Results 61 to 70 of about 73,460 (305)
Keratoglobus with ARCL1B (EFEMP2 gene) cutis laxa
Purpose: To report a case of keratoglobus in a patient with autosomal recessive (AR) cutis laxa. Observations: A 38 year old male presented with decreased vision in both eyes uncorrectable with spectacles and a history of corneal rupture in the left eye ...
Thomas F. Mauger +3 more
doaj +1 more source
Introdução:A cutis laxa é uma doença rara do tecido conjuntivo provocada por alterações da elastina. Caracteriza-se por pele sem elasticidade, flácida, mole e enrugada, dando aos doentes um aspecto envelhecido; o envolvimento sistémico é variável ...
Afonso, A +5 more
core
Activity of different desoximetasone preparations compared to other topical corticosteroids in the vasoconstriction assay [PDF]
Introduction: We report on a double-blind, vehicle-controlled, single-center confirmatory study with random assignment. The purpose of the study was to investigate the topical bioavailability of different topical corticosteroid formulations in healthy ...
Ashton RE +17 more
core +1 more source
Concurrent Psoriasis and Dermatomyositis: Retrospective Analysis and Literature Review
ABSTRACT Background Psoriasis (PsO) and dermatomyositis (DM) are both autoimmune‐mediated, inflammatory conditions. The concurrence of PsO and DM is rare, and literature on their relationship remains limited. Additionally, cutaneous DM can be challenging to clinically diagnosis, often presenting with psoriasiform clinical features.
Emily R. Gordon +5 more
wiley +1 more source
Narrar a própria história de vida e a prática docente pode contribuir para ações humanizadoras?
Este artigo é oriundo de uma dissertação de mestrado que teve, como objetivo, compreender o processo de humanização nas histórias de vida, na formação e na prática docente de professores(as) de Educação Física (EF).
Raphael Cutis Dias, Eliana Ayoub
doaj +1 more source
Background In human subcutaneous adipose tissue, the superficial fascia distinguishes superficial and deep microenvironments showing extensions called retinacula cutis.
Leandra Santos Baptista +7 more
doaj +1 more source
Novel deletions causing pseudoxanthoma elasticum underscore the genomic instability of the ABCC6 region [PDF]
Mutations in ABCC6 cause pseudoxanthoma elasticum (PXE), a heritable disease that affects elastic fibers. Thus far, >200 mutations have been characterized by various PCR-based techniques (primarily direct sequencing), identifying up to 90% of PXE-causing
Chassaing, N +9 more
core +2 more sources
Null.
Aamer, Aleem, Farjah, Algahtani
openaire +2 more sources
Here we describe two new species of Inocybe from pine forests of Pakistan; I. hazarensisand I. shimlaensis. Morphological and molecular data show that these species have not been described before and hence need to be described as new. Both species are smooth‐spored and pruinose only in the apical part of the stipe.
Arooj Naseer +7 more
wiley +1 more source
Cutis Verticis Gyrata Secondary to Cerebriform Intradermal Naevus: A rare entity and its Management
Cutis verticis gyrata (CVG) is a rare skin disorder characterised by thick skin folds and grooves, resembling the gyri and sulci of the cerebral cortex. It can be classified as primary essential, primary non-essential and secondary CVG. The rarity of the
Jia Yuan Lee +4 more
doaj +1 more source

