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The Turkish Journal of Pediatrics
|
February 24, 1999
Neuronal migration disorders. Part I: Terminology, classification, pathophysiology, EEG and epilepsy
G Turanli, D Yalnizoğlu, Y Renda
The Turkish Journal of Pediatrics
|
October 1, 1996
Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactyly
G 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 literature
L 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 patients
H Erdem, S Pehlivan, H Topaloğlu, et al.
The Turkish Journal of Pediatrics
|
January 1, 1997
Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosis
S 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 disease
B 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.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
The Turkish Journal of Pediatrics
|
February 24, 1999
Neuronal migration disorders. Part I: Terminology, classification, pathophysiology, EEG and epilepsy
G Turanli, D Yalnizoğlu, Y Renda
The Turkish Journal of Pediatrics
|
October 1, 1996
Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactyly
G 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 literature
L 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 patients
H Erdem, S Pehlivan, H Topaloğlu, et al.
The Turkish Journal of Pediatrics
|
January 1, 1997
Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosis
S 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 disease
B 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.
Page
of 1