(Q48166370)

9 February 2018

title

Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred. (English)

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9 February 2018

8

Keats B

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9 February 2018

author name string

Butinar D

1

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9 February 2018

Zidar J

2

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9 February 2018

Leonardis L

3

1 reference

9 February 2018

Popovic M

4

1 reference

9 February 2018

Kalaydjieva L

5

1 reference

9 February 2018

Angelicheva D

6

1 reference

9 February 2018

Sininger Y

7

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9 February 2018

Starr A

9

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9 February 2018

publication date

1 July 1999

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9 February 2018

published in

Annals of Neurology

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9 February 2018

volume

46

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9 February 2018

page(s)

36-44

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9 February 2018

issue

1

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9 February 2018

Absence of both auditory evoked potentials and auditory percepts dependent on timing cues

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

21 January 2018

1 reference

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Does type I afferent neuron dysfunction reveal itself through lack of efferent suppression?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

Hereditary motor and sensory neuropathy--Lom, a novel demyelinating neuropathy associated with deafness in gypsies. Clinical, electrophysiological and nerve biopsy findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

HMSNL in a 13-year-old Bulgarian girl

21 January 2018

1 reference

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Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 gene

21 January 2018

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

21 January 2018

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The phenotypic manifestations of chromosome 17p11.2 duplication.

21 January 2018

1 reference

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Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

Autosomal recessive forms of hereditary motor and sensory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199907%2946%3A1%3C36%3A%3AAID-ANA7%3E3.0.CO%3B2-J

10.1002/1531-8249(199907)46:1<36::AID-ANA7>3.0.CO;2-J

21 January 2018

Identifiers

DOI

1 reference

9 February 2018

PubMed ID

10401778

1 reference

9 February 2018