004010051016. Acta Neuropathol. 1999. PMID: 10334484

6

Complex alternative splicing of the myelin oligodendrocyte glycoprotein gene is unique to human and non-human primates.

Delarasse C, Della Gaspera B, Lu CW, Lachapelle F, Gelot A, Rodriguez D, Dautigny A, Genain C, Pham-Dinh D. Delarasse C, et al. J Neurochem. 2006 Sep;98(6):1707-17. doi: 10.1111/j.1471-4159.2006.04053.x. Epub 2006 Aug 11. J Neurochem. 2006. PMID: 16903876 Free article.

7

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

8

Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.

Pham-Dinh D, Popot JL, Boespflug-Tanguy O, Landrieu P, Deleuze JF, Boué J, Jollès P, Dautigny A. Pham-Dinh D, et al. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7562-6. doi: 10.1073/pnas.88.17.7562. Proc Natl Acad Sci U S A. 1991. PMID: 1715570 Free PMC article.

9

Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.

Boespflug-Tanguy O, Mimault C, Melki J, Cavagna A, Giraud G, Pham Dinh D, Dastugue B, Dautigny A. Boespflug-Tanguy O, et al. Am J Hum Genet. 1994 Sep;55(3):461-7. Am J Hum Genet. 1994. PMID: 7915877 Free PMC article.

10

Identification of a Val 145 Ile substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis. The Réseau de Recherche Clinique INSERM sur la Susceptibilité Génétique à la Sclérose en Plaques.

Rodriguez D, Della Gaspera B, Zalc B, Hauw JJ, Fontaine B, Edan G, Clanet M, Dautigny A, Pham-Dinh D. Rodriguez D, et al. Mult Scler. 1997 Dec;3(6):377-81. doi: 10.1177/135245859700300603. Mult Scler. 1997. PMID: 9493637

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