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Items: 1 to 20 of 21

1.
2.

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome.

Tyson J, Ellis D, Fairbrother U, King RH, Muntoni F, Jacobs J, Malcolm S, Harding AE, Thomas PK.

Brain. 1997 Jan;120 ( Pt 1):47-63.

PMID:
9055797
3.

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

LeGuern E, Guilbot A, Kessali M, Ravisé N, Tassin J, Maisonobe T, Grid D, Brice A.

Hum Mol Genet. 1996 Oct;5(10):1685-8.

PMID:
8894708
5.

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

Kalaydjieva L, Hallmayer J, Chandler D, Savov A, Nikolova A, Angelicheva D, King RH, Ishpekova B, Honeyman K, Calafell F, Shmarov A, Petrova J, Turnev I, Hristova A, Moskov M, Stancheva S, Petkova I, Bittles AH, Georgieva V, Middleton L, Thomas PK.

Nat Genet. 1996 Oct;14(2):214-7.

PMID:
8841199
6.

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

Bolino A, Brancolini V, Bono F, Bruni A, Gambardella A, Romeo G, Quattrone A, Devoto M.

Hum Mol Genet. 1996 Jul;5(7):1051-4.

PMID:
8817346
7.

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

Quattrone A, Gambardella A, Bono F, Aguglia U, Bolino A, Bruni AC, Montesi MP, Oliveri RL, Sabatelli M, Tamburrini O, Valentino P, Van Broeckhoven C, Zappia M.

Neurology. 1996 May;46(5):1318-24.

PMID:
8628474
8.

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1.

Mariman EC, Gabreëls-Festen AA, van Beersum SE, Jongen PJ, Ropers HH, Gabreëls FJ.

Hum Genet. 1993 Aug;92(1):87-90.

PMID:
8396068
9.

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

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM.

Hum Mol Genet. 1993 Oct;2(10):1625-8.

PMID:
8268915
10.

The status of HMSN type III.

Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.

Neuromuscul Disord. 1994 Jan;4(1):63-9.

PMID:
8173353
11.

Autosomal recessive forms of hereditary motor and sensory neuropathy.

Harding AE, Thomas PK.

J Neurol Neurosurg Psychiatry. 1980 Aug;43(8):669-78.

12.

Hereditary motor and sensory neuropathies in Swedish children. III. De- and remyelinating type in 10 sporadic cases.

Hagberg B, Westerberg B, Hagne I, Selldén U.

Acta Paediatr Scand. 1983 Jul;72(4):537-44.

PMID:
6578668
14.

Charcot-Marie-Tooth disease associated with hypertrophic neuropathy: a neuropathologic study of two cases.

Smith TW, Bhawan J, Keller RB, DeGirolami U.

J Neuropathol Exp Neurol. 1980 Jul;39(4):420-40.

PMID:
6260904
15.

Spinocerebellar ataxia with neural myatrophy.

Hopf HC, Volles E.

Neuropadiatrie. 1971 Jul;3(1):97-105. No abstract available.

PMID:
5170970
16.

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

Joosten E, Gabreëls F, Gabrèèls-Festen A, Vrensen G, Korten J, Notermans S.

Acta Neuropathol. 1974 Feb 28;27(2):105-18. No abstract available.

PMID:
4152255
17.

Crossover counts and likelihood in multipoint linkage analysis.

Thompson EA.

IMA J Math Appl Med Biol. 1987;4(2):93-108.

PMID:
3503093
18.

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

Gal A, Mücke J, Theile H, Wieacker PF, Ropers HH, Wienker TF.

Hum Genet. 1985;70(1):38-42.

PMID:
2987105
19.

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding.

Ohnishi A, Murai Y, Ikeda M, Fujita T, Furuya H, Kuroiwa Y.

Muscle Nerve. 1989 Jul;12(7):568-75.

PMID:
2779605
20.

Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Stegeman DF, Vos AJ, Busch HF.

Brain. 1990 Dec;113 ( Pt 6):1629-43.

PMID:
2276038

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