Results 121 to 130 of about 1,408,479 (244)
Autosomal Dominant Optic Atrophy In Singapore
, 2015 Autosomal dominant optic atrophy (ADOA) is a ubiquitous condition causing bilateral visual loss, most commonly related to mutations in the OPA1 gene, mapped on the chromosome 3q28-q29. Recent data suggests a minimum prevalence of 4.07/100 000 in northern
Sharon L. Tow; Jing-Liang Loo; P. Amati-Bonneau; D. Bonneau; V. Procaccio; P. Reynier; Dan Milea +1 more
core
Metastable Polymers for Circular 3D Printing
Advanced Materials, EarlyView.3D‐printed polymers are usually permanent and hard to recycle. Here, metastable polymers are designed to fall apart on demand. A chemical trigger unzips the printed material back into its original building blocks within minutes at room temperature.
Johannes Markhart +2 more
wiley +1 more source
Hereditary Optic Neuropathy (Leber\u27s Hereditary Optic Neuropathy)
, 2022 Hereditary Optic Neuropathy - A hereditary optic neuropathy is caused by a genetic variant (or mutation) that causes dysfunction of the neurons (nerve cells) which form the optic nerve.
NANOS
core
Advanced Materials, EarlyView.A hierarchical flexible ceramic nanofiber membrane integrates a La‐stabilized ZrO2 scaffold with superhydrophobic UiO‐66‐NH2/CdS heterojunctions. The gas–liquid–solid interfacial architecture sustains vapor‐selective desalination, visible‐light charge separation, and rapid H2 extraction, enabling simultaneous freshwater production and photocatalytic ...
Pengfei Lin +9 more
wiley +1 more source
Decoding Synergistic Pathways in Bimetallic MOFs for Advanced Oxidation Processes
Advanced Materials, EarlyView.This review presents a unified framework linking metal pairing and framework design with electronic structure, redox cycling, oxidant activation, reactive‐species generation, and catalytic performance across photocatalytic and oxidant‐based BMOF‐AOPs. The resulting design principles guide the development of hydrolytically stable and efficient BMOFs for
Karim El‐Naggar +2 more
wiley +1 more source
IF203a Temporal Cupping with Dominant Hereditary Optic Atrophy
Right eye shows pallor and temporal cupping. Pair with IF2_3b. 1994. Anatomy: Optic disc. Pathology: Dominant hereditary optic atrophy. Disease/ Diagnosis: Dominant hereditary optic atrophy.
William F. Hoyt, MD
core
Introduction: Ubiquitin C-terminal hydrolase L1 (UCHL1) has been associated with a severe, complex autosomal recessive spastic paraplegia (HSP79) [1] [2] [3] [4].
Koenig, M. +15 more
core +1 more source
Bioengineered Interfaces for Peripheral Nerve Sensory Restoration
Advanced Materials, EarlyView.Half of amputees abandon their prosthetics for lack of feeling. This review charts the full path from peripheral nerve injury to restored sensation, through surgical, regenerative, noninvasive, and implanted approaches, and shows how injury type and interface material properties determine which strategy can deliver naturalistic feedback, and why ...
Sydney Swedick +4 more
wiley +1 more source
IF203b Temporal Cupping with Dominant Hereditary Optic Atrophy
Left disc is hypoplastic and smaller with temporal pallor. Pair with IF2_3a. 1994. Anatomy: Optic disc. Pathology: Dominant hereditary optic atrophy. Disease/ Diagnosis: Dominant hereditary optic atrophy.
William F. Hoyt, MD
core
OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets. [PDF]
J Neuroophthalmol, 2023 Wong DCS +6 more
europepmc +1 more source