病原性大腸菌O157による完全型HUSで認められた神経合併症のリスク因子
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-04-01
著者
-
OZONO Keiichi
Department of Developmental Medicine (Pediatrics), Osaka University Graduate School of Medicine
-
Okada Shintaro
Department Of Developmental Medicine (pediatrics) D-5 Osaka University Graduate School Of Medicine.
-
山本 威久
Department Of Pediatrics Minoh City Hospital
-
Okada Shintaro
Department Of Pediatrics Osaka University Graduate School Of Medicine
-
SATOMURA Kenichi
Department of Pediatric Nephrology and Metabolism, Osaka Medical Center and Research Institute for M
-
Satomura Kenichi
Department Of Pediatric Nephrology And Metabolism Osaka Medical Center And Research Institute For Ma
-
Ozono Keiichi
Department Of Developmental Medicine (pediatrics) D-5 Osaka University Graduate School Of Medicine
関連論文
- Pediatric myeloid/NK cell precursor lymphoma/leukemia expressing T/NK immunophenotype markers
- Allogeneic hematopoietic stem cell transplantation with reduced intensity conditioning for a child with recurrent anaplastic large cell lymphoma
- Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene
- Endocrinological Analysis of 122 Japanese Childhood Cancer Survivors in a Single Hospital
- Tacrolimus-Related Encephalopathy following Allogeneic Stem Cell Transplantation in Children
- Pediatric post-transplant diffuse large B cell lymphoma after cardiac transplantation
- A case of congenital bone marrow failure with radio-ulnar synostosis
- Sleep disordered breathing in childhood-onset acid maltase deficiency
- Causes and Differential Diagnosis of Hypocalcemia : Recommendation Proposed by Expert Panel Supported by Ministry of Health, Labour and Welfare, Japan
- Hereditary hypophosphatemic rickets with hypercalciuria : a study for the phosphate transporter gene type IIc and osteoblastic function
- A Case of Persistent Hyperinsulinemic Hypoglycemia of Infancy Successfully Managed with Subcutaneous Octreotide Injection and Nocturnal Intravenous Glucose Supply
- Biological Activities of 2α-Substituted Analogues of 1α, 25-Dihydroxyvitamin D_3 in Transcriptional Regulation and Human Promyelocytic Leukemia (HL-60) Cell Proliferation and Differentiation(Medicinal Chemistry)
- Application of Signal-Averaged Electrocardiogram to Myocardial Damage in the Late Stage of Kawasaki Disease
- Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia : New Understanding
- Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss
- Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome
- Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype-phenotype correlation
- A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency
- Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease
- Epilepsy in Wolf-Hirschhorn Syndrome (4p-)
- Longitudinal Observation of a Patient with Leri-Weill Dyschondrosteosis and SHOX Haploinsufficiency
- Hormonal and Genetical Assessment of a Japanese Girl with Weaver Syndrome
- In Vitro Biological Activities of a Series of 2β-Substituted Analogues of 1α, 25-Dihydroxyvitamin D_3
- Singly Dehydroxylated A-Ring Analogues of 19-Nor-1α, 25-dihydroxyvitamin D_3 and 19-Nor-22-oxa-1α, 25-dihydroxyvitamin D_3 : Novel Vitamin D_3 Analogues with Potent Transcriptional Activity but Extremely Low Affinity for Vitamin D Receptor
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia
- A Case of Pediatric Virilizing Adrenocortical Tumor Resulting in Hypothalamic-pituitary Activation and Central Precocious Puberty Following Surgical Removal
- Late-onset differentiation syndrome in a child with acute promyelocytic leukemia
- Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B_1 and B_2
- Functional and Morphological Abnormalities of Mitochondria in Human Cells Containing Mitochondrial DNA with Pathogenic Point Mutations in tRNA Genes
- Alendronate and pharmacological doses of 1α OHD_3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
- A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period
- Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia
- Blunted effect of parathyroid hormone on adenosine 3',5'-cyclic monophosphate production is derived from ATP depletion in proximal convoluted tubules of hypophosphatemic mice
- The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets
- Follow-Up Study of Hypervariable Region Sequences of the Hepatitis C Virus (HCV) Genome in an Infant with Delayed Anti-HCV Antibody Responses
- Difficulty in differential diagnosis of atypical absence seizures and complex partial seizures in childhood
- Postural change and pulmonary ventilation-perfusion distribution after Fontan operation
- -0476-ASSESSMENT OF EXERCISE TOLERANCE BY ANAEROBIC THRESHOLD IN POST-OPERATIVE PATIENTS WITH CONGENITAL HEART DISEASE
- Mutation analysis of Japanese patient with fucosidosis
- A novel type X collagen gene mutation (G595R) associated with Schmid-type metaphyseal chondrodysplasia
- Genetic association of a polymorphism of the cAMP-responsive element binding protein-binding protein with steroid-induced osteonecrosis after kidney transplantation
- Hypersensitivity to Mosquito Bites Conceals Clonal Lymphoproliferation of Epstein-Barr Viral DNA-positive Natural Killer Cells
- Scheie syndrome (MPS-IS) presented as bilateral trigger thumb
- Skeletal development of achondroplasia : Analysis of genotyped patients
- Zonisamide Monotherapy in Newly Diagnosed Infantile Spasms
- Human herpesvirus-6 infection in neonates : Not protected by only humoral immunity
- Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
- Ictal Video-EEG Recording of Three Partial Seizures in a Patient with the Benign Infantile Convulsions Associated with Mild Gastroenteritis
- Remission of progressive multifocal leukoencephalopathy following highly active antiretroviral therapy in a patient with HIV infection
- Isolated Iissencephaly sequence with balanced chromosome translocation involving 17p13.3
- Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates
- Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
- A Patient with Sotos Syndrome Who Reached Final Height
- 136 Excessive Growth in a Japanese Girl with Weaver Syndrome
- Gene therapy in Duchenne muscular dystrophy
- AN EcoRI RFLP IN HUMAN APC GENE
- EFFECTS OF SUCROSE IN CULTURED HUMAN SKIN FIBROBLASTS
- Wnt signaling in bone metabolism
- Hepatitis C virus infection and interferon therapy in patients with Down syndrome
- Diseases Associated with Abnormal Skeletal Maturity
- G-protein Stimulatory α Subunit is Involved in Osteogenic Activity in Osteoblastic Cell Line SaOS-2 Cells
- Phenotype and genotype analysis of severe skeletal dysplasia
- A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
- A case of giant axonal neuropathy showing focal aggregation and hypophosphorylation of intermediate filaments
- CORRELATION OF SUBCELLULAR LOCALIZATION OF DISEASE-SPECIFIC INCLUSIONS AND SPHINGOLIPID ACTIVATOR PROTEIN-1(SAP-1)IN SULFATIDE SULFATASE-DEFICIENT FIBROBLASTS
- Localization of SAP-1 in fibroblasts of metachromatic leukodystrophy
- Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome
- A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria
- A Case of Chaotic Atrial Tachycardia and Noonan's Syndrome
- Hyperintensity of Posterior Pituitary on MR T1WI in a Boy with Central Diabetes Insipidus Caused by Missense Mutation of Neurophysin II Gene
- Pediatric post-transplant lymphoproliferative disorder after cardiac transplantation
- ALLELE FREQUENCIES OF INTRAGENIC, AND 5' AND 3' MARKERS OF THE DYSTROPHIN GENE IN JAPANESE FAMILIES AFFLICTED WITH DUCHENNE OR BECKER MUSCULAR DYSTROPHY
- Indigogenic Method for β-galactosidase in Cultured Skin Fibroblasts and its Application to Single Cell Analysis
- The application of a simple assay method for lysosomal hydrolase in a single cultured skin fibroblast: Cytogenetic study of Mucolipidosis by cell fusion.
- A case of chronic infantile type of fucosidosis : clinical and magnetic resonance in image findings
- 病原性大腸菌O157による完全型HUSで認められた神経合併症のリスク因子
- Clinical aspects and adrenal functions in eleven Japanese children with X-linked adrenoleukodystrophy
- Anthracyclines for acute lymphoblastic leukemia in a child with congenital long QT syndrome
- Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
- SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome
- Mucolipidosis II and III alpha/beta : mutation analysis of 40 Japanese patients showed genotype-phenotype correlation
- Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta
- Hypophosphatasia now draws more attention of both clinicians and researchers : A Commentary on prevelance of c. 1559deIT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasias in Japanese and effects of the mutation on he
- Clinicogenetical features of a Japanese patient with giant axonal neuropathy
- Drastic Shift From Positive to Negative Estrogen Effect on Bone Morphogenetic Protein Signaling in Pulmonary Arterial Endothelial Cells Under Hypoxia
- Synergistic Effect of 1,25-Dihydroxyvitamin D3 and Retinoic Acid in Inducing U937 Cell Differentiation.
- Major role of apolipoprotein B in cycloheximide-induced acute hepatic steatosis in mice
- Regional Left Ventricnlar Motion during Early Filling Phase in Patients with Right Ventricular Pressure Overload.
- Effect of Growth Hormone Treatment on Quality of Life in Japanese Children with Growth Hormone Deficiency: An Analysis from a Prospective Observational Study
- Drastic Shift From Positive to Negative Estrogen Effect on Bone Morphogenetic Protein Signaling in Pulmonary Arterial Endothelial Cells Under Hypoxia
- Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome