Ikeda Shu-ichi | Third Department Of Medicine Shinshu University School Of Medicine

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概要

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著作論文

Serum Levels of Free Light Chain before and after Chemotherapy in Primary Systemic AL Amyloidosis
Choroidal Vascular Lesions Identified by ICG Angiography in a Case of Familial Amyloidotic Polyneuropathy
Risk of Worsened Encephalopathy after Intravenous Glycerol Therapy in Patients with Adult-onset Type II Citrullinemia (CTLN2)
Hepatocellular Carcinoma in a Case of Adult-onset Type II Citrullinemia
Myasthenia Gravis with Anti-MuSK Antibody, Showing Progressive Muscular Atrophy without Blepharoptosis
Reactive Arthritis Due to Asymptomatic Infection of Chlamydia trachomatis
Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan : Outcomes of Living Donor Liver Transplantations
Increase in Incidence of Elderly-onset Patients with Myasthenia Gravis in Nagano Prefecture, Japan
High-dose Melphalan Followed by Autologous Stem Cell Support in Primary Systemic AL Amyloidosis with Multiple Organ Involvement
Serum Amyloid A as a Potent Therapeutic Marker in a Refractory Patient with Polymyalgia Rheumatica
Intractable Skin Necrosis and Interstitial Pneumonia in Amyopathic Dermatomyositis, Successfully Treated with Cyclosporin A
Hemolysis, Elevated Liver Enzymes and Low Platelet (HELLP) Syndrome Associated with Systemic Lupus Erythematosus
Abdominal Fat Aspiration Biopsy and Genotyping of Serum Amyloid A Contribute to Early Diagnosis of Reactive AA Amyloidosis Secondary to Rheumatoid Arthritis
Malignant Lymphoma Associated with Rheumatoid Arthritis, Developing Shortly after Initiation of Oral Methotrexate
Senile Systemic Amyloidosis Starting as Bilateral Carpal and Left Ulnar Tunnel Syndrome
Primary Cardiac Malignant Fibrous Histiocytoma in the Right Ventricular Infundibulum Treated With a Cavo-Pulmonary Shunt and Coronary Embolization
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano
Unilateral Oculomotor Nerve Palsy Induced by Combination Therapy of Interferon-α2b and Ribavirin
Tacrolimus Related Brady and Tachyarrhythmias in a Familial Amyloid Polyneuropathy Patient who Underwent Partial Liver Transplantation
Tacrolimus Related Brady and Tachyarrhythmias in a Familial Amyloid Polyneuropathy Patient who Underwent Partial Liver Transplantation
Regional features of autosomal-dominant cerebellar ataxia in Nagano : clinical and molecular genetic analysis of 86 families
An 80-year-old Mitochondrial Disease Patient with A3243G tRNA^ Gene Presenting Cardiac Dysfunction as the Main Symptom
Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)
Emotional Stress-Induced 'Ampulla Cardiomyopathy' : Discrepancy Between the Metabolic and Sympathetic Innervation Imaging Performed During the Recovery Course
Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome)
Characteristic Spinal MRI Findings of HIV-associated Myelopathy in an AIDS Patient
Fasciitis in Mixed Connective Tissue Disease Successfully Treated with High-dose Intravenous Immunoglobulin
Paraneoplastic Neurologic Syndrome Associated with Small Breast Cancer : Diagnostic Value of FDG-PET for Detection of Underlying Malignancy
Osmotic Demyelination Syndrome : Reversible MRI Findings in Bilateral Cortical Lesions
A Japanese Case of Familial Mediterranean Fever with Homozygosity for the Pyrin E148Q Mutation
A Japanese Patient with Familial Mediterranean Fever Associated with Compound Heterozygosity for Pyrin Variant E148Q/M694I
Fatal Acute Pancreatitis with Cystic Formation in Reactive Systemic AA Amyloidosis Secondary to Rheumatoid Arthritis
Cardiac Amyloidosis : Heterogenous Pathogenic Backgrounds

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