Danielle Pham-Dinh - Concepedia

Author

Danielle Pham-Dinh

Also Known As

D Pham-Dinh, D. Pham-Dinh, D. Pham‐Dinh, DANIELLE PHAM-DINH, Danielle Pham-Dinh, Danielle Pham-dinh, Pham-Dinh, Danielle

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

Inserm Sorbonne Université Université Paris Cité Centre National de la Recherche Scientifique Charing Cross Hospital

About

Danielle Pham-Dinh is an author at Inserm specializing in medicine, neurology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	23	1.7K
2	Social Sciences	7	7	250
3	Natural Sciences	2	2	120
4	Engineering	1	1	47
5	Public Health	1	1	27

Danielle Pham-Dinh

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex. Danielle Pham-Dinh, Marie‐Geneviève Mattéi, J.L. Nussbaum, Proceedings of the National Academy of Sciences GlycoproteomicsImmunogeneticsDevelopmental BiologyAutoimmune DiseaseMedicine	1993	220
The response of NG2-expressing oligodendrocyte progenitors to demyelination in MOG-EAE and MS Richard Reynolds, Mary R.L. Dawson, Dimitrios Papadopoulos, Journal of Neurocytology	2002	172
Antibodies to native myelin oligodendrocyte glycoprotein are serologic markers of early inflammation in multiple sclerosis Patrice H. Lalive, Til Menge, Cécile Delarasse, Proceedings of the National Academy of Sciences Neurological DisorderImmunologyPathologyOther Myelin ConstituentsNeuroinflammation	2006	172
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice A. Dautigny, Marie‐Geneviève Mattéi, D. Morello, Nature Knockout MouseMolecular NeuroscienceDevelopmental BiologySignal TransductionStructural Gene	1986	154
Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation Diana Rodriguez, Fernande Gauthier, Enrico Bertini, The American Journal of Human Genetics Developmental AnomalyMendelian DisorderInfantile Alexander DiseaseGenetic DisorderGenetics	2001	150
Myelin/oligodendrocyte glycoprotein–deficient (MOG-deficient) mice reveal lack of immune tolerance to MOG in wild-type mice Cécile Delarasse, Philippe Daubas, Lennart T. Mars, Journal of Clinical Investigation	2003	143
Estradiol inhibits ongoing autoimmune neuroinflammation and NFκB-dependent CCL2 expression in reactive astrocytes Sébastien N. Giraud, Cécile M. Caron, Danielle Pham-Dinh, Proceedings of the National Academy of Sciences	2010	142
Axon loss is responsible for chronic neurological deficit following inflammatory demyelination in the rat Dimitrios Papadopoulos, Danielle Pham-Dinh, Richard Reynolds Experimental Neurology Inflammatory DemyelinationNeurodegenerative DiseasesMedicineExperimental NeuropathologyNeurological Function	2005	113
Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene Eva Nelis, Vincent Timmerman, Peter De Jonghe, Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsClinical Genetics	1994	98
Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases Diana Rodriguez, A. Gélot, Bruno Della Gaspera, Acta Neuropathologica Neurological DisorderExperimental NeuropathologyDiffuse Central HypomyelinationNeurologyNeuroscience	1999	88

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