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 *

180 related articles for article (PubMed ID: 12483859)

  • 21. Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophy.
    Tunc S; Tadic V; Zühlke C; Hellenbroich Y; Brüggemann N
    Neurology; 2018 Jan; 90(3):142-143. PubMed ID: 29335306
    [No Abstract]   [Full Text] [Related]  

  • 22. [From gene to disease; progressive myoclonus epilepsy of Unverricht-Lundborg and mutations in the cystatin B gene].
    de Haan GJ; Halley DJ; Deelen WH; Lindhout D
    Ned Tijdschr Geneeskd; 2002 May; 146(18):846-8. PubMed ID: 12038222
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Postoperative seizure in an epileptic patient with dentatorubral pallidoluysian atrophy].
    Yanagidate F; Dohi S; Hamaya Y; Ueda N
    Masui; 2002 May; 51(5):532-4. PubMed ID: 12058442
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Dentatorubral-pallidoluysian atrophy (DRPLA: differential diagnosis of chorea)].
    Tsuji S
    Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):101-3. PubMed ID: 10434603
    [No Abstract]   [Full Text] [Related]  

  • 25. [Dentatorubral-pallidoluysian atrophy (DRPLA: Naito-Oyanagi disease)].
    Tsuji S
    Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):275-9. PubMed ID: 10434650
    [No Abstract]   [Full Text] [Related]  

  • 26. Periodic Epileptiform Discharges in Children With Advanced Stages of Progressive Myoclonic Epilepsy.
    Isobe N; Sakai Y; Kira R; Sanefuji M; Ishizaki Y; Sakata A; Sasazuki M; Torio M; Akamine S; Torisu H; Hara T
    Clin EEG Neurosci; 2016 Oct; 47(4):317-323. PubMed ID: 25828483
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A pediatric patient with sporadic dentatorubral pallidoluysian atrophy.
    Takano T; Okuno K; Maruo Y; Takeuchi Y
    Pediatr Neurol; 2003 Jan; 28(1):72-3. PubMed ID: 12657426
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italy.
    Grimaldi S; Cupidi C; Smirne N; Bernardi L; Giacalone F; Piccione G; Basiricò S; Mangano GD; Nardello R; Orsi L; Grosso E; Laganà V; Mitolo M; Maletta RG; Bruni AC
    Mov Disord; 2019 Dec; 34(12):1919-1924. PubMed ID: 31755148
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Importance of CAG repeat length in childhood-onset dentatorubral-pallidoluysian atrophy.
    Maruyama S; Saito Y; Nakagawa E; Saito T; Komaki H; Sugai K; Sasaki M; Kumada S; Saito Y; Tanaka H; Minami N; Goto Y
    J Neurol; 2012 Nov; 259(11):2329-34. PubMed ID: 22527233
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Head tremor in dentatorubral-pallidoluysian atrophy.
    Ohizumi H; Okuma Y; Fukae J; Fujishima K; Goto K; Mizuno Y
    Acta Neurol Scand; 2002 Nov; 106(5):319-21. PubMed ID: 12371928
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Progressive myoclonic epilepsy: myoclonic epilepsy and ataxia due to KCNC1 mutation (MEAK): a case report and review of the literature.
    Barot N; Margiotta M; Nei M; Skidmore C
    Epileptic Disord; 2020 Oct; 22(5):654-658. PubMed ID: 32972906
    [TBL] [Abstract][Full Text] [Related]  

  • 32. SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
    Faruq M; Scaria V; Singh I; Tyagi S; Srivastava AK; Mukerji M
    Hum Mutat; 2009 Jul; 30(7):1037-42. PubMed ID: 19370769
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Glyceraldehyde 3-phosphate dehydrogenase and endothelin-1 immunoreactivity is associated with cerebral white matter damage in dentatorubral-pallidoluysian atrophy.
    Shiozawa M; Fukutani Y; Arai N; Cairns NJ; Mizutani T; Isaki K; Lantos PL; Wada Y
    Neuropathology; 2003 Mar; 23(1):36-43. PubMed ID: 12722924
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An established case of dentatorubral pallidoluysian atrophy (DRPLA) with unusual features on muscle biopsy.
    Cox H; Costin-Kelly NM; Ramani P; Whitehouse WP
    Eur J Paediatr Neurol; 2000; 4(3):119-23. PubMed ID: 10872107
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Oligodendrocytic polyglutamine pathology in dentatorubral-pallidoluysian atrophy.
    Yamada M; Sato T; Tsuji S; Takahashi H
    Ann Neurol; 2002 Nov; 52(5):670-4. PubMed ID: 12402270
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Is cerebral white matter involvement helpful in the diagnosis of dentatorubral-pallidoluysian atrophy?
    Yoon WT; Youn J; Cho JW
    J Neurol; 2012 Aug; 259(8):1694-7. PubMed ID: 22286658
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA).
    Bidollari E; Rotundo G; Altieri F; Amicucci M; Wiquel D; Ferrari D; Goldoni M; Bernardini L; Consoli F; De Luca A; Fanelli S; Lamorte G; D'Agruma L; Vescovi AL; Squitieri F; Rosati J
    Stem Cell Res; 2019 Oct; 40():101551. PubMed ID: 31493762
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cervical dystonia in dentatorubral-pallidoluysian atrophy.
    Hatano T; Okuma Y; Iijima M; Fujishima K; Goto K; Mizuno Y
    Acta Neurol Scand; 2003 Oct; 108(4):287-9. PubMed ID: 12956864
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Electroclinical features of epilepsy in patients with juvenile type dentatorubral-pallidoluysian atrophy.
    Egawa K; Takahashi Y; Kubota Y; Kubota H; Inoue Y; Fujiwara T; Onodera O
    Epilepsia; 2008 Dec; 49(12):2041-9. PubMed ID: 18616556
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Dentatorubral-pallidoluysian atrophy (DRPLA)].
    Tsuji S
    Rinsho Shinkeigaku; 2007 Nov; 47(11):932-3. PubMed ID: 18210839
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.