Charcot-Marie-Tooth disease, Type 4B1

Known as: Charcot-Marie-Tooth disease, Type 4B, CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B1, Charcot-Marie-Tooth Disease, Autosomal Recessive, With Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4b1 
 
National Institutes of Health

Papers overview

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2016
2016
Charcot-Marie-Tooth neuropathy type 4B1 (CMT4B1) disease is a rare subtype of CMT4 with reported association of facial weakness… (More)
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2014
2014
Design and development of a high power, wide-bandwidth W-band travelling wave tube (TWT) is presented in this paper. The design… (More)
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2013
2013
Charcot-Marie-Tooth type 4B1 (CMT4B1) is a rare autosomal recessive demyelinating neuropathy caused by mutation of the… (More)
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2007
2007
Charcot-Marie-Tooth (CMT) disease denotes a large group of genetically heterogeneous hereditary motor and sensory neuropathies… (More)
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2006
2006
A new 4-pole bandpass tiller design based on a folded-waveguide (FWG) resonator structure is presented. The filter uses an… (More)
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2005
2005
Charcot-Marie-Tooth disease (CMT) comprises a family of clinically and genetically very heterogeneous hereditary peripheral… (More)
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2004
2004
The authors report a Japanese family segregating autosomal recessive Charcot-Marie-Tooth disease (CMT) with focally folded myelin… (More)
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2003
2003
Charcot-Marie-Tooth disease type 4B1, CMT4B1, is a severe, autosomal-recessive, demyelinating peripheral neuropathy, due to… (More)
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2001
2001
The concept of Dejerine-Sottas disease, which corresponds to presumed recessive demyelinating neuropathies with onset in infancy… (More)
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1993
1993
Alternating purine and pyrimidine repeats (RY(i)) are an abundant source of polymorphism. The subset with long tandem repeats of… (More)
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