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Research 961–990 of 1000+
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Neonatal lupus syndrome in a Nigerian child
- Faun tail nevus: A series of 15 cases and their management with Intense Pulse Light
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Idiopathic isolated adrenocorticotropic hormone deficiency combined with testicular germ cell tumor: Case report
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Monilethrix
- Knowledge, Attitude, and Practice of Polycystic Ovarian Syndrome Diagnosis among Health Care Providers in Addis Ababa, Ethiopia
- Micronutrient Deficiencies and Digital Computerized Phototrichogram Analysis in Telogen Effluvium: A Retrospective Correlation Study in a Tertiary Medical Center
- Identification of Beta-Sitosterol and Stigmasterol as Possible Inhibitors of 5 Alpha-Reductase 1: An In-Silico Study
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The developmental basis of fingerprint pattern formation and variation
- Ichthyosis with confetti: clinics, molecular genetics and management
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Rooster feathering, androgenic alopecia, and hormone-dependent tumor growth: What is in common?
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Hair Keratin
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- The color of skin: white diseases of the skin, nails, and mucosa
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland
- Treatment of Nonclassic 11-Hydroxylase Deficiency with Ashwagandha Root
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Synthesis and Actions of 5α-Reduced Metabolites of Testosterone in the Nervous System