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9
Brain & Dev
Supplement 1
Development of the nigrostriatal dopamine neuron and the pathways in the basal ganglia.
Neural circuits and topographic organization of the basal ganglia and related regions.
Possible pathways through which neurons of the shell of the nucleus accumbens influence the outflow of the core of the nucleus accumbens.
The cat neostriatum. Relative distribution of cholinergic neurons versus serotonergic fibers.
Postnatal development of the dopaminergic neurons in the rat mesencephalon.
Alterations of tetrahydrobiopterin biosynthesis and pteridine levels in mouse tissues during growth and aging.
Studies on the genotype-phenotype relation in the hph-1 mouse mutant deficient in guanosine triphosphate (CTP) cyclohydrolase I activity.
Dopamine deficiency in mice.
Gradual changes in environmental light intensity and entrainment of circadian rhythms.
Hereditary progressive dystonia with marked diurnal fluctuation.
Development of the nosological analysis of juvenile parkinsonism.
Autosomal recessive early-onset parkinsonism with diurnal fluctuation. Clinicopathologic characteristics and molecular genetic identification.
Two phenotypes and anticipation observed in Japanese cases with early onset torsion dystonia (DYT1) - pathophysiological consideration.
Gene mutation in hereditary progressive dystonia with marked diumal fluctuation (HPD), strictly defined dopa-responsive dystonia.
Molecular mechanisms of hereditary progressive dystonia with marked diumal fluctuation, Segawa's disease.
Missense mutants inactivate guanosine triphosphate cyclohydrolase I in hereditary progressive dystonia.
Autosomal recessive juvenile parkinsonism.
Diagnosis and treatment of 6-pyruvoyl-tetrahydropterin synthase deficiency.
Neurotransmitter changes in the pathophysiology of Lesch-Nyhan syndrome.
Intracortical inhibition of the motor cortex in movement disorders.
REM sleep atonia. Responsible brain regions, quantification, and clinical implication.
Approach to ex vivo gene therapy in the treatment of Parkinson's disease.
22
1
The neurological complications of achondroplasia.
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.
Reading of Kana (phonetic symbols for syllables) in Japanese children with spastic diplegia and periventricular leukomalacia.
The perfusion defect seen with SPECT in West syndrome is not correlated with seizure prognosis or developmental outcome.
A neurodegenerative disorder with early myoclonic encephalopathy, retinal pigmentary degeneration and nephronophthisis.
Mental retardation subsequent to refractory partial seizures in infancy.
Phenytoin administration in the newborn and infant.
Developmental changes of distortion product and transient evoked otoacoustic emissions in different age groups.
A case of chronic infantile type of fucosidosis: clinical and magnetic resonance image findings.
Transient seizure disappearance due to bilateral striatal necrosis in a patient with intractable epilepsy.
Successful control with bromide of two patients with malignant migrating partial seizures in infancy.
Chronic fatigue syndrome in childhood.
Perturbation in dystrophin-associated glycoprotein complex in a boy with Becker muscular dystrophy.
2
When antiepileptic drugs aggravate epilepsy.
Medical education and postgraduate training in the USA: Special reference to children's hospital.
Sleep in subjects with autistic disorder: A neurophysiological and psychological study.
Benign partial epilepsy in infancy and early childhood with vertex spikes and waves during sleep: A new epileptic form.
Head stability during whole body movements in spastic diplegia.
Epilepsy in adolescents and young adults with autistic disorder.
Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation.
Ethical attitudes of Japanese physicians regarding life-sustaining treatment for children with severe neurological disabilities.
Age-related changes in the posterior limb of the internal capsule revealed by magnetic resonance imaging.
Plasmapheresis in a child affected by acute disseminated encephalomyelitis.
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography(FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; A progressive neurometabolic disease.
Congenital myotonic dystrophy: Report of paternal transmission.
Suppression-burst patterns in intractable epilepsy with focal cortical dysplasia.
3
Fetal pain?
Autonomic nervous system functions in obese children.
Brain distribution and efficacy of carbamazepine in kainic acid induced seizure in rats.
A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency.
Perceptual-motor, visual and cognitive ability in very low birthweight preschool children without neonatal ultrasound abnormalities.
Benign paroxysmal torticollis of infancy.
Development of voluntary control of saccadic eye movements. I. Age-related changes in normal children.
The serum nitric oxide levels in patients with Duchenne muscular dystrophy.
Bipolar affective disorder heralding cerebral demyelination in adreno-myelo-leukodystrophy.
Pontocerebellar hypoplasia type 2(PCH2): Report of two siblings.
Acute transient pseudoatrophy of the brain accompanying measles infection.
Ganglioside patterns in neuroepithelial tumors of childhood.
4
The therapeutics of melatonin: a paediatric perspective.
Otocerebral anomalies associated with topical tretinoin use.
Infantile bilateral striatal necrosis following measles.
On chronological changes in the basic EEG rhythm in persons with Down syndrome - with special reference to slowing of alpha waves.
Zonisamide - induced urinary lithiasis in patients with intractable epilepsy.
Unique astrocytic inclusion in a 2 month-old baby showing Leigh-like brain lesions with lactic acidosis.
Midazolam as a first-line agent for status epilepticus in children.
Seizure-inducing paradoxical reaction to antiepileptic drugs.
Long-term medical, educational, and social prognoses of childhood-onset epilepsy: a population-based study in a rural district of Japan.
Haloperidol-induced rhabdomyolysis without neuroleptic malignant syndrome in a handicapped child.
Acute disseminated encephalomyelitis after live rubella vaccination.
Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family.
Hypoxic-ischemic encephalopathy with cystic brain stem necroses and thalamic calcifications in a preterm twin.
Empty sella syndrome in nevoid basal cell carcinoma syndrome.
5
The spectrum of neuropsychiatric abnormalities associated with electrical status epilepticus in sleep.
Benign partial epilepsies in infancy.
Infantile convulsions with mild gastroenteritis.
Central nervous system complications in human herpesvirus-6 infection.
Repetitive intermittent hypoxia-ischemia and brain damage in neonatal rats.
Gene expression related to cholesterol metabolism in mouse brain during development.
Otoacoustic emission in patients with neurological disorders who have auditory brainstem response abnormality.
Focal polymicrogyria in mother and son.
Neonatal intracranial teratoma.
6
Intranasal midazolam for prolonged convulsive seizures.
Spatial cognition in children. I. Development of drawing-related (visuospatial and constructional) abilities in preschool and early school years.
Spatial cognition in children. II. Visuospatial and constructional skills in developmental reading disability.
Combined therapy with hypothermia and anticytokine agents in influenza A encephalopathy.
The test of variables of attention (TOVA) is useful in the diagnosis of Japanese male children with attention deficit hyperactivity disorder.
Adenylosuccinase deficiency: an unusual cause of early-onset epilepsy associated with acquired microcephaly.
Partial seizures in leukoencephalopathy with swelling and a discrepantly mild clinical course.
Sneddon syndrome, arylsulfatase A pseudodeficiency and impairment of cerebral white matter.
An autopsy case of atypical adrenoleukomyeloneuropathy in childhood.
Ictal increased writing preceded by dysphasic seizures.
Lyme borreliosis mimicking central nervous system malignancy: the diagnostic pitfall of cerebrospinal fluid cytology.
7
Neurological bases of behavioral development in infancy.
Assessment of brainstem function in Chiari II malformation utilizing brainstem auditory evoked potentials(BAEP), blink reflex and masseter reflex.
Cognitive and neurophysiological evaluation of Japanese dyslexia.
Cerebrospinal fluid purine metabolite and neuron-specific enolase concentrations after febrile seizures.
Co-segregation of benign infantile convulsions and paroxysmal kinesigenic choreoathetosis.
Developmental sequence of postural control in prone position in children with spastic diplegia.
Complex regional pain syndrome in childhood: report of three cases.
Infantile convulsions and paroxysmal kinesigenic choreoathetosis in a patient with idiopathic hypoparathyroidism.
Diagnostic usefulness of diffusion-weighted magnetic resonance imaging in influenza-associated acute encephalopathy or encephalitis.
A case of Walker-Warburg syndrome.
8
Friedreich's ataxia and iron metabolism.
Neurotuberculosis among Filipino children: an 11 years experience at the Philippine Children's Medical Center.
Schizencephaly: clinical and imaging features in 30 infantile cases.
Unprovoked seizures after complex febrile convulsions.
MRI spectrum of cortical malformations in tuberous sclerosis complex.
Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings.
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