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Browsing Radyoloji Anabilim Dalı by Author "Aslan, Mehmet"

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Atlanto axial subluxation associated with rubinstein taybi syndrome

Sığırcı, Ahmet; Yakıncı, Mehmet Cengiz; Alkan, Alpay; Aslan, Mehmet; Sığırcı, Aykut; Kutlu, Ramazan (Eur J Radiol Extra, 2003)

A case of atlanto-axial subluxation in a 5-year-old boy with Rubinstein /Taybi syndrome (RTS) is presented and the imaging findings are evaluated. To the best of our knowledge, atlanto-axial subluxation has not been ...
Delayed myelination in a rhizomelic chondrodysplasia punctata case MR spectroscopy findings

Alkan, Alpay; Kutlu, Ramazan; Yakıncı, Mehmet Cengiz; Sığırcı, Ahmet; Aslan, Mehmet; Saraç, Kaya (Magn Reson Imaging, 2003)

Rhizomelic chondrodysplasia punctata is a member of genetic peroxisomal disorders. Delayed myelination, which is probably related to the inadequacy of plasmalogens biosynthesis, is an important feature of this disorder. ...
Early and late state subacute sclerosing panencephalitis chemical shift imaging and single voxel MR spectroscopy

Alkan, Alpay; Saraç, Kaya; Kutlu, Ramazan; Yakıncı, Mehmet Cengiz; Sığırcı, Ahmet; Aslan, Mehmet; Baysal, Tamer (AJNR, 2003)

Subacute sclerosing panencephalitis (SSPE) is a rare, progressive, inflammatory neurodegenerative disease. Our aim was to determine the metabolic abnormalities of brain in early- and late-stage SSPE by using MR spectroscopy ...
Proton MR spectroscopy features of normal appearing white matter neurofibromatosis type 1

Alkan, Alpay; Saraç, Kaya; Kutlu, Ramazan; Yakıncı, Mehmet Cengiz; Sığırcı, Ahmet; Aslan, Mehmet; Özcan, Hamdi; Yoloğlu, Saim (Magn Reson Imaging, 2003)

To determine whether differences exist between neurofibromatosis type 1 (NF1) patients with or without focal lesions and healthy normal volunteers in the metabolite ratios of normal appearing white matter, 27 patients ...
Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings

Alkan, Alpay; Kutlu, Ramazan; Yakıncı, Mehmet Cengiz; Sığırcı, Ahmet; Aslan, Mehmet; Saraç, Kaya (J Child Neurol, 2003)

Sandhoff’s disease is a rare, genetic lysosomal storage disease leading to delayed myelination or demyelination. Although neuroimaging findings in this disease have been reported previously, magnetic resonance spectroscopy ...
Subacute sclerosing panencephalitis with fulminating course follow up magnetic resonance spectroscopy MRS findings

Alkan, Alpay; Kutlu, Ramazan; Sığırcı, Ahmet; Aslan, Mehmet; Saraç, Kaya; Yakıncı, Mehmet Cengiz (J Child Neurol, 2004)

The fulminating form of subacute sclerosing panencephalitis is an extremely rare condition. Imaging findings are usually not correlated with clinical staging. We describe a 4-year-old girl with severe neuronal loss, ...
Brain MR spectroscopy in children with a history of rheumatic fever with a special emphasis on neuropsychiatric complications

Alkan, Alpay; Kutlu, Ramazan; Koçak, Gülendam; Sığırcı, Ahmet; Emul, Murat; Doğan, Selda; Aslan, Mehmet; Saraç, Kaya; Yakıncı, Mehmet Cengiz (Eur J Radiol, 2004)

Purpose: To investigate whether there are metabolite changes in basal ganglia of children with complete healing of rheumatic fever (RF), history of Syndenham chorea (SC) and obsessive compulsive-tic disorder (OCTD) developed ...
Neurofibromatosis type 1 diffusion weighted imaging findings of brain

Alkan, Alpay; Sığırcı, Ahmet; Kutlu, Ramazan; Özcan, Hamdi; Erdem, Gülnur; Aslan, Mehmet; Ateş, Özkan; Yakıncı, Mehmet Cengiz; Eğri, Mücahit (Eur J Radiol, 2005)

Purpose: The purposes of this study were to evaluate the differences in apparent diffusion coefficient (ADC) values between infra and supratentorial unidentified bright objects (UBOs), between UBOs and normal appearing ...
Renal interlobar artery parameters with duplex Doppler sonography and correlations with age plasma renin and aldosterone levels in healthy children

Sığırcı, Ahmet; Hallaç, Tarık; Akıncı, Ayşehan; Temel, İsmail; Gülcan, Hande; Aslan, Mehmet; Koçer, Muzaffer; Kahraman, Bayram; Alkan, Alpay; Kutlu, Ramazan (AJR, 2006)

The objectives of this study were to compare and make correlations between age and Doppler parameters of the interlobar arteries, including synchronously obtained plasma renin and aldosterone levels and to obtain new ...
Merosin negative congenital muscular dystrophy diffusion weighted imaging findings of brain

Alkan, Alpay; Sığırcı, Ahmet; Kutlu, Ramazan; Aslan, Mehmet; Doğanay, Selim; Yakıncı, Mehmet Cengiz (J Child Neurol, 2007)

Merosin-negative congenital muscular dystrophy is a rare genetic disease of childhood involving the central and peripheral nervous system. There were high signal intensities throughout the centrum semiovale, periventricular, ...

Now showing items 1-10 of 10

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Browsing Radyoloji Anabilim Dalı by Author "Aslan, Mehmet"

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