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Research 661–690 of 1000+
- Diagnostic approach to low‐renin hypertension
- Congenital adrenal hyperplasia
- Transcriptomic inspection revealed a possible pathway regulating the formation of the high-quality brush hair in Chinese Haimen goat ( <i>Capra hircus</i> )
- Biotinidase deficiency characterized by skin and hair findings
- Skin Deep and Deeper: Multiple Pathways in Basal Cell Carcinogenesis
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Traditional and Integrative Approaches to the Treatment of Alopecia
- Biology of Human Hair: Know Your Hair to Control It
- The Clinical Presentation of Systemic Lupus Erythematosus
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Managing polycystic ovary syndrome in primary care
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Role of skin enzymes in metabolism of topical drugs
- Ether: Fiction or Reality? A Review
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Hashimoto Thyroiditis - A Comprehensive Review
- Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments
- Hypertension and Cicatricial Hair Loss: Defining High Value Symptom Clusters within Reproductive Aging
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair and nail involvement in lupus erythematosus