Published in Acta Paediatr on January 01, 2001
The role of epilepsy and epileptiform EEGs in autism spectrum disorders. Pediatr Res (2009) 2.01
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. Am J Hum Genet (2004) 1.88
Epilepsy and the natural history of Rett syndrome. Neurology (2010) 1.40
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients. J Med Genet (2006) 1.35
Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging. J Neurophysiol (2011) 1.33
Describing the phenotype in Rett syndrome using a population database. Arch Dis Child (2003) 1.33
Autism-lessons from the X chromosome. Soc Cogn Affect Neurosci (2006) 1.18
Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment. J Neurosci (2012) 1.18
The relationship of Rett syndrome and MECP2 disorders to autism. Dialogues Clin Neurosci (2012) 1.18
Seizures in Rett syndrome: an overview from a one-year calendar study. Eur J Paediatr Neurol (2007) 1.17
Convulsing toward the pathophysiology of autism. Brain Dev (2008) 1.15
Rett syndrome: genes, synapses, circuits, and therapeutics. Front Psychiatry (2012) 1.14
Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice. Hippocampus (2014) 1.02
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome. Neurology (2009) 0.97
Clinical and biological progress over 50 years in Rett syndrome. Nat Rev Neurol (2016) 0.95
Selective impact of MeCP2 and associated histone deacetylases on the dynamics of evoked excitatory neurotransmission. J Neurophysiol (2011) 0.93
Rett Syndrome. Mol Syndromol (2012) 0.91
Investigating mechanisms underlying neurodevelopmental phenotypes of autistic and intellectual disability disorders: a perspective. Front Syst Neurosci (2013) 0.89
Potential therapeutic use of the ketogenic diet in autism spectrum disorders. Front Pediatr (2014) 0.83
Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders. Elife (2016) 0.82
Characteristics of late-onset epilepsy and EEG findings in children with autism spectrum disorders. Korean J Pediatr (2011) 0.80
Epilepsy and other central nervous system diseases in atypical autism: a case control study. J Neural Transm (Vienna) (2011) 0.80
Epilepsy in individuals with a history of Asperger's syndrome: a Danish nationwide register-based cohort study. J Autism Dev Disord (2013) 0.80
Longitudinal course of epilepsy in Rett syndrome and related disorders. Brain (2016) 0.80
The role of GABAergic system in neurodevelopmental disorders: a focus on autism and epilepsy. Int J Physiol Pathophysiol Pharmacol (2011) 0.78
Genetic and epileptic features in Rett syndrome. Yonsei Med J (2012) 0.77
A review of Rett syndrome (RTT) with induced pluripotent stem cells. Stem Cell Investig (2016) 0.76
Analysis of the Serotonergic System in a Mouse Model of Rett Syndrome Reveals Unusual Upregulation of Serotonin Receptor 5b. Front Mol Neurosci (2017) 0.75
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann Neurol (1983) 6.80
National character does not reflect mean personality trait levels in 49 cultures. Science (2005) 3.56
The changing panorama of cerebral palsy in Sweden 1954-1970. I. Analysis of the general changes. Acta Paediatr Scand (1975) 3.21
Cerebral palsy epidemiology: where are we now and where are we going? Dev Med Child Neurol (1992) 2.96
Changing panorama of cerebral palsy in Sweden. VIII. Prevalence and origin in the birth year period 1991-94. Acta Paediatr (2001) 2.33
Dyskinetic cerebral palsy in Europe: trends in prevalence and severity. Arch Dis Child (2009) 2.17
The changing panorama of cerebral palsy in Sweden. IV. Epidemiological trends 1959-78. Acta Paediatr Scand (1984) 2.15
The changing panorama of cerebral palsy in Sweden. V. The birth year period 1979-82. Acta Paediatr Scand (1989) 2.07
Cerebral palsy and restricted growth status at birth: population-based case-control study. BJOG (2008) 1.90
Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls. Acta Paediatr Scand (1985) 1.81
The changing panorama of cerebral palsy in Sweden. IX. Prevalence and origin in the birth-year period 1995-1998. Acta Paediatr (2005) 1.61
Segregation analysis of the X-chromosome in a family with Rett syndrome in two generations. Am J Med Genet (1990) 1.54
The chronic brain syndrome of infantile hydrocephalus. A follow-up study of 63 spontaneously arrested cases. Am J Dis Child (1966) 1.52
The changing panorama of cerebral palsy in Sweden. VI. Prevalence and origin during the birth year period 1983-1986. Acta Paediatr (1993) 1.50
Dyskinetic cerebral palsy: a population-based study of children born between 1991 and 1998. Dev Med Child Neurol (2007) 1.50
Bilateral spastic cerebral palsy--a collaborative study between southwest Germany and western Sweden. III: Aetiology. Dev Med Child Neurol (1995) 1.50
Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents. Neuroreport (1994) 1.49
Gains and hazards of intensive neonatal care: an analysis from Swedish Cerebral palsy epidemiology. Dev Med Child Neurol (1982) 1.49
Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence. Am J Med Genet Suppl (1986) 1.48
Recurrences after initial dislocation of the shoulder. Results of a prospective study of treatment. J Bone Joint Surg Am (1983) 1.47
Rett syndrome: criteria for inclusion and exclusion. Brain Dev (1985) 1.46
The changing panorama of cerebral palsy in Sweden 1954-1970. II. Analysis of the various syndromes. Acta Paediatr Scand (1975) 1.44
Disialotransferrin developmental deficiency syndrome. Arch Dis Child (1989) 1.43
Carbohydrate-deficient glycoprotein (CDG) syndrome--a new variant, type III. Neuropediatrics (1993) 1.42
Brief report: autism and Asperger syndrome in seven-year-old children: a total population study. J Autism Dev Disord (1999) 1.42
Gross and fine motor function and accompanying impairments in cerebral palsy. Dev Med Child Neurol (2006) 1.41
Neurophysiological findings in the Rett syndrome, I: EMG, conduction velocity, EEG and somatosensory-evoked potential studies. Brain Dev (1989) 1.40
Psychotropic drug use in pregnancy and perinatal death. Acta Obstet Gynecol Scand (1992) 1.39
The Swedish Centenarian Study: a multidisciplinary study of five consecutive cohorts at the age of 100. Int J Aging Hum Dev (1997) 1.35
Bilateral spastic cerebral palsy--MRI pathology and origin. Analysis from a representative series of 56 cases. Dev Med Child Neurol (1995) 1.30
Rett syndrome: epidemiology and geographical variability. Eur Child Adolesc Psychiatry (1997) 1.25
Gaucher disease--Norrbottnian type. I. General clinical description. Eur J Pediatr (1980) 1.24
The incidence and genetics of metachromatic leucodystrophy in northern Sweden. Acta Paediatr Scand (1971) 1.23
Arthroscopy in acute injuries of the knee joint. Acta Orthop Scand (1977) 1.22
Increased dopamine synthesis rate in medial prefrontal cortex and striatum in schizophrenia indicated by L-(beta-11C) DOPA and PET. Biol Psychiatry (1999) 1.21
Mild mental retardation in Swedish school children. II. Etiologic and pathogenetic aspects. Acta Paediatr Scand (1981) 1.19
The changing panorama of cerebral palsy in Sweden. VII. Prevalence and origin in the birth year period 1987-90. Acta Paediatr (1996) 1.19
The changing panorama of cerebral palsy in Sweden 1954-1970. III. The importance of foetal deprivation of supply. Acta Paediatr Scand (1976) 1.16
Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease. J Neurol Neurosurg Psychiatry (1994) 1.15
Pre-, peri- and postnatal prevention of major neuropediatric handicaps. Neuropadiatrie (1975) 1.14
The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement. Acta Paediatr Scand Suppl (1991) 1.11
Morphological study of neocortical areas in Rett syndrome. Acta Neuropathol (1997) 1.10
Cerebral palsy in preterm infants: a population-based case-control study of antenatal and intrapartal risk factors. Acta Paediatr (2002) 1.08
Severe mental retardation in a Swedish county. II. Etiologic and pathogenetic aspects of children born 1959--1970. Neuropadiatrie (1977) 1.08
The dysequilibrium syndrome in cerebral palsy. Clinical aspects and treatment. Acta Paediatr Scand Suppl (1972) 1.07
Ocular pathology in disialotransferrin developmental deficiency syndrome. Ophthalmic Paediatr Genet (1990) 1.07
Correlation between ICIDH handicap code and Gross Motor Function Classification System in children with cerebral palsy. Dev Med Child Neurol (2000) 1.07
Identical syndromes of cerebral palsy in the same family. Acta Paediatr Scand (1969) 1.05
The changing panorama of cerebral palsy in Sweden. X. Prevalence and origin in the birth-year period 1999-2002. Acta Paediatr (2010) 1.05
Therapeutic arthroscopy of the knee. Injury (1978) 1.04
Infantile hydrocephalus epidemiology: an indicator of enhanced survival. Arch Dis Child Fetal Neonatal Ed (1994) 1.03
Epidemiology of infantile hydrocephalus in Sweden. I. Birth prevalence and general data. Acta Paediatr Scand (1986) 1.03
Familial ataxic diplegia with deficient cellular immunity. A new clinical entity. Acta Paediatr Scand (1970) 1.02
EEG and cognitive impairment in presenile dementia. Acta Neurol Scand (1979) 1.02
Serial proton MR spectroscopy of contrast-enhancing multiple sclerosis plaques: absolute metabolic values over 2 years during a clinical pharmacological study. AJNR Am J Neuroradiol (2000) 1.02
Mosaic trisomy of an autosome in the 6-12 group in a patient with multiple congenital anomalies. Acta Paediatr Scand (1967) 1.01
Attention deficits and autistic spectrum problems in children exposed to alcohol during gestation: a follow-up study. Dev Med Child Neurol (1997) 1.00
[CDGS-1--a recently discovered hereditary metabolic disease. Multiple organ manifestations, incidence 1/80,000, difficult to treat]. Lakartidningen (1998) 0.99
Epidemiology of infantile hydrocephalus in Sweden: a clinical follow-up study in children born at term. Neuropediatrics (1988) 0.97
Benign intracranial hypertension (pseudotumor cerebri). Review and report of 18 cases. Acta Paediatr Scand (1970) 0.97
Mild mental retardation in Swedish school children. I. Prevalence. Acta Paediatr Scand (1981) 0.96
A new modification of the technique of arthroscopy of the knee joint. Acta Chir Scand (1976) 0.95
Ataxic syndrome in congenital hypothyroidism. Acta Paediatr Scand (1970) 0.95
Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases. Acta Neuropathol (1984) 0.95
Intravenous physostigmine treatment of Alzheimer's disease evaluated by psychometric testing, regional cerebral blood flow (rCBF) measurement, and EEG. Psychopharmacology (Berl) (1987) 0.94
The changing panorama of infantile hydrocephalus and cerebral palsy over forty years--a Swedish survey. Brain Dev (1989) 0.94
Infantile globoid cell leucodystrophy (Krabbe's disease). A clinical and genetic study of 32 Swedish cases 1953--1967. Neuropadiatrie (1972) 0.94
Epidemiological and preventive aspects of cerebral palsy and severe mental retardation in Sweden. Eur J Pediatr (1979) 0.93
Rett syndrome: a search for gene sources. Am J Med Genet (1992) 0.93
Tryptophan load tests and pyridoxal-5-phosphate levels in epileptic children. II. Cryptogenic epilepsy. Acta Paediatr Scand (1966) 0.93
Social relationships and health as predictors of life satisfaction in advanced old age: results from a Swedish longitudinal study. Int J Aging Hum Dev (1999) 0.92
In vivo multiple spin echoes imaging of trabecular bone on a clinical 1.5 T MR scanner. Magn Reson Imaging (2002) 0.92
Infantile hydrocephalus--the impact of enhanced preterm survival. Acta Paediatr Scand (1990) 0.91
Large alterations in ganglioside and neutral glycosphingolipid patterns in brains from cases with infantile neuronal ceroid lipofuscinosis/polyunsaturated fatty acid lipidosis. J Neurochem (1987) 0.91
Epidemiology of infantile hydrocephalus in Sweden. III. Origin in preterm infants. Acta Paediatr Scand (1987) 0.91
Neurophysiological findings in the Rett syndrome, II: Visual and auditory brainstem, middle and late evoked responses. Brain Dev (1989) 0.91
Elevated CSF glutamate in Rett syndrome. Neuropediatrics (1992) 0.91
Arthroscopic examination of the posteromedial compartment of the knee joint. Int Orthop (1979) 0.91
Neuropsychological disorders in children exposed to alcohol during pregnancy: a follow-up study of 24 children to alcoholic mothers in Göteborg, Sweden. Alcohol Clin Exp Res (1998) 0.90
Insomnia in an 80-year-old population: relationship to medical, psychological and social factors. J Sleep Res (1998) 0.89
Symptomatology of late onset Krabbe's leukodystrophy: the European experience. Dev Neurosci (1991) 0.89
Amnestic-confabulatory syndrome in hydrocephalic dementia and Korsakoff's psychosis in alcoholism. Acta Psychiatr Scand (1979) 0.89
Epidemiology of mental retardation--a Swedish survey. Brain Dev (1983) 0.89