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Research 841–870 of 1000+
- Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Scientific Highlights from the Society for Investigative Dermatology 2010 Annual Meeting
- Unexpected Autocrine Role of Vascular Endothelial Growth Factor in Squamous Cell Carcinoma
- Models for Skin Cancer
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- This month in JAAD Case Reports: October 2023—Central centrifugal cicatricial alopecia in Black men
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- STAT3 Inhibits Cell Proliferation at Least in Part Via Directly Negatively Regulating FST Gene Expression
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Clouston’s syndrome: a rare case report
- KRT16 wt Allele
- Roles of the Hedgehog Signaling Pathway in Cutaneous Physiology and Oncology
- 890 Development of pigmented reconstructed human epidermis model containing human melanoblasts from keratinocyte culture
- Acne-Associated Syndromes
- Follicular Neutrophilic Inflammation (Hidradenitis Suppurativa)
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- Trichothiodystrophy in a child with occult learning disorder
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- News in brief
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Syndromes of Severe Insulin Resistance (SSIRs)
- One Transgene: Two Outcomes
- One Transgene: Two Outcomes