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Results 1 - 10 of 596 for Neurol
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  1. Lennox-Gastaut syndrome 
    ... on diagnosis, assessment, management, and trial methodology. Lancet Neurol. 2009 Jan;8(1):82-93. doi: 10. ... Lennox-Gastaut syndrome and infantile spasms. J Child Neurol. 2010 Apr;25(4):441-7. doi: 10. ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  2. NF1 gene 
    ... Recent advances in neurofibromatosis type 1. Curr Opin Neurol. 2004 Apr;17(2):101-5. doi: 10. ... role of tumor suppressor mutations. J Neuropathol Exp Neurol. 2004 Nov;63(11):1115-23. doi: 10. ...
    https://medlineplus.gov/genetics/gene/nf1 - Genetics
  3. Charcot-Marie-Tooth disease 
    ... with Charcot-Marie-Tooth disease. Ann Clin Transl Neurol. 2022 Jul;9(7):902-911. doi: 10. ... disease: an electrophysiological reappraisal and systematic review. J Neurol. 2017 Aug;264(8):1655-1677. doi: 10. ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  4. Mitochondrial DNA 
    ... phenotypes of the mitochondrial DNA A3243G mutation. Arch Neurol. 2001 Nov;58(11):1885-8. doi: 10. ... the molecular diagnosis of mitochondrial disorders. Eur J Neurol. 2009 Dec;16(12):1255-64. doi: 10. ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  5. SNCA gene 
    ... Synuclein and Parkinsonism: Updates and Future Perspectives. Curr Neurol Neurosci Rep. 2017 Apr;17(4):31. doi: ... with increased risk for multiple system atrophy. Ann Neurol. 2009 May;65(5):610-4. doi: 10. ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  6. Prion disease 
    ... Mastrianni JA. The prion diseases. J Geriatr Psychiatry Neurol. 2010 Dec;23(4):277-98. doi: 10. ... Human prion diseases: molecular and clinical aspects. Arch Neurol. 2005 Apr;62(4):545-52. doi: 10. ...
    https://medlineplus.gov/genetics/condition/prion-disease - Genetics
  7. Fatty acid hydroxylase-associated neurodegeneration 
    ... Genetics of neurodegeneration with brain iron accumulation. Curr Neurol Neurosci Rep. 2011 Jun;11(3):254-61. ... P. Neurodegeneration with brain iron accumulation. Handb Clin Neurol. 2018;147:293-305. doi: 10.1016/B978- ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  8. CDKL5 deficiency disorder 
    ... Improving our understanding of a rare neurologic disorder. Neurol Genet. 2017 Dec 15;3(6):e200. doi: ... long-term course in 4 patients. J Child Neurol. 2013 Jul;28(7):937-41. doi: 10. ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  9. TH gene 
    ... dystonia due to mild tyrosine hydroxylase deficiency. Ann Neurol. 2004 Jan;55(1):147-8. doi: 10. ... causes progressive encephalopathy and dopa-nonresponsive dystonia. Ann Neurol. 2003;54 Suppl 6:S56-65. doi: 10. ...
    https://medlineplus.gov/genetics/gene/th - Genetics
  10. TTN gene 
    ... novel early-onset myopathy with fatal cardiomyopathy. Ann Neurol. 2007 Apr;61(4):340-51. doi: 10.1002/ana.21089. Erratum In: Ann Neurol. 2012 May;71(5):728. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
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