Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-12-02
著者
-
Matsuishi Toyojiro
Department Of Pediatrics And Child Health Kurume University School Of Medicine
-
Matsuishi Toyojiro
Department Of Pediatrics Kurume University
-
Ozawa Yuri
Department Of Clinical Laboratory National Center Hospital For Mental Nervous And Muscular Disorders
-
Saito Yoshiaki
Department Of Child Neurology National Center Hospital Of Neurology And Psychiatry National Center O
-
Takashima Sachio
National Institute Of Neuroscience National Center Of Neurology And Psychiatry
-
Hamano Kenzo
Department Of Pediatrics Tsukuba University
-
ITO Masayuki
National Institute of Neurology
-
Takashima Sachio
National Institute Of Neurology
-
Takashima Sachio
National Center Of Neurology And Psychiatry
-
Saito Yoshiaki
Department Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Univers
-
MATSUISHI Toyojiro
Department of Pediatrics & Child Health, Kurume University School of Medicine
関連論文
- 小児期発症自己免疫性肝炎4例の臨床・病理像
- Multicenter and Retrospective Case Study of Warfarin and Aspirin Combination Therapy in Patients With Giant Coronary Aneurysms Caused by Kawasaki Disease
- Impact of intravenous immunoglobulin infusion on longitudinal left ventricular performance in patients with acute Kawasaki disease of usual course
- PE-066 High Intensity Transient Signals Measured by Transcranial Doppler Study during Transcatheter Closure of Atrial Septal Defect Using Amplatzer Septal Occluder(PE011,Congenital Heart Disease (M),Poster Session (English),The 73rd Annual Scientific Meet
- Effect of Revision of Japanese Diagnostic Criterion for Fever in Kawasaki Disease on Treatment and Cardiovascular Outcome
- PE-554 Long-term Prognosis of Kawasaki Syndrome with Giant Coronary Aneurysms is Acceptable with Multiple Catheter and Surgical Interventions(Congenital heart disease/Kawasaki's disease-2 (M) PE94,Poster Session (English),The 70th Anniversary Annual Scien
- Scale properties of the Japanese version of the Strengths and Difficulties Questionnaire (SDQ) : A study of infant and school children in community samples
- Prefrontal cerebral blood volume patterns while playing video games : A near-infrared spectroscopy study
- Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome : pathological mutations and polymorphisms
- Neurobiology and neurochemistry of Rett syndrome
- Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech
- The test of variables of attention (TOVA) is useful in the diagnosis of Japanese male children with attention deficit hyperactivity disorder
- Sleep disorder in Rett syndrome and melatonin treatment
- Cerebral oxygenation and hemodynamics during hyperventilation and sleep in patients with Rett syndrome
- Balo's concentric sclerosis in a 4-year-old Japanese infant
- Early intervention for very-low-birth-weight infants
- Heat stroke-like episode in child caused by zonisamide
- In vivo quantitative ultrasonic evaluation of neonatal brain with a real time integrated backscatter imaging system
- 肥満児における摂食中枢制御蛋白の免疫・肝機能修飾作用についての検討
- Management of and prophylaxis against status epilepticus in children with severe myoclonic epilepsy in infancy (SMEI ; Dravet syndrome) - A nationwide questionnaire survey in Japan
- A pilot study on the changes in immunity after ACTH therapy in patients with West syndrome
- Impaired Nitric Oxide-Independent Dilation of Renal Afferent Arterioles in Spontaneously Hypertensive Rats
- Early head cooling in newborn piglets is neuroprotective even in the absence of profound systemic hypothermia
- Pyruvate dehydrogenase E1α subunit deficiency in a female patient : evidence of antenatal origin of brain damage and possible etiology of infantile spasms
- Long-term Follow-up Results in Catheter Intervention for Kawasaki Disease : Quantitative Coronary Artery Angiography and Intravascular Ultrasound Imaging Study
- Quantitative assessment of severity of infants with ventricular septal defect by natriuretic peptides
- Hyperkinetic movement disorder in a child treated by globus pallidus stimulation
- Conjunctival Vasculature Patterns Influencing the Filtering Bleb Shape Following Trabeculectomy with Limbal-Based Conjunctival Flaps
- Menatetrenone plus alfacalcidol treatment for bone problems in eight children with skeletal unloading
- Transthoracic echocardiography-assisted valve perforation in pulmonary atresia
- PJ-434 Impaired Endothelial Function in Adult Patients with Cyanotic Heart Disease(Congenital Heart Disease/Kawasaki's Disease 2 (M) : PJ73)(Poster Session (Japanese))
- Left Ventricular Performance During Pregnancy in Patients With Repaired Tetralogy of Fallot : Prospective Evaluation Using the Tei Index
- Incidence and Clinical Features of Asymptomatic Atrial Septal Defect in School Children Diagnosed by Heart Disease Screening
- Perinatal bile acid metabolism : bile acid analysis of meconium of preterm and full-term infants
- Acute severe hepatitis : Successful prevention of fulminant hepatic failure with early intensive medical therapy
- Transient encephalopathy with reversible white matter lesions : A case report
- Magnetic Resonance in an Amorphous Slag:8CaO・8SiO_2・3Fe_2O_3・2FeO
- Role of protein kinase C in Ca channel blocker-induced renal arteriolar dilation in spontaneously hypertensive rats : Studies in the isolated perfused hydronephrotic kidney
- Serial Magnetic Resonance Imaging and Single Photon Emission Computed Tomography Study of Acute Disseminated Encephalomyelitis Patient after Japanese Encephalitis Vaccination
- 小児気管支喘息治療における長期入院療法の現状と未来
- Neuropathology of early-infantile epileptic encephalopathy with suppression-bursts ; comparison with those of early myoclonic encephalopathy and West syndrome
- Short-term effect of American summer treatment program for Japanese children with attention deficit hyperactivity disorder
- Arthrogryposis multiplex congenita with callosal agenesis and dentato-olivary dysplasia
- Activity of neurons in ventrolateral respiratory groups during swallowing in decerebrate rats
- Brainstem and spinal projections of augmenting expiratory neurons in the rat
- Morphology of the decrementing expiratory neurons in the brainstem of the rat
- Brain MRI findings of older patients with Pallister-Killian syndrome
- Laryngeal dystonia in xeroderma pigmentosum
- DETECTION OF REGIONAL CARDIAC WALL MOTION ABNORMALITIES BY CARDIAC WALL KYMOGRAPHY : Echocardiography II : IIIrd Auditorium : Proceedings of the 43rd Annual Meeting of the Japanese Circulation Society, Tokyo, 1979
- Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy
- Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency
- Characteristic prefrontal blood volume patterns when imaging body type, high-calorie food, and mother-child attachment in childhood anorexia nervosa : A near infrared spectroscopy study
- Polysomnographic studies of Lesch-Nyhan syndrome
- Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms
- Thiamine-deficient encephalopathy due to excessive intake of isotonic drink or overstrict diet therapy in Japanese children
- Postnatal evolution of cortical malformation in the "non-affected" hemisphere of hemimegalencephaly
- Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan
- IV D2 A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures
- Molecular Genetics of Febrile Seizures
- Fukutin expression in mouse non-muscle somatic organs : its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
- Regional cerebral blood flow changes in early-onset anorexia nervosa before and after weight gain
- Comparison of the strengths and difficulties questionnaire (SDQ) scores between children with high-functioning autism spectrum disorder (HFASD) and attention-deficit/hyperactivity disorder (AD/HD)
- Developmental characteristics of visual cognitive function during childhood according to exploratory eye movements
- Excessive expression of synaptojanin in brains with Down syndrome
- Effect of L-arginine on synaptosomal mitochondrial function
- Inappropriate intracranial hemodynamics in the natural course of MELAS
- 早期産児における尿中胆汁酸組成の発達的推移
- Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome
- Merosin-negative non-Fukuyama-type congenital muscular dystrophy: a case report
- Canada and Japan
- Neuropathology of tuberous sclerosis
- Imaging and pathology in pediatric neurological disorders
- Reflections on the brainstem dysfunction in neurologically disabled children
- Prefrontal brain function in children with anorexia nervosa : A near-infrared spectroscopy study
- Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome
- Augmented startle responses in opsoclonus-myoclonus syndrome
- Juvenile myelomonocytic leukemia characterized by cutaneous lesion containing Langerhans cell histiocytosis-like cells
- Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination
- Summer treatment program for children with attention deficit hyperactivity disorder : Japanese experience in 5 years
- CD4^+ CD25^ regulatory T cell in childhood ocular myasthenia gravis
- Effects of low-dose hydrochlorothiazide on urolithiasis and bone metabolism in severely disabled individuals : A pilot study
- Pyruvate dehydrogenase E1 alpha subunit deficiency in a female patient: evidence of antenatal origin of brain damage and possible etiology of infantile spasms
- Effects of Indomethacin and Hyperventilation on Cerebral Hemodynamics and Oxygenation in Newborn Piglets
- Rho-kinase/nuclear factor-κβ/angiotensinogen axis in angiotensin II-induced renal injury
- Neurotransmitter changes in the pathophysiology of Lesch-Nyhan syndrome
- Clinical evaluation of non-Descemet stripping automated endothelial keratoplasty (nDSAEK)
- Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene
- Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies
- Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes
- Profiles of blood biomarkers in alternating hemiplegia of childhood-Increased MMP-9 and decreased substance P indicates its pathophysiology
- Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination
- A case of clinically mild encephalitis with a reversible splenial lesion (MERS) after mumps vaccination
- A case of congenital axonal neuropathy associated with West syndrome
- Rett syndrome : The state of clinical and basic research, and future perspectives
- Pitfalls in diagnosing psychogenic nonepileptic seizures in a sexually abused child
- Role of the basal ganglia and thalamus in extrapontine myelinolysis and thiamine deficiency
- A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder
- Calcium Antagonists Protect against Nephrosclerosis in Partially Nephrectomized Spontaneously Hypertensive Rats
- Transient Haemophilus Influenzae Type b Bacteremia in a Healthy Child
- West Syndrome Associated with Administration of a Histamine H1 Antagonist, Oxatomide