BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 32874040)

  • 1. Electronegative Electroretinograms in the United Arab Emirates.
    Alsalamah AK; Khan AO
    Middle East Afr J Ophthalmol; 2020; 27(2):86-90. PubMed ID: 32874040
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram.
    Renner AB; Kellner U; Cropp E; Foerster MH
    Graefes Arch Clin Exp Ophthalmol; 2006 Nov; 244(11):1467-73. PubMed ID: 16612636
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
    Hayashi T; Hosono K; Kurata K; Katagiri S; Mizobuchi K; Ueno S; Kondo M; Nakano T; Hotta Y
    Doc Ophthalmol; 2020 Apr; 140(2):147-157. PubMed ID: 31583501
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Negative electroretinograms in the pediatric and adult population.
    Kim JM; Payne JF; Yan J; Barnes CS
    Doc Ophthalmol; 2012 Feb; 124(1):41-8. PubMed ID: 22246197
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differentiation of murine models of "negative ERG" by single and repetitive light stimuli.
    Tanimoto N; Akula JD; Fulton AB; Weber BH; Seeliger MW
    Doc Ophthalmol; 2016 Apr; 132(2):101-9. PubMed ID: 26996188
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
    Marmor MF; Zeitz C
    Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
    Oh A; Loew ER; Foster ML; Davidson MG; English RV; Gervais KJ; Herring IP; Mowat FM
    Doc Ophthalmol; 2018 Oct; 137(2):87-101. PubMed ID: 30051304
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
    Bijveld MM; Florijn RJ; Bergen AA; van den Born LI; Kamermans M; Prick L; Riemslag FC; van Schooneveld MJ; Kappers AM; van Genderen MM
    Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Long-term follow-up of retinal function and structure in
    Al-Hujaili H; Taskintuna I; Neuhaus C; Bergmann C; Schatz P
    Mol Vis; 2019; 25():851-858. PubMed ID: 31908403
    [TBL] [Abstract][Full Text] [Related]  

  • 10. In vivo electroretinographic differentiation of rod, short-wavelength and long/medium-wavelength cone responses in dogs using silent substitution stimuli.
    Mowat FM; Wise E; Oh A; Foster ML; Kremers J
    Exp Eye Res; 2019 Aug; 185():107673. PubMed ID: 31128103
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.
    McAnany JJ; Alexander KR; Kumar NM; Ying H; Anastasakis A; Fishman GA
    Ophthalmic Genet; 2013 Sep; 34(3):167-73. PubMed ID: 23289809
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complete congenital stationary night blindness associated with a novel
    Hayashi T; Murakami Y; Mizobuchi K; Koyanagi Y; Sonoda KH; Nakano T
    Ophthalmic Genet; 2021 Aug; 42(4):412-419. PubMed ID: 33769208
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A phenotype-genotype correlation study of X-linked retinoschisis.
    Vincent A; Robson AG; Neveu MM; Wright GA; Moore AT; Webster AR; Holder GE
    Ophthalmology; 2013 Jul; 120(7):1454-64. PubMed ID: 23453514
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ISCEV extended protocol for the stimulus-response series for light-adapted full-field ERG.
    McCulloch DL; Kondo M; Hamilton R; Lachapelle P; Messias AMV; Robson AG; Ueno S
    Doc Ophthalmol; 2019 Jun; 138(3):205-215. PubMed ID: 30929108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia.
    Almutairi F; Almeshari N; Ahmad K; Magliyah MS; Schatz P
    Acta Ophthalmol; 2021 Sep; 99(6):581-591. PubMed ID: 33369259
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort.
    Malaichamy S; Sen P; Sachidanandam R; Arokiasamy T; Lancelot ME; Audo I; Zeitz C; Soumittra N
    Mol Vis; 2014; 20():341-51. PubMed ID: 24715752
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extracting the ON and OFF contributions to the full-field photopic flash electroretinogram using summed growth curves.
    Akula JD; Ambrosio L; Howard FI; Hansen RM; Fulton AB
    Exp Eye Res; 2019 Dec; 189():107827. PubMed ID: 31600486
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
    Smirnov VM; Zeitz C; Soumittra N; Audo I; Defoort-Dhellemmes S
    Doc Ophthalmol; 2018 Apr; 136(2):135-143. PubMed ID: 29525873
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis.
    Zeng Y; Takada Y; Kjellstrom S; Hiriyanna K; Tanikawa A; Wawrousek E; Smaoui N; Caruso R; Bush RA; Sieving PA
    Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):3279-85. PubMed ID: 15326152
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.
    Sustar M; Perovšek D; Cima I; Stirn-Kranjc B; Hawlina M; Brecelj J
    Doc Ophthalmol; 2015 Jun; 130(3):165-77. PubMed ID: 25663266
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.