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List of Jounal Titles
A to Z index of Journal Title. Choose a letter.
Brain & Dev
- 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.
Supplement 1
22
- 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.
1
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