• A new UHPLC-MS/MS method for the screening of urinary oligosaccharides expands the detection of storage disorders
• Analysis of urinary oligosaccharide excretion patterns by UHPLC/HRAM mass spectrometry for screening of lysosomal storage disorders
• beta-Mannosidosis caused by a novel homozygous intragenic inverted duplication in MANBA
• Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA
• beta-Mannosidosis in German Shepherd Dogs
• Beta-Mannosidosis Is a Cause of Hypomyelination
• Beta-mannosidosis presenting predominantly with recurrent pulmonary infections, hemorrhage, and cystic lesions
• Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis
• Familial Global Developmental Delay Secondary to beta-Mannosidosis
• Familial Global Developmental Delay Secondary to β-Mannosidosis
• Hereditary beta-mannosidosis in a dog: Clinicopathological and molecular genetic characterization
• Hereditary β-mannosidosis in a dog: Clinicopathological and molecular genetic characterization
• Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation
• Large animal models contribute to the development of therapies for central and peripheral nervous system dysfunction in patients with lysosomal storage diseases
• Oral manifestation and dental treatment of pediatric patient with beta-mannosidosis: A case report
• The Role of Hematopoietic Cell Transplant in the Glycoprotein Diseases
• The structure of mammalian β-mannosidase provides insight into β-mannosidosis and nystagmus
• Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant
• Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant
• β-Mannosidosis caused by a novel homozygous intragenic inverted duplication in <em>MANBA</em>
• β-Mannosidosis in German Shepherd Dogs