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Changes in olfactory bulbus volume and olfactory sulcus depth in the chronic period after COVID-19 infection
(Taylor and Francis Ltd., 2021)
Background: Although there are a limited number of studies investigating the changes in olfactory bulb volume (OBV) and olfactory sulcus depth (OSD) values in the acute and subacute periods after COVID-19 infection, there ...
Evaluation of iron status in COVID-19 pneumonia
(A. CARBONE Editore, 2021)
Introduction: In late 2019, a new coronavirus disease was detected in Wuhan, China and called COVID-19. Iron metabolism is one of the topics have to be investigated for the development of therapeutic strategies for COVID-19. ...
A case of B.1.1.7 SARS-CoV-2 UK strain with an atypical radiological presentation
(2021)
The new UK strain was first described in December 2020. It was seen for the first time in Turkey in February 2021. It is not yet known whether the new strain has different CT patterns compared to the classical type. We ...
An unexpected diagnosis in early pediatric age group: Fahr syndrome manifested with epileptic seizure
(Editura Medicala, 2021)
Intracerebral calcifications are one of the essential parameters in the diagnosis of some neurological diseases. Fahr group is a rare pathologic entity presenting with basal ganglion calcifications. Symmetrical basal ...
Total Aplasia of Paranasal Sinus Associated With a Syndromic Condition
(ALLIANCE COMMUNICATIONS GROUP DIVISION ALLEN PRESS, 2022)
Total aplasia of paranasal sinus (TAPS) is extremely rare, although the fact that partial aplasia is very common. TAPS seems to be limited to only 5 case reports in the literature until now. We present the case of a ...
Bilateral Petrous Apex Cephalocele Associated with a Wide Sella
(Wolters Kluwer, 2021)
Petrous apex cephalocele (PAC) is a rare type of cephalocele. It is usually asymptomatic. It can be unilateral or bilateral. Bilateral cases are less common. They are etiologically and clinically different entities from ...
The terminal period findings of late-diagnosed fibrodysplasia ossificans progressiva
(Association of the Scientific Medical Societies in Germany, 2023)
Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant rare disease characterized by foot deformities and concomitant hetero-topic ossifications. Theoretically, in the absence of early diagnosis and medication, ...