نتایج جستجو برای: polycystic

تعداد نتایج: 19013  

2017
Sebastião Freitas de-Medeiros Márcia Marly Winck Yamamoto Matheus Antônio Souto de-Medeiros Jacklyne Silva Barbosa Robert John Norman

BACKGROUND The purpose of the study was to examine whether patients with subclinical hypothyroidism (SCH) should be excluded before making a diagnosis of polycystic ovary syndrome (PCOS). METHODS Seven hundred sixteen patients, 462 with true PCOS, 31 with PCOS-SCH, and 223 normal cycling women were enrolled. Clinical, metabolic, and hormonal parameters among the groups were investigated. Cont...

Journal: :Hepatology 2003
Qi Qian Airong Li Bernard F King Patrick S Kamath Donna J Lager John Huston Clarence Shub Sonia Davila Stefan Somlo Vicente E Torres

Most reports on the natural history, manifestations, and treatment of polycystic liver disease are based on the disease as it manifests in patients with autosomal dominant polycystic kidney disease (ADPKD). The purpose of this study was to develop a clinical profile of isolated autosomal dominant polycystic liver disease (ADPLD) using nonaffected family members as controls. The study included 1...

Journal: :Journal of obstetrics and woman disease 2021

Polycystic ovary syndrome occupies a leading place in the structure of endocrine infertility. This article presents and metabolic features polycystic phenotypes, as well modern concepts efficiency complications use assisted reproductive technologies, depending on specific phenotype. The issues influence selecting method possible that occur during vitro fertilization pregnancy course remain unre...

Journal: :Reproductive biology and endocrinology : RB&E 2008
Marla E Lujan Donna R Chizen Andrew K Peppin Stefan Kriegler David A Leswick Terri G Bloski Roger A Pierson

BACKGROUND We recently reported poor inter-observer agreement in identifying and quantifying individual ultrasonographic features of polycystic ovaries. Our objective was to determine the effect of a training workshop on reducing inter-observer variation in the ultrasonographic evaluation of polycystic ovaries. METHODS Transvaginal ultrasound recordings from thirty women with polycystic ovary...

2008

This guideline has been produced to provide information, based on clinical evidence, to assist clinicians with a special interest and for updating the generalist who manages women with polycystic ovary syndrome, to allow them to advise women about the long-term health consequences of the syndrome. This guideline does not cover infertility associated with polycystic ovary syndrome (PCOS), which ...

2015
CA Stănescu DN Păduraru C Cirimbei E Brătucu

The hepatic polycystic disease represents a hereditary condition with a reduced prevalence in the general population, sometimes associated with polycystic kidney disease. We present a retrospective observational study applied to 49 patients. The study aimed to observe the laparoscopic surgery of simple hepatic cysts. Laparoscopic approach is a simple and successful surgery management of these t...

Journal: :Journal of clinical pathology 1998
D R Gouldesbrough S Fleming

Unilateral and segmental localised polycystic disease is a rare type of cystic disease of the kidney. It takes the form of a segmental cystic abnormality in one kidney morphologically identical to the autosomal dominant adult form of polycystic kidney disease. The clinical, radiological, and pathological appearances of a case are described. The differential diagnosis and a possible pathogenic m...

2016
Ahmed M Kabel

Polycystic ovarian syndrome (PCOS) is one of the most common female endocrine disorders. PCOS is a complex heterogeneous disorder of uncertain etiology, but there is strong evidence that it can, to a large degree, be classified as a genetic disease. Other names for this syndrome include polycystic ovary disease, functional ovarian hyperandrogenism, ovarian hyperthecosis, sclerocystic ovary synd...

2013
Izabela Cwojdzińska-Jankowska Anna Plewa

Autosomal dominant polycystic kidney disease is a genetic disorder which results in the development of multiple cysts in the kidneys and other parenchymal organs. The two genes in which mutations are known to cause autosomal dominant polycystic kidney disease are PKD1 and PKD2. Approximately 50% of individuals with autosomal dominant polycystic kidney disease will develop end-stage renal diseas...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2011
Maliha Sadick Ulrike Attenberger Bettina Kraenzlin Hany Kayed Stefan O Schoenberg Norbert Gretz Daniel Schock-Kusch

BACKGROUND The aim of this study was the assessment of kidney morphology and glomerular filtration rate (GFR) in rat models of polycystic kidney disease and a healthy control group of Sprague-Dawley rats (SD rats). The performance of two non-invasive GFR estimation methods-3.0 Tesla magnetic resonance imaging (MRI) and optical imaging were investigated. Data of GFR assessment was compared to su...

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