Results 261 to 270 of about 310,806 (291)

Neurometabolic Hereditary Diseases of Adults.

Journal of Inherited Metabolic Disease, 2019
Springer International Publishing AG 2018, ISBN 978-3-319-76148-0, ISBN 978-3-319-76148-0 (ebook) Growing up is a fascinating journey. The book "Neurometabolic Hereditary Diseases of Adults" designed and edited by Dr. Allessandro P.
G. Hoffmann
semanticscholar   +1 more source

Application of prime editing to the correction of mutations and phenotypes in adult mice with liver and eye diseases

Nature Biomedical Engineering, 2021
Hyewon Jang, D. Jo, Chang Sik Cho, J. Shin, J. Seo, Goosang Yu, Ramu Gopalappa, Daesik Kim, Sung-Rae Cho, J. H. Kim, H. Kim   +10 more
semanticscholar   +1 more source

A Comprehensive Review of Leber Hereditary Optic Neuropathy and Its Association with Multiple Sclerosis-Like Phenotypes Known as Harding’s Disease

Eye and Brain
Leber Hereditary Optic Neuropathy (LHON) stands as a distinctive maternally inherited mitochondrial disorder marked by painless, subacute central vision loss, primarily affecting young males.
J. Alorainy, Yara Alorfi, R. Karanjia, N. Badeeb   +3 more
semanticscholar   +1 more source

Gene therapy for Leber hereditary optic neuropathy

Expert Opinion on Biological Therapy
Introduction Leber hereditary optic neuropathy (LHON) is among the most frequent inherited mitochondrial disease, causing a severe visual impairment, mostly in young-adult males.
Marco Battista, Valerio Carelli, Leonardo Bottazzi, F. Bandello, M. Cascavilla, P. Barboni   +5 more
semanticscholar   +1 more source

[The research advances and applications of genome editing in hereditary eye diseases].

[Zhonghua yan ke za zhi] Chinese journal of ophthalmology, 2017
S. Cai, Y. Zhang, M. Hou, Y. Liu, X. Li
semanticscholar   +1 more source

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  

Japan Eye Genetics Consortium (JEGC) for Hereditary Retinal Diseases

, 2017
T. Iwata
semanticscholar   +1 more source

[Retinitis pigmentosa, symmetrical inner ear deafness, typical inverse vascular fistula symptom without fistula and vestibular sensitivity disease; combined hereditary ear and eye diseases].

Archiv für Klinische und Experimentelle Ohren- Nasen- und Kehlkopfheilkunde, 1956
H. Stenger
semanticscholar   +1 more source

Congenital and hereditary eye diseases.

The Sight-saving review, 1949
H. Falls
semanticscholar   +1 more source

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