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Research 661–690 of 1000+
- Immunological aspects and gender bias during respiratory viral infections including novel Coronavirus disease‐19 (COVID‐19): A scoping review
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Abstracts
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Inhibitory effect of tianeptine on catagen induction in alopecia areata-like lesions induced by ultrasonic wave stress in mice
- A newborn presenting with congenital blistering
- Alopecia in children
- Alcohol extract from Vernonia anthelmintica willd (L.) seed counteracts stress-induced murine hair follicle growth inhibition
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Global Trends in Research of Androgen Receptor Associated With Breast Cancer From 2011 to 2020: A Scientometric Analysis
- Circadian rhythm sleep-wake disorders (CRSWDs): Linking circadian misalignment to adverse health outcomes.
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Werner′s syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Telogen elongation in the hair cycle of <i>ob/ob</i> mice
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Congenital atrichia with papular lesions
- Hypotrichosis with juvenile macular dystrophy
- Le gène<i>hairless</i>de la souris
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- 277 An open label pilot clinical trial of the JAK inhibitor tofacitinib for alopecia areata
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Generation of iPS-derived model cells for analyses of hair shaft differentiation
- An unusual presentation of X-linked adrenoleukodystrophy
- A 40-Year-Old Woman With Facial Papules and Flank Pain