Results 71 to 80 of about 2,048 (238)
Sebaceous gland: Milestones of 30‐year modelling research dedicated to the “brain of the skin”
Experimental Dermatology, Volume 29, Issue 11, Page 1069-1079, November 2020., 2020 Abstract In 2018, Schneider and Zouboulis analysed the available tools for studying sebaceous gland pathophysiology in vitro. Since then, the interest in this field remains unbroken, as demonstrated by recent reviews on sebaceous gland physiology, endocrinology and neurobiology, the role of sebaceous glands beyond acne, and several original works on ...
Christos C. Zouboulis +4 more
wiley +1 more source
Revista Brasileira de Reumatologia, 2009 A osteoartropatia hipertrófica primária é uma síndrome rara, caracterizada pela presença de baqueteamento digital de mãos e pés, aumento das extremidades e de tecidos periarticulares secundários à proliferação óssea, fisionomia facial grosseira, dor e ...
Aline Biral Zanon +4 more
doaj +1 more source
Whole-Exome Sequencing Enables Rapid Determination of Xeroderma Pigmentosum Molecular Etiology [PDF]
, 2013 Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder haracterized by extreme sensitivity to actinic pigmentation changes in the skin and increased incidence of skin cancer. In some cases, patients are affected by neurological alterations. XP
Bermúdez, Olga +10 more
core +2 more sources
Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome? [PDF]
, 2011 Ectopic liver is a very uncommon developmental anomaly that predisposes to the development of hepatocellular carcinoma. We describe the second documented case of a hepatocellular carcinoma developing in the primary liver of a patient with a rare and ...
Cathomas, Gieri +5 more
core +7 more sources
Indian journal of dermatology, venereology and leprology, 2012 I, Hassan +3 more
openaire +3 more sources
Touraine-Solente-Gole Syndrome: A Rare Case Report
Delhi Journal of Ophthalmology, 2017 Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi +2 more
doaj +1 more source
Hypertrophic osteopathy in a cat with a concurrent injection-site sarcoma. [PDF]
, 2015 Case summary An 11-year old neutered female domestic shorthair cat presented for investigation of a large, partially ulcerated skin mass in the area of the left scapula. The cat had been vaccinated 6 weeks previously in the same area.
Constantino-Casas, Fernando +3 more
core +2 more sources
Revista Brasileira de Reumatologia, 2007 Apresentamos o caso de um paciente com baqueteamento digital e artrite que foi diagnosticado como tendo osteoartropatia hipertrófica primária. Essa é uma doença rara e benigna.
Aldo Lainetti +3 more
doaj +1 more source
Sclerosing bone dysplasia from 16th century Sardinia (Italy): a possible case of Camurati-Engelmann disease [PDF]
, 2016 The skeletal remains of a male aged 45–55 years displaying several bone anomalies were unearthed from the Alghero (Sardinia) plague cemetery ‘lo Quarter’, a burial site dating back to the 1582–1583 AD outbreak.
BANDIERA P. +7 more
core +1 more source
Pachydermoperiostosis-Like Disease In Captive Red Ruffled Lemurs (Varecia Variegatus Rubra) [PDF]
, 2011 Pachydermatoperiostosis, a rare form of hypertrophic osteoarthropathy, is of unknown etiology and previously thought limited to humans. The only periosteal reaction previously reported in prosimians is related to renal disease.
Bruce Rothschild +2 more
core +1 more source