(Q35489565)

8 August 2017

title

Age associated axonal features in HNPP with 17p11.2 deletion in Japan (English)

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8 August 2017

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Koike H

1

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8 August 2017

Hirayama M

2

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8 August 2017

Yamamoto M

3

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8 August 2017

Ito H

4

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8 August 2017

Hattori N

5

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8 August 2017

Umehara F

6

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8 August 2017

Arimura K

7

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8 August 2017

Ikeda S

8

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8 August 2017

Ando Y

9

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8 August 2017

Nakazato M

10

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8 August 2017

Kaji R

11

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8 August 2017

Hayasaka K

12

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8 August 2017

Nakagawa M

13

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8 August 2017

Sakoda S

14

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8 August 2017

Matsumura K

15

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8 August 2017

Onodera O

16

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8 August 2017

Baba M

17

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8 August 2017

Yasuda H

18

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8 August 2017

Saito T

19

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8 August 2017

Kira J

20

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8 August 2017

Nakashima K

21

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8 August 2017

Oka N

22

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8 August 2017

Sobue G

23

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8 August 2017

language of work or name

English

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publication date

1 August 2005

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Journal of Neurology, Neurosurgery and Psychiatry

8 August 2017

published in

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8 August 2017

volume

76

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8 August 2017

issue

8

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8 August 2017

page(s)

1109-1114

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A STUDY OF NORMAL NERVE ACTION POTENTIALS USING AN AVERAGING TECHNIQUE (BARRIER GRID STORAGE TUBE).

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Electrodiagnostic features of hereditary neuropathy with liability to pressure palsies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Clinicopathological features of Churg-Strauss syndrome-associated neuropathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Relation between size of compound sensory or muscle action potentials, and length of nerve segment

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

A computer simulation of conduction block: effects produced by actual block versus interphase cancellation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Hereditary pressure-sensitive neuropathy: demonstration of “tomacula” in motor nerve fibers

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Alcoholic neuropathy is clinicopathologically distinct from thiamine-deficiency neuropathy.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739771

Family with inflammatory demyelinating polyneuropathy and the HNPP 17p12 deletion

7 December 2018

1 reference

12 December 2020

Deletions of chromosome 17p11.2 in multifocal neuropathies

1 reference

12 December 2020

Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeat

1 reference

12 December 2020

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells

1 reference

12 December 2020

X-linked recessive bulbospinal neuronopathy. A clinicopathological study

1 reference

12 December 2020

HEREDITARY NEUROPATHY, WITH LIABILITY TO PRESSURE PALSIES; A CLINICAL AND ELECTROPHYSIOLOGICAL STUDY OF FOUR FAMILIES

1 reference

12 December 2020

Expression of nerve growth factor receptor in human peripheral neuropathies

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary neuropathy with liability to pressure palsy: the electrophysiology fits the name

1 reference

12 December 2020

Effects of PMP22 duplication and deletions on the axonal cytoskeleton

1 reference

12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Recurrent peripheral nerve palsies in a family

1 reference

12 December 2020

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

1 reference

12 December 2020

The carpal tunnel syndrome: localization of conduction abnormalities within the distal segment of the median nerve

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.2004.048140

1 reference

8 August 2017

1 reference

8 August 2017

1 reference