Results 161 to 170 of about 67,593 (295)

A Case Report of Unilateral <i>OPA3</i>-Related Dominant Optic Atrophy. [PDF]

Case Rep Ophthalmol
Ware MA, Li HC, Micieli J.
europepmc   +1 more source

Optic Atrophy in Thalassemia Intermedia

, 2011
A 21-year-old man with thalassemia intermedia presented with progressive decrease in vision and was found to have severe bilateral optic atrophy. Orbital and brain neuroimaging revealed massive diffuse expansion of the diploe of the craniofacial bones ...
Farzad Pakdel, MD; Niloofar Pirmarzdashty, MD; Mostafa Soltan Sanjari, MD; Mohsen Bahmani Kashkouli, MD; Hoshyar Sarhadi, MD
core  

Epidermal Patch Technologies for Integrated Healthcare and Infection Management

Advanced Healthcare Materials, EarlyView.
Epidermal patches have evolved from simple wound coverings into multifunctional, skin‐conformable platforms integrating drug delivery, biosensing, and therapeutic functionalities. This review highlights their material innovations, fabrication strategies, and intelligent designs, including hydrogels, microneedles, and flexible electronics, while ...
Yuqi Wang, Atakan Tevlek, Pawel L. Urban, Boaz Mizrahi, Onome Ejeromedoghene, Roshan Deen, Yuanjing Lin, Jagan Mohan Dodda   +7 more
wiley   +1 more source

Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy. [PDF]

Orphanet J Rare Dis
Roberts JP, Tang AF, Hernandez D, Carman B, Oiknine L, Brown C, Hurst S, Tang Y, Urano F.   +8 more
europepmc   +1 more source

IF201a Temporal Cupping with Dominant Hereditary Optic Atrophy

1969. Dominant hereditary optic atrophy (Kjer) Pair with IF2_1b. Right eye. Boy with reduced central acuity since childhood. Discs are pale temporally and the temporal nerve fiber layer is thin. Anatomy: Optic disc.
William F. Hoyt, MD
core  

A Systematic Study of GelMA‐Carbopol Bioinks for High‐Fidelity Extrusion 3D Bioprinting at Physiological Temperatures

Advanced Healthcare Materials, EarlyView.
Gonzalez Martinez and collaborators develop a strategy to formulate high performance GelMA‐based bioinks with low solids contents. The resulting bioinks enable 3D bioprinting at 37 °C of high‐fidelity structures with tunable mechanical properties that support high cell viability and function.
David A. González‐Martínez, Aidee V. Arizpe Tafoya, Eduardo González‐Martínez, Mabel Barreiro Carpio, Laura Daniela Serrano Andrade, Christopher T. N. Chow, Mohammadhossein Dabaghi, Jeremy A. Hirota, Jose M. Moran‐Mirabal   +8 more
wiley   +1 more source

IF201b Temporal Cupping with Dominant Hereditary Optic Atrophy

1969. Dominant hereditary optic atrophy (Kjer) Pair with IF2_1a. Left eye. Boy with reduced central acuity since childhood. and the temporal nerve fiber layer is thin. Anatomy: Optic disc. Pathology: Dominant hereditary optic atrophy. Disease/ Diagnosis:
William F. Hoyt, MD
core  

3D‐Printed Piezoionic/Bioelectronic Hydrogel for Electro‐Metabolic Regulation of Osteogenic Differentiation

Advanced Healthcare Materials, EarlyView.
A 3D‐printed piezoionic GPMx hydrogel enables stable electromechanical signal generation under mechanical loading, exhibiting long‐term durability and low fatigue. As a bioactive patch, it restores endogenous bioelectricity to stimulate osteogenesis via Ca2+ influx and mitochondrial activation, while simultaneously enabling label‐free alkaline ...
Sayan Deb Dutta, Myoung Joon Jeon, Youjin Seol, Ki‐Taek Lim   +3 more
wiley   +1 more source

Volumetric brain analysis and associated retinal thinning in autosomal dominant optic atrophy patients. [PDF]

Neuroimage Rep
Pajareeyapong P, Buathong S, Thammasarnsophon S, Sathianvichitr K, Rattanathamsakul N, Eiamsamarng A, Chirapapaisan N, Ngamsombat C.   +7 more
europepmc   +1 more source

IF205a Temporal Cupping with Dominant Hereditary Optic Atrophy

1970. Right eye. Pair with IF2_5b. 55 year old woman with deficient vision all her life. Typical pattern of dominant hereditary atrophy. Temporal pallor and shallow cupping. Anatomy: Optic disc. Pathology: Dominant hereditary optic atrophy.
William F. Hoyt, MD
core