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Research 211–240 of 237
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Changes in bone mineral density in women with early-onset androgenetik alopecia and their correlations with hair-loss stages: a cross-sectional study
- 66-Year-Old Woman With Painless Vesicular Lesions
- TONGUE, RED
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Autoimmunity: Alopecia Areata
- COVID-19 and endocrine and metabolic diseases. An updated statement from the European Society of Endocrinology
- FOXN1 deficient nude severe combined immunodeficiency
- Pregnancy and Skin
- 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
- 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
- Association of Acne Tarda with Endocrinological Disorders
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- DIETHYLPROPION
- Parathyroid adenoma with coeliac disease: primary or quaternary hyperparathyroidism? Gruczolak przytarczyc i choroba trzewna: pierwotna czy czwartorzędowa nadczynność przytarczyc?
- Idiopathic hypoparathyroidism with extensive intracranial calcification in children
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1