BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 35243593)

  • 1. Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia.
    Gouvêa LA; Raslan IR; Rosa ABR; Silva TYT; Campos RM; Aragão MM; Barsottini OGP; Pedroso JL
    Cerebellum; 2023 Apr; 22(2):316-318. PubMed ID: 35243593
    [No Abstract]   [Full Text] [Related]  

  • 2. Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral Neuropathy.
    Spagnoli C; Frattini D; Gozzi F; Rizzi S; Salerno GG; Cimino L; Fusco C
    Cerebellum; 2021 Jun; 20(3):481-483. PubMed ID: 33188499
    [No Abstract]   [Full Text] [Related]  

  • 3. Spinocerebellar ataxia type 23 (SCA23): a review.
    Wu F; Wang X; Li X; Teng H; Tian T; Bai J
    J Neurol; 2021 Dec; 268(12):4630-4645. PubMed ID: 33175256
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Expanding the Landscape of Spinocerebellar Ataxia Type 5.
    Benevides ML; França M
    Neuropediatrics; 2022 Oct; 53(5):358-360. PubMed ID: 35545114
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral Palsy.
    Rea G; Tirupathi S; Williams J; Clouston P; Morrison PJ
    Cerebellum; 2020 Feb; 19(1):161-163. PubMed ID: 31721007
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HEREDITARY SPASTIC ATAXIA SIMULATING DISSEMINATED SCLEROSIS.
    MAHLOUDJI M
    J Neurol Neurosurg Psychiatry; 1963 Dec; 26(6):511-3. PubMed ID: 14083222
    [No Abstract]   [Full Text] [Related]  

  • 8. Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report.
    Mizuno T; Kashimada A; Nomura T; Moriyama K; Yokoyama H; Hasegawa S; Takagi M; Mizutani S
    Brain Dev; 2019 Aug; 41(7):630-633. PubMed ID: 30898343
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar ataxia 13 and 25.
    Stevanin G; Dürr A
    Handb Clin Neurol; 2012; 103():549-53. PubMed ID: 21827913
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare forms of autosomal recessive neurodegenerative ataxia.
    Koenig M
    Semin Pediatr Neurol; 2003 Sep; 10(3):183-92. PubMed ID: 14653406
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Generation of induced pluripotent stem cell line (ZZUi0021-A) from a patient with spinocerebellar ataxia type 19.
    Liu F; Fan Y; Fan L; Li M; Zhang Q; Mao C; Wu J; Zhang S; Hu Z; Shi C; Xu Y
    Stem Cell Res; 2021 May; 53():102320. PubMed ID: 34087979
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
    Vural A; Şimşir G; Tekgül Ş; Koçoğlu C; Akçimen F; Kartal E; Şen NE; Lahut S; Ömür Ö; Saner N; Gül T; Bayraktar E; Palvadeau R; Tunca C; Pirkevi Çetinkaya C; Gündoğdu Eken A; Şahbaz I; Kovancılar Koç M; Öztop Çakmak Ö; Hanağası H; Bilgiç B; Eraksoy M; Gündüz A; Apaydın H; Kızıltan G; Özekmekçi S; Siva A; Altıntaş A; Kaya Güleç ZE; Parman Y; Oflazer P; Deymeer F; Durmuş H; Şahin E; Çakar A; Tüfekçioğlu Z; Tektürk P; Çorbalı MO; Tireli H; Akdal G; Yiş U; Hız S; Şengün İ; Bora E; Serdaroğlu G; Erer Özbek S; Ağan K; İnce Günal D; Us Ö; Kurt SG; Aksoy D; Bora Tokçaer A; Elmas M; Gültekin M; Kumandaş S; Acer H; Kaya Özçora GD; Yayla V; Soysal A; Genç G; Güllüoğlu H; Kotan D; Özözen Ayas Z; Şahin HA; Tan E; Topçu M; Topçuoğlu ES; Akbostancı C; Koç F; Ertan S; Elibol B; Başak AN
    Mov Disord; 2021 Jul; 36(7):1676-1688. PubMed ID: 33624863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hereditary ataxias-overview].
    Nishizawa M
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1114-6. PubMed ID: 12235812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Problems and possibilities in the differential diagnosis of Syndrome Spinocerebellar Ataxia.
    Zumrová A
    Neuro Endocrinol Lett; 2005 Apr; 26(2):98-108. PubMed ID: 15855879
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxias.
    Nikali K; Koskinen T; Suomalainen A; Pihko H; Peltonen L
    Pediatr Res; 1994 Nov; 36(5):607-12. PubMed ID: 7877879
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary congenital spinocerebellar ataxia accompanied by congenital cataract and oligophrenia; a genetic and clinical investigation.
    SJOGREN T
    Confin Neurol; 1950; 10(5):293-308. PubMed ID: 14792949
    [No Abstract]   [Full Text] [Related]  

  • 17. [Spinocerebellar ataxia type 8 in Russian patients].
    Nuzhnyi EP; Abramycheva NY; Chkhartishvili IA; Protopopova AO; Fedotova EY; Illarioshkin SN
    Zh Nevrol Psikhiatr Im S S Korsakova; 2022; 122(8):106-111. PubMed ID: 36036411
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinocerebellar ataxia type 31 exists in northeast China.
    Ouyang Y; He Z; Li L; Qin X; Zhao Y; Yuan L
    J Neurol Sci; 2012 May; 316(1-2):164-7. PubMed ID: 22353852
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of spinocerebellar ataxia types 1,2,3,6,7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia.
    Jin DK; Oh MR; Song SM; Koh SW; Lee M; Kim GM; Lee WY; Chung CS; Lee KH; Im JH; Lee MJ; Kim JW; Lee MS
    J Neurol; 1999 Mar; 246(3):207-10. PubMed ID: 10323319
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Chinese Han pedigree with Huntington disease mimicking spinocerebellar ataxia.
    Mao C; Su Y; Wang H; Fan L; Zheng H; Wang T; Li X; Zhang S; Hu Z; Luo H; Yang J; Shi C; Xu Y
    J Neurol Sci; 2021 Nov; 430():119985. PubMed ID: 34543932
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.