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Phenotypic diversity associated with the MT-TV gene m.1644G>A mutation, a matter of quantity.
Mitochondrion. 2014 Mar;15:34-9. doi: 10.1016/j.mito.2014.03.010. Epub 2014 Mar 29.
Mitochondrion. 2014.
PMID: 24691472
Free article.
Ischemic stroke in young women: risk of recurrence during subsequent pregnancies. French Study Group on Stroke in Pregnancy.
Lamy C, Hamon JB, Coste J, Mas JL.
Lamy C, et al. Among authors: hamon jb.
Neurology. 2000 Jul 25;55(2):269-74. doi: 10.1212/wnl.55.2.269.
Neurology. 2000.
PMID: 10908903
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Five-year outcome in the copaxone observatory: a nationwide cohort of patients with multiple sclerosis starting treatment with glatiramer acetate in France.
Lebrun-Frenay C, Moulignier A, Pierrot-Deseilligny C, Benrabah R, Moreau T, Lubetzki C, Monchecourt F; Copaxone Observatory.
Lebrun-Frenay C, et al.
J Neurol. 2019 Apr;266(4):888-901. doi: 10.1007/s00415-019-09211-5. Epub 2019 Feb 7.
J Neurol. 2019.
PMID: 30730008
Free PMC article.
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The 2008-2012 French Alzheimer plan: description of the national Alzheimer information system.
Le Duff F, Develay AE, Quetel J, Lafay P, Schück S, Pradier C, Robert P; French National Alzheimer dataBank (BNA).
Le Duff F, et al.
J Alzheimers Dis. 2012;29(4):891-902. doi: 10.3233/JAD-2012-111943.
J Alzheimers Dis. 2012.
PMID: 22366771
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[Interhemispheric disconnection caused by callosal infarction in the territory of the splenium artery].
Hamon JB, Medjbeur S, Cohen L, Tassan P, Pierrot-Deseilligny C.
Hamon JB, et al.
Rev Neurol (Paris). 1997 Feb;153(1):69-70.
Rev Neurol (Paris). 1997.
PMID: 9296161
French.
No abstract available.
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