Published in Turk J Pediatr on July 22, 1980
Optic neuritis and myelitis after booster tetanus toxoid vaccination. Lancet (1992) 2.02
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome. J Med Genet (2005) 1.58
Intraventricular interferon and oral inosiplex in the treatment of subacute sclerosing panencephalitis. Neurology (1992) 1.47
Association of antiphospholipid antibodies with systemic lupus erythematosus in a child presenting with chorea: a case report. Eur J Pediatr (1994) 1.38
Parietal lipoma associated with cortical dysplasia and abnormal vasculature: case report and review of the literature. AJNR Am J Neuroradiol (2000) 1.20
Giant axonal neuropathy: clinical and genetic study in six cases. J Neurol Neurosurg Psychiatry (2005) 1.10
Clinical and magnetic resonance imaging features of L-2-hydroxyglutaric acidemia: report of three cases in comparison with Canavan disease. J Child Neurol (1996) 1.00
Cranial MR findings in Wilson's disease. Acta Radiol (1997) 0.97
Vogt-Koyanagi-Harada syndrome in siblings (with a brief review of the literature). Eur J Pediatr (1980) 0.96
Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature. Neuropediatrics (2002) 0.93
Occidental type cerebromuscular dystrophy: a report of eleven cases. J Neurol Neurosurg Psychiatry (1991) 0.90
Sandhoff disease in the Turkish population. Brain Dev (1997) 0.89
Subacute sclerosing panencephalitis in Turkey: epidemiological features. J Trop Pediatr (1988) 0.88
Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia. Neurology (2002) 0.87
Unilateral agenesis of the sternocleidomastoid muscle. Turk J Pediatr (1996) 0.86
Tremor of tongue and dysarthria as the sole manifestation of Wilson's disease. Clin Neurol Neurosurg (1990) 0.84
Mucormycosis in a diabetic child and its treatment with fluconazole: a case report. Turk J Pediatr (1995) 0.83
Neurologic findings of vitamin B12 deficiency: presentation of 7 cases. Turk J Pediatr (1996) 0.81
Weight gain associated with valproate in childhood. Pediatr Neurol (2000) 0.81
Hot water epilepsy. Clin Electroencephalogr (1992) 0.81
Multiple sclerosis in childhood: report of 16 cases. Eur Neurol (1996) 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
Tissue inflammatory response in subacute sclerosing panencephalitis (SSPE). J Child Neurol (2001) 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
Arylsulfatase A pseudodeficiency incidence in Turkey. Turk J Pediatr (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
A case of adenosine deaminase-negative severe combined immunodeficiency with neurological abnormalities. Turk J Pediatr (1996) 0.77
Alice in Wonderland syndrome as an initial manifestation of Epstein-Barr virus infection. Br J Ophthalmol (1992) 0.77
Evoked potentials in Guillain-Barré syndrome. Turk J Pediatr (1994) 0.77
Mental retardation with rare fragile site expressed at 2q11. Brain Dev (2000) 0.77
Apoptosis in brain biopsies of subacute sclerosing panencephalitis patients. Neuropediatrics (1999) 0.77
Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling. Genet Couns (2009) 0.77
Arteriovenous fistula: a cause of torticollis. Pediatr Neurol (1999) 0.77
Evaluation of neuronal damage following hypoxic-ischaemic brain injury in acute and early chronic periods in neonatal rats. Cell Biochem Funct (2006) 0.76
Selective involvement of the quadriceps muscle in congenital muscular dystrophies: an ultrasonographic study. Brain Dev (1992) 0.76
Factor V Q 506 mutation in children with thrombosis. Am J Hematol (1996) 0.75
Classification of congenital muscular dystrophy. J Pediatr (1990) 0.75
The Rett syndrome in males. Brain Dev (1991) 0.75
Tongue dyskinesia in Wilson disease. Brain Dev (1992) 0.75
Cardiovascular evaluation of syncope. J Child Neurol (2001) 0.75
Spontaneous cytotoxicity against measles virus infected and K562 cells in normal subjects and subacute sclerosing panencephalitis. Boll Ist Sieroter Milan (1985) 0.75
Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation. Brain Dev (1989) 0.75
Electroencephalographic study in acute rheumatic carditis. Am Heart J (1976) 0.75
Cell mediated immunity in patients with subacute sclerosing panencephalitis. Brain Dev (1984) 0.75
Myasthenia gravis in childhood. Acta Paediatr (1996) 0.75
EEG findings of posterior fossa tumors. Turk J Pediatr (1972) 0.75
Cardiorespiratory function in Duchenne and Becker muscular dystrophy. Turk J Pediatr (1996) 0.75
Muscular dystrophy or spinal muscular atrophy? Lancet (1989) 0.75
Deletion analysis of Duchenne muscular dystrophy. Turk J Pediatr (1993) 0.75
Atypical EEG findings in subacute sclerosing panencephalitis. Clin Electroencephalogr (1995) 0.75
A case of Sandifer's syndrome with hand tremor. Turk J Pediatr (2001) 0.75
Monomelic amyotrophy in siblings. Pediatr Neurol (1991) 0.75
Hereditary sensory radicular neuropathy (HSN). Turk J Pediatr (1981) 0.75
N-acetylaspartic aciduria in Canavan disease: another proof in two infants. Neuropediatrics (1990) 0.75
Rubinstein-Taybi syndrome. Turk J Pediatr (1972) 0.75
Therapy and prognosis of subdural collections. Turk J Pediatr (1972) 0.75
Neurobrucellosis in children. Paediatr Indones (1989) 0.75
Asphyxia and birth injuries as the cause of spasticity among premature infants. Turk J Pediatr (1964) 0.75
Functional significance of dystrophin-positive fibers in Duchenne and Becker muscular dystrophy. Pediatr Pathol Lab Med (1997) 0.75
Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactyly. Turk J Pediatr (1997) 0.75
Intestinal lymphangiectasia in a patient with Zellweger cerebrohepatorenal syndrome. Am J Med Genet (1995) 0.75
Subpopulations of T lymphocytes in subacute sclerosing panencephalitis (SSPE). Turk J Pediatr (1986) 0.75
Neuronal migration disorders presenting with mild clinical symptoms. Pediatr Neurol (1996) 0.75
Computerized tomographic findings of complex partial seizures in childhood and adolescence. Turk J Pediatr (1988) 0.75
Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients. Brain Dev (1996) 0.75
Familial corpus callosum agenesis. Turk J Pediatr (1980) 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
Brainstem tumor with infantile spasms. J Child Neurol (1997) 0.75
Neurologic complications in chronic renal failure: a retrospective study. Clin Pediatr (Phila) (1990) 0.75
Neuronal migration disorders. Part II: Magnetic resonance imaging. Turk J Pediatr (1999) 0.75
Systemic lupus erythematosus with chorea. Turk J Pediatr (1979) 0.75
Microgliomatosis presenting as sustained hyperventilation. Turk J Pediatr (1982) 0.75
Neuronal migration disorders. Part I: Terminology, classification, pathophysiology, EEG and epilepsy. Turk J Pediatr (1999) 0.75
Paraneoplastic syndrome manifesting as chronic cerebellar ataxia in a child with Hodgkin disease. J Pediatr (1992) 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
Computerized tomography findings of the posterior fossa in children: etiology and clinical correlation. Turk J Pediatr (1990) 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
Multiple sclerosis in a six-year-old boy (case report). Turk J Pediatr (1994) 0.75