Results 231 to 240 of about 91,474 (255)

Metformin may alter the course of Leber's hereditary optic neuropathy: a case report. [PDF]

Front Med (Lausanne)
Elmaseh SA, Gauthier DA, Golmohammadi M, Pargalava N, Carelli V, Sadun AA.   +5 more
europepmc   +1 more source

Utilization of an automated machine learning approach for the detection of granular corneal dystrophy via slit lamp photographs. [PDF]

BMC Ophthalmol
Yavari N, Mohammadi SS, Sokol JT, Feky DE, Rajabi M, Hung JH, Or C, Elaraby O, Anover FA, Saengsirinavin AO, Akhavanrezayat A, Mobasserian A, Than NTT, Guo J, Bai Y, Yasar C, Afshari NA, Lin CC, Nguyen QD.   +18 more
europepmc   +1 more source

Tips of family history taking in diagnosing Alport syndrome: a report of six cases. [PDF]

CEN Case Rep
Mori T.
europepmc   +1 more source

Advanced therapies for inherited optic neuropathies. [PDF]

Eye (Lond)
Wong DCS, Makam R, Yu-Wai-Man P.
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Genetic testing in prostate cancer management: Considerations informing primary care

Ca-A Cancer Journal for Clinicians, 2022
Veda N Giri, Jacob E Berchuck, Mary-Ellen Taplin   +2 more
exaly  

Efficacy and safety of garadacimab, a factor XIIa inhibitor for hereditary angioedema prevention (VANGUARD): a global, multicentre, randomised, double-blind, placebo-controlled, phase 3 trial

Lancet, The, 2023
exaly  

Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis

New England Journal of Medicine, 2018
Márcia Waddington Cruz, John L Berk, Fabio A Barroso   +2 more
exaly  

150 years of Darwin’s theory of intercellular flow of hereditary information

Nature Reviews Molecular Cell Biology, 2018
Yongsheng Liu, Qi Chen
exaly  

Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis

New England Journal of Medicine, 2018
Alejandra Gonzalez-Duarte, Chih-Chao Yang, Mitsuharu Ueda   +2 more
exaly