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Results 71 - 80 of 81 for Miller syndrome
  1. Amyotrophic lateral sclerosis 
    ... PubMed McGeer PL, Steele JC. The ALS/PDC syndrome of Guam: ... G, de Belleroche J, Gallo JM, Miller CC, Shaw CE. Mutations in FUS, an RNA ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  2. Chromosome 16 
    ... Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome: an ... JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  3. ATP1A3 gene 
    ... the variant causes the specific features of CAPOS syndrome. ... KJ, Suerken CK, Cook JF, Ozelius LJ, Miller C, McCall WV, Whitlow CT, Brashear A. Revising ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  4. Adolescent idiopathic scoliosis 
    ... of other conditions, including a variety of genetic syndromes. However, adolescent idiopathic scoliosis ... on PubMed Miller NH. Idiopathic scoliosis: cracking the genetic code and ...
    https://medlineplus.gov/.../adolescent-idiopathic-scoliosis - Genetics
  5. OPA1 gene 
    ... Amati-Bonneau P, Reynier P. Early-onset Behr syndrome due to compound ... Tallaksen CM, Duffey P, Miller J, Whittaker RG, Baker MR, Jackson MJ, Clarke ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  6. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... of bone Pagetoid amyotrophic lateral sclerosis Pagetoid neuroskeletal syndrome ... MA, Shanks CA, Gregg G, Al-Lozi MT, Miller T, Rakowicz W, Lopate G, Florence J, Glosser ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  7. Very long-chain acyl-CoA dehydrogenase deficiency 
    ... chicken pox or flu. Most cases of Reye syndrome occur in children who take aspirin during these viral ... Mar 26. Citation on PubMed Miller MJ, Burrage LC, Gibson JB, Strenk ME, Lose ...
    https://medlineplus.gov/...g-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  8. Facioscapulohumeral muscular dystrophy 
    Facioscapulohumeral muscular dystrophy is a disorder characterized by muscle weakness and wasting (atrophy). This condition gets its name from the muscles that are affected ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  9. GRN-related frontotemporal lobar degeneration 
    ... develop movement disorders, such as parkinsonism and corticobasal syndrome. The signs and ... C, Mackenzie I, Mendez MF, Miller BL, Onyike C, Pantelyat A, Pearlman R, Petrucelli ...
    https://medlineplus.gov/...related-frontotemporal-lobar-degeneration - Genetics
  10. Fanconi anemia 
    ... People with Fanconi anemia may also develop myelodysplastic syndrome, a condition in which ... LM, Phelan R, Barbus C, Rayannavar A, Miller BS, Reardon EE, Theis-Mahon N, MacMillan ML. ...
    https://medlineplus.gov/genetics/condition/fanconi-anemia - Genetics
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