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Research 151–180 of 305
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Androgen Treatment in Women
- Androgen treatment in women
- Ethical Principles for Everyone
- Blinding in Placebo-Controlled Trials
- Dermatologic therapy: December 1986 to December 1987
- Transforming growth factor-β in stem cells and tissue homeostasis
- Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments
- Hardwiring Stem Cell Communication through Tissue Structure
- AMINOPTERIN IN TREATMENT OF LEUKEMIA IN CHILDREN
- Pegylated-interferon-α<sub>2a</sub>in clinical practice: how to manage patients suffering from side effects
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Testosterone Treatment in Women – An Overview
- Dermal Mucinosis in the Eosinophilia-Myalgia Syndrome
- Application of Platelet-Rich Plasma as a Stem Cell Treatment - anAttempt to Clarify a Common Public Misconception
- Techniques d'épargne cutanée dans la chirurgie de la gynécomastie
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Human Wharton’s Jelly Mesenchymal Stem Cells Plasticity Augments Scar-Free Skin Wound Healing with Hair Growth
- Abstract 14
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Disorders of Sex Development
- Sperm extraction in nonmosaic Klinefelter syndrome patients: A case series and literature review of sperm extraction in Klinefelter syndrome patients
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Iatrogenic Cushing's Syndrome in a Patient With Salt-Wasting Congenital Adrenal Hyperplasia (SWCAH)
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Treatment of Alopecia Universalis in a Child with Down Syndrome
- Development of Heritable Melanoma in Transgenic Mice