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Peripheral myelin protein

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2010
01219952010

Related topics

Related topics

1 relation
MPZ gene

Related mentions per year

Related mentions per year

1947-2018
19401960198020002020
Peripheral myelin protein
MPZ gene

Papers overview

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2010
2010
Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A.
We have previously shown that in two distinct models for inherited neuropathies of the Charcot-Marie-Tooth (CMT) type, T… (More)
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2008
2008
A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome
JO N 2896 A 58-year-old man (Case 1) presented with progressive gait unsteadiness since age 8. Examination showed scoliosis, pes… (More)
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2002
2002
Decreased GFAP-mRNA expression in spinal cord of cobalamin-deficient rats.
We have demonstrated previously that chronic vitamin B12 [cobalamin (Cbl)] deficiency preferentially affects glial cells in the… (More)
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2000
2000
Small axons relative to number of myelin lamellae in Charcot-Marie-Tooth disease 1A with peripheral myelin protein 22 gene duplication.
In myelinated fibers of the sural nerves in Charcot-Marie-Tooth disease 1A (CMT 1A), with peripheral myelin protein (PMP) 22 gene… (More)
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1999
1999
Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice.
Peripheral nerves of P0-deficient (P0(-)) mice show a severe dysmyelination and altered expression of several cell surface… (More)
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1999
1999
[A family of hereditary neuropathy with liability to pressure palsies with a proband who developed right and left foot drop successively following the left radial nerve palsy].
A 41-year-old man developed multifocal mononeuropathies manifesting right and left foot drop successively, following the left… (More)
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1997
1997
Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy.
Hereditary neuropathy with liability to pressure palsy (HNPP) is associated with a heterozygous 1.5 megabase deletion on… (More)
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Review
1997
Review
1997
Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules.
Several glia-associated cell surface molecules have been implicated in myelin formation in the central (CNS) and peripheral… (More)
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1995
1995
[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation].
A 16-year-old school boy suffered from an insidious foot deformity. Slight degrees of symmetrical muscular weakness of the distal… (More)
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