• A capillary electrophoresis procedure for the screening of oligosaccharidoses and related diseases
• A new case of alpha-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum, with Ménière's syndrome and without mental retardation
• A New Case of Schindler Disease
• A Novel Homozygous Missense Variant in the NAGA Gene with Extreme Intrafamilial Phenotypic Heterogeneity
• Application of ion mobility tandem mass spectrometry to compositional and structural analysis of glycopeptides extracted from the urine of a patient diagnosed with Schindler disease
• Association between complete revascularization of the coronary artery and clinical outcomes in peripheral artery disease: a sub-analysis of the I-PAD Nagano registry
• Association of abnormal glucose tolerance with liver-related disease and cardiovascular diseases in patients with chronic hepatitis C
• Automated chip-nanoelectrospray mass spectrometry for glycourinomics in Schindler disease type I
• Barrier Factors of Adherence to Dupilumab Self-Injection for Severe Allergic Disease: A Non-Interventional Open-Label Study
• Blood group A glycosphingolipid accumulation in the hair of patients with alpha-N-acetylgalactosaminidase deficiency
• Chemoradiotherapy for Small-Cell Prostate Carcinoma: A Case Report
• Early diagnosis leading to improvement of critical illness polyneuropathy associated with severe Staphylococcus aureus infection in a patient on hemodialysis
• Early recurrence of IgA nephropathy after kidney transplantation in a patient with Down syndrome
• High Albumin Clearance Predicts the Minimal Change Nephrotic Syndrome Relapse
• Hyperprogressive disease during atezolizumab plus bevacizumab treatment in patients with advanced hepatocellular carcinoma from Japanese real-world practice
• Identification and structural characterization of novel O- and N-glycoforms in the urine of a Schindler disease patient by Orbitrap mass spectrometry
• Matrisomic characterization of HCC to inform individualized patient management
• Neurologic manifestations of Kanzaki disease
• Neurological presentations of lysosomal diseases in adult patients
• Pharmacological chaperones for human α-N-acetylgalactosaminidase
• Post-traumatic Aeromonas hydrophila Osteomyelitis caused by an Infected Gustilo-Anderson Grade 3B Tibial Fracture: A Case Report with a 7-year Follow-up
• Quantitative Analyses of Retinal Traction Force and Metamorphopsia in Lamellar Macular Hole and Related Diseases
• Schindler-disease/Kanzaki disease
• Seasonal variations in renal biopsy numbers and primary glomerular disease features based on the Japan renal biopsy registry
• Single-Nephron GFR in Different Glomerular Basement Membrane Stages of Membranous Nephropathy
• Soluble Sema4D cleaved from osteoclast precursors by TACE suppresses osteoblastogenesis
• Structural and immunocytochemical studies on alpha-N-acetylgalactosaminidase deficiency (Schindler/Kanzaki disease)
• The 1.9 a structure of human alpha-N-acetylgalactosaminidase: The molecular basis of Schindler and Kanzaki diseases
• Three dimensional structural studies of alpha-N-acetylgalactosaminidase (alpha-NAGA) in alpha-NAGA deficiency (Kanzaki disease): different gene mutations cause peculiar structural changes in alpha-NAGAs resulting in different substrate specificities and c
• Varicella-zoster virus infection with concomitant lower cranial polyneuropathy in the absence of fever, headache and meningeal signs