Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies. (Q34341671)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11513338%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

review article

1 reference

title

Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11513338%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

T J Benstead

1

1 reference

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10 November 2019

I A Grant

series ordinal

2

1 reference

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10 November 2019

publication date

1 August 2001

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Canadian Journal of Neurological Sciences

10 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11513338%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

28

1 reference

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10 November 2019

issue

3

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10 November 2019

page(s)

199-214

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Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Human nerve pathology caused by different mutational mechanisms of the PMP22 gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A distinct pattern of trophic factor expression in myelin-deficient nerves of Trembler mice: implications for trophic support by Schwann cells

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Regulation of myelin-specific gene expression. Relevance to CMT1.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary neuropathy with liability to pressure palsies: a clinical, electroneurophysiological and morphological study

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Autosomal recessive forms of hereditary motor and sensory neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Ultrastructural PMP22 expression in inherited demyelinating neuropathies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

THE HYPERTROPHIC FORMS OF HEREDITARY MOTOR AND SENSORY NEUROPATHY

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Charcot-Marie-Tooth disease in northern Sweden: an epidemiological and clinical study

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Clinical and electrophysiological phenotype of a homozygously duplicated Charcot-Marie-Tooth (type 1A) disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Long-lasting conduction block in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Connexin32-null mice develop demyelinating peripheral neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Early onset cerebellar ataxia with retained tendon reflexes: foot deformity in a first grade family member

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Connexin32 is a myelin-related protein in the PNS and CNS

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The electrophysiologic profile of Dejerine-Sottas disease (HMSN III)

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Penetrance of the hereditary motor and sensory neuropathy Ia mutation: assessment by nerve conduction studies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Decreased axon caliber and neurofilaments in hereditary motor and sensory neuropathy, type I

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Deletions of chromosome 17p11.2 in multifocal neuropathies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Prevalence of hereditary motor and sensory neuropathy in Cantabria

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The phenotypic manifestations of chromosome 17p11.2 duplication

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Demyelinating X-linked Charcot-Marie-Tooth disease: unusual electrophysiological findings

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Role of myelin Po protein as a homophilic adhesion molecule

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Electron-microscopic heterogeneity of onion-bulb neuropathies of the Déjerine-Sottas type. Two patients in one family with the variant described by Lyon (1969).

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Longitudinal studies of the duplication form of Charcot-Marie-Tooth polyneuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Physiological tremor analysis of patients with anti-myelin-associated glycoprotein associated neuropathy and tremor

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary motor and sensory neuropathy with myelin outfolding: Clinical, genetic and neuropathological study of three cases

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Abnormalities in the axonal cytoskeleton induced by a connexin32 mutation in nerve xenografts

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A Novel Mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1)

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The peripheral myelin protein 22 and epithelial membrane protein family

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Ultrastructural study of a nerve biopsy from a case of early infantile chronic neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Homozygous expression of a dominant gene for charcot-marie-tooth neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

X-linked dominant hereditary motor and sensory neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The Roussy-Lévy family: from the original description to the gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Autosomal recessive hypermyelinating neuropathy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Electrodiagnostic findings in CMTX: a disorder of the Schwann cell and peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1).

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Thin axons relative to myelin spiral length in hereditary motor and sensory neuropathy, type I

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Tomaculous neuropathy: a clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p11.2.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

A case of congenital hypomyelination neuropathy. Clinical, morphological, and chemical studies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding in two siblings

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Uncompacted inner myelin lamellae in inherited tendency to pressure palsy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The status of HMSN type III.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Effects of PMP22 duplication and deletions on the axonal cytoskeleton

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Electrodiagnostic features of hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Recurrent polyradiculoneuropathy with the 17p11.2 deletion.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Tremor as a feature of chronic relapsing and dysgammaglobulinemic polyneuropathies. Incidence and management

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Genotype/Phenotype Correlations in X-Linked Dominant Charcot-Marie-Tooth Disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100001347

7 January 2021

10.1017/S0317167100001347

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11513338%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference