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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

270 related items for PubMed ID: 18348718

  • 21.
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  • 22. Hereditary sensory autonomic neuropathy type II: Report of two novel mutations in the FAM134B gene.
    Falcão de Campos C, Vidailhet M, Toutain A, de Becdelièvre A, Funalot B, Bonello-Palot N, Stojkovic T.
    J Peripher Nerv Syst; 2019 Dec; 24(4):354-358. PubMed ID: 31596031
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  • 26. Hereditary sensory and autonomic neuropathies: types II, III, and IV.
    Axelrod FB, Gold-von Simson G.
    Orphanet J Rare Dis; 2007 Oct 03; 2():39. PubMed ID: 17915006
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  • 27. Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness.
    Dubourg O, Barhoumi C, Azzedine H, Birouk N, Brice A, Bouche P, Leguern E.
    Muscle Nerve; 2000 Oct 03; 23(10):1508-14. PubMed ID: 11003785
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  • 28. Hereditary sensory and autonomic neuropathy type I in a Chinese family: British C133W mutation exists in the Chinese.
    Bi H, Gao Y, Yao S, Dong M, Headley AP, Yuan Y.
    Neuropathology; 2007 Oct 03; 27(5):429-33. PubMed ID: 18018475
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  • 31. [Hereditary sensory and autonomic neuropathy type II A: early neurological and skeletal findings].
    Esmer C, Díaz Zambrano S, Santos Díaz MA, González Huerta LM, Cuevas Covarrubias SA, Bravo Oro A.
    An Pediatr (Barc); 2014 Apr 03; 80(4):254-8. PubMed ID: 23831200
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  • 32. Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings.
    Lindahl AJ, Lhatoo SD, Campbell MJ, Nicholson G, Love S.
    Clin Neurol Neurosurg; 2006 Dec 03; 108(8):780-3. PubMed ID: 16271825
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  • 35. Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1-->q22.3: exclusion of GAS1 and XPA.
    Blair IP, Dawkins JL, Nicholson GA.
    Cytogenet Cell Genet; 1997 Dec 03; 78(2):140-4. PubMed ID: 9371409
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  • 36. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.
    Bellone E, Rodolico C, Toscano A, Di Maria E, Cassandrini D, Pizzuti A, Pigullo S, Mazzeo A, Macaione V, Girlanda P, Vita G, Ajmar F, Mandich P.
    Neuromuscul Disord; 2002 Mar 03; 12(3):286-91. PubMed ID: 11801401
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  • 38. Spectrum of SPTLC1-related disorders: a novel case of 'Ser331 syndrome' that expand the phenotype of hereditary sensory and autonomic neuropathy type 1A and motor neuron diseases.
    Lorenzoni PJ, Bayer DL, Ducci RD, Fustes OJH, do Vale Pascoal Rodrigues PR, Werneck LC, Kay CSK, Scola RH.
    Neurol Sci; 2023 Jul 03; 44(7):2551-2554. PubMed ID: 36964315
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  • 39. Hereditary sensory and autonomic neuropathy type IC accompanied by upper motor neuron abnormalities and type II juxtafoveal retinal telangiectasias.
    Triplett J, Nicholson G, Sue C, Hornemann T, Yiannikas C.
    J Peripher Nerv Syst; 2019 Jun 03; 24(2):224-229. PubMed ID: 30866134
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