BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 34021019)

  • 1. Hiding in plain sight: genetic deaf-blindness is not always Usher syndrome.
    Medina G; Perry J; Oza A; Kenna M
    Cold Spring Harb Mol Case Stud; 2021 Aug; 7(4):. PubMed ID: 34021019
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Review of Genotype-Phenotype Correlations in Usher Syndrome.
    Nisenbaum E; Thielhelm TP; Nourbakhsh A; Yan D; Blanton SH; Shu Y; Koehler KR; El-Amraoui A; Chen Z; Lam BL; Liu X
    Ear Hear; 2022; 43(1):1-8. PubMed ID: 34039936
    [TBL] [Abstract][Full Text] [Related]  

  • 3. "Minimized rotational vestibular testing" as a screening procedure detecting vestibular areflexy in deaf children: screening cochlear implant candidates for Usher syndrome type I.
    Teschner M; Neuburger J; Gockeln R; Lenarz T; Lesinski-Schiedat A
    Eur Arch Otorhinolaryngol; 2008 Jul; 265(7):759-63. PubMed ID: 18058117
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome.
    Igelman AD; Ku C; da Palma MM; Georgiou M; Schiff ER; Lam BL; Sankila EM; Ahn J; Pyers L; Vincent A; Ferraz Sallum JM; Zein WM; Oh JK; Maldonado RS; Ryu J; Tsang SH; Gorin MB; Webster AR; Michaelides M; Yang P; Pennesi ME
    Ophthalmic Genet; 2021 Dec; 42(6):664-673. PubMed ID: 34223797
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing loss.
    Stiff HA; Sloan-Heggen CM; Ko A; Pfeifer WL; Kolbe DL; Nishimura CJ; Frees KL; Booth KT; Wang D; Weaver AE; Azaiez H; Kamholz J; Smith RJH; Drack AV
    Ophthalmic Genet; 2020 Apr; 41(2):151-158. PubMed ID: 32281467
    [No Abstract]   [Full Text] [Related]  

  • 6. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
    Reiners J; Nagel-Wolfrum K; Jürgens K; Märker T; Wolfrum U
    Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Perform vestibular test among all small deaf children! Early detection of Usher syndrome improves the possibilities of communication in the event of later deaf-blindness].
    Konrádsson K; Magnusson M; Andréasson S
    Lakartidningen; 1998 Jan; 95(5):379-81. PubMed ID: 9492482
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review.
    Stephenson KAJ; Whelan L; Zhu J; Dockery A; Wynne NC; Cairns RM; Kirk C; Turner J; Duignan ES; O'Byrne JJ; Silvestri G; Kenna PF; Farrar GJ; Keegan DJ
    Invest Ophthalmol Vis Sci; 2023 Jul; 64(10):23. PubMed ID: 37466950
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Usher syndrome: hearing loss with vision loss.
    Friedman TB; Schultz JM; Ahmed ZM; Tsilou ET; Brewer CC
    Adv Otorhinolaryngol; 2011; 70():56-65. PubMed ID: 21358186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome.
    Kletke S; Batmanabane V; Dai T; Vincent A; Li S; Gordon KA; Papsin BC; Cushing SL; Héon E
    Clin Genet; 2017 Jul; 92(1):26-33. PubMed ID: 27743452
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification.
    Delmaghani S; El-Amraoui A
    Hum Genet; 2022 Apr; 141(3-4):709-735. PubMed ID: 35353227
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss.
    Pater JA; Green J; O'Rielly DD; Griffin A; Squires J; Burt T; Fernandez S; Fernandez B; Houston J; Zhou J; Roslin NM; Young TL
    BMC Med Genet; 2019 May; 20(1):68. PubMed ID: 31046701
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.
    Khalaileh A; Abu-Diab A; Ben-Yosef T; Raas-Rothschild A; Lerer I; Alswaiti Y; Chowers I; Banin E; Sharon D; Khateb S
    Invest Ophthalmol Vis Sci; 2018 Feb; 59(2):1095-1104. PubMed ID: 29490346
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive Molecular Screening in Chinese Usher Syndrome Patients.
    Sun T; Xu K; Ren Y; Xie Y; Zhang X; Tian L; Li Y
    Invest Ophthalmol Vis Sci; 2018 Mar; 59(3):1229-1237. PubMed ID: 29625443
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Current updates on genetic spectrum of usher syndrome.
    Ullah F; Zeeshan Ali M; Ahmad S; Muzammal M; Khan S; Khan J; Ahmad Khan M
    Nucleosides Nucleotides Nucleic Acids; 2024 May; ():1-24. PubMed ID: 38718411
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A nationwide epidemiologic, clinical, genetic study of Usher syndrome in Japan.
    Yoshimura H; Nishio SY; Isaka Y; Kurokawa T; Usami SI;
    Acta Otolaryngol; 2021 Sep; 141(9):841-846. PubMed ID: 34452594
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variants in CIB2 cause DFNB48 and not USH1J.
    Booth KT; Kahrizi K; Babanejad M; Daghagh H; Bademci G; Arzhangi S; Zareabdollahi D; Duman D; El-Amraoui A; Tekin M; Najmabadi H; Azaiez H; Smith RJ
    Clin Genet; 2018 Apr; 93(4):812-821. PubMed ID: 29112224
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromes.
    Grotz S; Schäfer J; Wunderlich KA; Ellederova Z; Auch H; Bähr A; Runa-Vochozkova P; Fadl J; Arnold V; Ardan T; Veith M; Santamaria G; Dhom G; Hitzl W; Kessler B; Eckardt C; Klein J; Brymova A; Linnert J; Kurome M; Zakharchenko V; Fischer A; Blutke A; Döring A; Suchankova S; Popelar J; Rodríguez-Bocanegra E; Dlugaiczyk J; Straka H; May-Simera H; Wang W; Laugwitz KL; Vandenberghe LH; Wolf E; Nagel-Wolfrum K; Peters T; Motlik J; Fischer MD; Wolfrum U; Klymiuk N
    EMBO Mol Med; 2022 Apr; 14(4):e14817. PubMed ID: 35254721
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher Syndrome.
    Daich Varela M; Wong SW; Kiray G; Schlottmann PG; Arno G; Shams ANA; Mahroo OA; Webster AR; AlTalbishi A; Michaelides M
    Am J Ophthalmol; 2023 Dec; 256():186-195. PubMed ID: 37422204
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular genetics of Usher syndrome].
    Tazetdinov AM; Dzhemileva LU; Khusnutdinova EK
    Genetika; 2008 Jun; 44(6):725-33. PubMed ID: 18727382
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.