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Results 1 - 8 of 8 for "Leukodystrophy," "hypomyelination," 27
  1. ... subunit of Pol III, cause a rare hypomyelinating leukodystrophy. Am J Hum Genet. ... R. More than hypomyelination in Pol-III disorder. J Neuropathol Exp Neurol. ...
  2. ... subunit of Pol III, cause a rare hypomyelinating leukodystrophy. Am J Hum Genet. ... R. More than hypomyelination in Pol-III disorder. J Neuropathol Exp Neurol. ...
  3. ... hypogonadotropic hypogonadism (4H syndrome); tremor-ataxia with central hypomyelination (TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy ...
  4. ... R, Elroy-Stein O. Childhood ataxia with CNS hypomyelination/vanishing white matter disease--a common leukodystrophy caused by abnormal control of protein synthesis. Mol ...
  5. ... McDonough JA, Pleasure D. Ablating N-acetylaspartate prevents leukodystrophy in a Canavan disease model. Ann Neurol. 2015 May;77(5):884-8. doi: 10.1002/ana.24392. Epub 2015 Mar 27. Citation on PubMed Janson CG, McPhee SW, Francis ...
  6. ... particular, Pelizaeus-Merzbacher-like disease type 1 involves hypomyelination, which means that the nervous system has a reduced ability to form myelin. The signs and symptoms of this condition are very similar to another leukodystrophy called Pelizaeus-Merzbacher disease, but the two disorders ...
  7. Leukodystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Start Here ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... Leukodystrophy refers to genetic diseases that predominantly ...
  8. Adult Refsum disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Specifics ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... Leukodystrophy refers to genetic diseases that predominantly ...