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Research 331–360 of 1000+
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Polycystic Ovarian Syndrome - What is New
- Congenital adrenal hyperplasia
- Regulation and dysregulation of hair regeneration: aiming for clinical application
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- Congenital Adrenal Hyperplasia
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health
- A Comprehensive Review on Skin Pigmentation-Types, Causes, and Treatment
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- The PI3K-Akt-mTOR and Associated Signaling Pathways as Molecular Drivers of Immune-Mediated Inflammatory Skin Diseases: Update on Therapeutic Strategy Using Natural and Synthetic Compounds
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Scalp hair cortisol concentration in patients with alopecia areata and correlate its level with the disease variables
- Current understanding and treatment of sex hormone-related hair diseases
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Syndromes of Severe Insulin Resistance (SSIRs)
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Clinical biochemistry of dihydrotestosterone
- A missing piece: the spiny mouse and the puzzle of menstruating species
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials