Results 71 to 80 of about 880 (178)
The Interconnected World of Dermatology and Ophthalmology
Medical science, is an integrated field that shares intricate relationship between various organ systems. Similarly, dermatology is inter‐related with various other specialties including ophthalmology. This article depicts the correlation of ophthalmology and dermatology iterating on the genetic diseases, autoimmune diseases, systemic disorders ...
Gyanesh Rathore +4 more
wiley +1 more source
The Lost Large Mammals of Arabia
ABSTRACT Aim If successful, plans to restore the vegetation of the Arabian Peninsula (AP) as announced by the Middle East and Saudi Green Initiatives will see the greatest increase in vegetation cover since the beginning of the Holocene Humid Phase (HHP), roughly 9–10,000 years ago.
Christopher Clarke, Sultan M. Alsharif
wiley +1 more source
Simplified cellular grafting for treatment of vitiligo and piebaldism: the '6-well plate' technique
: BACKGROUND Vitiligo is a disfiguring depigmenting dermatosis that affects approximately 0.5% to 1% of the general population regardless of race and sex.
Chua, Xuey-Mii +4 more
core +1 more source
Southern right whales (SRWs, Eubalena australis) are polymorphic for an X-linked pigmentation pattern known as grey morphism. Most SRWs have completely black skin with white patches on their bellies and occasionally on their backs; these patches remain ...
Guy D Eroh +10 more
doaj +1 more source
A new bicornuate model of rat uterus transplantation
Our study introduces a bicornuate uterus transplantation model in Lewis rats, comparable in safety and feasibility to the unicornuate model, enabling longitudinal graft health monitoring for UTx research. Abstract Introduction Uterus transplantation has revolutionized reproductive medicine for women with absolute uterine factor infertility, resulting ...
Dietrich Polenz +10 more
wiley +1 more source
Anomalous colourations occur in many tropical vertebrates. However, they are considered rare in wild populations, with very few records for the majority of animal taxa. We report two new cases of anomalous colouration in mammals.
MSL. Abreu +4 more
doaj
Research of genomic loci of piebaldism.
Research of Genomic Loci of Piebaldism Piebaldism is a rare, autosomal dominant genetic disorder, characterised by the congenital absence of melanocytes in the affected areas of the skin and hair.
Dilytė, Evelina,
core
Mutations in the Ligand-Binding Domain of the Kit Receptor: An Uncommon Site in Human Piebaldism
Heterozygous mutations in the gene for the Kit transmembrane receptor have been identified recently in human piebaldism and mouse “dominant spotting”. Interestingly, all of the 14 known missense mutations that cause depigmentation in these species map to
Gallardo, Teresa +2 more
core +1 more source
We present 9-year-old fraternal twins from a family with piebaldism, having congenital depigmented macules and meeting the diagnostic criteria for neurofibromatosis type 1 (NF1) due to the multiple cafe-au-lait macules (CALMs) and intertriginous ...
Avci, CEYLAN +3 more
core +1 more source

