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Research 811–840 of 1000+
- Effects of Selenium and Other Micronutrient Intake on Human Health
- Factors associated with early-onset androgenetic alopecia: A scoping review
- Correlation between sebum level and severity of male androgenetic alopecia
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Cutaneous findings and systemic associations in women with polycystic ovary syndrome
- Dermatology consultations significantly contribute to efficient care of hospitalized patients: A prospective study of dermatology inpatient consults at a tertiary care center
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- Non-Neoplastic Disorders of Hair
- National scientific medical meeting 1996 abstracts
- Molecular genetics of androgen insensitivity
- A Child with Nonscarring Alopecia
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- AVALIAÇÃO DO USO DE TELAS DIGITAIS POR CRIANÇAS E ADOLESCENTES EM TEMPOS DE PANDEMIA
- Farmácia dos Clérigos - Porto e nos Serviços Farmacêuticos da University College Hospital - Londres, Reino Unido, ao abrigo do programa Erasmus+
- Farmácia Padrão da Légua, Custóias e nos Serviços Farmacêuticos da Klinicka Bolnica Dubrava, Croácia
- Millets as a Novel Solution for PCOS Management: a Review
- Modelling androgen synthesis and action during human sexual differentiation
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis