Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome (Q28285809)

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R V Lebo

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G Rosoklija

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X S Ding

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R E Lovelace

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N Latov

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A P Hays

Demonstration of Fc gamma receptors on human peripheral nerve fibres

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language of work or name

English

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publication date

1994

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published in

Acta Neuropathologica

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volume

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issue

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page(s)

91-7

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cites work

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12 December 2020

Sex-linked recessive inheritance in Charcot-Marie-tooth disease with partial clinical manifestations in female carriers

1 reference

12 December 2020

Peripheral neuropathy associated with immunoglobulin disorders an immunological and ultrastructural study

1 reference

12 December 2020

Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13

1 reference

12 December 2020

Myelin Po‐protein, more than just a structural protein?

1 reference

12 December 2020

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding

1 reference

12 December 2020

Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy

1 reference

12 December 2020

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

1 reference

12 December 2020

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

1 reference

12 December 2020

Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients

1 reference

12 December 2020

Recurrent brachial plexus neuropathy

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12 December 2020

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region

1 reference

12 December 2020

Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects

1 reference

12 December 2020

A phorbol ester-sensitive kinase catalyzes the phosphorylation of P0 glycoprotein in myelin

1 reference

12 December 2020

Experimental allergic neuritis. Ultrastructure of serum-induced myelin aberrations in peripheral nervous system cultures

1 reference

12 December 2020

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

12 December 2020

Solubilization of human peripheral nerve Fc gamma receptors and purification of a functional 40 kDa receptor

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12 December 2020

Ehlers-Danlos in association with tomaculous neuropathy

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12 December 2020

Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein Po

1 reference

12 December 2020

Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.

1 reference

12 December 2020

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B

1 reference

12 December 2020

Developing Myelin in Human Peripheral Nerve

1 reference

12 December 2020

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Immunofluorescence study of patients with neuropathy and IgM M proteins

1 reference

12 December 2020

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

1 reference

12 December 2020

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

1 reference

12 December 2020

Tomaculous neuropathy presenting as acute recurrent polyneuropathy

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12 December 2020

Congenital hypo- and hypermyelination neuropathy. Two cases

1 reference

12 December 2020

Charcot-Marie-Tooth neuropathy related to chromosome 1.

1 reference

12 December 2020

Protein composition of myelin of the peripheral nervous system

1 reference

12 December 2020

X-linked neuropathy: gene localization with DNA probes

1 reference

12 December 2020

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17

1 reference

12 December 2020

Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

1 reference

12 December 2020

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A

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12 December 2020

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers

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12 December 2020

Globular neuropathy. A disorder of axons and Schwann cells

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12 December 2020

Characterization of HNK-1 bearing glycoproteins in human peripheral nerve myelin

1 reference

12 December 2020

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

1 reference

12 December 2020

Phosphorylation of P0Glycoprotein in Peripheral Nerve Myelin

1 reference

12 December 2020

Comparison of the N-linked oligosaccharide structures of the two major human myelin glycoproteins MAG and P0: assessment of the structures bearing the epitope for HNK-1 and human monoclonal immunoglobulin M found in demyelinating neuropathy

1 reference

12 December 2020

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

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12 December 2020

Multicolor fluorescence in situ hybridization and pulsed field electrophoresis dissect CMT1B gene region

1 reference

12 December 2020

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

12 December 2020

Isolation and analysis of the gene encoding peripheral myelin protein zero

1 reference

12 December 2020

The sural nerve of the human foetus: electron microscope observations and counts of axons

1 reference

12 December 2020

Role of myelin Po protein as a homophilic adhesion molecule

1 reference

12 December 2020

Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases

1 reference

12 December 2020

X-linked dominant charcot-marie-tooth neuropathy with 15 cases in a family genetic linkage study

1 reference

12 December 2020

Protein zero of peripheral nerve myelin: biosynthesis, membrane insertion, and evidence for homotypic interaction.

1 reference

12 December 2020

Comparison of the N-linked oligosaccharide structures of the two major human myelin glycoproteins MAG and P0: assessment and relative occurrence of oligosaccharide structures by serial lectin affinity chromatography of 14C-glycopeptides

1 reference

12 December 2020

[Hypermyelination in a case of peripheral neuropathy with benign IgM monoclonal gammopathy]

1 reference

12 December 2020

An ultrastructural study of experimental demyelination and remyelination. II. Chronic experimental allergic encephalomyelitis in the peripheral nervous system

1 reference

12 December 2020

Evidence for linkage of type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1

1 reference

12 December 2020