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Charcot-Marie-Tooth disease, Type 1D (disorder)

Known as: Charcot-Marie-Tooth Neuropathy, Type 1D, Hereditary motor and sensory neuropathy 1D, Charcot-Marie-Tooth disease, Type 1D 
 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal dominant inheritanceFootdrop

Broader (1)

Charcot-Marie-Tooth Disease

Papers overview

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Highly Cited
2012
Highly Cited
2012
BZS1, a B-box protein, promotes photomorphogenesis downstream of both brassinosteroid and light signaling pathways.
Photomorphogenesis is controlled by multiple signaling pathways, including the light and brassinosteroid (BR) pathways. BR… Expand
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Highly Cited
2010
Highly Cited
2010
Brassinosteroids control AtEXPA5 gene expression in Arabidopsis thaliana.
To elucidate the spatial and temporal roles of EXPANSIN A5 (AtEXPA5) in growth and development of Arabidopsis thaliana… Expand
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Highly Cited
2009
Highly Cited
2009
Alpha- to beta-(dmes)BiI(5) (dmes = dimethyl(2-ethylammonium)sulfonium dication): umbrella reversal of sulfonium in the solid state and short I...I interchain contacts--crystal structures, optical…
Syntheses, X-ray structural characterization, optical properties, and electronic structures of 1D metal(III) iodide hybrids… Expand
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Highly Cited
2008
Highly Cited
2008
Pre-SAT180, a simple and effective method for residual water suppression.
Water located outside the NMR detection coil experiences a reduced RF field intensity. This "faraway water" is known to be very… Expand
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2008
2008
Dynamics of paramagnetic metallofullerenes in carbon nanotube peapods.
We filled SWNTs with the paramagnetic fullerene Sc@C82 to form peapods. The interfullerene 1D packing distance measured using TEM… Expand
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2006
2006
Stability analysis for inverse heat conduction problems
In this paper, two matrix algebraic tools are provided for studying the solution-stabilities of inverse heat conduction problems… Expand
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2004
2004
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous group of disorders that involve the peripheral… Expand
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Review
2004
Review
2004
Genetic evaluation of inherited motor/sensory neuropathy.
  • P. Chance
  • Supplements to Clinical neurophysiology
  • 2004
    • Corpus ID: 21682844
Inherited disorders of peripheral nerves represent a common group of neurologic diseases. Charcot-Marie-Tooth neuropathy type 1… Expand
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2003
2003
Formation of a novel 1D supramolecule [HgCl2(ptz)]2.HgCl2 (ptz = phenothiazine): a new precursor to submicrometer Hg2Cl2 rods.
A novel supramolecule [HgCl(2)(ptz)](2).HgCl(2) (ptz = phenothiazine) with uncoordinated inorganic salt HgCl(2) presented in a 1D… Expand
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1999
1999
Immunochemical characterization and taxonomic evaluation of the O polysaccharides of the lipopolysaccharides of Pseudomonas syringae serogroup O1 strains.
The O polysaccharide (OPS) of the lipopolysaccharide (LPS) of Pseudomonas syringae pv. atrofaciens IMV 7836 and some other… Expand
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