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Research 931–960 of 1000+
- Central nervous system involvement in autoimmune polyglandular syndrome
- Collodion baby case series: the success of oral retinoic acid
- Vulvovaginal involvement in Netherton syndrome: A case report
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Treatment of Keratosis Pilaris With 810-nm Diode Laser
- Ovarian steroid cell tumor in a teenager masquerading as polycystic ovary syndrome: a case report and literature review
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
- Congenital atrichia associated with situs inversus and mesocardia
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Topical niacinamide 4% and desonide 0.05% for treatment of axillary hyperpigmentation: a randomized, double-blind, placebo-controlled study
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Varying Presentation of Type 1 Polyglandular Failure in India
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- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Mixed Form of Hirsutism in Adolescent Females and Laser Therapy
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Ehlers-Danlos syndrome: From bedside to bench