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Huseyin Per

Showing results (11-20 of 61) with videos related to

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Saudi Medical Journal|September 12, 2012
Serum and urine boron and selenium levels in children with resistant epilepsyHuseyin Per, Mehmet Canpolat, Ugur Sahin, et al.
Seizure|June 19, 2014
Prevalence and risk factors of epilepsy among school children in Kayseri City Center, an urban area in Central Anatolia, TurkeyMehmet Canpolat, Sefer Kumandas, Hatice Gamze Poyrazoglu, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 20, 2011
Late-type vitamin K deficiency bleeding: experience from 120 patientsMehmet Akif Ozdemir, Musa Karakukcu, Huseyin Per, et al.
Case Reports in Neurology|February 28, 2014
A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23Fatih Bayrakli, Mehmet Canpolat, Huseyin Per, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 29, 2012
Diffusion-weighted imaging in Sydenham's choreaHakan Gumus, Gulsum Gumus, Huseyin Per, et al.
Journal of Pediatric Hematology/Oncology|April 6, 2018
Neutropenia and Increased Mean Corpuscular Volume (MCV) With Abnormal Neurologic Findings: A Case of Cobalamin D DeficiencyPembe Soylu Ustkoyuncu, Mustafa Kendirci, Fatih Kardas, et al.
Renal Failure|December 17, 2004
The effects of pentoxifylline on diabetic renal changes in streptozotocin-induced diabetes mellitusZubeyde Gunduz, Ozlem Canoz, Huseyin Per, et al.
Neurogenetics|December 26, 2024
Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotypeEmine Karatas, Ayten Gulec, Maide Korkmaz, et al.
Turkish Neurosurgery|August 17, 2011
Surgical timing of the subependymal giant cell astrocytoma (SEGA) with the patients of tuberous sclerosis complexMehmet Ali Ekici, Sefer Kumandas, Huseyin Per, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 17, 2015
Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical featuresAyşe Kaçar Bayram, Ebru Yilmaz, Huseyin Per, et al.
Pageof 7

Showing results (11-20 of 61) with videos related to

Sort By:
Pageof 7
Saudi Medical Journal|September 12, 2012
Serum and urine boron and selenium levels in children with resistant epilepsyHuseyin Per, Mehmet Canpolat, Ugur Sahin, et al.
Seizure|June 19, 2014
Prevalence and risk factors of epilepsy among school children in Kayseri City Center, an urban area in Central Anatolia, TurkeyMehmet Canpolat, Sefer Kumandas, Hatice Gamze Poyrazoglu, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 20, 2011
Late-type vitamin K deficiency bleeding: experience from 120 patientsMehmet Akif Ozdemir, Musa Karakukcu, Huseyin Per, et al.
Case Reports in Neurology|February 28, 2014
A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23Fatih Bayrakli, Mehmet Canpolat, Huseyin Per, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 29, 2012
Diffusion-weighted imaging in Sydenham's choreaHakan Gumus, Gulsum Gumus, Huseyin Per, et al.
Journal of Pediatric Hematology/Oncology|April 6, 2018
Neutropenia and Increased Mean Corpuscular Volume (MCV) With Abnormal Neurologic Findings: A Case of Cobalamin D DeficiencyPembe Soylu Ustkoyuncu, Mustafa Kendirci, Fatih Kardas, et al.
Renal Failure|December 17, 2004
The effects of pentoxifylline on diabetic renal changes in streptozotocin-induced diabetes mellitusZubeyde Gunduz, Ozlem Canoz, Huseyin Per, et al.
Neurogenetics|December 26, 2024
Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotypeEmine Karatas, Ayten Gulec, Maide Korkmaz, et al.
Turkish Neurosurgery|August 17, 2011
Surgical timing of the subependymal giant cell astrocytoma (SEGA) with the patients of tuberous sclerosis complexMehmet Ali Ekici, Sefer Kumandas, Huseyin Per, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 17, 2015
Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical featuresAyşe Kaçar Bayram, Ebru Yilmaz, Huseyin Per, et al.
Pageof 7