Search Results - "OZLEM HERGÜNER, M"

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

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

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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…”
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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…”
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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…”
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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…”
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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…”
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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…”
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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…”
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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…”
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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…”
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Limbic encephalitis with antibodies to glutamic acid decarboxylase presenting with brainstem symptoms by Incecik, Faruk, Hergüner, Ozlem M, Yıldızdaş, Dincer, Horoz, Ozden, Besen, Seyda

“…Limbic encephalitis (LE) is a neurological syndrome that may present in association with cancer, infection, or as an isolate clinical condition often…”
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Guillain–Barré syndrome in children by Incecik, Faruk, Ozlem Hergüner, M., Altunbasak, Sakir

“…Guillain–Barré syndrome (GBS) is one of the reasons of acute polyneuropathy causing severe morbidity and mortality. Forty-six patients with GBS were included…”
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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…”
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Dysarthria, ataxia, and dystonia associated with COX20 (FAM36A) gene mutation: A case report of a Turkish child by Ozcanyuz, Duygu, Incecik, Faruk, Herguner, Ozlem, Mungan, Neslihan, Bozdogan, Sevcan

“…Complex IV is the final component of the respiratory chain and is responsible for the reduction of molecular oxygen and oxidation of cytochrome C.[1] Several…”
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Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series by Incecik, Faruk, Balci, Sibel, Kisla Ekinci, Rabia, Herguner, Ozlem, Bisgin, Atil, Yilmaz, Mustafa

“…Three prime repair exonuclease 1 (TREX1) degrades single- and double-stranded DNA with 3'-5' exonuclease activity. TREX1 mutations are related to type 1…”
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Acute disseminated encephalomyelitis: an evaluation of 15 cases in childhood by Incecik, Faruk, Hergüner, M Özlem, Altunbasak, Sakir

“…To describe our experience with acute disseminated encephalomyelitis (ADEM) and the relationships between the clinical course, magnetic resonance imaging (MRI)…”
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