BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

364 related articles for article (PubMed ID: 24787759)

  • 1. Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?
    Wictorin K; Brådvik B; Nilsson K; Soller M; van Westen D; Bynke G; Bauer P; Schöls L; Puschmann A
    Parkinsonism Relat Disord; 2014 Jul; 20(7):748-54. PubMed ID: 24787759
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
    Le Ber I; Moreira MC; Rivaud-Péchoux S; Chamayou C; Ochsner F; Kuntzer T; Tardieu M; Saïd G; Habert MO; Demarquay G; Tannier C; Beis JM; Brice A; Koenig M; Dürr A
    Brain; 2003 Dec; 126(Pt 12):2761-72. PubMed ID: 14506070
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z; Fernandez M; Matsushita M; Lipe H; Wolff J; Bird TD; Raskind WH
    Am J Med Genet; 2002 May; 114(4):450-7. PubMed ID: 11992570
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inherited ataxia with slow saccades.
    Chakor RT; Bharote H
    J Postgrad Med; 2012; 58(4):318-25. PubMed ID: 23298936
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias.
    Federighi P; Cevenini G; Dotti MT; Rosini F; Pretegiani E; Federico A; Rufa A
    Brain; 2011 Mar; 134(Pt 3):879-91. PubMed ID: 21354979
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
    Serrano-Munuera C; Corral-Juan M; Stevanin G; San Nicolás H; Roig C; Corral J; Campos B; de Jorge L; Morcillo-Suárez C; Navarro A; Forlani S; Durr A; Kulisevsky J; Brice A; Sánchez I; Volpini V; Matilla-Dueñas A
    JAMA Neurol; 2013 Jun; 70(6):764-71. PubMed ID: 23700170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ocular motor characteristics of different subtypes of spinocerebellar ataxia: distinguishing features.
    Kim JS; Kim JS; Youn J; Seo DW; Jeong Y; Kang JH; Park JH; Cho JW
    Mov Disord; 2013 Aug; 28(9):1271-7. PubMed ID: 23609488
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical picture of spinocerebellar ataxia type I (SCA1)].
    Milewska D; Piłkowska E; Jakubowska T; Rakowicz M; Niewiadomska M; Niedzielska K; Walinowska E; Wochnik-Dyjas D; Rejnowski G; Zdzienicka E; Mierzewska H; Hoffman-Zacharska D; Zaremba J
    Neurol Neurochir Pol; 2001; 35(6):993-1011. PubMed ID: 11987714
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.
    Ozaki K; Doi H; Mitsui J; Sato N; Iikuni Y; Majima T; Yamane K; Irioka T; Ishiura H; Doi K; Morishita S; Higashi M; Sekiguchi T; Koyama K; Ueda N; Miura Y; Miyatake S; Matsumoto N; Yokota T; Tanaka F; Tsuji S; Mizusawa H; Ishikawa K
    JAMA Neurol; 2015 Jul; 72(7):797-805. PubMed ID: 26010696
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease.
    Wallenius J; Kafantari E; Jhaveri E; Gorcenco S; Ameur A; Karremo C; Dobloug S; Karrman K; de Koning T; Ilinca A; Landqvist Waldö M; Arvidsson A; Persson S; Englund E; Ehrencrona H; Puschmann A
    Am J Hum Genet; 2024 Jan; 111(1):82-95. PubMed ID: 38035881
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Spinocerebellar ataxia type 7: clinical and molecular genetic analysis of a Mexican family].
    Rolón Lacarriere O; Rasmussen Almaraz A; Hernández Cruz H; Carranza del Río J; González Cruz M; Gutiérrez Moctezuma J
    Rev Neurol; 2004 Apr 16-30; 38(8):736-40. PubMed ID: 15122543
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Eye movements in a familial vestibulocerebellar disorder.
    Harris CM; Walker J; Shawkat F; Wilson J; Russell-Eggitt I
    Neuropediatrics; 1993 Jun; 24(3):117-22. PubMed ID: 8355816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impaired eye movements in presymptomatic spinocerebellar ataxia type 6.
    Christova P; Anderson JH; Gomez CM
    Arch Neurol; 2008 Apr; 65(4):530-6. PubMed ID: 18413478
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients.
    Tazir M; Ali-Pacha L; M'Zahem A; Delaunoy JP; Fritsch M; Nouioua S; Benhassine T; Assami S; Grid D; Vallat JM; Hamri A; Koenig M
    J Neurol Sci; 2009 Mar; 278(1-2):77-81. PubMed ID: 19141356
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A large family with spinocerebellar ataxia type 6 in Iran: a clinical and genetic study.
    Shimazaki H; Vazifehmand R; Heidari MH; Khorram-Khorshid HR; Saber S; Hejazi S; Aghakhani-Moghadam F; Ouyang Y; Honda J; Nakano I; Takiyama Y
    Arch Iran Med; 2008 Jul; 11(4):459-62. PubMed ID: 18588381
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) - a case report and review of literature.
    Figura M; Gaweł M; Kolasa A; Janik P
    Neurol Neurochir Pol; 2014; 48(5):368-72. PubMed ID: 25440017
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ocular and oculomotor signs in Joubert syndrome.
    Tusa RJ; Hove MT
    J Child Neurol; 1999 Oct; 14(10):621-7. PubMed ID: 10511333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI; Koenig M
    Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline.
    Castrioto A; Prontera P; Di Gregorio E; Rossi V; Parnetti L; Rossi A; Donti E; Brusco A; Calabresi P; Tambasco N
    Eur J Neurol; 2011 Oct; 18(10):1263-5. PubMed ID: 21382133
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
    Hiramoto K; Kawakami H; Inoue K; Seki T; Maruyama H; Morino H; Matsumoto M; Kurisu K; Sakai N
    Mov Disord; 2006 Sep; 21(9):1355-60. PubMed ID: 16763984
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.