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 *

191 related articles for article (PubMed ID: 32338350)

  • 1. Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14.
    Ihl T; Kadas EM; Oberwahrenbrock T; Endres M; Klockgether T; Schroeter J; Brandt AU; Paul F; Minnerop M; Doss S; Schmitz-Hübsch T; Zimmermann HG
    Cerebellum; 2020 Aug; 19(4):469-482. PubMed ID: 32338350
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Vision related quality of life in spinocerebellar ataxia.
    Kedar S; Ghate D; Murray EL; Corbett JJ; Subramony SH
    J Neurol Sci; 2015 Nov; 358(1-2):404-8. PubMed ID: 26474795
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder.
    Schmitz-Hübsch T; Lux S; Bauer P; Brandt AU; Schlapakow E; Greschus S; Scheel M; Gärtner H; Kirlangic ME; Gras V; Timmann D; Synofzik M; Giorgetti A; Carloni P; Shah JN; Schöls L; Kopp U; Bußenius L; Oberwahrenbrock T; Zimmermann H; Pfueller C; Kadas EM; Rönnefarth M; Grosch AS; Endres M; Amunts K; Paul F; Doss S; Minnerop M
    Ann Clin Transl Neurol; 2021 Apr; 8(4):774-789. PubMed ID: 33739604
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
    Yabe I; Sasaki H; Chen DH; Raskind WH; Bird TD; Yamashita I; Tsuji S; Kikuchi S; Tashiro K
    Arch Neurol; 2003 Dec; 60(12):1749-51. PubMed ID: 14676051
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased biological activity of protein Kinase C gamma is not required in Spinocerebellar ataxia 14.
    Shimobayashi E; Kapfhammer JP
    Mol Brain; 2017 Jul; 10(1):34. PubMed ID: 28738819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparison of two families with and without ataxia harboring novel variants in PRKCG.
    Tada Y; Kume K; Noguchi S; Sekiya T; Nishinaka K; Ishiguchi H; Koh J; Emori S; Nakayama Y; Kurashige T; Izumi Y; Ito H; Sakai N; Kawakami H
    J Hum Genet; 2022 Oct; 67(10):595-599. PubMed ID: 35760954
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The King-Devick (K-D) test of rapid eye movements: a bedside correlate of disability and quality of life in MS.
    Moster S; Wilson JA; Galetta SL; Balcer LJ
    J Neurol Sci; 2014 Aug; 343(1-2):105-9. PubMed ID: 24954088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.
    Chelban V; Wiethoff S; Fabian-Jessing BK; Haridy NA; Khan A; Efthymiou S; Becker EBE; O'Connor E; Hersheson J; Newland K; Hojland AT; Gregersen PA; Lindquist SG; Petersen MB; Nielsen JE; Nielsen M; Wood NW; Giunti P; Houlden H
    Mov Disord; 2018 Jul; 33(7):1119-1129. PubMed ID: 29603387
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Association between progressive retinal nerve fiber layer loss and longitudinal change in quality of life in glaucoma.
    Gracitelli CP; Abe RY; Tatham AJ; Rosen PN; Zangwill LM; Boer ER; Weinreb RN; Medeiros FA
    JAMA Ophthalmol; 2015 Apr; 133(4):384-90. PubMed ID: 25569808
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Severe structural and functional visual system damage leads to profound loss of vision-related quality of life in patients with neuromyelitis optica spectrum disorders.
    Schmidt F; Zimmermann H; Mikolajczak J; Oertel FC; Pache F; Weinhold M; Schinzel J; Bellmann-Strobl J; Ruprecht K; Paul F; Brandt AU
    Mult Scler Relat Disord; 2017 Jan; 11():45-50. PubMed ID: 28104256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
    Stevanin G; Hahn V; Lohmann E; Bouslam N; Gouttard M; Soumphonphakdy C; Welter ML; Ollagnon-Roman E; Lemainque A; Ruberg M; Brice A; Durr A
    Arch Neurol; 2004 Aug; 61(8):1242-8. PubMed ID: 15313841
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
    Hugosson T; Gränse L; Ponjavic V; Andréasson S
    Ophthalmic Genet; 2009 Mar; 30(1):1-6. PubMed ID: 19172503
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of Glaucoma-Related, Optical Coherence Tomography-Measured Macular Damage With Vision-Related Quality of Life.
    Prager AJ; Hood DC; Liebmann JM; De Moraes CG; Al-Aswad LA; Yu Q; Cioffi GA; Blumberg DM
    JAMA Ophthalmol; 2017 Jul; 135(7):783-788. PubMed ID: 28594977
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ophthalmological and Neurologic Manifestations in Pre-clinical and Clinical Phases of Spinocerebellar Ataxia Type 7.
    Azevedo PB; Rocha AG; Keim LMN; Lavinsky D; Furtado GV; de Mattos EP; Vargas FR; Leotti VB; Saraiva-Pereira ML; Jardim LB;
    Cerebellum; 2019 Jun; 18(3):388-396. PubMed ID: 30637674
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ganglion cell loss in relation to visual disability in multiple sclerosis.
    Walter SD; Ishikawa H; Galetta KM; Sakai RE; Feller DJ; Henderson SB; Wilson JA; Maguire MG; Galetta SL; Frohman E; Calabresi PA; Schuman JS; Balcer LJ
    Ophthalmology; 2012 Jun; 119(6):1250-7. PubMed ID: 22365058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregation.
    Wong MMK; Hoekstra SD; Vowles J; Watson LM; Fuller G; Németh AH; Cowley SA; Ansorge O; Talbot K; Becker EBE
    Acta Neuropathol Commun; 2018 Sep; 6(1):99. PubMed ID: 30249303
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations.
    De Michele G; Galatolo D; Galosi S; Mignarri A; Silvestri G; Casali C; Leuzzi V; Ricca I; Barghigiani M; Tessa A; Cioffi E; Caputi C; Riso V; Dotti MT; Saccà F; De Michele G; Cocozza S; Filla A; Santorelli FM
    J Neurol; 2022 Mar; 269(3):1476-1484. PubMed ID: 34292398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 20/40 or Better Visual Acuity After Optic Neuritis: Not as Good as We Once Thought?
    Sabadia SB; Nolan RC; Galetta KM; Narayana KM; Wilson JA; Calabresi PA; Frohman EM; Galetta SL; Balcer LJ
    J Neuroophthalmol; 2016 Dec; 36(4):369-376. PubMed ID: 27472185
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel maculopathy in patients with spinocerebellar ataxia type 1 autofluorescence findings and functional characteristics.
    Vaclavik V; Borruat FX; Ambresin A; Munier FL
    JAMA Ophthalmol; 2013 Apr; 131(4):536-8. PubMed ID: 23579607
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.