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Research 301–330 of 1000+
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Loose anagen syndrome in one identical twin girl
- The autoimmune basis of alopecia areata: A comprehensive review
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Inborn Errors of Biotin Metabolism
- <i>CCDC47</i> gene and trichohepatoneurodevelopmental syndrome: Report of the fifth and sixth cases from Saudi Arabia
- Alopecia Areata in Children
- Alopezien und Hypotrichosen im Kindesalter
- What is behind the ‘swarm of bees’ in alopecia areata
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Evaluation of the Environmental Risk Factors and Comorbidities in Patients with Lichen Planopilaris: A Case-Control Study
- The Pathogenesis of Primary Cicatricial Alopecias
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Cutaneous Manifestations of Mucopolysaccharidoses
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Autoimmune Disease Induction in a Healthy Human Organ: A Humanized Mouse Model of Alopecia Areata
- Monilethrix in three generations
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Management of congenital ichthyoses: European guidelines of care, part two
- <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
- Nonclassic 21-hydroxylase deficiency
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Alopecia Areata - Current and Emerging Therapies
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2