dejerine-klumpke syndrome 是什么意思，中文意思 | 德热里纳-克隆普克综合征英文怎么说医学英语中英文词汇翻译

Déjerine‐Sottas syndrome with a silent nucleotide change of myelin protein zero gene

F Taioli, I Cabrini, T Cavallaro… - Journal of the …, 2011 - Wiley Online Library
Charcot-Marie-Tooth disease type 1B (CMT1B) and Déjerine-Sottas syndrome type B
(DSSB) are caused by missense or frameshift mutations of myelin protein zero (MPZ) gene. We
identified an apparently silent synonymous c.411C>T transition in MPZ exon 3 ...
Related articles - All 2 versions

The identification of Landouzy-Dejerine disease: An investigative history.

M Jacqueline - Neuromuscular disorders: NMD, 2011 - ncbi.nlm.nih.gov
1. Neuromuscul Disord. 2011 Feb 11. [Epub ahead of print] The identification of
Landouzy-Dejerine disease: An investigative history. Jacqueline M. Paris 7, Denis Diderot
University, Paris, France. PMID: 21316966 [PubMed - as supplied by publisher].
Related articles - All 3 versions

The Impossible Succession of Charcot–The Quest for a Suitable Heir

L Tatu… - European Neurology, 2011 - content.karger.com
... There were a number of potential successors, but only three were officially declared: Brissaud,
Jules Déjerine (1849–1917) and Fulgence Raymond (1844–1910). ... In 1917, at the age of 65,
Pierre Marie would finally occupy Charcot's chair following the death of Déjerine. ...
Cited by 1 - Related articles - All 2 versions

A case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years

VFML Ramos… - Age and Ageing, 2011 - Br Geriatrics Soc
... retrospective review of 107 cases. FSHD is also known as Landouzy-Dejerine muscular
dystrophy, as first described by Louis Theophile Joseph Landouzy and Joseph Jules
Dejerine in 1885 [2–4]. Clinical features include progression ...

[HTML] Alexia without Agraphia

[HTML] from imj.ieE Mulroy, S Murphy… - Instructions for Authors, 2011 - imj.ie
... Déjerine in 1892 reported a patient who developed this syndrome after an infarct of the
left occipital lobe and splenium of the corpus callosum. ... Brain Lang 1974; 1:215-26. 7.
Dejerine J. Sur un cas de cécité verbale avec agraphie, suivi d'autopsie. ...
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Déjerine‐Sottas syndrome with a silent nucleotide change of myelin protein zero gene

F Taioli, I Cabrini, T Cavallaro… - Journal of the …, 2011 - Wiley Online Library
Charcot-Marie-Tooth disease type 1B (CMT1B) and Déjerine-Sottas syndrome type B
(DSSB) are caused by missense or frameshift mutations of myelin protein zero (MPZ) gene. We
identified an apparently silent synonymous c.411C>T transition in MPZ exon 3 ...
Related articles - All 2 versions

The identification of Landouzy-Dejerine disease: An investigative history.

M Jacqueline - Neuromuscular disorders: NMD, 2011 - ncbi.nlm.nih.gov
1. Neuromuscul Disord. 2011 Feb 11. [Epub ahead of print] The identification of
Landouzy-Dejerine disease: An investigative history. Jacqueline M. Paris 7, Denis Diderot
University, Paris, France. PMID: 21316966 [PubMed - as supplied by publisher].
Related articles - All 3 versions

The Impossible Succession of Charcot–The Quest for a Suitable Heir

L Tatu… - European Neurology, 2011 - content.karger.com
... There were a number of potential successors, but only three were officially declared: Brissaud,
Jules Déjerine (1849–1917) and Fulgence Raymond (1844–1910). ... In 1917, at the age of 65,
Pierre Marie would finally occupy Charcot's chair following the death of Déjerine. ...
Cited by 1 - Related articles - All 2 versions

A case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years

VFML Ramos… - Age and Ageing, 2011 - Br Geriatrics Soc
... retrospective review of 107 cases. FSHD is also known as Landouzy-Dejerine muscular
dystrophy, as first described by Louis Theophile Joseph Landouzy and Joseph Jules
Dejerine in 1885 [2–4]. Clinical features include progression ...

[HTML] Alexia without Agraphia

[HTML] from imj.ieE Mulroy, S Murphy… - Instructions for Authors, 2011 - imj.ie
... Déjerine in 1892 reported a patient who developed this syndrome after an infarct of the
left occipital lobe and splenium of the corpus callosum. ... Brain Lang 1974; 1:215-26. 7.
Dejerine J. Sur un cas de cécité verbale avec agraphie, suivi d'autopsie. ...
Related articles - Cached - All 3 versions

A Case of Thalamic Pain Successfully Treated with Kampo Medicine

K Ueda, T Namiki, Y Kasahara… - The Journal of …, 2011 - liebertonline.com
... T halamic pain, one of the symptoms of Déjerine-Roussy syndrome 1,2 and included in the
concept of central post-stroke pain, is an unrelenting and often intolerable pain. ... In addition,
these symptoms were diagnosed as Déjerine-Roussy syndrome. 1,2. ...
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Vaginal allodynia as the presentation of a thalamic tumor

DL Silbergeld, AO Hebb… - Pain, 2011 - Elsevier
... Article | PDF (195 K) | View Record in Scopus | Cited By in Scopus (5). [6] J. Cambier,
Dejerine–Roussy syndrome, Rev Neurol (Paris) 138 (1982), pp. 979–988. View Record in Scopus |
Cited By in Scopus (3). [7] S. Canavero and V. Bonicalzi, Bilaterality of central pain. ...
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The Experience of Pain and the Putamen: A New Link Found With Functional MRI and Diffusion Tensor Imaging

ND Tomycz… - Neurosurgery, 2011 - journals.lww.com
... Although neurosurgeons are well aware of chronic pain syndromes following stroke (most
notably the Dejerine-Roussy syndrome following thalamic stroke), it is not common to think
of decreased pain sensitivity following small basal ganglia strokes. ...

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome

V Bonadona, B Bonaïti, S Olschwang… - JAMA: The Journal of …, 2011 - Am Med Assoc
... Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch
Syndrome. ... CHU) Toulouse (Dr Guimbaud), Toulouse; CHU, Nantes (Dr Buecher); Centre Jean
Perrin, Clermont-Ferrand (Dr Bignon); Institut Gustave Roussy, Villejuif (Dr Caron ...
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METHOD FOR DETERMINING A PREDISPOSITION TO BASAL CELL CARCINOMA AND FOR SCREENING TREATMENTS THEREOF

A Valin… - US Patent 20,110,136,685, 2011 - freepatentsonline.com
... INSTITUT GUSTAVE ROUSSY (VILLEJUIF CEDEX, FR) CENTRE NATIONAL DE LA
RECHERCHE SCIENTIFIQUE (PARIS, FR) UNIVERSITE PARIS DIDEROT ... under-expressed
in a human subject having a predisposition to nevoid basal cell carcinoma syndrome (NBCCS) ...
Cached

Déjerine‐Sottas syndrome with a silent nucleotide change of myelin protein zero gene

F Taioli, I Cabrini, T Cavallaro… - Journal of the …, 2011 - Wiley Online Library
Charcot-Marie-Tooth disease type 1B (CMT1B) and Déjerine-Sottas syndrome type B
(DSSB) are caused by missense or frameshift mutations of myelin protein zero (MPZ) gene. We
identified an apparently silent synonymous c.411C>T transition in MPZ exon 3 ...
Related articles - All 2 versions

The identification of Landouzy-Dejerine disease: An investigative history.

M Jacqueline - Neuromuscular disorders: NMD, 2011 - ncbi.nlm.nih.gov
1. Neuromuscul Disord. 2011 Feb 11. [Epub ahead of print] The identification of
Landouzy-Dejerine disease: An investigative history. Jacqueline M. Paris 7, Denis Diderot
University, Paris, France. PMID: 21316966 [PubMed - as supplied by publisher].
Related articles - All 3 versions

The Impossible Succession of Charcot–The Quest for a Suitable Heir

L Tatu… - European Neurology, 2011 - content.karger.com
... There were a number of potential successors, but only three were officially declared: Brissaud,
Jules Déjerine (1849–1917) and Fulgence Raymond (1844–1910). ... In 1917, at the age of 65,
Pierre Marie would finally occupy Charcot's chair following the death of Déjerine. ...
Cited by 1 - Related articles - All 2 versions

A case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years

VFML Ramos… - Age and Ageing, 2011 - Br Geriatrics Soc
... retrospective review of 107 cases. FSHD is also known as Landouzy-Dejerine muscular
dystrophy, as first described by Louis Theophile Joseph Landouzy and Joseph Jules
Dejerine in 1885 [2–4]. Clinical features include progression ...

[HTML] Alexia without Agraphia

[HTML] from imj.ieE Mulroy, S Murphy… - Instructions for Authors, 2011 - imj.ie
... Déjerine in 1892 reported a patient who developed this syndrome after an infarct of the
left occipital lobe and splenium of the corpus callosum. ... Brain Lang 1974; 1:215-26. 7.
Dejerine J. Sur un cas de cécité verbale avec agraphie, suivi d'autopsie. ...
Related articles - Cached - All 3 versions

T cell responses to gangliosides in patients with inflammatory neuropathy

PA McCombe, AA Sullivan… - Xth International …, 2011 - espace.library.uq.edu.au
skip nav. ...
Cached

Molecular diagnosis and clinical onset of Charcot–Marie–Tooth disease in Japan

A Abe, C Numakura, K Kijima, M Hayashi… - Journal of human …, 2011 - nature.com
... Novel mutations of the peripheral myelin protein 22 gene in two pedigrees with Dejerine-Sottas
disease. Hum. ... De novo mutation of the myelin Po gene in Dejerine-Sottas disease (hereditary
motor and sensory neuropathy type III): two amino acid insertion after Asp 118. Hum. ...
Related articles - All 4 versions

The Homozygous Ganglioside-Induced Differentiation-Associated Protein 1 Mutation c. 373C> T Causes a Very Early-Onset Neuropathy: Case Report and Literature …

C Fusco, V Ucchino, G Barbon… - Journal of Child …, 2011 - jcn.sagepub.com
... criteria; the type 1 demyelinating form is characterized by slow motor median nerve conduction
velocities (less than 38 m/s), whereas the type 2 axonal form displays a normal or slightly reduced
nerve conduction velocity.3 Dejerine-Sottas disease and congenital hypomyeli ...
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Charcot-Marie-Tooth disease: a review with emphasis on the pathophysiology of pes cavus

J Berciano, E Gallardo, A García… - Revista Española de …, 2011 - Elsevier
... Revisamos el diagnóstico y tratamiento de la enfermedad. Keywords: Axon; Charcot-Marie-
Tooth disease; Dejerine-Sottas disease; Gene mutation; Genetic neuropathy; Pes cavus;
Magnetic resonance; Myelin; Nerve conduction velocity; Vitamin C. ...
All 2 versions

Genetic spectrum of hereditary neuropathies with onset in the first year of life

J Baets, T Deconinck, E De Vriendt, M Zimoń… - Brain, 2011 - Oxford Univ Press
... Hereditary motor and sensory neuropathies with onset in infancy are rare disorders that were
first described by Dejerine and Sottas, 1893 in the late 19th century as a separate disease, distinct
from the more commonly occurring Charcot–Marie–Tooth neuropathy (Gabreels ...

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[HTML] Alexia without Agraphia

[HTML] Alexia without Agraphia

[HTML] Alexia without Agraphia