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Browsing Tıp Fakültesi Makale Koleksiyonu by Title

Browsing Tıp Fakültesi Makale Koleksiyonu by Title

Now showing items 1-20 of 1200

1H-magnetic resonance spectroscopy in first episode and chronic schizophrenia patients

Kirtaş, D.; Karadağ, R.F.; Balcı Şengül, Melike Ceyhan; Kiroğlu, Y. (Turkiye Klinikleri Journal of Medical Sciences, 2016)

Background/aim: The aim of this study was to compare metabolite levels of the dorsolateral prefrontal cortex (DLPFC), anterior cingulate gyrus (ACG), thalamus, and hippocampus in patients with chronic schizophrenia (CSPs) ...
A 26-yr-old female with persistent cough

Başer, Sevin; Fişekçi, Fatma Evyapan; Özkurt, Sibel; Kiter, Göksel; Kıraç, Suna; Alper, H. (European Respiratory Society, 2003)
A basketball player with marfan syndrome and high risk of fall detected by posturography

Akkaya, Nuray; Fındıkoğlu, Gülin; Akkaya, Semih; Alemdaroğlu, Bilal Utku (GALENOS YAYINCILIK, 2011)

Marfan syndrome is an inherited disorder of connective tissue involving various organs. There is no data in the literature regarding balance disturbance or fall risk for sportsmen with Marfan syndrome. In this case report, ...
A cadaveric histological investigation of the prostate with three-dimensional reconstruction for better results in continence and erectile function after radical prostatectomy

Özdemir, Mehmet Bülent; Eskiçorapçı, Saadet Yılmaz; Baydar, D.E.; Cumhur, M.; Önderoǧlu, S.; Özen, H. (2007)

In this study our aim is to increase the understanding of the prostate and related organs anatomy for better continence and erectile function results after urological surgery. Prostate and related organs were dissected ...
A case of acute lymphoblastic leukemia with isolated orbital relapse

Polat, Aziz; Akpınar, Funda Özgürler; Balcı, Yasemin Işık; Acer, Semra; Koçyiğit, Ali; Evrengül, Havva (GALENOS YAYINCILIK, 2018)

Acute lymphoblastic leukemia (ALL) is the most common malignancy of childhood. Central nervous system is the most frequent place of both at the onset and relapse of the disease, but orbital involvement is rarely seen. A ...
A case of cephalosporin-induced autoimmune hemolytic anemia

Candemir, Maşallah.; Polat, Aziz.; Kılıç, İlknur.; Balcı, Yasemin Işık.; İnan, Murat.; Halis, Hülya. (2006)

Drug-induced autoimmune hemolytic anemia is a quite rare state in childhood. Currently, most of the reported cases of drug-induced hemolytic anemia are those caused by the second and third generation cephalosporins. In ...
A case of congenital chylothorax treated with octreotide

Özdemir, Özmert Muhammet Ali; Ergin, H.; Küçüktaşçı, K.; Şahin, Ö.; Çördük, N.; Karadağlı, E.; Yıldırım, B. (Galenos Yayincilik,, 2015)

Congenital chylothorax, an abnormal accumulation of chylous fluid in the pleural space, is a common cause of pleural effusion in the neonatal period. The traditional management of chylothorax is conservative. Conservative ...
A case of eosinophilic pneumonia that developed secondary to bleomycin in testicular carcinoma treatment

Değirmencioğlu, Serkan.; Değirmencioğlu, B.; Ünal, E.Y.; Uğurlu, E. (Anatolian Journal of Clinical Investigation, 2015)

Bleomycin is an antibiotic agent that has anti-tumor efficiency. Dose limiting toxicity depends on pulmonary complications which can be diagnosed by clinical and radiological findings. Positron emission tomography/computed ...
A case of familial lichen amyloidosis

Ergin, Şeniz; Demirkan, Neşe; Kaçar, Nida; Erdoǧan, Berna Şanlı; Akman, Hatice (2008)

Familial lichen amyloidosis which is also referred to familial primary cutaneous amyloidosis is a rare clinical variant of cutaneous amyloidosis. Lichen amyloidosis is characterized by persistent, pruritic, small brown ...
A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain

Ergin, Hacer; Başkan, Merve; Akalın, Necdet; Gürses, Dolunay (2003)

Hereditary angioedema (HAE) results from a congenital deficiency of C1 inhibitor and is characterized by submucosal and subcutaneous edema of skin, larynx and abdomen. Occasional reports have appeared linking HAE with ...
A case of idiopathic subglottic and bilateral bronchial stenosis

Aydoğmuş, Ümit; Yüncü, Gökhan; Türk, Figen (BILIMSEL TIP PUBLISHING HOUSE, 2016)

Subglottic stenosis is rarely idiopathic. In this case report, a 40-year-old female patient presented with subglottic stenosis with an unidentified etiology along with bilateral bronchial stenosis. Hoarseness arose in the ...
A case of multiple coronary microfistulas to the left ventricle and apical myocardial hypertrophy coexisting with stable angina

Yildiz, B.S.; Bilgin, M.; Alihanoğlu, Yusuf İzzettin; Evrengül, Harun (2013)

A coronary artery fistula consists of a communication between a coronary artery and a cardiac chamber, a great artery or the vena cava. It is the most common congenital anomaly that can affect coronary perfusion. However, ...
A case of PICA infarction presenting as vestibuler neuritis

Öncel, Çağatay.; Şahiner, T.; Kıroǧlu, Yılmaz.; Cam, M.; Tokgöz, F. (Turkish Society of Cerebrovascular Diseases, 2008)

We reported a patient of 50 years old men, who presented with severe acute vertigo and nausea such as vestibuler neuritis without usually symptom or signs of cerebellar dysfunction. Cranial MRI of patient showed acute left ...
A case of symptomatic idiopathic thrombocytopenic purpura during mumps

Polat, Aziz.; İnan, Murat.; Çakaloz, İnanç.; Karakuş, Yasin Tuğrul. (2005)
A case report of surgically treated drug resistant epilepsy associated with subependymal nodular heterotopia

Acar, Göksemin; Acar, Feridun; Öztura, I.; Baklan, B. (2012)

Subependymal nodular heterotopia (SNH) is a cortical development malformation that is commonly associated with medically resistant epilepsy. Cases of SNH are challenging to treat surgically because there are typically ...
A case with bloom syndrome

Kaçar, Nida; Erdoǧan, Murat Kadri; Erdoǧan, Berna Şanlı; Atmaca, Münevver; Düzcan, Füsun (2008)

BS is a rare, autosomal recessive disorder characterized by telangiectasias, photosensitivity, growth deficiency of prenatal onset, immunodeficiency, increased susceptibility to malignancies and diabetes mellitus. There ...
A case with rheumatod arthritis and atraumatic odontoid fracture: disappearence of bony landmarks

Fındıkoğlu, Gülin; Ardic, F.; Akkaya, N.; Sahin, F.; Sabir, N.; Cirak, B. (Blackwell Publishing, 2018)

We aim to draw attention to occult, atraumatic fractures of the odontoid process in patients with rheumatoid arthritis (RA) and to underline difficulties encountered during clinical and radiological diagnosis. A forty-seven ...
A child case of acute brucellosis presenting with coombs-positive autoimmune hemolytic anemia. Case report

Akın, Mehmet; Küçüktaşçı, Kazım; Karaca, Abdullah; Güçtürk, I.; Kaya, Burçin; Halis, Hülya (2012)

Human brucellosis is a multisystem disease with a wide spectrum of clinical manifestations. Brucellosis can mimic several primary hematological diseases. Several non-specific hematologic abnormalities have been reported ...
A combination of topographic and pachymetric parameters in keratoconus diagnosis

Toprak, İbrahim; Yaylalı, Volkan; Yıldırım, Cem (Elsevier, 2015)

Purpose: To evaluate the utility of topographic and pachymetric parameters of Scheimpflug system in keratoconus diagnosis. Methods: This study included 183 eyes of 183 patients with keratoconus (keratoconus group) and 131 ...
A comparative biomechanical analysis of suprapectineal and infrapectineal fixation oacetabular anterior column fracture by finite element modeling

Yücens, Mehmet.; Alemdaroğlu, K.B.; Özmeriç, A.; İltar, S.; Yildirim, A.Ö.; Aydoğan, N.H. (Turkiye Klinikleri Journal of Medical Sciences, 2019)

Background/aim: The aim of this study is to compare the stability and implant stresses of suprapectineal plate with infrapectineal plate in three subconfigurations of the screw types. Materials and methods: The stabilities ...

Now showing items 1-20 of 1200

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