Search
for
Sort by
Research 511–540 of 1000+
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- Endocrinology
- Use of Contact Immunotherapy in the Treatment of Skin Diseases Other than Alopecia Areata
- Conference 2022, The Sequel
- Proteomics as a tool to improve novel insights into skin diseases: what we know and where we should be going
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital hair loss disorders: Rare, but not too rare
- 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
- 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
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- 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].
- Natural hair patterns
- AN UPDATE OF HAIR SHAFT DISORDERS