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Research 661–690 of 1000+
- Approach to Alopecia in Dogs in Clinical Practice
- Lifestyle changes and Nutrition in Polycystic Ovarian Disorder: A Holistic Review
- Hashimoto Thyroiditis - A Comprehensive Review
- The Skin at Different Ages
- Inflammatory and non-melanocytic tumoral pathology of the nail
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Association of Insulin Resistance with Hyperandrogenia in Women
- Hair and Nail Relationship
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- RETRACTED: Thyroid Dysfunction and Alopecia Areata: A Genetic Prediction Causality Analysis Study
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Interleukins gene polymorphism in alopecia areata patients: a systematic review
- Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels
- Current issues on the genetic implications and treatment of androgenic alopecia
- [Visual field defect in a patient given sodium valporate then carbamazepine: possible effect of aminotransferase inhibition].
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- 8242 A Case of Ayme Gripp Syndrome
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Alopecia Universalis with Frequently Relapsing Nephrotic Syndrome of Infantile Onset: A Rare Presentation
- Exosomes derived from uMSCs promote hair regrowth in alopecia areata through accelerating human hair follicular keratinocyte proliferation and migration
- 19-Year-Old Female with Hair Thinning and Heavy Periods
- Adult Onset Isolated Hypogonadotropic Hypogonadism- a Cause of Secondary Amenorrhea
- Ocular manifestation in progeria: A case report
- Hair Disorders
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Фрактальный обнаружитель эхo-сигнала
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Referee report. For: Hair greying in castrated mice [version 1; peer review: 1 approved with reservations]
- Updates in the understanding and treatments of skin & hair disorders in women of color