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Research 301–330 of 1000+
- Management of congenital ichthyoses: European guidelines of care, part two
- Female Pattern Hair Loss and Androgen Excess: A Report From the Multidisciplinary Androgen Excess and PCOS Committee
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Acne and hidradenitis suppurativa
- Assessment of a Bidirectional Association Between Major Depressive Disorder and Alopecia Areata
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Central centrifugal cicatricial alopecia: possible familial aetiology in two African families from South Africa
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- Acquired progressive kinking of the hair in a prepubertal boy
- Frontal fibrosing alopecia: a disease that remains enigmatic
- Alopecia in children
- Conditions simulating androgenetic alopecia
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Scalp basal cell carcinoma: A different entity?
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Alopecias in humans: biology, pathomechanisms and emerging therapies
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Hair, Hormones, and High-Risk Prostate Cancer
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Etiopathogenesis of Alopecia Areata
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Genomic Analysis of Trichotillomania
- Congenital Lipedematous Alopecia in a 6-Year-Old Asian Boy
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Assessment and treatment of adolescent hair loss
- Berardinelli–Seip syndrome
- Global Burden of Alopecia Areata and Associated Diseases: A Trend Analysis From 1990 to 2021.