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Research 511–540 of 1000+
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Precocious Puberty
- Androgenetic alopecia: a review
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- Secondary Sexual Characteristics and Menses in Young Girls
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- Epidemiology, Treatment Patterns, and Healthcare Resource Utilization Study of Patients With Alopecia Areata in Taiwan’s National Health Insurance Research Database
- Quoi de neuf en recherche dermatologique ?
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- Akala Palitya: An Ayurvedic Review
- The Review On "Alopecia Areata: A Compressive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- POLYCYSTIC OVARY SYNDROME (PCOS): DIAGNOSIS, PATHOPHYSIOLOGY AND CONTEMPORARY THERAPEUTIC APPROACHES
- Epidemiologic Study of Gene Distribution in Romanian and Brazilian Patients with Non-Cicatricial Alopecia
- Oral Presentations
- British Society for Dermatopathology
- Serum Ferritin Levels amongst Individuals with Androgenetic Alopecia in Ile-Ife, Nigeria.
- HAIR LOSS IN WOMEN
- Alopecia Areata. Current situation and perspectives
- Low prevalence of twisted hair in anorexia nervosa
- Alopecia areata. Actualidad y perspectivas
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- POLY CYSTIC OVARIAN SYNDROME: AN UPDATED REVIEW
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- Exploring Clinical and Imaging Differences in COVID-19: an Observational Approach to the IFITM3 rs12252 Polymorphism
- Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency