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Research 511–540 of 1000+
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- Penis Endocrinology
- Decades of progressive red and yellow nodules
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Hair and Nail Relationship
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Insulin resistance is increased in alopecia areata patients
- CLINICAL UPDATES IN HAIR
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Evidence based homoeopathy: A case report on androgenic alopecia in 23 year old male
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- Review Article - Changing trends in hair restoration surgery
- Alopecia and its medical management
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Gestational diabetes mellitus and COVID-19, clinical characteristics and review of the literature
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Alopecia and Hirsuties
- Congenital atrichia and hypotrichosis
- The clinical spectrum of parathyroid disease
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases