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Research 451–480 of 1000+
- What is behind the ‘swarm of bees’ in alopecia areata
- Alopecia Areata - Current and Emerging Therapies
- Acne
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Molecular basis of androgen receptor diseases
- Bioengineered Plants Can Be a Useful Source of Omega-3 Fatty Acids
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Ulcerative colitis and total alopecia in a mother and her son
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Keratins: the hair shaft's backbone revealed
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Cutaneous Manifestations of Mucopolysaccharidoses
- Taiwanese Dermatological Association consensus on the diagnosis and management of alopecia areata
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Abstracts
- Androgenic Alopecia: A Comprehensive Literature Review of Epidemiology, Pathophysiology, Diagnosis, and Management
- The Specific Dermatoses of Pregnancy
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Lipedematous scalp with lipedematous alopecia: A case report
- Perspectives of Kennedy's disease
- PCOS: update and diagnostic approach
- Open questions in hidradenitis suppurativa research: a hair biologist's perspective
- VITILIGO: WHAT’S OLD, WHAT’S NEW?
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Insulin Resistance Syndrome- the Sensitive IRS
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I