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Research 121–150 of 1000+
- Idiopathic Hirsutism*
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- SUCCESSFUL 28-DAY COMBINATION THERAPY OF MALASSEZIA DERMATITIS IN A 1-YEAR-OLD MIXED SMALL-BREED DOG: A CASE REPORT
- Pharmacology of anabolic steroids
- Green and Emerging Microextraction Strategies for Bioanalytical Determination of Hormones: Trends, Challenges, and Applications
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Management of “hyperandrogenism” confounded by dermatology biotin prescriptions
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- Primary cutaneous diffuse large B‑cell lymphoma of the scalp: A case report and brief review of the literature
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Werner's syndrome: incidental finding during pregnancy
- Role of Extracellular Vesicles as Mediators of Cell Communication and Novel Biomarkers in Sepsis
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Mycobacteriosis in a Pet Ferret (Mustela putorius furo) Caused by Mycobacterium xenopi: A Case Report on Neglected Risk of Zoonotic Transmission
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- E-Poster
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Trailing the Path to Preventive Oncology
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Definition criteria and diagnostic assessments