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Research 361–390 of 1000+
- Current Status of Hair Restoration Surgery
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- The incidental pore: Ca<sub>V</sub>1.2 and stem cell activation in quiescent hair follicles
- Ulerythema Ophryogenes in a Saudi Male: A Case Report
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- Triangular temporal alopecia: a rare case in adulthood
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Lichen Planopilaris
- Hypotrichosis in a child with olmsted syndrome
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- FGF5 is a crucial regulator of hair length in humans
- Interventions for androgenic alopecia in women
- Interventions for androgenic alopecia in women
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Nilotinib-induced generalized keratosis pilaris: Report of a rare case
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Genetic Basis of Male Pattern Baldness
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- A rare case of woolly hair with unusual associations
- Molecular Basis of Androgenetic Alopecia
- Androgenetische Alopezie
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Analogs of human genetic skin disease in domesticated animals