EEG-Veränderungen bei metabolischen Erkrankungen im Kindesalter
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[1] T. Nakayama,et al. Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in Japan , 2005, Brain and Development.
[2] T. Coşkun,et al. Inherited metabolic disorders in Turkey , 1990, Journal of Inherited Metabolic Disease.
[3] S. Felber,et al. EEG-alterations in patients with propionic acidemia , 2004 .
[4] M. Connolly,et al. Spasms in children with definite and probable mitochondrial disease * , 2004, European journal of neurology.
[5] S. Kan,et al. Slowly progressive spread of the stroke-like lesions in MELAS , 2003, Neurology.
[6] O. Dulac,et al. Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation. , 2003, Neuropediatrics.
[7] K. Engelstad,et al. Seizure Characterization and Electroencephalographic Features in Glut‐1 Deficiency Syndrome , 2003, Epilepsia.
[8] M. Fukuda,et al. Neuronal hyperexcitability in stroke-like episodes of MELAS syndrome , 2002, Neurology.
[9] P. Huppke,et al. EEG Features of Glut‐1 Deficiency Syndrome , 2002, Epilepsia.
[10] R. Boles,et al. Mitochondrial Disorders: A Potentially Under-recognized Etiology of Infantile Spasms , 2002, Journal of child neurology.
[11] P. Crumrine,et al. Degenerative disorders of the central nervous system. , 2001, Pediatrics in review.
[12] M. Zeviani,et al. Epileptic phenotypes associated with mitochondrial disorders , 2001, Neurology.
[13] F. Panzica,et al. Electroencephalographic features in a series of patients with neuronal ceroid lipofuscinoses , 2000, Neurological Sciences.
[14] M. Seashore,et al. Glucose transporter type 1 deficiency: a study of two cases with video-EEG , 1999, European Journal of Pediatrics.
[15] A. Leff,et al. Brief Communication Complex Partial Status Epilepticus in Late‐Onset MELAS , 1998, Epilepsia.
[16] T. Yasuda,et al. Periodic lateralized epileptiform discharges in mitochondrial encephalomyopathy. , 1997, Electroencephalography and clinical neurophysiology.
[17] Jean Aicardi,et al. Diseases of the Nervous System in Childhood , 1993 .
[18] B. Tharp. Unique EEG pattern (comb-like rhythm) in neonatal maple syrup urine disease. , 1992, Pediatric neurology.
[19] G. Pampiglione,et al. Progressive Neuronal Degeneration of Childhood with Liver Disease("Alpers' Disease"): Characteristic Neurophysiological Features , 1986, Neuropediatrics.
[20] E. Paulsen,et al. Valproate in the treatment of seizures associated with propionic acidemia. , 1981, Pediatrics.
[21] D N Donker,et al. Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria. , 1979, Electroencephalography and clinical neurophysiology.
[22] G. Pampiglione,et al. So-called neuronal ceroid lipofuscinosis , 1977, Journal of neurology, neurosurgery, and psychiatry.
[23] G. Pampiglione,et al. Some E.E.G. Observations in Patients with Krabbe's Disease , 1969, Developmental medicine and child neurology.