Showing 1 - 11 results of 11 for search 'Semra Hiz-Kurul', query time: 0.02s Refine Results
  1. 1
    Anti-GQ1b-negative Miller Fisher syndrome presented with one-sided horizontal gaze palsy

    Anti-GQ1b-negative Miller Fisher syndrome presented with one-sided horizontal gaze palsy by Gülçin Akinci, Ibrahim Oztura, Semra Hiz-Kurul

    Published 2010-06-01
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  2. 2
    A case of atypical Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G and importance of H reflex

    A case of atypical Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G and importance of H reflex by Uluç Yiş, Erhan Bayram, Yasemin Topçu, Pakize Karakaya, Semra Hız Kurul

    Published 2013-04-01
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  3. 3
    Expanding spectrum of SCN1A-related phenotype with novel mutations

    Expanding spectrum of SCN1A-related phenotype with novel mutations by Semra Hız-Kurul, Semra Gürsoy, Müge Ayanoğlu, Uluç Yiş, Derya Erçal

    Published 2017-10-01
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  4. 4
    Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases

    Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases by Çağatay Günay, Pınar Edem, Ayşe Semra Hız-Kurul, Elif Yaşar, Uluç Yiş

    Published 2022-06-01
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  5. 5
    Pneumatosis intestinalis due to rotavirus infection in a child with Prader-Willi syndrome

    Pneumatosis intestinalis due to rotavirus infection in a child with Prader-Willi syndrome by Uluç Yiş, Yasemin Topçu, Erhan Bayram, Pakize Karakaya, Handan Cakmakçı, Semra Hız-Kurul

    Published 2012-12-01
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  6. 6
    Fibromuscular dysplasia as a cause of stroke in a 9-year-old girl

    Fibromuscular dysplasia as a cause of stroke in a 9-year-old girl by Uluç Yiş, Süleyman Men, Handan Cakmakçi, Fatih Demircioğlu, Semra Hiz Kurul, Hale Oren, Eray Dirik

    Published 2011-10-01
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  7. 7
    Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature

    Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature by Cem Paketçi, Pınar Edem, Derya Okur, Fatma Ceren Sarıoğlu, Handan Güleryüz, Erhan Bayram, Semra Hız Kurul, Uluç Yiş

    Published 2020-02-01
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  8. 8
    Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2

    Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2 by Uluç Yiş, Vishal Dixit, Sedat Işıkay, Mert Karakaya, Figen Baydan, Gülden Diniz, İpek Polat, Semra Hız-Kurul, Sebahattin Çırak

    Published 2017-06-01
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  9. 9
    Optic neuritis in CD59 deficiency: an extremely rare presentation

    Optic neuritis in CD59 deficiency: an extremely rare presentation by Çağatay Günay, Elvan Yardım, Elif Yaşar, Ayse Semra Hız-Kurul, Gamze Sarıkaya Uzan, Taylan Öztürk, Aylin Yaman, Uluç Yiş

    Published 2022-08-01
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  10. 10
    Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish population

    Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish population by Uluç Yiş, Gert C Scheper, Nedret Uran, Aycan Unalp, Handan Cakmakçi, Semra Hiz-Kurul, Eray Dirik, Marjo S Van Der Knaap

    Published 2010-04-01
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  11. 11
    GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria

    GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria by Tülay Öncü-Öner, Semra Hız-Kurul, Bayram Yüksel, Bekir Ergüner, Aydan Saraç, Handan Güleryüz, Sinem Ağılkaya, İlknur Porsuk-Doru, Aycan Ünalp, Sultan Cingöz

    Published 2018-06-01
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