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Research 181–210 of 1000+
- Hair Loss: Diagnosis and Treatment.
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Gynecomastia and Premature Thelarche
- Current systemic treatment strategies for hidradenitis suppurativa
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Genes for Hair and Avian Keratins
- Tracing the cellular origin of cancer
- The Mossman–Pacey Paradox
- Transcriptomic analyses of regenerating adult feathers in chicken
- Case Report: Postmenopausal hyperandrogenism misled by adrenal incidentaloma: a rare case of androgen-secreting ovarian adult granulosa cell tumor and clinical implications
- Evo Devo of the Vertebrates Integument
- A review of modern surgical hair restoration techniques
- De novo assembly and annotation of Asiatic lion (<i>Panthera leo persica</i>) genome
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Avanços terapêuticos no tratamento da alopecia androgenética: Uma revisão das evidências científicas atuais
- Who Tells the Story of the Treatment of Androgenetic Alopecia?—A Bibliometric Analysis From 2003 to 2023
- Lymphoproliferative Disorders: Hot Topics in Dermatology 2019
- CRISPR–Cas9: A History of Its Discovery and Ethical Considerations of Its Use in Genome Editing
- The role of multiomics in revealing the mechanism of skin repair and regeneration
- Androgenetic alopecia and risk of coronary artery disease
- Immunodeficiency Disorders
- Biology of hair pigmentation and its role in premature canities
- Diseases of Periocular Hair
- 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation
- Ubiquity and Diversity of Human-Associated Demodex Mites
- Isolation and Characterization of Mouse High-glycine/Tyrosine Proteins
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome