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hereditary vitreoretinal degeneration相关文献:
Current Clinical Applications of In Vivo Gene Therapy with AAVs.
Mendell JR, Al-Zaidy SA, Rodino-Klapac LR, Goodspeed K, Gray SJ, Kay CN, Boye SL, Boye SE, George LA, Salabarria S, Corti M, Byrne BJ, Tremblay JP.
Mol Ther. 2021 Feb 3;29(2):464-488. doi: 10.1016/j.ymthe.2020.12.007. Epub 2020 Dec 10.
PMID:33309881
Revolution in evolution.
Honavar SG.
Indian J Ophthalmol. 2018 Dec;66(12):1667. doi: 10.4103/ijo.IJO_1894_18.
PMID:30451160
Snowflake degeneration in hereditary vitreoretinal degeneration.
Hirose T, Lee KY, Schepens CL.
Am J Ophthalmol. 1974 Feb;77(2):143-53. doi: 10.1016/0002-9394(74)90665-5.
PMID:4812083
Hereditary snowflake vitreoretinal degeneration.
Gheiler M, Pollack A, Uchenik D, Godel V, Oliver M.
Birth Defects Orig Artic Ser. 1982;18(6):577-80.
PMID:7171777
Goldmann-Favre vitreoretinal degeneration.
Batioğlu F.
Eur J Ophthalmol. 2003 Apr;13(3):307-10. doi: 10.1177/112067210301300311.
PMID:12747653
Hereditary vitreoretinal degeneration and night blindness.
Feiler-Ofry V, Adam A, Regenbogen L, Godel V, Stein R.
Am J Ophthalmol. 1969 Apr;67(4):553-8. doi: 10.1016/0002-9394(69)94263-9.
PMID:5305106
Optical Coherence Tomography.
Enaholo ES, Musa MJ, Zeppieri M.
2024 Oct 6. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:39163419
Wagner's hereditary vitreoretinal degeneration.
Manning LM.
Aust J Ophthalmol. 1980 Feb;8(1):29-33. doi: 10.1111/j.1442-9071.1980.tb00885.x.
PMID:7387542
Safety and efficacy of ATSN-101 in patients with Leber congenital amaurosis caused by biallelic mutations in GUCY2D: a phase 1/2, multicentre, open-label, unilateral dose escalation study.
Yang P, Pardon LP, Ho AC, Lauer AK, Yoon D, Boye SE, Boye SL, Roman AJ, Wu V, Garafalo AV, Sumaroka A, Swider M, Viarbitskaya I, Aleman TS, Pennesi ME, Kay CN, Fujita KP, Cideciyan AV.
Lancet. 2024 Sep 7;404(10456):962-970. doi: 10.1016/S0140-6736(24)01447-8.
PMID:39244273
Hereditary vitreoretinal diseases.
Neetens A.
Bull Soc Belge Ophtalmol. 1987;223 Pt 1:241-72. doi: 10.1007/978-1-4757-1901-7_16.
PMID:3307967
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