Results 21 to 30 of about 1,061,223 (312)
European evidence-based guidelines on pancreatic cystic neoplasms
Gut, 2018 Evidence-based guidelines on the management of pancreatic cystic neoplasms (PCN) are lacking. This guideline is a joint initiative of the European Study Group on Cystic Tumours of the Pancreas, United European Gastroenterology, European Pancreatic Club ...
Marco Marc Lianne Marco J Djuna L Thomas M Jeanin E Mark Del Chiaro Besselink Scholten Bruno Cahen Gress va
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Recurrent Cerebral Astroblastoma with Aggressive Histology: An Uncommon Case
Indian Journal of Neurosurgery, 2017 Astroblastomas are uncommon tumors of uncertain histogenesis. Recently tanycyte is postulated to be the cell of origin. These occur predominantly in the cerebral hemisphere of young adults and children. Astroblastoma constitutes approximately 0.45 to 2.8%
Sumit Bansal +3 more
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Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation
Jornal de Pediatria, 2017 Objective Cystic fibrosis (CF), caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, continues to present diagnostic challenges.
P. Farrell +13 more
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Purely Cystic Desmoplastic Ganglioglioma: An Incidental Finding in a Giant Cyst
Indian Journal of Neurosurgery, 2017 Desmoplastic infantile ganglioglioma (DIG) is a rare supratentorial brain tumor occurring mostly before the age of 2 years. It has a good prognosis and total excision of the tumor is curative, necessitating no further treatment.
Sumit Bansal +3 more
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Expert consensus for the diagnosis and treatment of cystic and alveolar echinococcosis in humans.
Acta Tropica, 2010 The earlier recommendations of the WHO-Informal Working Group on Echinococcosis (WHO-IWGE) for the treatment of human echinococcosis have had considerable impact in different settings worldwide, but the last major revision was published more than 10 ...
E. Brunetti, P. Kern, D. Vuitton
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Nephronophthisis and medullary cystic kidney disease complex [PDF]
Vojnosanitetski Pregled, 2005 Background. Nephronophthisis and medullary cystic kidney disease complex refers to the genetic heterogeneous group of inherited tubulointerstital nephritis. Nephronophthisis comprises at last 3 clinical manifestations, has the autosomal recessive pattern
Stanišić Marijana +3 more
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대한영상의학회지, 2017 Purpose To evaluate the results of two-injection ethanol sclerotherapy in simple renal cysts performed with 5-minute ethanol exposure time. Materials and Methods We retrospectively reviewed 30 renal cysts in 30 patients treated by ethanol ...
Seung Eun Lee, Jae Ho Cho
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Mucinous cystadenoma of pancreas with honeycombing appearance: Radiological-Pathological correlation
Indian Journal of Radiology and Imaging, 2018 Most mucinous cystadenomas of pancreas are solitary and multilocular with a few large compartments. Serous cystadenomas usually have a polycystic or microcystic (honeycomb) pattern consisting of collection of cysts (usually >6) that range from few ...
Beno Jefferson +4 more
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Role of ultrasonography and fine-needle aspiration cytology in the evaluation of neck masses
Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2020 Objective: The objective of the study is to study the efficacy of ultrasonography (USG) and fine- needle aspiration cytology (FNAC) in the evaluation of neck masses and differentiating between cystic, inflammatory, benign, and malignant neck masses with ...
Gaveshani Mantri +3 more
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VX-445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles
New England Journal of Medicine, 2018 BACKGROUND VX‐445 is a next‐generation cystic fibrosis transmembrane conductance regulator (CFTR) corrector designed to restore Phe508del CFTR protein function in patients with cystic fibrosis when administered with tezacaftor and ivacaftor (VX‐445 ...
D. Keating +19 more
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