BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 38587696)

  • 1. Genetic aspects of ataxias in a cohort of Turkish patients.
    Gogus B; Elmas M; Turk Boru U
    Neurol Sci; 2024 Apr; ():. PubMed ID: 38587696
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective.
    da Graça FF; Peluzzo TM; Bonadia LC; Martinez ARM; Diniz de Lima F; Pedroso JL; Barsottini OGP; Gama MTD; Akçimen F; Dion PA; Rouleau GA; Marques W; França MC
    Cerebellum; 2022 Feb; 21(1):49-54. PubMed ID: 33956305
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model.
    Németh AH; Kwasniewska AC; Lise S; Parolin Schnekenberg R; Becker EB; Bera KD; Shanks ME; Gregory L; Buck D; Zameel Cader M; Talbot K; de Silva R; Fletcher N; Hastings R; Jayawant S; Morrison PJ; Worth P; Taylor M; Tolmie J; O'Regan M; ; Valentine R; Packham E; Evans J; Seller A; Ragoussis J
    Brain; 2013 Oct; 136(Pt 10):3106-18. PubMed ID: 24030952
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population.
    Incecik F; Herguner OM; Mungan NO
    J Pediatr Neurosci; 2020; 15(2):86-89. PubMed ID: 33042236
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Ataxias. Diagnostic procedure and treatment].
    Klockgether T
    Nervenarzt; 2005 Oct; 76(10):1275-83; quiz 1284-5. PubMed ID: 16175415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations.
    Chakravarty A; Mukherjee SC
    Neurol India; 2003 Jun; 51(2):227-34. PubMed ID: 14571010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.
    Atadzhanov M; Smith DC; Mwaba MH; Siddiqi OK; Bryer A; Greenberg LJ
    Cerebellum Ataxias; 2017; 4():17. PubMed ID: 29214039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
    Hamza W; Ali Pacha L; Hamadouche T; Muller J; Drouot N; Ferrat F; Makri S; Chaouch M; Tazir M; Koenig M; Benhassine T
    BMC Med Genet; 2015 Jun; 16():36. PubMed ID: 26068213
    [TBL] [Abstract][Full Text] [Related]  

  • 10. EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
    van de Warrenburg BP; van Gaalen J; Boesch S; Burgunder JM; Dürr A; Giunti P; Klockgether T; Mariotti C; Pandolfo M; Riess O
    Eur J Neurol; 2014 Apr; 21(4):552-62. PubMed ID: 24418350
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17.
    Algahtani H; Shirah B; Almatrafi S; Al-Qahtani MH; Abdulkareem AA; Naseer MI
    Neurol Res; 2021 Feb; 43(2):141-147. PubMed ID: 33012273
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal recessive cerebellar ataxias.
    Palau F; Espinós C
    Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia.
    Eidhof I; Baets J; Kamsteeg EJ; Deconinck T; van Ninhuijs L; Martin JJ; Schüle R; Züchner S; De Jonghe P; Schenck A; van de Warrenburg BP
    Brain; 2018 Sep; 141(9):2592-2604. PubMed ID: 30084953
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias.
    Wan N; Chen Z; Wan L; Yuan H; Tang Z; Liu M; Peng Y; Peng L; Lei L; Xie Y; Deng Q; Wang S; Wang C; Peng H; Hou X; Shi Y; Long Z; Qiu R; Xia K; Tang B; Jiang H
    Parkinsonism Relat Disord; 2021 Aug; 89():120-127. PubMed ID: 34284285
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adult-onset Niemann-Pick disease type C masquerading as spinocerebellar ataxia.
    Vo ML; Levy T; Lakhani S; Wang C; Ross ME
    Mol Genet Genomic Med; 2022 Apr; 10(4):e1906. PubMed ID: 35192242
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.
    Ashrafi MR; Mohammadi P; Tavasoli AR; Heidari M; Hosseinpour S; Rasulinejad M; Rohani M; Akbari MG; Malamiri RA; Badv RS; Fathi D; Dehnavi AZ; Savad S; Rabbani A; Synofzik M; Mahdieh N; Rezaei Z
    Cerebellum; 2023 Aug; 22(4):640-650. PubMed ID: 35731353
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Rare Phenotype of Inherited Cerebellar Ataxia.
    Raval DM; Rathod VM; Dobariya RK; Dave MP; Patel NS
    Cureus; 2022 Sep; 14(9):e28831. PubMed ID: 36225512
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.
    Cheng HL; Shao YR; Dong Y; Dong HL; Yang L; Ma Y; Shen Y; Wu ZY
    Transl Neurodegener; 2021 Oct; 10(1):40. PubMed ID: 34663476
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.