Results 151 to 160 of about 1,166 (222)

Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress. [PDF]

Int J Mol Sci
Yang TH, Kang EY, Lin PH, Yu BB, Wang JH, Chen V, Wang NK.   +6 more
europepmc   +1 more source

Efficient Direct Recycling of Spent Batteries: Integrated Lithiation and Delamination

Advanced Science, EarlyView.
An integrated process for the delamination and relithiation of spent cathodes, LixNi0.6Co0.2Mn0.2O2 and LixFePO4, under open‐air conditions is proposed. The transition‐metal (Ni) oxidation state in the cathode is reduced by the oxidation of diethylene glycol, facilitating relithiation. Glycol aldehyde formation induces 100% electrode delamination.
Jeonghwan Song, Seok Hyun Song, Dokyeong Han, Jaehyun Noh, Jayoung Kim, Min Jeong Kim, Hayong Song, Jeong‐Sun Park, Jaekook Kim, Jiyoung Ma, Jinju Song, Jung‐Je Woo   +11 more
wiley   +1 more source

Cascade testing in mitochondrial diseases: a cross-sectional retrospective study. [PDF]

BMC Neurol
Haque S, Crawley K, Schofield D, Shrestha R, Sue CM.   +4 more
europepmc   +1 more source

Axonal Transport Deficits in Parkinson's Disease: Insights from Neurotoxin, Genetic, and Sporadic Models. [PDF]

Brain Sci
Wang X, Liu Z, Smith WW.
europepmc   +1 more source

Hereditary optic atrophy (Leber's disease).

Indian pediatrics, 1970
K V, Devadiga, K G, Nayak
openaire   +1 more source

State of the Art on Inherited Retinal Dystrophies: Management and Molecular Genetics. [PDF]

J Clin Med
Nebbioso M, Artico M, Gharbiya M, Mannocci A, Limoli PG, Iannetta D, Donato L.   +6 more
europepmc   +1 more source

Review of the Genetic Spectrum of Hereditary Spastic Paraplegias in the Middle East and North Africa Regions. [PDF]

Neurol Genet
Salari M, Hojjatipour F, Etemadifar M, Soleimani S.   +3 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Leber's hereditary optic atrophy

Ophthalmic Paediatrics and Genetics, 1989
Leber described a particular type of hereditary optic atrophy in 1871. The clinical features of all cases since reported are reviewed. There is characteristically acute visual loss, circumpapillary teleangiectatic micropathy, tortuosity of the retinal vessels and oedema in the retinal nerve fibres.
T A, Berninger, A C, Bird, G B, Arden
openaire   +2 more sources