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Research 841–870 of 1000+
- Congenital adrenal hyperplasia
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Autoimmunity: Alopecia Areata
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Human epidermal neural crest stem cells as a source of Schwann cells
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Crystalline Cataract and Uncombable Hair
- Hair and Nail Relationship
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Analyzing Big EHR Data—Optimal Cox Regression Subsampling Procedure with Rare Events
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- ACE1 rs1799752 polymorphism is not associated with long-COVID symptomatology in previously hospitalized COVID-19 survivors
- Alopecia and hirsutism*
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- Patologías dermatológicas de origen nutricional en los pequeños animales: una revisión
- Genomics
- Coexistence of psoriasis, and alopecia areata with trachyonychia in a pediatric patient with Turner Syndrome
- A guide to diagnosis and management of hypertrichosis
- Melanocytes and Vitiligo (and Hair Graying)
- REVIEW ON PREMATURELY GREYING OF HAIR IN CHILDREN: CLINICAL ASPECTS, ETIOPATHOGENESIS AND HOMOEOPATHIC MANAGEMENT
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- POLYCYSTIC OVARY SYNDROME (PCOS): DIAGNOSIS, PATHOPHYSIOLOGY AND CONTEMPORARY THERAPEUTIC APPROACHES
- Mitochondrial dysfunction in metabolic syndrome and inflammatory skin disease
- Vitiligo
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies