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Research 871–900 of 1000+
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Focal and Generalized Alopecia
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Hair loss in children.
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- 5-Alpha-reductase deficiency in a Saudi "girl"
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- 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
- 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
- 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
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Gestational diabetes mellitus and COVID-19, clinical characteristics and review of the literature
- Oral Manifestations of Hematologic and Nutritional Diseases
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family