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Research 30 of 37
- Cantú syndrome with coexisting familial pituitary adenoma
- Inherited Disorders of the Hair
- Cutaneous drug reactions
- Main Plenary Sessions: Summaries of Papers
- Dermatologic manifestations of endocrine disorders
- The eye and the skin in endocrine metabolic diseases
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- E-Poster
- Polycystic Ovary Syndrome in the Context of Pituitary Adenomas: Prevalence, Pathophysiology and Clinical Management
- TONGUE, RED
- Acromegaloid Facial Appearance: Case Report and Literature Review
- [Hirsutism and hypertrichosis in adults: investigations and treatment].
- Pseudoacromegaly induced by the long-term use of minoxidil
- Menstrual Irregularity in Women with Acromegaly
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Cutaneous Manifestations of Eating Disorders
- Cutaneous Manifestations of Eating Disorders
- Endocrinopathies and Other Disorders Inducing a Polycystic Ovary Syndrome Phenotype
- Syndromes of Severe Insulin Resistance (SSIRs)
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Biology of Hair Growth
- Diffuse idiopathic skeletal hyperostosis in a 33-year-old woman with PCOS and metabolic syndrome: a rare scenario
- Evaluación clínica del pelo corporal en una población de mujeres colombianas: determinación del punto de corte para el diagnóstico de hirsutismo
- The Case of the Elusive Androgen
- Endocrinologia e Medicina Estética Ed. X
- Iperandrogenismo della donna in menopausa
- Evaluación endocrinológica en el acné
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature