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Research 451–480 of 1000+
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- Endocrinology
- Association of Acne Tarda with Endocrinological Disorders
- Table of Contents
- Ameliorative Impact of High Inositol Diet on the Insulin Resistance and Metabolite Hormones among Women with Polycystic Ovary Syndrome
- Systemic Antifungals
- Significance of stress keratin expression in normal and diseased epithelia
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- Testosterone: The Male Sex Hormone
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz
- Congenital Hypotrichosis with Hair and Dental Ectodermal Features Responsive to Sublingual Minoxidil
- A Hairy Paradox: Congenital Triangular Alopecia with a Central Hair Tuft
- Scalp hair 17‐hydroxyprogesterone and androstenedione as a long‐term therapy monitoring tool in congenital adrenal hyperplasia
- Congenital hypotrichosis - treatment with topical minoxidil and hair dye
- Regrowth of hair in congenital triangular alopecia induced by sublingual minoxidil
- Steroid 17-Hydroxyprogesterone in Hair Is a Potential Long-Term Biomarker of Androgen Control in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
- Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
- A Congenital Hair Defect: Trichoschisis With Alternating Birefringence and Low Sulfur Content
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- 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
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].
- Hair follicles and their role in skin health
- Natural hair patterns