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Serdar Ceylaner

Showing results (41-50 of 244) with videos related to

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Case Reports in Immunology|March 28, 2025
Coexistence of a Leaky SCID Phenotype With Hyperphenylalaninemia in an Adult CaseUgur Musabak, Tuba Erdogan, Muserref Sule Akcay, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 8, 2026
Spinocerebellar ataxia type 40 presenting with isolated cervical dystonia: expanding the phenotypic spectrumHalil Onder, Haktan Bagis Erdem, Serdar Ceylaner, et al.
Journal of Pediatric Neurosciences|February 3, 2021
Hypomyelination and Congenital Cataract: Three Siblings PresentationZeynep Selen Karalok, Esra Gurkasb, Kursad Aydinc, et al.
Prenatal Diagnosis|December 23, 2004
Prenatal sonographic findings in a case of Varadi-Papp syndromeMelih Atahan Guven, Serdar Ceylaner, Federico Prefumo, et al.
Journal of Pediatric Neurosciences|March 11, 2016
Merosin-negative congenital muscular dystrophy: Report of five casesFaruk Incecik, Ozlem M Herguner, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 17, 2016
Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior VermisFatih Gürbüz, Serdar Ceylaner, Ali Kemal Topaloğlu, et al.
Journal of Pediatric Hematology/Oncology|February 3, 2025
Rare Etiology of Isolated Macrocytosis: Adenosine Kinase Deficiency With a Novel MutationAyşe Öz, Ayşe Mavi Özdemir, Serdar Ceylaner, et al.
Journal of Pediatric Neurosciences|November 19, 2016
Mitochondrial membrane protein-associated neurodegeneration in a Turkish patientFaruk Incecik, Ozlem M Hergüner, Seyda Besen, et al.
Epilepsy & Behavior Case Reports|July 29, 2017
Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1Yalcin Celik, Cetin Okuyaz, Ali Ertug Arslankoylu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 9, 2003
Asymmetric crying facies associated with hemihypertrophy: report of one caseHüseyin Caksen, Türkan Patiroğlu, Ahmet Ciftçi, et al.
Pageof 25

Showing results (41-50 of 244) with videos related to

Sort By:
Pageof 25
Case Reports in Immunology|March 28, 2025
Coexistence of a Leaky SCID Phenotype With Hyperphenylalaninemia in an Adult CaseUgur Musabak, Tuba Erdogan, Muserref Sule Akcay, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 8, 2026
Spinocerebellar ataxia type 40 presenting with isolated cervical dystonia: expanding the phenotypic spectrumHalil Onder, Haktan Bagis Erdem, Serdar Ceylaner, et al.
Journal of Pediatric Neurosciences|February 3, 2021
Hypomyelination and Congenital Cataract: Three Siblings PresentationZeynep Selen Karalok, Esra Gurkasb, Kursad Aydinc, et al.
Prenatal Diagnosis|December 23, 2004
Prenatal sonographic findings in a case of Varadi-Papp syndromeMelih Atahan Guven, Serdar Ceylaner, Federico Prefumo, et al.
Journal of Pediatric Neurosciences|March 11, 2016
Merosin-negative congenital muscular dystrophy: Report of five casesFaruk Incecik, Ozlem M Herguner, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 17, 2016
Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior VermisFatih Gürbüz, Serdar Ceylaner, Ali Kemal Topaloğlu, et al.
Journal of Pediatric Hematology/Oncology|February 3, 2025
Rare Etiology of Isolated Macrocytosis: Adenosine Kinase Deficiency With a Novel MutationAyşe Öz, Ayşe Mavi Özdemir, Serdar Ceylaner, et al.
Journal of Pediatric Neurosciences|November 19, 2016
Mitochondrial membrane protein-associated neurodegeneration in a Turkish patientFaruk Incecik, Ozlem M Hergüner, Seyda Besen, et al.
Epilepsy & Behavior Case Reports|July 29, 2017
Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1Yalcin Celik, Cetin Okuyaz, Ali Ertug Arslankoylu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 9, 2003
Asymmetric crying facies associated with hemihypertrophy: report of one caseHüseyin Caksen, Türkan Patiroğlu, Ahmet Ciftçi, et al.
Pageof 25