Results 121 to 130 of about 9,151,829 (395)

The accuracy of 18F-Fluorodeoxyglucose positron emission tomography/computed tomography in the evaluation of bone lesions of undetermined origin

open access: yesWorld Journal of Nuclear Medicine, 2016
The aim of the current study was to determine the diagnostic accuracy of whole-body fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) in detecting carcinoma of unknown primary (CUP) with bone metastases.
Cuneyt Tamam   +2 more
doaj   +1 more source

Mechanisms to Evade the Phagocyte Respiratory Burst Arose by Convergent Evolution in Typhoidal Salmonella Serovars. [PDF]

open access: yes, 2018
Typhoid fever caused by Salmonella enterica serovar (S.) Typhi differs in its clinical presentation from gastroenteritis caused by S. Typhimurium and other non-typhoidal Salmonella serovars.
Bäumler, Andreas J   +6 more
core   +2 more sources

Treatment Survival in Patients With Hidradenitis Suppurativa

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Background Despite the existence of therapeutic approaches, effective management of hidradenitis suppurativa (HS) remains elusive in many cases. In addition, most of the current studies focus on treatment response in a cross‐sectional analysis of patients, and therefore a proper study analysing different treatment strategies longitudinally in ...
Lea Schulte‐Oestrich   +3 more
wiley   +1 more source

Report of 2 Cases of Chronic Granulomatous Disease in Adults

open access: yesپزشکی بالینی ابن سینا, 2007
Introduction: Chronic granulomatous disease (CGD) is an inherited disorder of phagocyte function . The defect of intracellular killing in phagocytes is the cause of recurrent pyogenic infection of patients .
Mahdi Eskandarlou   +5 more
doaj  

Atypical Presentation of Chronic Granulomatous Disease in a Child

open access: yesAtti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, 2017
Chronic granulomatous disease is a rare, inherited immunodeficiency caused by deletions or mutations in genes that encode subunits of the NADPH oxidase complex. The pattern of chronic granulomatous disease inheritance can be X-linked (about 70% of cases)
Chiara Cuzzupè   +7 more
doaj   +1 more source

Autoinflammatory granulomatous diseases: from Blau syndrome and early-onset sarcoidosis to NOD2-mediated disease and Crohn's disease

open access: yesRMD Open, 2015
The recent identification of genetic mutations leading to dysfunction of inflammatory and apoptotic pathways, has allowed to characterise a group of diseases, recognised as monogenic autoinflammatory syndromes.
F. Caso   +5 more
semanticscholar   +1 more source

Granulomatous liver diseases: A review

open access: yesJournal of the Formosan Medical Association, 2012
Granulomas that consist of focal accumulations of macrophages are commonly found in the liver due to stimulation of the immune system by a number of agents. Manifestations are variable depending on whether the underlying cause is a systemic disease or a primary hepatic granulomatous reaction.
George Y. Wu   +3 more
openaire   +4 more sources

Granulomatous infiltration of a parathyroid adenoma presenting as primary hyperparathyroidism in a woman: a case report

open access: yesJournal of Medical Case Reports, 2010
Introduction Hypercalcemia can be associated with vitamin D (1,25(OH)2D3) -mediated granulomatous disorders in addition to primary hyperparathyroidism (PHPT).
Algün Ekrem   +3 more
doaj   +1 more source

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