Charcot's disease
ELA · esclerosis lateral amiotrófica
Charcot disease oor Spaans
Charcot disease
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esclerosis lateral amiotrófica
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My father had Charcot's disease, a degenerative nerve disorder.
No me des la charlaOpenSubtitles2018.v3 OpenSubtitles2018.v3
(Also called Charcot’s Disease; Lou Gehrig’s Disease; Lytico)
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ALS is also sometimes referred to as Charcot’s disease, after Jean-Martin Charcot, the French neurologist who first described it in 1869.
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This result confirms the diagnosis of Charcot-Marie-Tooth disease, type 4A.
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Its close relation to Friedreich ataxia and the amyotrophy of Charcot-Marie-Tooth disease was recognized.
Espera ¿ Ella no habla francés?Literature Literature
We confirmed through the DNA in your biopsy that you have something called Charcot-Marie-Tooth disease.
Para ello debe tener una puerta abierta al malOpenSubtitles2018.v3 OpenSubtitles2018.v3
has Charcot-Marie-Tooth disease.
¡ Acaba con él!OpenSubtitles2018.v3 OpenSubtitles2018.v3
Tonic pupil has also been reported in young children with Charcot-Marie-Tooth disease.
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Charcot-Marie-Tooth Disease Type 1A 9.
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This patient developed progressive polyneuropathy resembling Charcot-Marie-Tooth disease type 2.
Pero ella no me amaLiterature Literature
This test confirmed that J.T. had a duplicated PMP22 allele and type 1A Charcot-Marie-Tooth disease.
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The genetic locus of 17p11.2 is identical to that of HMSN type I or Charcot-Marie-Tooth disease.
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Charcot-Marie-Tooth disease.
TEXTOS APROBADOSOpenSubtitles2018.v3 OpenSubtitles2018.v3
Charcot Marie Tooth disease (CMT4A) due to GDAP1 mutation: report of a colombian family
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The majority are associated with an underlying neurologic disorder such as Charcot-Marie-Tooth disease.
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The genetic locus of 17p11.2 is identical to that of HMSN type I or Charcot-Marie-Tooth disease.
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The initial diagnosis has been confused with Charcot-Marie-Tooth disease.
Vamos, Eric, debes tomar estoLiterature Literature
Aims and purposes of the organization: The aims of the organization are to support patients and their families while showing respect for their diversity, circumstances and wishes, to support research on amyotrophic lateral sclerosis, also known as Charcot’s disease, and other motor neuron diseases and to encourage all initiatives to combat these diseases and address the disabilities they cause.
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A link with neurodegenerative disorders and mitochondria-associated conditions such as Charcot-Marie-Tooth disease should be made in future studies.
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Mutations of GDAP1 gene cause autosomal dominant and autosomal recessive Charcot-Marie-Tooth disease and more than 40 different mutations have been reported.
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HNPP is part of the group of hereditary motor and sensory neuropathy (HMSN) disorders and is linked to Charcot–Marie–Tooth disease (CMT).
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James Lupski, a medical geneticist who has Charcot-Marie-Tooth (CMT) disease.
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Background: Mutations of GDAP1 gene cause autosomal dominant and autosomal recessive Charcot-Marie-Tooth disease and more than 40 different mutations have been reported.
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Known human disorders include Charcot-Marie-Tooth disease type 1A, which may be caused by duplication of the gene encoding peripheral myelin protein 22 (PMP22) on chromosome 17.
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Jean-Martin Charcot coined the term "Parkinson's disease" some 60 years later.
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199 sinne gevind in 15 ms. Hulle kom uit baie bronne en word nie nagegaan nie.