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Research 151–180 of 235
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- Risk of Acute Pancreatitis in Users of Finasteride
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- Pincer Nails – A Rare Manifestation of Systemic Lupus Erythematosus
- The skin manifestations in end-stage renal disease patients in Jordan, single-center experience
- Serum Vitamin D Level in Pediatric Alopecia Areata
- THU471 Resolution Of Elevated Alkaline Phosphatase After Joint Replacement In Severe Osteoarthritis
- Calcified Epidermal Cyst on the Neck
- Bone Health - Running. Can You Outrun Your Past?
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity
- Autoimmunity: Alopecia Areata
- Madarosis: A marker of many Maladies
- FOXN1 deficient nude severe combined immunodeficiency
- Pernicious anemia in a patient with Type 1 diabetes mellitus and alopecia areata universalis
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Testosterone therapy for women with low sexual desire: a position statement from the Brazilian Society of Endocrinology and Metabolism
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Diphenylcyclopropenone-Induced Vitiligo in a Patient with Alopecia Universalis
- Study of the Thyroid Profile of Patients with Alopecia
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Where is the data? Delayed and chronic irAE surveillance and management after cessation of ICIs: expert insights from SITC on survivorship care and the need for long-term data
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Autoimmune Polyglandular Syndrome Type 2 Presentation with Alopecia Universalis, Hashimoto’s Disease, and Addison’s Disease
- Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents
- Intracranial hypertension as the first manifestation of systemic lupus erythematosus: A case report
- E-Poster
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association