The juvenile gangliosidoses: A timeline of clinical change

The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention

(2019) Carlos R. Ferreira et al.   BONE

The natural history of Type 1 infantile GM1 gangliosidosis: A literature-based meta-analysis

(2019) Frederick M. Lang et al.   MOLECULAR GENETICS AND METABOLISM

Diagnostic challenge for the rare lysosomal storage disease: Late infantile GM1 gangliosidosis

(2018) Jin Sook Lee et al.   BRAIN & DEVELOPMENT

Distinct progression patterns of brain disease in infantile and juvenile gangliosidoses: Volumetric quantitative MRI study

(2018) Igor Nestrasil et al.   MOLECULAR GENETICS AND METABOLISM

Infantile gangliosidoses: Mapping a timeline of clinical changes

(2017) Jeanine R. Jarnes Utz et al.   MOLECULAR GENETICS AND METABOLISM

White matter changes in GM1 gangliosidosis

(2015) Moni Tuteja et al.   INDIAN PEDIATRICS

GM1 Gangliosidosis, Late Infantile Onset Dystonia, and T2 Hypointensity in the Globus Pallidus and Substantia Nigra

(2013) José Pedro Vieira et al.   PEDIATRIC NEUROLOGY

GM2 gangliosidosis in a UK study of children with progressive neurodegeneration: 73 cases reviewed

(2011) NICHOLAS J SMITH et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Natural History of Infantile GM2 Gangliosidosis

(2011) A. E. Bley et al.   PEDIATRICS

Pharmacokinetics, safety and tolerability of miglustat in the treatment of pediatric patients with GM2 gangliosidosis

(2009) Gustavo H.B. Maegawa et al.   MOLECULAR GENETICS AND METABOLISM