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D Yalnizoğlu

Showing results (1-10 of 7) with videos related to

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The Turkish Journal of Pediatrics|February 24, 1999
Neuronal migration disorders. Part I: Terminology, classification, pathophysiology, EEG and epilepsyG Turanli, D Yalnizoğlu, Y Renda
The Turkish Journal of Pediatrics|October 1, 1996
Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactylyG Turanli, M Aynaci, D Yalnizoğlu, et al.
The Turkish Journal of Pediatrics|January 1, 1995
Fatal agranulocytosis developed in the course of carbamazepine therapy. A case report and review of the literatureL Olcay, S Pekcan, D Yalnizoğlu, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Deletions in the survival motor neuron gene in Turkish spinal muscular atrophy patientsH Erdem, S Pehlivan, H Topaloğlu, et al.
The Turkish Journal of Pediatrics|January 1, 1997
Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosisS Göğüş, F Sarikayalar, Z Akçören, et al.
Revista Espanola De Medicina Nuclear E Imagen Molecular|September 18, 2012
The role of brain perfusion SPECT in Moyamoya diseaseB Volkan-Salanci, E Lay Ergün, Ç Genc Sel, et al.
Neuropediatrics|April 1, 1994
Analysis of "pure" congenital muscular dystrophies in thirty-eight cases. How different is the classical type 1 from the occidental type cerebromuscular dystrophy?H Topaloğlu, G Kale, D Yalnizoğlu, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The Turkish Journal of Pediatrics|February 24, 1999
Neuronal migration disorders. Part I: Terminology, classification, pathophysiology, EEG and epilepsyG Turanli, D Yalnizoğlu, Y Renda
The Turkish Journal of Pediatrics|October 1, 1996
Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactylyG Turanli, M Aynaci, D Yalnizoğlu, et al.
The Turkish Journal of Pediatrics|January 1, 1995
Fatal agranulocytosis developed in the course of carbamazepine therapy. A case report and review of the literatureL Olcay, S Pekcan, D Yalnizoğlu, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Deletions in the survival motor neuron gene in Turkish spinal muscular atrophy patientsH Erdem, S Pehlivan, H Topaloğlu, et al.
The Turkish Journal of Pediatrics|January 1, 1997
Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosisS Göğüş, F Sarikayalar, Z Akçören, et al.
Revista Espanola De Medicina Nuclear E Imagen Molecular|September 18, 2012
The role of brain perfusion SPECT in Moyamoya diseaseB Volkan-Salanci, E Lay Ergün, Ç Genc Sel, et al.
Neuropediatrics|April 1, 1994
Analysis of "pure" congenital muscular dystrophies in thirty-eight cases. How different is the classical type 1 from the occidental type cerebromuscular dystrophy?H Topaloğlu, G Kale, D Yalnizoğlu, et al.
Pageof 1