Search Results - "Poyrazoglu, Hatıce Gamze"

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  1. 1

    Renal manifestations in children with neurofibromatosis type 1 by Celik, Binnaz, Aksoy, Ozlem Yuksel, Bastug, Funda, Poyrazoglu, Hatice Gamze

    Published in European journal of pediatrics (01-12-2021)
    “…Neurofibromatosis type 1 (NF1) is an autosomal-dominant neurocutaneous syndrome affecting various parts of the body, including the renovascular and urinary…”
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  2. 2

    Assessment of Psychopathology and Quality of Life in Children and Adolescents With Migraine by Öztop, Didem Behice, Taşdelen, Bedia İnce, PoyrazoğLu, Hatıce Gamze, Ozsoy, Saliha, Yilmaz, Rabia, Şahın, Nilfer, Per, Hüseyin, Bozkurt, Selma

    Published in Journal of child neurology (01-06-2016)
    “…Aim: The aims of this study were to investigate comorbid psychiatric disorders and to identify anxiety and depression levels and quality of life in children…”
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  3. 3

    Clinical spectrum of the pseudotumor cerebri in children: Etiological, clinical features, treatment and prognosis by Per, Hüseyin, Canpolat, Mehmet, Gümüş, Hakan, Poyrazoğlu, Hatice Gamze, Yıkılmaz, Ali, Karaküçük, Sarper, Doğan, Hakkı, Kumandaş, Sefer

    Published in Brain & development (Tokyo. 1979) (01-06-2013)
    “…Abstract Objective: Pseudotumor cerebri (PTC) is a clinical condition characterized by signs and symptoms of increased intracranial pressure, such as headache…”
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    Bone mineral density and bone metabolic markers' status in children with neurofibromatosis type 1 by Poyrazoğlu, Hatice Gamze, Baş, Veysel Nijat, Arslan, Alev, Bastug, Funda, Canpolat, Mehmet, Per, Hüseyin, Gümüs, Hakan, Kumandas, Sefer

    “…Neurofibromatosis type 1 (NF1) is a multisystem disorder characterized by progressive manifestations, which is inherited in an autosomal dominant manner. The…”
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    Effects of L-thyroxine treatment on heart functions in infants with congenital hypothyroidism by Arslan, Alev, Baş, Veysel Nijat, Uytun, Salih, Poyrazoğlu, Hatice Gamze

    “…Impaired heart functions in newborns with hypothyroidism should be reversed by levothyroxine substitution therapy. The aim of the study was to investigate…”
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  8. 8

    Postnatal outcome of isolated, nonprogressive, mild borderline fetal ventriculomegaly by Kutuk, Mehmet Serdar, Ozgun, Mahmut Tuncay, Uludag, Semih, Dolanbay, Mehmet, Poyrazoglu, Hatice Gamze, Tas, Mustafa

    Published in Child's nervous system (01-05-2013)
    “…Background This study aimed to evaluate postnatal outcome of fetuses affected by nonprogressive, isolated, mild (≥10 and ≤12 mm) borderline ventriculomegaly…”
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    A Rare Cause of Spasticity and Microcephaly: Argininemia by Soylu Üstkoyuncu, Pembe, Kendirci, Mustafa, Gökay, Songül, Kardaş, Fatih, Gümüş, Hakan, Per, Hüseyin, Poyrazoğlu, Hatice Gamze, Kaçar Bayram, Ayşe, Canpolat, Mehmet, Kumandaş, Sefer

    Published in Türk nöroloji dergisi (01-09-2020)
    “…Argininemia is an autosomal recessive urea cycle disorder caused by the deficiency of arginase. Our first case presented with psychomotor retardation,…”
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  11. 11

    Tyrosinemia type II: Novel mutations in TAT in a boy with unusual presentation by Gokay, Songul, Kendirci, Mustafa, Ustkoyuncu, Pembe Soylu, Kardas, Fatih, Bayram, Ayse Kacar, Per, Hüseyin, Poyrazoğlu, Hatice Gamze

    Published in Pediatrics international (01-10-2016)
    “…Tyrosinemia type II is a rare autosomal recessive disorder caused by deficiency of tyrosine aminotransferase (TAT). It may occur with ocular and cutaneous…”
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  12. 12

    Screening Inherited Metabolic Disorder in Children with Intellectual Disability and Epilepsy by Soylu Üstkoyuncu, Pembe, Güven, Ahmet Sami, Poyrazoğlu, Hatice Gamze, Gökay, Songül, Kardaş, Fatih, Kendirci, Mustafa, Gökçek, İkbal, Altuner Torun, Yasemin

    Published in Türk nöroloji dergisi (01-01-2019)
    “…Objective: To indicate the benefits of the screening of inherited metabolic disorders in patients with epilepsy, global developmental delay, and intellectual…”
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  13. 13

    Transverse myelitis and acute motor sensory axonal neuropathy due to Legionella pneumophila: A case report by Canpolat, Mehmet, Kumandas, Sefer, Yikilmaz, Ali, Gumus, Hakan, Koseoglu, Emel, Poyrazoğlu, Hatice Gamze, Kose, Mehmet, Per, Huseyin

    Published in Pediatrics international (01-12-2013)
    “…Guillain–Barré syndrome is a rapidly progressive symmetrical muscle weakness associated with acute inflammatory disease. Transverse myelitis (TM) is the…”
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  14. 14

    Combination of two different homozygote mutations in Pompe disease by Arslan, Alev, Poyrazoğlu, Hatice Gamze, Kiraz, Aslihan, Özcan, Alper, Işık, Halid, Ergul, Ayse Betül, Mungan, Neslihan Önenli, Streubel, Berthold, Ceylaner, Serdar, Altuner Torun, Yasemin

    Published in Pediatrics international (01-03-2016)
    “…Pompe disease (OMIM no 232300) is an autosomal recessive inherited metabolic disorder, caused by glycogen accumulation in the lysosome due to deficiency of the…”
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    Iron status of pregnant women and their newborns and the necessity of iron supplementation in infants in eastern turkey by Poyrazoglu, Hatice Gamze, Aygun, A. Denizmen, Ustundag, Bilal, Akarsu, Saadet, Yildirmaz, Serap

    Published in Turk Pediatri Arsivi (01-09-2011)
    “…Aim: Iron deficiency anemia is the most frequent cause of nutritional anemia in the first two years of life. The aim of this study is to evaluate iron status…”
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  16. 16

    Predictive value of laboratory parameters in childhood migraine by Poyrazoğlu, Hatice Gamze, Öztürk, Agah Bahadır

    Published in Acta neurologica Belgica (01-08-2020)
    “…Migraine is a neurovascular disease characterized by inflammation of the cerebral and extra cerebral vessels and appears in the form of attacks. Although the…”
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    Acute demyelinating encephalomyelitis and transverse myelitis in a child with COVID-19 by Poyrazoğlu, Hatice Gamze, Kırık, Serkan, Sarı, Mehmet Yusuf, Esen, İhsan, Toraman, Zülal Aşçı, Eroğlu, Yeşim

    Published in Turkish journal of pediatrics (01-01-2022)
    “…Corona virus disease 2019 (COVID-19) includes a wide range of diseases with varying pathophysiology in children and adults. Although the disease mainly affects…”
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  18. 18

    The Prevalence of Migraine and Tension-Type Headache Among Schoolchildren in Kayseri, Turkey: An Evaluation of Sensitivity and Specificity Using Multivariate Analysis by Poyrazoğlu, Hatice Gamze, Kumandas, Sefer, Canpolat, Mehmet, Gümüs, Hakan, Elmali, Ferhan, Kara, Ahu, Per, Hüseyin

    Published in Journal of child neurology (01-06-2015)
    “…This study aimed to determine the prevalence as well as psychosocial and demographic features of migraine and tension-type headache among school children…”
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    Different etiologies of acquired torticollis in childhood by Per, Hüseyin, Canpolat, Mehmet, Tümtürk, Abdülfettah, Gumuş, Hakan, Gokoglu, Abdulkerim, Yikilmaz, Ali, Özmen, Sevgi, Kaçar Bayram, Ayşe, Poyrazoğlu, Hatice Gamze, Kumandas, Sefer, Kurtsoy, Ali

    Published in Child's nervous system (01-03-2014)
    “…Introduction Torticollis can be congenital or may be acquired in childhood. Acquired torticollis occurs because of another problem and usually presents in…”
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    Three Patients With Lafora Disease: Different Clinical Presentations and a Novel Mutation by Poyrazoğlu, Hatice Gamze, Karaca, Emin, Per, Hüseyin, Gümüs, Hakan, Onay, Huseyin, Canpolat, Mehmet, Canöz, Özlem, Ozkınay, Ferda, Kumandas, Sefer

    Published in Journal of child neurology (01-05-2015)
    “…Lafora disease is a rare, fatal, autosomal recessive hereditary disease characterized by epilepsy, myoclonus and progressive neurological deterioration…”
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