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Meral Topçu

Showing results (1-10 of 65) with videos related to

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Brain & Development|July 28, 2004
Sphingolipidoses in TurkeyHatice Asuman Ozkara, Meral Topçu
Pediatric Neurology|May 29, 2004
Infantile convulsions and paroxysmal choreoathetosis in a consanguineous familyErcan Demir, Jean François Prud'homme, Meral Topçu
Clinical Biochemistry|May 17, 2011
Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote manBasak Celtikci, Meral Topçu, Hatice Asuman Ozkara
Journal of Child Neurology|March 23, 2004
Benign neonatal sleep myoclonus mimicking status epilepticusGüzide Turanli, Nesrin Senbil, Sakir Altunbaşak, et al.
Turk Psikiyatri Dergisi = Turkish Journal of Psychiatry|September 6, 2019
[Childhood Traumas, Attachment and Alexithymia in Adolescentswith Psychogenic Nonepileptic Seizure Type of Conversion Disorder]Özlem Uzun, Devrim Akdemir, Meral Topçu, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Usefulness of long-term video-EEG monitoring in children at a tertiary care centerSelin Onay, Dilek Yalnızoğlu, Meral Topçu, et al.
Journal of Child Neurology|September 15, 2005
Streptococcus oralis as a risk factor for middle cerebral artery thrombosisEbru Kazanci, Kader Karli Oguz, Aytemiz Gurgey, et al.
The Turkish Journal of Pediatrics|November 19, 2008
Osteoid osteoma in a 16-year-old boy presenting with atrophy of the left thigh: diagnostic difficultiesSinem Akgül, Akin Uzümcügil, M Fani Bozkurt, et al.
European Journal of Medical Genetics|December 15, 2010
Novel mutations of the MLC1 gene in Turkish patientsAyşe Yüzbaşioğlu, Meral Topçu, Y Cetin Kocaefe, et al.
Pediatric Neurosurgery|July 26, 2002
Medulloblastoma in a child with the metabolic disease L-2-hydroxyglutaric aciduriaPinar Akdemir Ozişik, Nejat Akalan, Selçuk Palaoğlu, et al.
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Brain & Development|July 28, 2004
Sphingolipidoses in TurkeyHatice Asuman Ozkara, Meral Topçu
Pediatric Neurology|May 29, 2004
Infantile convulsions and paroxysmal choreoathetosis in a consanguineous familyErcan Demir, Jean François Prud'homme, Meral Topçu
Clinical Biochemistry|May 17, 2011
Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote manBasak Celtikci, Meral Topçu, Hatice Asuman Ozkara
Journal of Child Neurology|March 23, 2004
Benign neonatal sleep myoclonus mimicking status epilepticusGüzide Turanli, Nesrin Senbil, Sakir Altunbaşak, et al.
Turk Psikiyatri Dergisi = Turkish Journal of Psychiatry|September 6, 2019
[Childhood Traumas, Attachment and Alexithymia in Adolescentswith Psychogenic Nonepileptic Seizure Type of Conversion Disorder]Özlem Uzun, Devrim Akdemir, Meral Topçu, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Usefulness of long-term video-EEG monitoring in children at a tertiary care centerSelin Onay, Dilek Yalnızoğlu, Meral Topçu, et al.
Journal of Child Neurology|September 15, 2005
Streptococcus oralis as a risk factor for middle cerebral artery thrombosisEbru Kazanci, Kader Karli Oguz, Aytemiz Gurgey, et al.
The Turkish Journal of Pediatrics|November 19, 2008
Osteoid osteoma in a 16-year-old boy presenting with atrophy of the left thigh: diagnostic difficultiesSinem Akgül, Akin Uzümcügil, M Fani Bozkurt, et al.
European Journal of Medical Genetics|December 15, 2010
Novel mutations of the MLC1 gene in Turkish patientsAyşe Yüzbaşioğlu, Meral Topçu, Y Cetin Kocaefe, et al.
Pediatric Neurosurgery|July 26, 2002
Medulloblastoma in a child with the metabolic disease L-2-hydroxyglutaric aciduriaPinar Akdemir Ozişik, Nejat Akalan, Selçuk Palaoğlu, et al.
Pageof 7