CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H

Known as: Charcot-Marie-Tooth Disease, Autosomal Recessive, Type 4H, Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4H, Charcot-Marie-Tooth Neuropathy, Type 4H 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2005-2017
01220052017

Papers overview

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2017
2017
Charcot-Marie-Tooth disease type 4H (CMT4H) is a rare variant of autosomal recessive hereditary neuropathy. It is caused by FGD4… (More)
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2015
2015
Charcot-Marie-Tooth disease type 4H (CMT4H) is an autosomal recessive demyelinating subtype of peripheral enuropathies caused by… (More)
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2013
2013
Charcot-Marie-Tooth disease type 4H (CMT4H) is an autosomal recessive demyelinating neuropathy. It presents as infancy or early… (More)
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2012
2012
By sequencing of the FGD4 coding sequence in a cohort of 101 patients affected by autosomal recessive demyelinating Charcot-Marie… (More)
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2009
2009
BACKGROUND Autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4H (CMT4H) manifests early onset, severe… (More)
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2007
2007
Charcot-Marie-Tooth (CMT) disorders are a clinically and genetically heterogeneous group of hereditary motor and sensory… (More)
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2005
2005
A De Sandre-Giovannoli, V Delague, T Hamadouche, M Chaouch, M Krahn, I Boccaccio, T Maisonobe, E Chouery, R Jabbour, S Atweh, D… (More)
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2005