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Research 211–240 of 1000+
- Pulse corticosteroid therapy with oral dexamethasone for the treatment of adult alopecia totalis and universalis
- Polycystic ovary syndrome (PCOS)
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- SWEET SYNDROME: AN UNUSUAL PRESENTATION OF CHRONIC GRANULOMATOUS DISEASE IN A CHILD
- Alopecia androgénica masculina y factores de riesgo cardiovascular: estudio de casos y controles
- Prevention of Frey syndrome with superficial temporal fascia interpositioning: a retrospective study
- Improvement of Satoyoshi syndrome with tacrolimus and corticosteroids
- Insulin resistance is increased in alopecia areata patients
- Satoyoshi syndrome: A rare multisystemic disorder requiring systemic and symptomatic treatment
- Follicular mucinosis in association with Sezary syndrome
- Localized cutaneous necrosis associated with the antiphospholipid syndrome
- Alopecia Universalis Associated with Cutaneous T Cell Lymphoma
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Down Syndrome and Autoimmune Disease
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Satoyoshi Syndrome
- Alopecia areata with white hair regrowth: case report and review of poliosis
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Successful induction of oral tolerance in Netherton syndrome
- Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- The coudability sign of alopecia areata: the real story
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Case Report: Rowell Syndrome–Like Flare of Cutaneous Lupus Erythematosus Following COVID-19 Infection
- Treatment of Satoyoshi syndrome: a systematic review
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia