Search Results - "Hergüner, M Özlem"

Neurofibromatosis type 1 and cardiac manifestations by Incecik, Faruk

“…Cardiac manifestations of neurofibromatosis type 1 (NF1) may include hypertension, congenital heart disease, and hypertrophic cardiomyopathy. The aim of this…”
Get full text

Pseudotumor Cerebri in a Child With Familial Mediterranean Fever by Incecik, Faruk, Herguner, Ozlem M, Yilmaz, Mustafa, Altunbasak, Sakir

“…Familial Mediterranean fever is an autosomal recessive polysystemic disease characterized by attacks of relapsing and self-limiting fever, peritonitis,…”
Get full text

A Presentation of Lyme Disease: Pseudotumor Cerebri by Şahin, Burcu, İncecik, Faruk, Hergüner, Özlem M, Alabaz, Derya, Beşen, Şeyda

“…Lyme disease is caused by a tick-transmitted spirochete, B. burgdorferi. It can present with both central and peripheral nervous system manifestations,…”
Get full text

Recurrent cerebral stroke in a thalassemic patient by Özlem Hergüner, M, Incecik, Faruk, Altunbaşak, Şakir, Şaşmaz, Ïlgen, Leblebisatan, Goksel

Get full text

Dynamic thiol/disulphide homeostasis in children with Duchenne muscular dystrophy by Incecik, Faruk, Avcıoğlu, Gamze, Erel, Özcan, Neşelioğlu, Salim, Hergüner, Ozlem M.

“…Duchenne muscular dystrophy (DMD) is a disorder that alter the expression of the dystrophin protein. Dystrophin deficiency alters the structural integrity of…”
Get full text

Autosomal-recessive spastic ataxia of Charlevoix-Saguenay: A Turkish child by Incecik, Faruk, Hergüner, Ozlem, Bisgin, Atil

“…Autosomal-recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by mutations of the SACS gene, characterized by late-infantile-onset spastic…”
Get full text

Fatal glioblastoma multiforme in a child with neurofibromatosis type 1 by Incecik, F, Ozlem Hergüner, M O, Bayram, I, Zorludemir, S, Altunbasak, S

Get full text

Limbic encephalitis associated with anti-leucine-rich glioma-inactivated-1 protein antibodies in a child by Incecik, Faruk, Hergüner, Ozlem, Besen, Seyda, Yılmaz, Mustafa, Altunbasak, Sakir

“…A serological panel for autoimmune disorders including antinuclear antibodies, double-stranded DNA antibody, rheumatoid factor, and complement levels was…”
Get full text

Mitochondrial membrane protein-associated neurodegeneration in a Turkish patient by Incecik, Faruk, Hergüner, Ozlem, Besen, Seyda, Ceylaner, Serdar

Get full text

Neurologic findings of nutritional vitamin B12 deficiency in children by Incecik, Faruk, Hergüner, M Ozlem, Altunbaşak, Sakir, Leblebisatan, Göksel

“…We report herein our interesting case series of 15 infants admitting with neurological symptoms who were found to have vitamin B12 deficiency. Infants who were…”
Get full text

Akut Karın ile Gelen Guillain-Barre Sendromu by İncecik, Faruk, Horoz, Özden Özgür, Hergüner, M. Özlem, Yıldızdaş, Dinçer

“…Guillain-Barre Sendromu (GBS), çocukluk çağındaki akut flask paralizinin en sık nedenidir. Simetrik güçsüzlük, baş ağrısı, solunum sıkıntısı, nöropatik ağrı,…”
Get full text

Türk Çocuklarında İdiopatik Çocukluk Çağı Oksipital Lob Epilepsisi by İncecik, Faruk, Hergüner, Özlem M., Mert, Gülen, Altunbaşak, Şakir

“…Amaç: İdiopatik çocukluk çağı oksipital lob epilepsisinin iki farklı tipi tanımlanmıştır: erken başlangıçlı veya Panayiotopoulos tip (PS) ve geç başlangıçlı…”
Get full text

Clinical Characteristics of 10 Patients With Continuous Spikes and Waves During Slow Sleep Syndrome by HERGIINER, M. Ozlem, INCECIK, Faruk, ALTUNBASAK, Sakir, KIRIS, Nurcihan

“…Continuous spikes and waves during slow sleep syndrome is characterized by the presence of spike-and-wave discharges in at least 85% of non–rapid eye movement…”
Get full text

Patients with acute, fulminant form of SSPE by Hergüner, M Ozlem, Altunbaşak, Sakir, Baytok, Vildan

“…Subacute sclerosing panencephalitis (SSPE) usually begins insidiously and follows a subacute course with relentless but slow progression to death. In recent…”
Get full text

A rare form of Guillain-Barré syndrome: pharyngeal-cervical-brachial variant by Hergüner, M Ozlem, Tepe, Tugay, Altunbaşak, Sakir, Baytok, Vildan

“…Guillain-Barré syndrome is clinically characterized by acute onset of generalized, symmetrical, and ascending muscle weakness and areflexia from peripheral…”
Get full text

Peripheral facial nerve palsy in children: clinical manifestations, treatment and prognosis by Bilge, Serap, Mert, Gülen Gül, Hergüner, M Özlem, İncecik, Faruk, Sürmelioğlu, Özgür, Bilen, Sevcan, Yılmaz, Levent

“…Sudden onset of unilateral weakness of the upper and lower muscles of one side of the face is defined as peripheral facial nerve palsy. Peripheral facial nerve…”
Get full text

Mitochondrial membrane protein-associated neurodegeneration: A case series of six children by Incecik, Faruk, Herguner, Ozlem, Bisgin, Atil

“…Neurodegeneration with brain iron accumulation (NBIA) is a group of genetic disorders with a progressive extrapyramidal syndrome and excessive iron deposition…”
Get full text

Giant axonal disease: Report of eight cases by Incecik, Faruk, Herguner, Ozlem M, Ceylaner, Serdar, Zorludemir, Suzan, Altunbasak, Sakir

“…Abstract Background Giant axonal neuropathy (GAN) is an autosomal recessive inherited progressive motor and sensory neuropathy with typical onset in early…”
Get full text

First-drug treatment failures in children with typical absence epilepsy by Incecik, Faruk, Altunbasak, Sakir, Herguner, Ozlem M

“…Abstract Background Childhood absence epilepsy (CAE) is a well-known syndrome with onset in middle childhood and is characterized by multiple typical absences…”
Get full text

Prognostic significance of failure of the initial antiepileptic drug in children with benign childhood epilepsy with centrotemporal spikes by Incecik, Faruk, Altunbasak, Sakir, Herguner, Ozlem M, Mert, Gulen, Sahan, Duygu

“…Abstract Background: Benign epilepsy with centrotemporal spikes is the most common partial epilepsy syndrome in children. The long-term prognosis for children…”
Get full text