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Research 121–150 of 1000+
- Cutaneous Clues to Metabolic Dysfunction: Dermatological Manifestations of Diabetes and Insulin Resistance in Clinical Practice
- Integrative homoeopathic management of acne vulgaris: A narrative review combining constitutional prescribing with targeted topical mother tincture
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Polycystic ovary syndrome — the skin as a mirror of endocrine disorders
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Immunological control of skin development: from homeostasis to developmental pathologies
- The Impact of Bariatric Surgery on the Development and Progression of Dermatologic Diseases: A Narrative Review
- SYSTEMATIC REVIEW OF PHARMACOTHERAPY STRATEGIES IN THE MANAGEMENT OF HIDRADENITIS SUPPURATIVA
- To evaluate the causes and possible treatments for alopecia seborrheic in adolescents
- Adrenal causes of endocrine hypertension in childhood or adolescence
- A Unique Acquired Athletic Dermatologic Condition in a Half Marathon Participant: An Autobiographical Case Report of Sports-Associated Clothing Related Axillary Tangled Clumped Hairs (SCRATCH)
- Effects of local and systemic medications on eye health: Adverse reactions
- Hormonal Influences on Women's Health and Athletic Performance: Insights into the Menstrual Cycle, Menopause, Contraception, and Anabolic Steroids
- If Women Just had Their Hormones Back the Way they Were!
- Hashimoto Thyroiditis - A Comprehensive Review
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- AN SYNOPTIC OVERVIEW ON AUTOIMMUNE DISORDERS AND ITS MANAGEMENT
- Complex Regional Pain Syndrome Type I : measurements and treatment
- CME examination for volume 43
- Neuroimmunology of Stress: Skin Takes Center Stage
- Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart
- Androgenetic alopecia: combing the hair follicle signaling pathways for new therapeutic targets and more effective treatment options
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A CASE REPORT OF PARANOID DELUSION WITH VENLAFAXINE USE
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations