Coexistent Charcot-Marie-Tooth type 1A and type 2 diabetes mellitus neuropathies in a Chinese family

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A case report of hereditary neuropathy with liability to pressure palsies accompanied by type 2 diabetes mellitus and psoriasis

P2860

Q41881301-E0AE26D4-E3C3-44B0-BD00-B24AEE664C8D

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Coexistent Charcot-Marie-Tooth type 1A and type 2 diabetes mellitus neuropathies in a Chinese family

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

@zh-hans

2015年学术文章

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2015年学术文章

@zh-sg

2015年學術文章

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2015年學術文章

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2015年學術文章

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name

Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

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Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

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Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

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Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

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Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

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Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

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P1476

Coexistent Charcot-Marie-Tooth ...... uropathies in a Chinese family

@en

P2093

A-Ping Sun

http://www.w3.org/2001/XMLSchema#string

Hui Zhang

http://www.w3.org/2001/XMLSchema#string

Lu Tang

http://www.w3.org/2001/XMLSchema#string

Qin Liao

http://www.w3.org/2001/XMLSchema#string

Ying-Shuang Zhang

http://www.w3.org/2001/XMLSchema#string

P2860

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromes.

Pathological mechanisms involved in diabetic neuropathy: can we slow the process?

Endoneurial microvascular pathology in feline diabetic neuropathy.

Marked improvement of glycaemic control with pioglitazone in a Type 2 diabetic patient associated with Charcot-Marie-Tooth disease.

The phenotypic manifestations of chromosome 17p11.2 duplication.

Combination of myotonic dystrophy and hereditary motor and sensory neuropathy.

Genetic epidemiology of Charcot-Marie-Tooth in the general population.

Diabetes mellitus exacerbates motor and sensory impairment in CMT1A.

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study

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1696-1699

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scholarly article

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10.4103/1673-5374.167771

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P407

English

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P478

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Jun Zhang

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2015-10-01T00:00:00Z

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26692872

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P921

type-2 diabetes

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4660768

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Coexistent Charcot-Marie-Tooth type 1A and type 2 diabetes mellitus neuropathies in a Chinese family

about

P2860

P2860

Coexistent Charcot-Marie-Tooth type 1A and type 2 diabetes mellitus neuropathies in a Chinese family

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932