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Acute disseminated encephalomyelitis in children: outcome and prognosis

Neuropediatrics, 2003-08, Vol.34 (4), p.194-199

2003

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Evaluation of corpus callosum morphometry in patients with mesial temporal lobe epilepsy with hippocampal sclerosis

Surgical and radiologic anatomy (English ed.), 2014, Vol.36 (1), p.47-54

2014

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POS0601 CRANIOCERVICAL JUNCTION INVOLVEMENT ASSESSED BY COMPUTED TOMOGRAPHY AND/OR MAGNETIC RESONANCE IMAGING IN INFLAMMATORY ARTHRITIS: SINGLE CENTER CASE-CONTROL STUDY

Annals of the rheumatic diseases, 2022-06, Vol.81 (Suppl 1), p.568-568

2022

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AB0548 A COMPARATIVE STUDY BETWEEN THE NEUROPSYCHIATRIC INVOLVEMENTS IN ADULT-ONSET AND CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS

Annals of the rheumatic diseases, 2022-06, Vol.81 (Suppl 1), p.1401-1402

2022

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Diffusion-Weighted Cranial MR Imaging Findings in a Patient with Hemophagocytic Syndrome

American Journal of Neuroradiology, 2006-06, Vol.27 (6), p.1312-1314

2006

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Paediatric Behçet's disease with sinus venous thrombosis: experience from three centres in Turkey

Clinical and experimental rheumatology, 2019-11, Vol.37 Suppl 121 (6), p.147

2019

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Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies

Genetic counseling, 2010, Vol.21 (1), p.19

2010

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P85 – 2818: Nonketotic hyperglycinemia: A cause of severe epileptic encephalopathy and hypotonia in children

European journal of paediatric neurology, 2015-05, Vol.19, p.S118-S118

2015

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G.O.21

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.921-921

2014

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Magnetic resonance imaging findings in Kimura's disease

Neuroradiology, 2004-10, Vol.46 (10), p.855-858

2004

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Nose-to-brain delivery of farnesylthiosalicylic acid loaded hybrid nanoparticles in the treatment of glioblastoma

Journal of the neurological sciences, 2017-10, Vol.381, p.171-172

2017

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Rim enhancement of meningiomas on fast FLAIR imaging

Neuroradiology, 2003-02, Vol.45 (2), p.78-81

2003

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P.P.1 06 Magnetic resonance imaging and spectroscopy findings in a patient with partial merosin deficiency

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.663-664

2006

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P.P.1 05 Magnetic resonance imaging findings in a newborn with merosin-deficient congenital muscular dystrophy

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.663-663

2006

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Congenital infiltrating lipomatosis of the face with ipsilateral hemimegalencephaly

Pediatric radiology, 2002-02, Vol.32 (2), p.106-109

2002

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PP05.7 – 2639: Horizontal gaze palsy with progressive scoliosis (HGPPS): The role of brain MRI and diffusion tensor imaging in diagnosis

European journal of paediatric neurology, 2015-05, Vol.19, p.S48-S48

2015

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P295 New onset neurological symptoms in patients with phenylketonuria owing to B12 deficiency

European journal of paediatric neurology, 2009, Vol.13, p.S113-S113

2009

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G.O.21: Relapsing immune mediated polyneuropathy, strokes and chronic haemolysis due to inherited CD59 deficiency

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.921-921

2014

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Defining thresholds for changes in size of simulated T2-hyperintense brain lesions on the basis of qualitative comparisons

American journal of roentgenology (1976), 2003-01, Vol.180 (1), p.65-69

2003

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MLO02 Dysmorphology in patients with pyridoxine-dependent seizures and mutations of the antiquitin (Aldh7a1) gene

European journal of paediatric neurology, 2007, Vol.11, p.30-31

2007

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P317 Cerebral creatine deficiency syndromes: clinical and laboratory follow-up in five patients with GAMT deficiency

European journal of paediatric neurology, 2009, Vol.13, p.S119-S119

2009

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P318 Unusual presentations in Niemann Pick disease type C: Clues for early diagnosis

European journal of paediatric neurology, 2009, Vol.13, p.S119-S120

2009

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P199 Clinical and molecular evaluation of 14 Turkish patients with Dravet syndrome

European journal of paediatric neurology, 2009, Vol.13, p.S82-S82

2009

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Radiologic aspects of abdominal hydatidosis in children: A study of 31 cases in Turkey

Clinical imaging, 2004-05, Vol.28 (3), p.196-200

2004

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The Anatomy of the Sigmoid-Transverse Junction According to the Tentorial Angle

The Journal of craniofacial surgery, 2019-10, Vol.30 (7), p.2280-2284

2019

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Acute disseminated encephalomyelitis in children: outcome and prognosis

Evaluation of corpus callosum morphometry in patients with mesial temporal lobe epilepsy with hippocampal sclerosis

POS0601 CRANIOCERVICAL JUNCTION INVOLVEMENT ASSESSED BY COMPUTED TOMOGRAPHY AND/OR MAGNETIC RESONANCE IMAGING IN INFLAMMATORY ARTHRITIS: SINGLE CENTER CASE-CONTROL STUDY

AB0548 A COMPARATIVE STUDY BETWEEN THE NEUROPSYCHIATRIC INVOLVEMENTS IN ADULT-ONSET AND CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS

Diffusion-Weighted Cranial MR Imaging Findings in a Patient with Hemophagocytic Syndrome

Paediatric Behçet's disease with sinus venous thrombosis: experience from three centres in Turkey

Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies

P85 – 2818: Nonketotic hyperglycinemia: A cause of severe epileptic encephalopathy and hypotonia in children

G.O.21

Magnetic resonance imaging findings in Kimura's disease

Nose-to-brain delivery of farnesylthiosalicylic acid loaded hybrid nanoparticles in the treatment of glioblastoma

Rim enhancement of meningiomas on fast FLAIR imaging

P.P.1 06 Magnetic resonance imaging and spectroscopy findings in a patient with partial merosin deficiency

P.P.1 05 Magnetic resonance imaging findings in a newborn with merosin-deficient congenital muscular dystrophy

Congenital infiltrating lipomatosis of the face with ipsilateral hemimegalencephaly

PP05.7 – 2639: Horizontal gaze palsy with progressive scoliosis (HGPPS): The role of brain MRI and diffusion tensor imaging in diagnosis

P295 New onset neurological symptoms in patients with phenylketonuria owing to B12 deficiency

G.O.21: Relapsing immune mediated polyneuropathy, strokes and chronic haemolysis due to inherited CD59 deficiency

Defining thresholds for changes in size of simulated T2-hyperintense brain lesions on the basis of qualitative comparisons

MLO02 Dysmorphology in patients with pyridoxine-dependent seizures and mutations of the antiquitin (Aldh7a1) gene

P317 Cerebral creatine deficiency syndromes: clinical and laboratory follow-up in five patients with GAMT deficiency

P318 Unusual presentations in Niemann Pick disease type C: Clues for early diagnosis

P199 Clinical and molecular evaluation of 14 Turkish patients with Dravet syndrome

Radiologic aspects of abdominal hydatidosis in children: A study of 31 cases in Turkey

The Anatomy of the Sigmoid-Transverse Junction According to the Tentorial Angle

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