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Research 61–90 of 1000+
- The clinical spectrum of parathyroid disease
- Vitamins
- Endocrinology
- Role of anabolic agents in colorectal carcinogenesis: Myths and realities (Review)
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Lab Quality Management and Methodology
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- Cytostatics and immunosuppressive drugs
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- Vitamin D levels in patients with seborrheic dermatitis
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Biology and Genetics of Hair
- Alopecia in Belgian Blue crossbred calves: a case series
- The Effect of Parathyroid Hormones on Hair Follicle Physiology: Implications for Treatment of Chemotherapy-Induced Alopecia
- Dermatoses of pregnancy
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Male fertility and skin diseases
- Pregnancy and Skin
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Mucocutaneous manifestations of acquired hypoparathyroidism: An observational study
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- The Effect of Drugs on Hair
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Topical minoxidil therapy in hereditary androgenetic alopecia
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor