CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F

Known as: CMT 2F, Charcot-Marie-Tooth disease, neuronal, Type 2F, Cmt2f 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2016
02420042016

Papers overview

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2017
2017
Heat shock protein beta-1 (HSPB1), is a ubiquitously expressed, multifunctional protein chaperone. Mutations in HSPB1 result in… (More)
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2016
2016
BACKGROUND Charcot-Marie-Tooth (CMT) and associated neuropathies, the most common inherited diseases of the peripheral nervous… (More)
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Review
2016
Review
2016
To date, there is no approved pharmacologic treatment for any form of Charcot-Marie-Tooth disease (CMT). However, some clinical… (More)
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2016
2016
The Charcot-Marie-Tooth disease 2F (CMT2F) and distal hereditary motor neuropathy 2B (dHMN2B) are caused by autosomal dominantly… (More)
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2014
2014
Charcot–Marie–Tooth disease (CMT) is a group of clinically and genetically heterogeneous peripheral neuropathies. We identified… (More)
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2013
2013
OBJECTIVE Preimplantation genetic diagnosis (PGD) is an assisted reproductive technique for couples carrying genetic risks… (More)
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2013
2013
Mutations in the small heat shock protein HSPB1 (HSP27) are a cause of axonal Charcot–Marie–Tooth neuropathy (CMT2F) and distal… (More)
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2012
2012
The small heat shock protein HSPB1 is a multifunctional, α-crystallin-based protein that has been shown to be neuroprotective in… (More)
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2011
2011
Researchers in Belgium have generated a mouse model of Charcot–Marie–Tooth disease (CMT), and have discovered that axonal… (More)
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2008
2008
Distal hereditary motor neuropathy (dHMN) is a heterogeneous disorder characterized by degeneration of motor nerves in the… (More)
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