Beta-Mannosidosis Latest Advances

Mucopolysaccharidosis IIID and Beta-Mannosidosis in Brazilian Anglo-Nubian Goats: Molecular and Genealogical Insights for the Development and Implementation of a Genetic Disease Eradication Program.

Journal: Animal genetics

Published: September 29, 2025

Screening of high risk children for lysosomal storage diseases and analysis of disease spectrum

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: May 20, 2025

Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA.

Journal: Gene

Published: August 30, 2023

Beta-Mannosidosis Is a Cause of Hypomyelination.

Journal: Pediatric neurology

Published: August 07, 2022

Beta-mannosidosis presenting predominantly with recurrent pulmonary infections, hemorrhage, and cystic lesions.

Journal: Pediatric pulmonology

Published: July 25, 2022

Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation.

Journal: International journal of molecular sciences

Published: June 15, 2022

Oral manifestation and dental treatment of pediatric patient with beta-mannosidosis: A case report.

Journal: SAGE open medical case reports

Published: July 29, 2021

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.

Journal: Orphanet journal of rare diseases

Published: June 15, 2020

β-Mannosidosis in German Shepherd Dogs.

Journal: Veterinary pathology

Published: April 16, 2019

Hereditary β-mannosidosis in a dog: Clinicopathological and molecular genetic characterization.

Journal: Molecular genetics and metabolism

Published: April 04, 2019

Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis.

Journal: Molecular genetics & genomic medicine

Published: March 13, 2019

β-Mannosidosis caused by a novel homozygous intragenic inverted duplication in MANBA.

Journal: Cold Spring Harbor molecular case studies

Published: January 11, 2019

Beta-Mannosidosis Latest Advances

Find the Latest Research About Beta-Mannosidosis

Mucopolysaccharidosis IIID and Beta-Mannosidosis in Brazilian Anglo-Nubian Goats: Molecular and Genealogical Insights for the Development and Implementation of a Genetic Disease Eradication Program.

Mucopolysaccharidosis IIID and Beta-Mannosidosis in Brazilian Anglo-Nubian Goats: Molecular and Genealogical Insights for the Development and Implementation of a Genetic Disease Eradication Program.

Screening of high risk children for lysosomal storage diseases and analysis of disease spectrum

Screening of high risk children for lysosomal storage diseases and analysis of disease spectrum

Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA.

Beta-mannosidosis in a domestic cat associated with a missense variant in MANBA.

Beta-Mannosidosis Is a Cause of Hypomyelination.

Beta-Mannosidosis Is a Cause of Hypomyelination.

Beta-mannosidosis presenting predominantly with recurrent pulmonary infections, hemorrhage, and cystic lesions.

Beta-mannosidosis presenting predominantly with recurrent pulmonary infections, hemorrhage, and cystic lesions.

Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation.

Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation.

Oral manifestation and dental treatment of pediatric patient with beta-mannosidosis: A case report.

Oral manifestation and dental treatment of pediatric patient with beta-mannosidosis: A case report.

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 in German Shepherd Dogs.

β-Mannosidosis in German Shepherd Dogs.

Hereditary β-mannosidosis in a dog: Clinicopathological and molecular genetic characterization.

Hereditary β-mannosidosis in a dog: Clinicopathological and molecular genetic characterization.

Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis.

Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis.

β-Mannosidosis caused by a novel homozygous intragenic inverted duplication in MANBA.

β-Mannosidosis caused by a novel homozygous intragenic inverted duplication in MANBA.