Ikeda Shu-ichi | Department Of Internal Medicine (neurology And Rheumatology) Shinshu University School Of Medicine

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著作論文

Biopsy-proven Tuberculous Meningitis Mimicking CNS Sarcoidosis
Flow Cytometric Analysis of Lymphocyte Subpopulations and Th1/Th2 Balance in Patients with Polymyositis and Dermatomyositis
Long-term Follow-up of Plasma Cells in Bone Marrow and Serum Free Light Chains in Primary Systemic AL Amyloidosis
A Rare Lung Nodule Consisting of Adenocarcinoma and Amyloid Deposition in a Patient with Primary Systemic AL Amyloidosis
Cytomegalovirus-induced Infectious Mononucleosis-like Syndrome in a Rheumatoid Arthritis Patient Treated with Methotrexate and Infliximab
Successful Treatment with Rituximab in a Patient with Stiff-Person Syndrome Complicated by Dysthyroid Ophthalmopathy
Takayasu's Arteritis in a Patient with Crohn's Disease: An Unexpected Association during Infliximab Therapy
Therapeutic outcome of cyclic VAD (vincristine, doxorubicin and dexamethasone) therapy in primary systemic AL amyloidosis patients
Successful treatment with infliximab and low-dose methotrexate in a Japanese patient with familial Mediterranean fever
Hemophagocytic syndrome associated with rheumatoid arthritis: A case report and review of the literature
Expression of Various Glutamate Receptors Including N-Methyl-D-Aspartate Receptor (NMDAR) in an Ovarian Teratoma Removed from a Young Woman with Anti-NMDAR Encephalitis
Huntington's disease with onset ages greater than 60 years
An Unusual Case of Klippel-Trenaunay-Weber Syndrome Presenting with Portosystemic Encephalopathy
Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis
Periodic Peritonitis due to Familial Mediterranean Fever in a Patient with Systemic Lupus Erythematosus
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan
The Characteristics of Food Intake in Patients with Type II Citrullinemia
A Japanese case of SCA14 with the Gly128Asp mutation
Intestinal Angina Due to Atherosclerosis in a 45-year-old Systemic Lupus Erythematosus Patient
4 Cardiac Amyloidosis : Heterogenous Pathogenic Backgrounds(New Insights of Specific Cardiomyopathies, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Leukoencephalopathy Induced by Low-dose Methotrexate in a Patient with Rheumatoid Arthritis
Buerger's disease manifesting nodular erythema with livedo reticularis
Spinal Epidural Abscess with Osteomyelitis as a Cause of Bacterial Meningitis
Intravenous Immunoglobulin (IVIg) with Methylprednisolone Pulse Therapy for Motor Impairment of Neuralgic Amyotrophy: Clinical Observations in 10 Cases
A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)
Cerebral hemorrhage in Fabry's disease
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene
A Case of Mikulicz's Disease Complicated by Malignant Lymphoma: A Postmortem Histopathological Finding
ANCA-associated Vasculitis with Central Retinal Artery Occlusion Developing during Treatment with Methimazole
Clinical and Serial MRI Findings of a Sialidosis Type I Patient with a Novel Missense Mutation in the NEU1 Gene
Liver Dysfunction and Thrombocytopenia Diagnosed as Intravascular Large B-cell Lymphoma Using a Timely and Accurate Transjugular Liver Biopsy
Adult Onset X-Linked Chronic Granulomatous Disease in a Woman Patient Caused by a de novo Mutation in Paternal-Origin CYBB Gene and Skewed Inactivation of Normal Maternal X Chromosome
Pure Red Cell Aplasia Developing after Treatment of Pleural Recurrence of Thymoma, Successfully Treated with Cyclosporin A but not with Tacrolimus
Corpus Callosum Atrophy in Patients with Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids: An MRI-based Study
Nephrotic Syndrome Due to Primary Systemic AL Amyloidosis, Successfully Treated with VAD (Vincristine, Doxorubicin and Dexamethasone) Alone
Systemic AL Amyloidosis Mimicking Rheumatoid Arthritis
An 85-year-old Case with Hashimoto's Encephalopathy, Showing Spontaneous Complete Remission
Patient with adult-onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma : Indication for liver transplantation
Marked and Rapid Regression of Hepatic Amyloid Deposition in a Patient with Systemic Light Chain (AL) Amyloidosis after High-dose Melphalan Therapy with Stem Cell Transplantation
Spinal Intradural Extramedullary Cavernous Angioma Presenting with Superficial Siderosis and Hydrocephalus: A Case Report and Review of the Literature

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