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Research 121–150 of 811
- Endocrinology
- Contents
- A review of hyperandrogenism state in polycystic ovarian syndrome
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- SUMMARIES OF PAPERS
- Cutaneous signals of immune system disease
- Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart
- Idiopathic CD4+ T-lymphocytopenia
- Congenital adrenal hyperplasia
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Neonatal Occipito-Lınear and Temporo-Fronto-Parıetal Alopecıa: Can Non-Marginal and Marginal forms of the Transient Neonatal Hair Loss be Found Together?
- DERMATOLOGICAL AND SYSTEMIC REACTIONS TO HAIR DYES: CURRENT EVIDENCE AND MANAGEMENT
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Reporting on Adverse Clinical Events
- Penis Endocrinology
- Genetic Defects of Female Sexual Differentiation
- The skin findings of pregnant women and our treatment choices. A Turkish experience: a 5-year survey.
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Endocrinologia e Medicina Estética Ed. X
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- Spontaneous hair hyperpigmentation in response to vitamin intake in pregnancy—A clue for homocystinuria
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Two parietal cephaloceles in a female neonate
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- Recommendations from the 2023 international evidence-based guideline for the assessment and management of polycystic ovary syndrome
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency