These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 1591746)

  • 21. Progressive myoclonic ataxia without ragged red fibres: Unverricht-Lundborg disease vs Ramsay Hunt syndrome.
    Shakir RA; Khan RA; al-Zuhair AG
    Acta Neurol Scand; 1992 Nov; 86(5):470-3. PubMed ID: 1336290
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hereditary essential myoclonus in a large Norwegian family.
    Fahn S; Sjaastad O
    Mov Disord; 1991; 6(3):237-47. PubMed ID: 1922129
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Partial motor epilepsy with "negative myoclonus".
    Cirignotta F; Lugaresi E
    Epilepsia; 1991; 32(1):54-8. PubMed ID: 1898721
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Myoclonic occipital photosensitive epilepsy with dystonia (MOPED): A familial epilepsy syndrome.
    Sadleir LG; Paterson S; Smith KR; Redshaw N; Ranta A; Kalnins R; Berkovic SF; Bahlo M; Hildebrand MS; Scheffer IE
    Epilepsy Res; 2015 Aug; 114():98-105. PubMed ID: 26088892
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linkage studies in alcohol-responsive myoclonic dystonia.
    Gasser T; Bereznai B; Müller B; Pruszak-Seel R; Damrich R; Deuschl G; Oertel WH
    Mov Disord; 1996 Jul; 11(4):363-70. PubMed ID: 8813214
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Action myoclonus after cerebral anoxia.
    Rizvi AH; Karetzky MS
    N J Med; 1993 Dec; 90(12):918-20. PubMed ID: 8309643
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Inherited myoclonus-dystonia.
    Saunders-Pullman R; Ozelius L; Bressman SB
    Adv Neurol; 2002; 89():185-91. PubMed ID: 11968443
    [No Abstract]   [Full Text] [Related]  

  • 28. Progressive myoclonic ataxia associated with celiac disease presenting as unilateral cortical tremor and dystonia.
    Fung VS; Duggins A; Morris JG; Lorentz IT
    Mov Disord; 2000 Jul; 15(4):732-4. PubMed ID: 10928587
    [No Abstract]   [Full Text] [Related]  

  • 29. Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome.
    Leuzzi V; Carducci C; Carducci C; Cardona F; Artiola C; Antonozzi I
    Neurology; 2002 Oct; 59(8):1241-3. PubMed ID: 12391354
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.
    Nygaard TG; Raymond D; Chen C; Nishino I; Greene PE; Jennings D; Heiman GA; Klein C; Saunders-Pullman RJ; Kramer P; Ozelius LJ; Bressman SB
    Ann Neurol; 1999 Nov; 46(5):794-8. PubMed ID: 10554001
    [TBL] [Abstract][Full Text] [Related]  

  • 31. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
    Asmus F; Langseth A; Doherty E; Nestor T; Munz M; Gasser T; Lynch T; King MD
    Mov Disord; 2009 Apr; 24(5):702-9. PubMed ID: 19117362
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hereditary spastic paraplegia with epileptic myoclonus.
    Sommerfelt K; Kyllerman M; Sanner G
    Acta Neurol Scand; 1991 Aug; 84(2):157-60. PubMed ID: 1950452
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Video-EEG study in an adult and a child with eyelid myoclonia with absences.
    Burneo JG; Miller S; Bebin EM; Prasad A
    Epileptic Disord; 2004 Dec; 6(4):287-91. PubMed ID: 15634626
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trihexyphenidyl in posthemorrhagic dystonia: motor and language effects.
    Pidcock FS; Hoon AH; Johnston MV
    Pediatr Neurol; 1999 Mar; 20(3):219-22. PubMed ID: 10207932
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Both thalamic and pallidal deep brain stimulation for myoclonic dystonia.
    Oropilla JQ; Diesta CC; Itthimathin P; Suchowersky O; Kiss ZH
    J Neurosurg; 2010 Jun; 112(6):1267-70. PubMed ID: 19929196
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q.
    Vidailhet M; Tassin J; Durif F; Nivelon-Chevallier A; Agid Y; Brice A; Dürr A
    Neurology; 2001 May; 56(9):1213-6. PubMed ID: 11342690
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: trunk tremor, myoclonus, and dystonia.
    Foncke EM; Beukers RJ; Tijssen CC; Koelman JH; Tijssen MA
    Parkinsonism Relat Disord; 2010 May; 16(4):288-9. PubMed ID: 19913450
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW
    Adv Neurol; 1986; 43():33-55. PubMed ID: 3080851
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Myoclonus in fraternal twin toddlers: a French family with a novel mutation in the SGCE gene.
    Thümmler S; Giuliano F; Pincemaille O; Saugier-Veber P; Perelman S
    Eur J Paediatr Neurol; 2009 Nov; 13(6):559-61. PubMed ID: 19147379
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic features of myoclonus-dystonia in three kindreds.
    Doheny DO; Brin MF; Morrison CE; Smith CJ; Walker RH; Abbasi S; Müller B; Garrels J; Liu L; De Carvalho Aguiar P; Schilling K; Kramer P; De Leon D; Raymond D; Saunders-Pullman R; Klein C; Bressman SB; Schmand B; Tijssen MA; Ozelius LJ; Silverman JM
    Neurology; 2002 Oct; 59(8):1187-96. PubMed ID: 12391346
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.