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Research 421–450 of 1000+
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- An Update of Congenital Adrenal Hyperplasia
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Hashimoto Thyroiditis - A Comprehensive Review
- Current and Emerging Approaches to Androgenetic Alopecia
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Melanocytes: The new Black
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Tatalaksana Alopesia Androgenetik
- AN OVERVIEW ON POLYCYSTIC OVARIAN SYNDROME
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Polycystic ovary syndrome
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Partial Reversal of Canities in a 22-Year-Old Normal Chinese Male
- Cleave but not leave: Astrotactin proteins in development and disease
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- A missense mutation in Lama3 causes androgen alopecia
- Ulcerative colitis and total alopecia in a mother and her son
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Oral Presentations
- HAIR KERATINIZATION IN HEALTH AND DISEASE