Results 71 to 80 of about 163,801 (186)
Pioneers for the Basic Understanding of Usher syndrome
After the first description of the inherited nature of bimodal deaf-blindness disease in mid nineteenth century by pioneering ophthalmologists Albrecht von Graefe (May 22, 1828 ± July 20, 1870) and Richard Liebreich (June 30, 1830 - January 19, 1917 ...
Ahuja, Satpal,, Lund University.
core
A rare type of Usher's syndrome.
A case is presented of a very rare type of Usher's syndrome detected in a 30-year-old woman in her 28th week of pregnancy. She reported left eye visual impairment with a one-month history. She underwent standard ophthalmologic examination with additional procedures scheduled after childbirth, including fluorescein angiography, visual field (Goldman and
Gverovic Antunica, Antonela +5 more
openaire +3 more sources
Prostate Cancer Development, Progression, and Therapy
This review provides an integrated overview of prostate cancer development, progression, and therapy, spanning historical milestones, molecular mechanisms, advanced research models, and emerging therapeutic strategies. It highlights recent advances in precision diagnosis, lineage plasticity, therapy resistance, and next‐generation treatments for ...
Xin Jin +9 more
wiley +1 more source
Letter from Congressman Usher Burdick to Senator Langer Regarding Petition from Elbowoods, July 27, 1953 [PDF]
In this letter, dated July 27, 1953, from United States (US) Representative Usher Burdick to US Senator William Langer, Burdick replies to Langer\u27s letter of July 13, regarding a petition Langer had received from residents of Elbowoods, North Dakota ...
Burdick, Usher
core +1 more source
Neurological disorders (NDs) are characterized by substantial loss of specific neurons, with Alzheimer's and Parkinson's diseases being the most frequent NDs and nearly 99% of all “foreign substances” are prohibited from entering the brain by the blood‐brain barrier (BBB) and the blood‐cerebrospinal fluid barrier (CFB).
Nnamdi Ikemefuna Okafor +3 more
wiley +1 more source
Abstract Congenital aniridia is a rare genetic disorder primarily caused by pathogenic variants of the PAX6 gene. It leads to various panocular anomalies, including aniridia‐associated keratopathy (AAK). This review highlights recent insights into its pathogenesis, focusing on clinical staging, microstructural changes in the cornea and molecular ...
N. Szentmáry +27 more
wiley +1 more source
There are many misconceptions about narcissistic personality disorder, not only in the public consciousness, but also in dermatological and aesthetic practice. Patients and their environment may both suffer from the symptoms. These conditions can be managed with psychotherapeutic interventions, but recognizing the psychological problem can be ...
Eszter Szlávicz +4 more
wiley +1 more source
Neuropathy With Demyelinating Features in a Patient With Biallelic HARS1 Variants
ABSTRACT Background and Aims The HARS1 gene encodes cytoplasmic histidyl‐tRNA synthetase, which catalyzes the ligation of histidine to tRNAHIS in the cytoplasm as an early step in protein biosynthesis and is essential for cell viability. Pathogenic variants in HARS1 have been associated with three phenotypes: autosomal dominant Charcot–Marie–Tooth (CMT)
Christina Del Greco +5 more
wiley +1 more source
Telegram from Usher Burdick to Charles Vogel Regarding Oil Rights, April 18, 1953 [PDF]
This telegram, dated April 18, 1953, from United States (US) Representative Usher Burdick to Judge Charles J. Vogel of the US District Court, District of North Dakota, reads as follows: JAMES BLACK DOG NECESSARY WITNESS YOUR HEARING TODAY NOW IN ...
Burdick, Usher L.
core +1 more source
Periods, Pains, Pills, and Performance—Fighting Blood, Bodies and Biology
ABSTRACT This paper draws on various data from long‐term immersion in combat sports to explore the period experiences of cis women fighters. We blend theoretical ideas from the social scientific literature on menstruation and the sociology of medicalization, pain and injury.
Reem AlHashmi +2 more
wiley +1 more source

