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Research 91–120 of 1000+
- Farmácia Sanches - Leiria e nos Serviços Farmacêuticos do Hospital Lusíadas - Porto
- Ovarian Leydig cell tumor and postmenopausal hirsutism with signs of virilisation
- Androgenisierung
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- Diabetes, ovarian tumor, hyperparathyroidism, and papillary cancer: A chance association?
- Hyperadrenocorticism in Ferrets
- Gonadal Sex Steroids: Production, Action and Interactions in Mammals
- The therapeutic use of androgens in women
- The Case of the Elusive Androgen
- Aging and Immortality: Quasi-Programmed Senescence and Its Pharmacologic Inhibition
- Ovarian Hilus-Cell Hyperplasia and High Serum Testosterone in a Patient With Postmenopausal Virilization
- Postmenopausal Hyperandrogenism due to Ovarian Hyperthecosis
- Immunohistochemical, pharmacovigilance, and omics analyses reveal the involvement of ATP-sensitive K+ channel subunits in cancers: role in drug–disease interactions
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Role of regeneration in tissue repairing and therapies
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Síndrome PRIDE: una práctica forma de identificar los efectos adversos cutáneos de los inhibidores del EGFR
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- Factores de riesgo cardiovascular en pacientes con alopecia androgenética: síndrome metabólico y ateromatosis carotidea
- Síndrome do nevo de Becker
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Syndrome des ovaires polykystiques : Point de vue contemporain
- Clinical characterization of men with long QT syndrome and torsades de pointes associated with hypogonadism: A review and pharmacovigilance study
- Gilles de la Tourette syndrome – A treatable condition?
- A meta-analysis of the relationship between vitamin D receptor gene ApaI polymorphisms and polycystic ovary syndrome
- Abordagens psicológicas e novas terapêuticas perante as escolhas do paciente portador da Síndrome de Morris
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Tratamento bem sucedido de síndrome dos cabelos anágenos frouxos: um relato de caso
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene