Results 61 to 70 of about 2,165 (170)

Efficacy of frontalis suspension with silicone rods in ptosis patients with poor Bell's phenomenon

Taiwan Journal of Ophthalmology, 2017
Purpose: The purpose of the study was to evaluate the efficacy of silicone rods as frontalis sling for correction of ptosis associated with poor Bell's phenomenon in specific situations.
Khyati P Shah, Bipasha Mukherjee
doaj   +1 more source

Green Electrospinning of Highly Concentrated Polyurethane Suspensions in Water: From the Rheology to the Fiber Morphology

Macromolecular Materials and Engineering, Volume 309, Issue 12, December 2024.
Green electrospinning of highly concentrated polyurethane suspensions in water can be achieved thanks to an in‐depth investigation of the rheological behavior in regard to the complex interactions occurring in the formulation. A fibrous membrane with a PU/PEO weight ratio equal to 50 under very stable and efficient production conditions is obtained ...
Bryan Gross, Guy Schlatter, Pascal Hébraud, Flavien Mouillard, Lotfi Chehma, Anne Hébraud, Emeline Lobry   +6 more
wiley   +1 more source

Outcome of Ptosis Surgery in Patients with Chronic Progressive External Ophthalmoplegia

Türk Oftalmoloji Dergisi, 2014
Objectives: To evaluate the clinical features and the outcome of ptosis surgery in patients with chronic progressive external ophthalmoplegia (CPEO). Materials and Methods: The demographic features, surgical approaches, anatomic and functional outcomes,
Şeyda Uğurlu, Sevinç Atik, Mehmet Reşit Işık, Gülden Diniz   +3 more
doaj   +1 more source

The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross‐sectional study

Clinical Genetics, Volume 106, Issue 6, Page 733-744, December 2024.
The epidemiological study of 1351 Chinese patients with mitochondrial disease reveals that the most prevalent phenotypes are mitochondrial encephalomyopathy with lactic acidosis and stroke‐like episodes (MELAS), chronic progressive external ophthalmoplegia (CPEO), and Leigh syndrome. Additionally, the study identified several rare phenotypes.
Yang Zhao, Xutong Zhao, Kunqian Ji, Junling Wang, Yuying Zhao, Jie Lin, Qiang Gang, Meng Yu, Yun Yuan, Haishan Jiang, Chong Sun, Fang Fang, Chuanzhu Yan, Zhaoxia Wang   +13 more
wiley   +1 more source

Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic Tissues

Frontiers in Genetics, 2020
It is generally accepted that patients with chronic progressive ophthalmoplegia caused by single large-scale deletion (SLD) of mitochondrial DNA (mtDNA) only harbor mutation in skeletal and eye muscles.
Tina D. Jeppesen, Morten Duno, John Vissing   +2 more
doaj   +1 more source

Structure designing, interface engineering, and application prospects for sodium‐ion inorganic solid electrolytes

InfoMat, Volume 6, Issue 9, September 2024.
All‐solid Na‐ion batteries (ASNIBs) have attracted extensive research interests owing to superior safety and energy density. Among various solid‐state batteries based on solid electrolytes (SEs), inorganic solid electrolytes (ISEs) present substantial potential due to their exceptional ionic conductivity and electrochemical stability.
Meng Wu, Hong Liu, Xiang Qi, Dabing Li, Chao Wang, Ce‐Wen Nan, Li‐Zhen Fan   +6 more
wiley   +1 more source

Skeletal muscle: molecular structure, myogenesis, biological functions, and diseases

MedComm, Volume 5, Issue 7, July 2024.
The article systematically and comprehensively reviews the physiological and pathological processes associated with skeletal muscles from five perspectives: molecule basis, myogenesis, biological function, poststimulation response, and myopathy. We primarily focus on nuclei‐related behaviors of skeletal muscle, cell–cell fusion, and nuclei migration in
Lan‐Ting Feng, Zhi‐Nan Chen, Huijie Bian   +2 more
wiley   +1 more source

The expanding phenotype of MELAS caused by the m.3291T>C mutation in the MT-TL1 gene

Molecular Genetics and Metabolism Reports, 2016
m.3291T>C mutation in the MT-TL1 gene has been infrequently encountered in association with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS), however remains poorly characterized from a clinical perspective. In the
E. Keilland, C.A. Rupar, Asuri N. Prasad, K.Y. Tay, A. Downie, C. Prasad   +5 more
doaj   +1 more source

Computational Hyperspectral Microflow Cytometry

Small, Volume 20, Issue 30, July 25, 2024.
The study presents a computational hyperspectral microflow cytometry capable of detecting the full fluorescence emission spectrum from individual flowing cells within the 450 to 650 nm spectral range, achieving a high spectral resolution of ≈3 nm in a compact form‐factor.
Hyo Geun Yun, Yoel Alonso Cadierno, Tae Won Kim, Arrate Muñoz‐Barrutia, Daniel Garica‐Gonzalez, Sungyoung Choi   +5 more
wiley   +1 more source

Primary mitochondrial disorders and mimics: Insights from a large French cohort

Annals of Clinical and Translational Neurology, Volume 11, Issue 6, Page 1478-1491, June 2024.
Abstract Objective The objective of this study was to evaluate the implementation of NGS within the French mitochondrial network, MitoDiag, from targeted gene panels to whole exome sequencing (WES) or whole genome sequencing (WGS) focusing on mitochondrial nuclear‐encoded genes.
Cécile Rouzier, Emmanuelle Pion, Annabelle Chaussenot, Céline Bris, Samira Ait‐El‐Mkadem Saadi, Valérie Desquiret‐Dumas, Naïg Gueguen, Konstantina Fragaki, Patrizia Amati‐Bonneau, Giulia Barcia, Pauline Gaignard, Julie Steffann, Alessandra Pennisi, Jean‐Paul Bonnefont, Elise Lebigot, Sylvie Bannwarth, Bruno Francou, Benoit Rucheton, Damien Sternberg, Marie‐Laure Martin‐Negrier, Aurélien Trimouille, Gaëlle Hardy, Stéphane Allouche, Cécile Acquaviva‐Bourdain, Cécile Pagan, Anne‐Sophie Lebre, Pascal Reynier, Mireille Cossee, Shahram Attarian, Véronique Paquis‐Flucklinger, MitoDiag's Network Collaborators, Vincent Procaccio   +31 more
wiley   +1 more source