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Research 121–150 of 1000+
- Potential adverse effects of long-term testosterone therapy
- Acne as a chronic systemic disease
- Dermatoscopy of hair shaft disorders
- Mechanism of Sleep Disturbance in Children with Atopic Dermatitis and the Role of the Circadian Rhythm and Melatonin
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- STEROIDS AND STEROID-LIKE COMPOUNDS
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Nonclassic Congenital Adrenal Hyperplasia
- Premature graying of hair
- Endocrine-skin interactions
- Toward a Diagnostic Score in Cushing's Syndrome
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- Current evaluation of amenorrhea
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- A Clinical Approach to Severe Insulin Resistance
- Nonclassic congenital adrenal hyperplasia
- Current evaluation of amenorrhea
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- What does acne genetics teach us about disease pathogenesis?
- Diagnostic approach to low‐renin hypertension
- Further Clinical Evidence for the Effect of IGF-1 on Hair Growth and Alopecia
- Trichotillomania in Children
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Congenital adrenal hyperplasia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Systematic review of the therapeutic roles of adipose tissue in dermatology
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Congenital adrenal hyperplasia
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain