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Research 271–300 of 1000+
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- Incorporation of Isotopically Labeled Cocaine and Metabolites into Human Hair: 1. Dose-Response Relationships
- Effects of in Utero Exposure to Finasteride on Androgen-Dependent Reproductive Development in the Male Rat
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Stability of opiates in hair fibers after exposure to cosmetic treatment
- Feline atopic dermatitis: a retrospective study of 45 cases (2001–2012)
- BIOLOGICAL ACTIVITY OF ANTIANDROGENS
- Toward a Diagnostic Score in Cushing's Syndrome
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Clinical picture, diagnosis, treatment and outcome of severe acute respiratory syndrome (SARS) in children
- Polycystic ovary syndrome (PCOS)
- Testosterone Is a Contraceptive and Should Not Be Used in Men Who Desire Fertility
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- (Un)targeted Scanning of Locks of Hair for Drugs of Abuse by Direct Analysis in Real Time–High-Resolution Mass Spectrometry
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- How to Diagnose Hair Loss
- Genetic Hair Disorders: A Review
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Contact allergy to essential oils cannot always be predicted from allergy to fragrance markers in the baseline series
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Generation of Skin Organoids: Potential Opportunities and Challenges
- Clinical Case Seminar: Postmenopausal androgen excess-challenges in diagnostic work-up and management of ovarian thecosis
- Stem and progenitor cells in sebaceous gland development, homeostasis and pathologies
- Pustular allergic contact dermatitis caused by fragrances
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Medical Options for Care of Gender Diverse and Transgender Youth
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis