Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy
スポンサーリンク
概要
- 論文の詳細を見る
- 2008-06-01
著者
-
GOTO Yu-ichi
Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, Nati
-
MORIMOTO Masafumi
Department of Cerebrovascular Surgery, National Cordiovascular Center
-
Goto Yu-ichi
Department Of Child Neurology National Center Hospital For Mental Nervous And Musculardisorders Nati
-
CHIYONOBU Tomohiro
Department of Pediatrics, Matsushita Memorial Hospital
-
YOSHIDA Michiko
Department of Clinical Nutrition, School of Medicine, Tokushima University
-
Morimoto Masafumi
Department Of Anatomy And Neurobiology Kyoto Prefectural University Of Medicine
-
NODA Rei
Department of Pediatrics, Akashi Municipal Hospital
-
FUJIKI Atsushi
Department of Pediatrics, Akashi Municipal Hospital
-
ISHII Rumiko
Department of Pediatrics, Akashi Municipal Hospital
-
NUKINA Sadayuki
Department of Pediatrics, Akashi Municipal Hospital
-
FUJITA Kinya
Department of Gastroenterology, Akashi Municipal Hospital
-
Noda Rei
Department Of Pediatrics Akashi Municipal Hospital
-
Ishii Rumiko
Department Of Pediatrics Akashi Municipal Hospital
-
Fujita Kinya
Department Of Gastroenterology Akashi Municipal Hospital
-
Fujita Kinya
Department Of Computer Information And Communication Sciences Tokyo University Of Agriculture And Te
-
Fujiki Atsushi
Department Of Pediatrics Akashi Municipal Hospital
-
Yoshida Michiko
Department Of Pediatrics Akashi Municipal Hospital
-
Goto Yu-ichi
Department Of Mental Retardation And Birth Defect Research National Institute Of Neuroscience Nation
-
Yoshida Michiko
Department Of Clinical Nutrition School Of Medicine Tokushima University
-
Noda Rei
Department Of Cardiovascular Surgery Social Insurance Chukyo Hospital
-
Chiyonobu Tomohiro
Department Of Pediatrics Akashi Municipal Hospital
-
Nukina Sadayuki
Department Of Pediatrics Akashi Municipal Hospital
関連論文
- Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions
- Orthostatic Hypotension Improved After Bilateral Carotid Endarterectomy : Case Report
- Early onset distal muscular dystrophy
- A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom
- Granulocytic Sarcoma Presenting with Severe Adenopathy (Cervical Lymph Nodes, Tonsils, and Adenoids) in a Child with Juvenile Myelomonocytic Leukemia and Successful Treatment with Allogeneic Bone Marrow Transplantation
- Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B_1 and B_2
- Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers(MERRF):a single-photon emission computed tomographic(SPECT)and electrophysiological study
- Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome
- Polymorphism in the caudal-related homeodomain protein Cdx-2 binding element in the human vitamin D receptor
- Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis
- A Patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency
- A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
- Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene
- Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
- Direct Evidence for Two Distinct Forms of the Flavoprotein Subunit of Human Mitochondrial Complex II (Succinate-Ubiquinone Reductase)
- Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle
- Leigh syndrome caused by mitochondrial DNA G13513A mutation : frequency and clinical features in Japan
- Distribution of glucocorticoid receptor immunoreactivity and mRNA in the rat brain: an immunohistochemical and in situ hybridization study
- Infantile Spasms in a Patient with Williams Syndrome and Craniosynostosis
- Progressive myoclonus epilepsy with unusual neuropathologic features
- Humanin expression in skeletal muscles of patients with chronic progressive external ophthalmoplegia
- Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy
- Abnormal glucose metabolism in aromatic L-amino acid decarboxylase deficiency
- Mitochondrial encephalomyopathy
- Ring Chromosome 14 with Localization-related Epilepsy : Three Cases
- Effects of stress of postnatal development on corticosterone, serotonin and behavioral changes
- Uptake of Iodine and Bromine by Ion-Exchange Resins in Aqueous Solution
- Atopic dermatitis and transient hypogammaglobulinemia of infancy improved simultaneously
- Infantile bilateral striatal necrosis associated with human herpes virus-6 (HHV-6) infection
- Treatment for Leigh syndrome by monitoring dichloroacetate concentration
- A haptic representation system for a virtual plain wall
- Retrograde coronary sinus cardioplegia cannula placement under short-time circulatory arrest in surgery for a ruptured type A dissection with a previous coronary artery bypass
- T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake
- Resuspension of the Uninfarcted Papillary Muscle at the Time of Mitral Valve Replacement in a Patient with Post Myocardial Infarction Papillary Muscle Rupture
- Mitochondrial Encephalomyopathy Associated with Diabetes Mellitus, Cataract, and Corpus Callosum Atrophy
- The emerging ST8 methicillin-resistant Staphylococcus aureus clone in the community in Japan : associated infections, genetic diversity, and comparative genomics
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
- Profiles of blood biomarkers in alternating hemiplegia of childhood-Increased MMP-9 and decreased substance P indicates its pathophysiology
- Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle