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Research 811–840 of 1000+
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- [Hormonal interaction and hair growth].
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Marie-unna hereditary hypotrichosis
- Monilethrix, a rare inherited hair shaft disorder in siblings
- A Brief Overview of the Role of Drugs and Novel Methodologies on the Stability and Growth of Hair Follicles: An Approach Towards Hair Regeneration
- Chapter 14 Principles of drug metabolism
- Alopecia Areata in Skin of Color Patients: New Considerations Sparked by the Approval of Baricitinib
- Male androgenetic alopecia
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Moderne Untersuchungsmethoden zur Evaluation von Haarausfall und Alopezie bei Frauen
- VINCENT BARRANCO, M.D., EDITOR 2121 EAST 21ST STREET, P.O. BOX 52588 TUESA, OK 74152-0588.
- Book review
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Recent advances in congenital ichthyoses
- ANDROGENETIC ALOPECIA
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- A clinical case of CNOT3 syndrome in a 10-year-old girl
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- FC056 The ideal catagen of the hair
- Prioritizing Susceptibility Genes for the Prognosis of Male-pattern Baldness with Transcriptome-wide Association Study
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Nonclassic 21-hydroxylase deficiency
- Update on Melasma—Part I: Pathogenesis
- ТУБЕРОЗНЫЙ СКЛЕРОЗ (БУРНЕВИЛЛЯ-ПРИНГЛА). ОБЗОР ЛИТЕРАТУРЫ
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- 10-Year-Old Female with an Irregularly Shaped Patch of Hair Loss