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 *

92 related articles for article (PubMed ID: 2368812)

  • 21. A novel family with an unusual early-onset generalized dystonia.
    Fabbrini G; Brancati F; Vacca L; Valente EM; Nemeth A; Meesaq A; Sykes N; Dallapiccola B; Berardelli A
    Mov Disord; 2005 Jan; 20(1):81-6. PubMed ID: 15390042
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dystonia in Spain: study of a Gypsy family and general survey.
    Giménez-Roldán S; López-Fraile IP; Esteban A
    Adv Neurol; 1976; 14():125-36. PubMed ID: 941766
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spread of symptoms in idiopathic torsion dystonia.
    Greene P; Kang UJ; Fahn S
    Mov Disord; 1995 Mar; 10(2):143-52. PubMed ID: 7753056
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The spectrum of disorders presenting as adult-onset focal lower extremity dystonia.
    McKeon A; Matsumoto JY; Bower JH; Ahlskog JE
    Parkinsonism Relat Disord; 2008 Dec; 14(8):613-9. PubMed ID: 18329318
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Neuropathology of lubag (x-linked dystonia parkinsonism).
    Waters CH; Faust PL; Powers J; Vinters H; Moskowitz C; Nygaard T; Hunt AL; Fahn S
    Mov Disord; 1993 Jul; 8(3):387-90. PubMed ID: 8341310
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dystonia in 61-year-old identical twins: observations over 45 years.
    Eldridge R; Ince SE; Chernow B; Milstien S; Lake CR
    Ann Neurol; 1984 Sep; 16(3):356-8. PubMed ID: 6486739
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.
    Klein C; Pramstaller PP; Castellan CC; Breakefield XO; Kramer PL; Ozelius LJ
    Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Torsion dystonia in Israel.
    Korczyn AD; Kahana E; Zilber N; Streifler M; Carasso R; Alter M
    Ann Neurol; 1980 Oct; 8(4):387-91. PubMed ID: 7436383
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome.
    Ha AD; Parratt KL; Rendtorff ND; Lodahl M; Ng K; Rowe DB; Sue CM; Hayes MW; Tranebjaerg L; Fung VS
    Mov Disord; 2012 Jul; 27(8):1034-40. PubMed ID: 22736418
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetics, geography and intelligence in the torsion dystonias.
    Eldridge R; Edgar A; Cooper IS
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):167-77. PubMed ID: 5173357
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Delayed-onset dystonia due to asphyxia in the perinatal period].
    Kostić VS; Covicković-Sternić N; Svetel-Stojanović M; Filipović S
    Srp Arh Celok Lek; 1997; 125(3-4):84-8. PubMed ID: 9221523
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
    Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness.
    Jin H; May M; Tranebjaerg L; Kendall E; Fontán G; Jackson J; Subramony SH; Arena F; Lubs H; Smith S; Stevenson R; Schwartz C; Vetrie D
    Nat Genet; 1996 Oct; 14(2):177-80. PubMed ID: 8841189
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical and genetic characterization of a large Dutch family with primary focal dystonia.
    Contarino MF; Berger-Plantinga E; Foncke EM; Ritz K; Mellema J; Baas F; Speelman JD; Tijssen MA
    Mov Disord; 2008 Oct; 23(14):1998-2003. PubMed ID: 18823044
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia.
    Slominsky PA; Markova ED; Shadrina MI; Illarioshkin SN; Miklina NI; Limborska SA; Ivanova-Smolenskaya IA
    Hum Mutat; 1999 Sep; 14(3):269. PubMed ID: 10477437
    [TBL] [Abstract][Full Text] [Related]  

  • 36. HLA antigens in bullous epidermolysis, congenital ichthyosis and ectodermal dysplasia.
    László A; Kaiser G; Simon M
    Acta Paediatr Acad Sci Hung; 1982; 23(4):447-58. PubMed ID: 7170955
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The natural history of sex-linked recessive dystonia parkinsonism of Panay, Philippines (XDP).
    Lee LV; Maranon E; Demaisip C; Peralta O; Borres-Icasiano R; Arancillo J; Rivera C; Munoz E; Tan K; Reyes MT
    Parkinsonism Relat Disord; 2002 Oct; 9(1):29-38. PubMed ID: 12217620
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A genetic study of idiopathic torsion dystonia in the United Kingdom.
    Fletcher NA; Harding AE; Marsden CD
    Brain; 1990 Apr; 113 ( Pt 2)():379-95. PubMed ID: 2183913
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A genetic study of torsion dystonia.
    Bundey S; Harrison MJ; Marsden CD
    J Med Genet; 1975 Mar; 12(1):12-9. PubMed ID: 1121020
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two women.
    Waters CH; Takahashi H; Wilhelmsen KC; Shubin R; Snow BJ; Nygaard TG; Moskowitz CB; Fahn S; Calne DB
    Neurology; 1993 Aug; 43(8):1555-8. PubMed ID: 8351010
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.