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Did you mean kuhn h (1,385 results)?
Current and emerging treatments for albinism.
Liu S, Kuht HJ, Moon EH, Maconachie GDE, Thomas MG. Liu S, et al. Among authors: kuht hj. Surv Ophthalmol. 2021 Mar-Apr;66(2):362-377. doi: 10.1016/j.survophthal.2020.10.007. Epub 2020 Oct 29. Surv Ophthalmol. 2021. PMID: 33129801 Review.
Normal and abnormal foveal development.
Thomas MG, Papageorgiou E, Kuht HJ, Gottlob I. Thomas MG, et al. Among authors: kuht hj. Br J Ophthalmol. 2022 May;106(5):593-599. doi: 10.1136/bjophthalmol-2020-316348. Epub 2020 Nov 4. Br J Ophthalmol. 2022. PMID: 33148537 Review.
Dorsal midbrain (Parinaud) syndrome.
Prakash E, Kuht HJ, Harieaswar S, Thomas MG. Prakash E, et al. Among authors: kuht hj. Pract Neurol. 2021 Dec;21(6):550-551. doi: 10.1136/practneurol-2021-003068. Epub 2021 Aug 25. Pract Neurol. 2021. PMID: 34433682 No abstract available.
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Kuht HJ, Maconachie GDE, Han J, Kessel L, van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, Jiao Y, Smirnov V, Choi JH, Tobin MD, Sheth V, Purohit R, Dawar B, Girach A, Strul S, May L, Chen FK, Heath Jeffery RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arveiler B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, Thomas MG. Kuht HJ, et al. Ophthalmology. 2022 Jun;129(6):708-718. doi: 10.1016/j.ophtha.2022.02.010. Epub 2022 Feb 11. Ophthalmology. 2022. PMID: 35157951 Free PMC article.
Ocular Manifestations of PNPT1-Related Neuropathy.
Kuht HJ, Thomas KA, Hisaund M, Maconachie GDE, Thomas MG. Kuht HJ, et al. J Neuroophthalmol. 2021 Sep 1;41(3):e293-e296. doi: 10.1097/WNO.0000000000001012. J Neuroophthalmol. 2021. PMID: 34415280 No abstract available.
Home-based screening tools for amblyopia: a systematic review.
Sii SSZ, Chean CS, Kuht H, Bunce C, Thomas MG, Rufai SR. Sii SSZ, et al. Among authors: kuht h. Eye (Lond). 2023 Sep;37(13):2649-2658. doi: 10.1038/s41433-023-02412-3. Epub 2023 Feb 24. Eye (Lond). 2023. PMID: 36828959 Free PMC article. Review.
Discordant phenotypes in twins with infantile nystagmus.
Aamir A, Kuht HJ, McLean RJ, Maconachie GDE, Sheth V, Dawar B, Purohit R, Sylvius N, Hisaund M, Zubcov-Iwantscheff A, Proudlock FA, Gottlob I, Thomas MG. Aamir A, et al. Among authors: kuht hj. Sci Rep. 2021 Feb 2;11(1):2826. doi: 10.1038/s41598-021-82368-0. Sci Rep. 2021. PMID: 33531592 Free PMC article.
Clinical utility gene card for FRMD7-related infantile nystagmus.
Dawar B, Kuht HJ, Han J, Maconachie GDE, Thomas MG. Dawar B, et al. Among authors: kuht hj. Eur J Hum Genet. 2021 Oct;29(10):1584-1588. doi: 10.1038/s41431-021-00826-9. Epub 2021 Feb 25. Eur J Hum Genet. 2021. PMID: 33633368 Free PMC article. No abstract available.
Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease.
Grove JI, Lo PCK, Shrine N, Barwell J, Wain LV, Tobin MD, Salter AM, Borkar AN, Cuevas-Ocaña S, Bennett N, John C, Ntalla I, Jones GE, Neal CP, Thomas MG, Kuht H, Gupta P, Vemala VM, Grant A, Adewoye AB, Shenoy KT, Balakumaran LK, Hollox EJ, Hannan NRF, Aithal GP. Grove JI, et al. Among authors: kuht h. JHEP Rep. 2023 Apr 23;5(8):100764. doi: 10.1016/j.jhepr.2023.100764. eCollection 2023 Aug. JHEP Rep. 2023. PMID: 37484212 Free PMC article.
28 results