371 related articles for article (PubMed ID: 18495953)
1. Late-onset hereditary axonal neuropathies.
Bennett CL; Lawson VH; Brickell KL; Isaacs K; Seltzer W; Lipe HP; Weiss MD; Carter GT; Flanigan KM; Chance PF; Bird TD
Neurology; 2008 Jul; 71(1):14-20. PubMed ID: 18495953
[TBL] [Abstract][Full Text] [Related]
2. Late-onset HMSN 2: further evidence of genetic heterogeneity.
Dyck PJ
Neurology; 2008 Jul; 71(1):9-10. PubMed ID: 18591500
[No Abstract] [Full Text] [Related]
3. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
4. Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.
Miltenberger-Miltenyi G; Janecke AR; Wanschitz JV; Timmerman V; Windpassinger C; Auer-Grumbach M; Löscher WN
Arch Neurol; 2007 Jul; 64(7):966-70. PubMed ID: 17620486
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.
Tang B; Liu X; Zhao G; Luo W; Xia K; Pan Q; Cai F; Hu Z; Zhang C; Chen B; Zhang F; Shen L; Zhang R; Jiang H
Arch Neurol; 2005 Aug; 62(8):1201-7. PubMed ID: 16087758
[TBL] [Abstract][Full Text] [Related]
6. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
[TBL] [Abstract][Full Text] [Related]
7. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
Pou Serradell A; Monells J; Téllez MJ; Fossas P; Löfgren A; Meuleman J; Timmerman V; De Jonghe P; Ceuterick C; Martin JJ
Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826
[TBL] [Abstract][Full Text] [Related]
8. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
Kobayashi S; Takuma H; Murayama S; Sakurai M; Kanazawa I
J Neurol Sci; 2007 Mar; 254(1-2):44-8. PubMed ID: 17258771
[TBL] [Abstract][Full Text] [Related]
9. Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies.
Sutton IJ; Mocroft AP; Lindley VH; Barber RM; Bryon RJ; Winer JB; MacDonald F
Neuromuscul Disord; 2004 Dec; 14(12):804-9. PubMed ID: 15564036
[TBL] [Abstract][Full Text] [Related]
10. Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy.
Passamonti L; Muglia M; Magariello A; Bellesi M; Conforti FL; Mazzei R; Patitucci A; Gabriele AL; Sprovieri T; Peluso G; Caracciolo M; Medici E; Logullo F; Provinciali L; Quattrone A
Neuromuscul Disord; 2004 Nov; 14(11):705-10. PubMed ID: 15482954
[TBL] [Abstract][Full Text] [Related]
11. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
Züchner S; De Jonghe P; Jordanova A; Claeys KG; Guergueltcheva V; Cherninkova S; Hamilton SR; Van Stavern G; Krajewski KM; Stajich J; Tournev I; Verhoeven K; Langerhorst CT; de Visser M; Baas F; Bird T; Timmerman V; Shy M; Vance JM
Ann Neurol; 2006 Feb; 59(2):276-81. PubMed ID: 16437557
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic clustering in MPZ mutations.
Shy ME; Jáni A; Krajewski K; Grandis M; Lewis RA; Li J; Shy RR; Balsamo J; Lilien J; Garbern JY; Kamholz J
Brain; 2004 Feb; 127(Pt 2):371-84. PubMed ID: 14711881
[TBL] [Abstract][Full Text] [Related]
13. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
Schüle R; Bonin M; Dürr A; Forlani S; Sperfeld AD; Klimpe S; Mueller JC; Seibel A; van de Warrenburg BP; Bauer P; Schöls L
Neurology; 2009 Jun; 72(22):1893-8. PubMed ID: 19357379
[TBL] [Abstract][Full Text] [Related]
14. Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
Sanahuja J; Franco E; Rojas-García R; Gallardo E; Combarros O; Begué R; Granés P; Illa I
Arch Neurol; 2005 Dec; 62(12):1911-4. PubMed ID: 16344349
[TBL] [Abstract][Full Text] [Related]
15. Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful neuropathy.
Burns TM; Phillips LH; Dimberg EL; Vaught BK; Klein CJ
Neuromuscul Disord; 2006 May; 16(5):308-10. PubMed ID: 16616847
[TBL] [Abstract][Full Text] [Related]
16. Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families.
Mazzeo A; Muglia M; Rodolico C; Toscano A; Patitucci A; Quattrone A; Messina C; Vita G
Acta Neurol Scand; 2008 Nov; 118(5):328-32. PubMed ID: 18422810
[TBL] [Abstract][Full Text] [Related]
17. Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3.
Berghoff C; Berghoff M; Leal A; Morera B; Barrantes R; Reis A; Neundörfer B; Rautenstrauss B; Del Valle G; Heuss D
Neuromuscul Disord; 2004 May; 14(5):301-6. PubMed ID: 15099588
[TBL] [Abstract][Full Text] [Related]
18. Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.
Li J; Ghandour K; Radovanovic D; Shy RR; Krajewski KM; Shy ME; Nicholson GA
Arch Neurol; 2007 Jul; 64(7):974-8. PubMed ID: 17620487
[TBL] [Abstract][Full Text] [Related]
19. Reliability and validity of the CMT neuropathy score as a measure of disability.
Shy ME; Blake J; Krajewski K; Fuerst DR; Laura M; Hahn AF; Li J; Lewis RA; Reilly M
Neurology; 2005 Apr; 64(7):1209-14. PubMed ID: 15824348
[TBL] [Abstract][Full Text] [Related]
20. Late-onset childhood occipital epilepsy (Gastaut type): a family study.
Grosso S; Vivarelli R; Gobbi G; Di Bartolo R; Berardi R; Balestri P
Eur J Paediatr Neurol; 2008 Sep; 12(5):421-6. PubMed ID: 18249143
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
