Decreased resting energy expenditure in patients with Duchenne muscular dystrophy
スポンサーリンク
概要
- 論文の詳細を見る
- 2012-03-01
著者
-
Kawai Mitsuru
Department of Neurology, National Hospital Organization Higashi-Saitama National Hospital
-
Goto Katsumasa
Department Of Physiology St. Marianna University School Of Medicine
-
Sugai Kenji
Department Of Child Neurology National Center Hospital For Mental Nervous And Muscular Disorders Nat
-
Ishikawa Tomoko
Department Of Anatomy Nippon Medical School
-
Ogata Katsuhisa
Department Of Neurology Graduate School Of Medicine The University Of Tokyo
-
Konagaya Masaaki
Department Of Neurology National Suzuka Hospital
-
Miyazaki Tatsushi
Department Of Pediatrics National Hospital Organization Tokushima Hospital
-
Mochizuki Hitoshi
Department Of Communication Systems Faculty Of Electro-communications The University Of Electro-comm
-
Kubota Norika
Department Of Paediatrics Tottori Prefectural Kaike Rehabilitation Center For Disabled Children
-
Tatara Katsunori
Department Of Pediatrics National Hospital Organization Tokushima Hospital
-
Nakagawa Eiji
Department Of Child Neurology National Center Hospital For Mental Nervous And Muscular Disorders Nat
-
Sasaki Masayuki
Department Of Anesthesiology Gunma University Graduate School Of Medicine
-
Komaki Hirofumi
Department Of Child Neurology National Center Hospital For Mental Nervous And Disorders National Cen
-
Oya Yasushi
Department Of Neurology National Center Hospital For Neurology And Psychiatry National Center Of Neu
-
Fujisaki Toshiyuki
Department Of Neurophysiology Brain Research Institute Niigata University Department Of Otorhinolary
-
TOKITA Yasuko
Department of Pediatrics, National Hospital Organization (NHO) Matsue Medical Center
-
KAWAI Mitsuru
Department of Neurology, NHO Higashisaitama National Hospital
-
SHIMIZU FUJIWARA
Department of Child Neurology, National Center Hospital of Neurology and Psychiatry, National Center of Neurology and Psychiatry
-
MORI YOSHIMURA
Department of Neurology, National Center Hospital of Neurology and Psychiatry, National Center of Neurology and Psychiatry (NCNP)
-
SHIMAZAKI Rie
Department of Neurology, NHO Nishibeppu National Hospital
-
SATO Kimiko
Department of Neurology, NHO Nishibeppu National Hospital
-
TAKANOHA Satoko
Nutrition Control Unit, National Center Hospital of Neurology and Psychiatry, National Center of Neurology and Psychiatry (NCNP)
-
KOMAKI Hirofumi
Department of Child Neurology, National Center Hospital of Neurology and Psychiatry, National Center of Neurology and Psychiatry
-
OYA Yasushi
Department of Neurology, National Center Hospital of Neurology and Psychiatry, National Center of Neurology and Psychiatry (NCNP)
-
KONAGAYA Masaaki
Department of Neurology, NHO Suzuka National Hospital
-
TATARA Katsunori
Department of Pediatrics, NHO Tokushima National Hospital
-
OGATA Katsuhisa
Department of Neurology, NHO Higashisaitama National Hospital
-
MIYAZAKI Tatsushi
Department of Pediatrics, NHO Tokushima National Hospital
-
KUBOTA Norika
Department of Pediatrics, National Hospital Organization (NHO) Matsue Medical Center
-
GOTO Katsumasa
Department of Neurology, NHO Nishibeppu National Hospital
-
Kawai Mitsuru
Department of Neurology, Higashi-Saitama National Hospital
-
SASAKI Masayuki
Department of Child Neurology, National Center Hospital of Neurology and Psychiatry, National Center of Neurology and Psychiatry
-
MOCHIZUKI Hitoshi
Department of Agricultural Chemistry, Faculty of Agriculture, Hokkaido University
関連論文
- Duchenne 型筋ジストロフィー患者における自律神経機能
- Segmental Myocardial Strain of the Left Ventricle in Patients With Duchenne Muscular Dystrophy Using Two-Dimensional Speckle Tracking Echocardiography
- An analysis of epilepsy with chromosomal abnormalities
- Carvedilol can Prevent Cardiac Events in Duchenne Muscular Dystrophy
- Mental Retardation and Lifetime Events of Duchenne Muscular Dystrophy in Japan
- Activities of Daily Living, Functional Capacity, and Life Satisfaction of Subacute Myelo-Optico-Neuropathy Patients in Japan
- S-13 Possible mechanism of the plasticity of skeletal muscle fibers(The Proceedings of the 13th Annual Meetings of Japan Society of Exercise and Sports Physiology July 30-31, (Tokyo))
- Role of Gravity in Mammalian Development : Effects of Hypergravity and/or Microgravity on the Development of Skeletal Muscles
- 3P271 ゼブラフィッシュクリプトクローム-DASHの円二色性分光測定(光生物-視覚・光受容,第48回日本生物物理学会年会)
- Functional Overloading Facilitates the Regeneration of Injured Soleus Muscles in Mice
- Heat stress facilitates the regeneration of injured skeletal muscle in rats
- 2AC3 Postnatal changes in the signal transduction pathways involved in the muscular hypertrophy of the rat plantaris muscle(The Proceeding of the 14th Annual Meeting of Japan Society of Exercise and Sports Physiology July 29-30, (Hiroshima))
- 2B-08 The influence of the different heat exposure time on signal transduction during the recovery from skeletal muscle atrophy(Muscular Function, The Proceedings of the 13th Annual Meetings of Japan Society of Exercise and Sports Physiology July 30-31, (
- Heat Stress as a Countermeasure for Prevention of Muscle Atrophy in Microgravity Environment
- P2-8 Estrogen administration attenuates skeletal muscle atrophy induced immobilization of male rats(The Proceedings of the 12th Annual Meetings of Japan Society of Exercise and Sports Physiology)
- Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome
- Extraosseous accumulation of ^Tc-HMDP to radiation nephropathy, mimicking recurrent neuroblastoma
- Alterations of tumor suppressor genes (Rb, p16, p27 and p53) and an increased FDG uptake in lung cancer
- Comparison of ^FDG-PET with ^Tc-HMDP scintigraphy for the detection of bone metastases in patients with breast cancer
- PET evaluation of the relationship between D_2 receptor binding and glucose metabolism in patients with parkinsonism
- Lesion detectability of a gamma camera based coincidence system with FDG in patients with malignant tumors : A comparison with dedicated positron emission tomography
- An analysis of the physiological FDG uptake pattern in the stomach
- Differential FDG accumulation associated with GLUT-1 expression in a patient with lymphoma
- Clinical impact of whole body FDG-PET on the staging and therapeutic decision making for malignant lymphoma
- ^C-methionine uptake in cerebrovascular disease : A comparison with ^F-FDG PET and ^Tc-HMPAO SPECT
- The usefulness of dipyridamole thallium-201 single photon emission computed tomography for predicting perioperative cardiac events in patients undergoing non-cardiac vascular surgery
- An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease)
- The genomic structure and expression of MJD, the Machado-Joseph disease gene
- Videofluorographic assessment of swallowing function in patients with Duchenne muscular dystrophy
- Salivary Chromogranin A: Useful and Quantitative Biochemical Marker of Affective State in Patients with Amyotrophic Lateral Sclerosis
- Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms
- Hyperkinetic movement disorder in a child treated by globus pallidus stimulation
- Surgical treatment of early-infantile epileptic encephalopathy with suppression-bursts associated with focal cortical dysplasia
- Surgical Treatment of a Case of Early Infantile Epileptic Encephalopathy with Suppression-Bursts Associated with Focal Cortical Dysplasia
- Tremor and seizures associated with chronic manganese intoxication
- III B11 Infantile spasms treated by peri-insular hemispherotomy : a Case report
- Early onset distal muscular dystrophy
- The Activity of Bisphenol A Depends on Both the Estrogen Receptor Subtype and the Cell Type
- Dilated Cardiomyopathy in Kugelberg-Welander Disease : Coexisting Sleep Disordered Breathing and Its Treatment with Continuous Positive Airway Pressure
- Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome
- Human skeletal muscle calcium channel α1S is expressed in the basal ganglia: distinctive expression pattern among L-type Ca^ channels
- Recovery function of and effects of hyperventilation on somatosensory evoked high-frequency oscillation in Parkinson's disease and myoclonus epilepsy
- Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
- Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduria
- Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability : Coexistence of auditory neuropathy and cochlear hearing loss
- II C12 Treatment of intractable epilepsies with supratherapeutic levels of phenobarbital
- Mechanical ventilation care in severe childhood neurological disorders
- Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
- A severely brain-damaged case of 3-hydroxyisobutyric aciduria
- Transient seizure disappearance due to bilateral striatal necrosis in a patient with intractable epilepsy
- Dietary Tocotrienol Reduces UVB-Induced Skin Damage and Sesamin Enhances Tocotrienol Effects in Hairless Mice
- Expression of heat shock protein 72 in rat quadriceps muscles following anterior cruciate ligament resection
- Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion
- Phosphory lated Sites of M_r 25,000 Protein, a Putative Protein Phosphatase 2A Modulator, and Phosphorylation of the Synthetic Peptide Containing These Sites by Protein Kinase C^1
- Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)
- Increased mid-left ventricular rotation in patients with Duchenne muscular dystrophy using two-dimensional speckle tracking echocardiography
- 2P-214 低温分光測定によるゼブラフィッシュクリプトクロームDASH光反応経路の決定(光生物-視覚・光受容,第47回日本生物物理学会年会)
- III B9 Resective epilepsy surgery in children : comparison between younger and older age groups
- Effective immunoglobulin therapy for brief tonic seizures in methylmalonic acidemia
- Callosal agenesis followed postnatally after prenatal diagnosis
- 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
- Tourette's syndrome in Taiwan : an epidemiological study of tic disorders in an elementary school at Taipei County
- Hemifacial seizures due to ganglioglioma of cerebellum
- Electroencephalography-Guided Resection of Dysembryoplastic Neuroepithelial Tumor
- Acute Necrotizing Encephalopathy of Childhood due to Influenza Type A Virus
- A Patient with Influenza A-associated Encephalopathy Treated with Mild Hypothermic Therapy and Methylprednisolone Pulse Therapy
- Prolonged central sensory conduction time in alcoholics with hypoactive aldehyde dehydrogenase-2
- Motor Dominant Neuropathy in Sjogren's Syndrome : Report of Two Cases
- An autopsy case of multiple sclerosis accompanying parkinsonism
- Computer Method for New Elliptical Abel Inversion Applied to Holographic Plasma Diagnostics
- Resonant Faraday Rotation and Holography for the Measurement of Spatial Magnetic Field and Atomic Density in a Plasma
- Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis
- Brain perfusion SPECT and EEG findings in children with autism spectrum disorders and medically intractable epilepsy
- Development of a convenient in vitro fertilization method using interspecific hybrids between Oryzias latipes and Oryzias curvinotus
- Current management of febrile seizures in Japan : An overview
- Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter
- Studies on a Ca2+- and Cyclic Nucleotide-Independent H1 Histone Kinase Purified from Rabbit Skeletal Muscle
- Role(s) of Mechanical Load and Satellite Cells in The Regulation of The Size of Soleus Muscle Fiber in Rats
- Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome
- Augmented startle responses in opsoclonus-myoclonus syndrome
- Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination
- 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
- Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
- Change in Activities of Daily Living, Functional Capacity, and Life Satisfaction in Japanese Patients with Subacute Myelo-Optico-Neuropathy
- A Novel SACS Mutation in an Atypical Case with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
- Some aspects of heat stress on the plasticity of skeletal muscle cells
- SISCOM technique with a variable Z score improves detectability of focal cortical dysplasia : a comparative study with MRI
- Decreased resting energy expenditure in patients with Duchenne muscular dystrophy
- Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies
- Gene Suppression of Mouse Testis In Vivo Using Small Interfering RNA Derived from Plasmid Vectors
- A case of congenital axonal neuropathy associated with West syndrome
- Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multilobar Cortical Dysplasia:—Three Case Reports—
- Biological Activity of the Constituents in Roots of Ezo-no-gishigishi (Rumex obtusifolius)
- Balloon Pulmonary Valvuloplasty for Infants with Severe Tetralogy of Fallot.
- Heart Rate Variability and Hypercapnia in Duchenne Muscular Dystrophy
- Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multilobar Cortical Dysplasia -Three Case Reports-