Search Results 81-90 of 16807 for ataxia

  1. Clinical Trials - Mayo Clinic Research

    ... Ataxia (+) Epicatechin to Treat Friedreich's Ataxia NCT ID: NCT02660112 POC ID: CLS-20258268; Title: Effects of N-Acetyl-L-Leucine on Niemann-Pick Disease ...

  2. Publications - Vanessa V. Marin Collazo, M.D. - Mayo Clinic

    Dominguez L, Collazo IVM, Sechi E, Bohm P, Chiriboga SL. Neurochondrin immunoglobulin G - Associated myelopathy - Ataxia syndrome. J Neurol Sci. 2022 Jan 15; ...

  3. The Influence of SSRI’s in Multiple System Atrophy - Mayo Clinic

    ... ataxia, parkinsonism, or parkinsonian features and autonomic dysfunction on coding or final diagnosis. This project does not involve experimentation of ...

  4. Neurology - Clinical trials

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  5. Neurology - Clinical trials

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  6. Publications - Jaimin S. Shah, M.D. - Mayo Clinic

    ... ataxia type 3. Parkinsonism Relat Disord. 2021 Aug; 89:151-154 Epub 2021 July 17. View PubMed; Oskarsson B, Mauricio EA, Shah JS, Li Z, Rogawski MA. Cortical ...

  7. Neurology - Clinical trials

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  8. Neurology - Clinical trials

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  9. Publications - Karthik Muthusamy, M.B.B.S. - Mayo Clinic

    Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinent. Eur J Med Genet. 2023 Jun; 66 (6):104766 ...

  10. Neurosciences Clinical Trials - Medical Professionals

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...