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Toplam kayıt 297, listelenen: 11-20
Smith-magenis syndrome: Clues in the clinic
(Georg Thieme Verlag KG, 2020)
As a multisystemic congenital mental retardation disorder/anomaly, Smith-Magenis syndrome (SMS) is commonly aroused from de novo interstitial deletion of the 17p11.2 chromosome. The deletion of this chromosome results with ...
Outcomes of the novolimus-eluting bioresorbable vascular scaffold in real world clinical practice
(Edizioni Minerva Medica, 2021)
BACKGROUND: Most of the current data regarding the use of bioresorbable scaffolds (BRS) come from everolimus-eluting stent platforms. Adverse events with the everolimus-eluting BRSs which are the most comprehensively ...
Balanced double aortic arch causing persistent respiratory symptoms mimicking asthma in an infant
(Georg Thieme Verlag KG, 2021)
Double aortic arch (DAA) is a common form of complete vascular ring. The condition leads to airway obstruction and compression of the esophagus. A balanced type of DAA is an extremely rare anomaly. The anatomical aberration ...
Individualized treatment of tinnitus during sleep using combined tinnitus signal and music
(Karger, 2021)
Introduction: Tinnitus is a widely seen otological symptom that interferes with daily activities and causes discomfort. Tinnitus treatments can be classified into 4 main groups: pharmacological treatments, cognitive and ...
Association of conductive hearing loss with the structural changes in the organ of corti
(Karger, 2021)
Objective: The aim of the study was to evaluate the association of conductive hearing loss (CHL) with the structural changes in the organ of Corti. Methods: Twenty ears of 10 healthy adult Wistar albino rats were included ...
Steroid hormone profiles and molecular diagnostic tools in pediatric patients with non-CAH primary adrenal insufficiency
(National Library of Medicine's (NLM) Medline, 2022)
CONTEXT: There is a significant challenge of attributing specific diagnoses to patients with primary adrenal insufficiency of unknown etiology other than congenital adrenal hyperplasia (non-CAH PAI). Specific diagnoses per ...
Anaesthesia recommendations for patients suffering from Alkaptonuria
(Aktiv Druck & Verlag GmbH, 2014)
Alkaptonuria (AKU) is a rare autosomal recessive disorder with an incidence of 1:250 000 to 1:1000 000 live births. AKU is caused by a deficiency of the enzyme homogentisate 1,2-dioxygenase (HGO). This enzyme converts ...
A case of infectious mononucleosis presenting with cholestatic hepatitis
(Galenos Publishing, 2012)
Although mild liver involvement is common in patients with Epstein-Barr virus (EBV) infection-induced infectious mononucleosis, acute cholestatic hepatitis is rare. In this report, we describe a 210-year-old previously ...
Three-corridors procedure to operate in the infralabyrinthine cervico-jugulo-carotico-tympanic area
(Karger, 2022)
Introduction: The aim of the study was to present the results of our experience in three-corridors procedures applied for the tumors and inflammatory lesions of the infralabyrinthine cervico-jugulo-carotico-tympanic area. ...
What a single electroencephalographic (EEG) channel can tell us about alzheimer's disease patients with mild cognitive impairment
(NLM (Medline), 2023)
Abnormalities in cortical sources of resting-state eyes closed electroencephalographic (rsEEG) rhythms recorded by hospital settings (10-20 montage) with 19 scalp electrodes characterized Alzheimer's disease (AD) from ...