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PUBMED FOR HANDHELDS

Journal Abstract Search

218 related items for PubMed ID: 29613898

  • 1. Hereditary Myelopathies.
    Hedera P.
    Continuum (Minneap Minn); 2018 Apr; 24(2, Spinal Cord Disorders):523-550. PubMed ID: 29613898
    [Abstract] [Full Text] [Related]

  • 2. Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation.
    Faruq M, Kumar D, Wadhwa S, Shamim U, Mathur A, Parveen S, Garg A, Srivastava AK.
    Clin Genet; 2019 Sep; 96(3):271-273. PubMed ID: 31286494
    [No Abstract] [Full Text] [Related]

  • 3. Subtle Imaging Findings Aid the Diagnosis of Adolescent Hereditary Spastic Paraplegia and Ataxia.
    Wagner F, Titelbaum DS, Engisch R, Coskun EK, Waugh JL.
    Clin Neuroradiol; 2019 Jun; 29(2):215-221. PubMed ID: 29379980
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  • 4. Two cases of early-onset autosomal recessive spastic ataxia of Charlevoix-Saguenay diagnosed in adulthood.
    Sahin T, Karaarslan FT, Yilmaz R, Tekgül Ş, Başak AN, Akbostanci MC.
    Clin Neurol Neurosurg; 2021 Feb; 201():106423. PubMed ID: 33348119
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  • 11. Neurological Phenotypes Associated with AAAS-Related Disorders: Spastic Ataxia and Complex Spastic Paraplegia.
    Lorea CF, Tenório RB, Koenig M, Huebner A, Koehler K, Devos D, Guissart C, Saute JAM.
    Cerebellum; 2020 Jun; 19(3):465-468. PubMed ID: 32146693
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  • 16. Hereditary and metabolic myelopathies.
    Hedera P.
    Handb Clin Neurol; 2016 Jun; 136():769-85. PubMed ID: 27430441
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  • 18. Exome sequencing & homozygosity mapping for identification of genetic aetiology for spastic ataxia in a consanguineous family.
    Dalal A, Bhowmik AD, Agarwal D, Phadke SR.
    Indian J Med Res; 2015 Aug; 142(2):220-4. PubMed ID: 26354221
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  • 19. Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1.
    Bettencourt C, de Yébenes JG, López-Sendón JL, Shomroni O, Zhang X, Qian SB, Bakker IM, Heetveld S, Ros R, Quintáns B, Sobrido MJ, Bevova MR, Jain S, Bugiani M, Heutink P, Rizzu P.
    Cerebellum; 2015 Jun; 14(3):378-81. PubMed ID: 25592071
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  • 20. CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia.
    Shetty A, Gan-Or Z, Ashtiani S, Ruskey JA, van de Warrenburg B, Wassenberg T, Kamsteeg EJ, Rouleau GA, Suchowersky O.
    Eur J Med Genet; 2019 Dec; 62(12):103605. PubMed ID: 30572172
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