Published in Turk J Pediatr on April 15, 1999
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Cranial MR findings in Wilson's disease. Acta Radiol (1997) 0.97
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Sandhoff disease in the Turkish population. Brain Dev (1997) 0.89
Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosis. Turk J Pediatr (2000) 0.89
Subacute sclerosing panencephalitis in Turkey: epidemiological features. J Trop Pediatr (1988) 0.88
Tremor of tongue and dysarthria as the sole manifestation of Wilson's disease. Clin Neurol Neurosurg (1990) 0.84
Multiple sclerosis in childhood: report of 16 cases. Eur Neurol (1996) 0.81
Hot water epilepsy. Clin Electroencephalogr (1992) 0.81
Long-term follow-up of indirect hyperbilirubinemia in full-term Turkish infants. Acta Paediatr (1996) 0.80
HLA antigens in subacute sclerosing panencephalitis. Arch Neurol (1983) 0.80
The role of brain perfusion SPECT in Moyamoya disease. Rev Esp Med Nucl Imagen Mol (2012) 0.79
Cimetidine as an immunomodulator in subacute sclerosing panencephalitis: a double blind, placebo-controlled study. Pediatr Infect Dis J (1993) 0.79
Evoked potentials in full-term and premature infants: a comparative study. Childs Nerv Syst (1993) 0.78
Mental retardation with rare fragile site expressed at 2q11. Brain Dev (2000) 0.77
Neurophysiological studies of patients with classical phenylketonuria: evaluation of results of IQ scores, EEG and evoked potentials. Turk J Pediatr (1993) 0.77
Arylsulfatase A pseudodeficiency incidence in Turkey. Turk J Pediatr (2000) 0.77
Evoked potentials in Guillain-Barré syndrome. Turk J Pediatr (1994) 0.77
Selective involvement of the quadriceps muscle in congenital muscular dystrophies: an ultrasonographic study. Brain Dev (1992) 0.76
Analysis of "pure" congenital muscular dystrophies in thirty-eight cases. How different is the classical type 1 from the occidental type cerebromuscular dystrophy? Neuropediatrics (1994) 0.76
Factor V Q 506 mutation in children with thrombosis. Am J Hematol (1996) 0.75
The Rett syndrome in males. Brain Dev (1991) 0.75
Classification of congenital muscular dystrophy. J Pediatr (1990) 0.75
Tongue dyskinesia in Wilson disease. Brain Dev (1992) 0.75
Asphyxia and birth injuries as the cause of spasticity among premature infants. Turk J Pediatr (1964) 0.75
Muscular dystrophy or spinal muscular atrophy? Lancet (1989) 0.75
Functional significance of dystrophin-positive fibers in Duchenne and Becker muscular dystrophy. Pediatr Pathol Lab Med (1997) 0.75
Deletions in the survival motor neuron gene in Turkish spinal muscular atrophy patients. J Inherit Metab Dis (1996) 0.75
The effect of clonazepam on myoclonic seizures in infancy and childhood. Turk J Pediatr (1980) 0.75
Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactyly. Turk J Pediatr (1997) 0.75
Cardiorespiratory function in Duchenne and Becker muscular dystrophy. Turk J Pediatr (1996) 0.75
Fatal agranulocytosis developed in the course of carbamazepine therapy. A case report and review of the literature. Turk J Pediatr (1995) 0.75
Intestinal lymphangiectasia in a patient with Zellweger cerebrohepatorenal syndrome. Am J Med Genet (1995) 0.75
EEG findings of posterior fossa tumors. Turk J Pediatr (1972) 0.75
N-acetylaspartic aciduria in Canavan disease: another proof in two infants. Neuropediatrics (1990) 0.75
Computerized tomographic findings of complex partial seizures in childhood and adolescence. Turk J Pediatr (1988) 0.75
Cognitive and behavioural characteristics of children with idiopathic epilepsy in a low-income area of Ankara, Turkey. Dev Med Child Neurol (1984) 0.75
Familial corpus callosum agenesis. Turk J Pediatr (1980) 0.75
Myasthenia gravis in childhood. Acta Paediatr (1996) 0.75
Cell mediated immunity in patients with subacute sclerosing panencephalitis. Brain Dev (1984) 0.75
Donor splice site mutation in intron 5 of the HEXA gene in a Turkish infant with Tay-Sachs disease. Hum Mutat (1995) 0.75
Acetylcholine receptor antibodies and single-fiber EMG in first-degree relatives of children with myasthenia gravis. Neuropediatrics (1995) 0.75
Neurologic complications in chronic renal failure: a retrospective study. Clin Pediatr (Phila) (1990) 0.75
Computerized tomography findings of the posterior fossa in children: etiology and clinical correlation. Turk J Pediatr (1990) 0.75
Neuronal migration disorders. Part II: Magnetic resonance imaging. Turk J Pediatr (1999) 0.75
Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation. Brain Dev (1989) 0.75
Paraneoplastic syndrome manifesting as chronic cerebellar ataxia in a child with Hodgkin disease. J Pediatr (1992) 0.75
Electroencephalographic study in acute rheumatic carditis. Am Heart J (1976) 0.75
A study on enzyme activities of some sphingolipidoses. Turk J Pediatr (1994) 0.75
Fukuyama type congenital muscular dystrophy in a Turkish child. Can J Neurol Sci (1990) 0.75
Cardiac dysrhythmia that simulates seizure disorder in two children. Turk J Pediatr (2000) 0.75
Hereditary sensory radicular neuropathy (HSN). Turk J Pediatr (1981) 0.75
Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients. Brain Dev (1996) 0.75
Multiple sclerosis in a six-year-old boy (case report). Turk J Pediatr (1994) 0.75
Atypical EEG findings in subacute sclerosing panencephalitis. Clin Electroencephalogr (1995) 0.75
Deletion analysis of Duchenne muscular dystrophy. Turk J Pediatr (1993) 0.75
Rubinstein-Taybi syndrome. Turk J Pediatr (1972) 0.75
Therapy and prognosis of subdural collections. Turk J Pediatr (1972) 0.75