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Research 691–720 of 1000+
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Histopathological evaluation of urethroplasty with buccal mucosa graft: an experimental study in rabbit
- Topical Cyclosporine in Alopecia Areata
- Temporal triangular alopecia and a review of 52 past cases
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Basics of androgen synthesis and action
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- Hair and Nail Relationship
- Epidermal dysplasia and <i>Malassezia</i> infection in two West Highland White Terrier siblings: an inherited skin disorder or reaction to severe <i>Malassezia</i> infection?
- Skin Development and Disease: A Molecular Perspective
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- Ectrodactyly, Soft‐Tissue Syndactyly, and Nodulocystic Acne: Coincidence or Association?
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- The role of cochlea extracellular matrix in age related hearing loss
- Secondary Amenorrhea and Clinical Hyperandrogenism in a 34-Year-Old Female: Polycystic Ovary Syndrome or Not?
- Birth Outcomes of Infants Born to Mothers with Alopecia Areata: A Nationwide Population-based Study in Korea
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- What Work-Up Should Be Done for Patients With Alopecia?
- 301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa
- Early Onset Werner Syndrome
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Abstracts
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Eflúvio telógeno após dermatite de contato no couro cabeludo
- Trichonodosis: a case report and literature review
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix