Atrophie multisystématisée (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Atrophie multisystématisée" in French language version.

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bmj.com

jnnp.bmj.com

Sakakibara R, Hattori T, Uchiyama T et al. Urinary dysfunction and orthostatic hypotension in multiple system atrophy: which is the more common and earlier manifestation?, J Neurol Neurosurg Psychiatry, 2000;68:65-69

jamanetwork.com

archneur.jamanetwork.com

Hara K, Momose Y, Tokiguchi S et al. Multiplex families with multiple system atrophy, Arch Neurol, 2007;64:545-551

nejm.org

Fanciulli A, Wenning GK, Multiple-system atrophy, N Engl J Med, 2015;372:249-263
The Multiple-System Atrophy Research Collaboration, Mutations in COQ2 in familial and sporadic multiple-system atrophy, N Engl J Med, 2013;369:233-244

neurology.org

Ben-Shlomo Y, Wenning GK, Tison F, Quinn NP, Survival of patients with pathologically proven multiple system atrophy: a meta-analysis, Neurology, 1997;48:384-393
Gilman S, Wenning GK, Low PA et al. Second consensus statement on the diagnosis of multiple system atrophy, Neurology, 2008;71:670-676

oxfordjournals.org

brain.oxfordjournals.org

Watanabe H, Saito Y, Terao S et al. Progression and prognosis in multiple system atrophy: an analysis of 230 Japanese patients, Brain, 2002;125:1070-1083

sciencedirect.com

Jecmenica-Lukic M, Poewe W, Tolosa E, Wenning GK, Premotor signs and symptoms of multiple system atrophy, Lancet Neurol, 2012;11:361-368
Papp MI, Kahn JE, Lantos PL, Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome), J Neurol Sci, 1989;94:79-100
Wenning GK, Geser F, Krismer F et al. The natural history of multiple system atrophy: a prospective European cohort study, Lancet Neurol, 2013;12:264-274

springer.com

rd.springer.com

Geser F, Seppi K, Stampfer-Kountchev M, The European Multiple System Atrophy-Study Group (EMSA-SG), J Neural Transm, 2005;112:1677-1686
Ferguson MC, Garland EM, Hedges L et al. SHC2 gene copy number in multiple system atrophy (MSA), Clin Auton Res, 2014;24:25-30

wiley.com

onlinelibrary.wiley.com

May S, Gilman S, Sowell BB et al. Potential outcome measures and trial design issues for multiple system atrophy, Mov Disord, 2007;22:2371-2377
Stankovic I, Krismer F, Jesic A et al. Cognitive impairment in multiple system atrophy: a position statement by the Neuropsychology Task Force of the MDS Multiple System Atrophy (MODIMSA) study group, Mov Disord, 2014;29:857-867
Ahmed Z, Asi YT, Sailer A et al. The neuropathology, pathophysiology and genetics of multiple system atrophy, Neuropathol Appl Neurobiol, 2012;38:4-24
Tu PH, Galvin JE, Baba M et al. Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein, Ann Neurol, 1998;44:415-422