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Research 421–450 of 1000+
- Hereditary, Congenital, and Acquired Alopecias
- Effects of androgen overproduction on skin target organs in children with congenital adrenal hyperplasia
- Mice Expressing a Mutant Krt75 (K6hf) Allele Develop Hair and Nail Defects Resembling Pachyonychia Congenita
- A novel point mutation of keratin 17 (<i>KRT17</i>) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb
- BENEFÍCIOS DO USO DA TOMOGRAFIA COMPUTADORIZADA NO DIAGNÓSTICO DE POSSÍVEL MICROCEFALIA DEVIDO À INFECÇÃO CONGÊNITA PELO ZIKA VÍRUS
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Structure and Expression of a New Complementary DNA Encoding the almost Exclusive 3β-Hydroxysteroid Dehydrogenase/Δ<sup>5</sup>-Δ<sup>4</sup>-lsomerase in Human Adrenals and Gonads
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Structural abnormalities of the hair shaft
- Hypertrichosis
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Critical Developmental Periods for Effects on Male Rat Genitalia Induced by Finasteride, a 5α-Reductase Inhibitor
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Acne as a chronic systemic disease
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The clinical evaluation of hirsutism
- The Use of Micrografts and Minigrafts in the Aesthetic Reconstruction of the Face and Scalp
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Adverse Reactions to Oral Retinoids An Update
- Diagnostic Criteria for Polycystic Ovarian Syndrome
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- Hirsutism: Diagnosis and management
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Vitamin D<sub>3</sub>Analogs Stimulate Hair Growth in Nude Mice