Globoid Cell Leukodystrophy

Globoid cell leukodystrophy (GLD) or Krabbe disease is a neurodegenerative disorder caused by the deficiency of the lysosomal enzyme galactocerebrosidase (GALC). Discover the latest research on globoid cell leukodystrophy here.

July 10, 2020

Intracranial calcifications in childhood: Part 2

Pediatric Radiology
Fabricio Guimarães GonçalvesArastoo Vossough
March 10, 2020

Thermal dehydration of urban biosolids with green liquor dregs from pulp and paper mill

Journal of Environmental Management
Luciano A GomesMargarida J Quina
April 8, 2020

Cell-autonomous expression of the acid hydrolase galactocerebrosidase

Proceedings of the National Academy of Sciences of the United States of America
Christina R MikulkaMark S Sands
September 12, 2020
Open Access

Natural history of Krabbe disease - a nationwide study in Germany using clinical and MRI data

Orphanet Journal of Rare Diseases
Sarah Isabel KriegChristiane Kehrer
March 22, 2020
Open Access

Spontaneous Third Ventriculostomy in Krabbe Disease

Pediatric Neurology
Giulio ZuccoliMaria Escolar
March 29, 2020
Open Access

Canine Models of Inherited Musculoskeletal and Neurodegenerative Diseases

Frontiers in Veterinary Science
Brett D StoryHeather L Gray-Edwards
February 27, 2020
Open Access

Lysosomal Ceramide Metabolism Disorders: Implications in Parkinson's Disease

Journal of Clinical Medicine
Silvia PaciottiTommaso Beccari
April 22, 2020
Open Access

Retinal ganglion cell topography predicts visual field function in spastic cerebral palsy

Developmental Medicine and Child Neurology
Lena JacobsonMaria Nilsson
August 22, 2020
Open Access

Ability of Macular Inner Retinal Layer Thickness Asymmetry Evaluated by Optical Coherence Tomography to Detect Preperimetric Glaucoma

Translational Vision Science & Technology
Daisuke TakemotoKazuhisa Sugiyama
May 7, 2020
Open Access

Neural differentiation footprints of mesenchymal stem cell by fetal brain extract

Iman Razeghian-JahromiAshkan Mowla

Sign up to follow this feed and discover related papers.

Related Feeds

Acute Disseminated Encephalomyelitis

Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disease of the central nervous system. Discover the latest research on acute disseminated encephalomyelitis here.


Adrenoleukodystrophy (ALD), the most frequent peroxisomal disorder, is an X-linked disorder caused by a defect in the metabolism of long chain fatty acids leading to demyelination, neurodegeneration, and death. Here is the latest research.

Alexander Disease

Alexander disease is a rare neurological disorder caused by mutations in the astrocyte-specific intermediate filament protein glial fibrillary acidic protein (GFAP). Here is the latest research.

Asperger Syndrome

Asperger syndrome (AS), also known as Asperger's, is a developmental disorder characterized by significant difficulties in social interaction and nonverbal communication, along with restricted and repetitive patterns of behavior and interests. Discover the latest research on Asperger syndrome here.


Autism spectrum disorder is associated with challenges with social skills, repetitive behaviors, and often accompanied by sensory sensitivities and medical issues. Here is the latest research.

Batten Disease

Batten Disease is a group of nervous system disorders known as neuronal ceroid lipfuscinosis. This feed focuses on neurobiological and neuropathological aspects of this disease. Discover more here.

Brain developing: Influences & Outcomes

This feed focuses on influences that affect the developing brain including genetics, fetal development, prenatal care, and gene-environment interactions. Here is the latest research in this field.

Canavan Disease

Canavan disease is an autosomal recessive degenerative disorder that causes progressive damage to nerve cells in the brain, and is one of the most common degenerative cerebral diseases of infancy. Discover the latest research on Canavan disease here.

Cerebral Palsy & Spasticity

Spactic cereberal palsy is one of the most common types of cerebral palsy that stems from an upper motor neuron lesion in the brain. Discover the latest research on cerebral palsy and spasticity here.

Congenital Brain Malformations

Congenital brain malformations are a major cause of morbidity and mortality in pediatric patients younger than 2 years. Discover the latest research on congenital brain malformations here.

© 2020 Meta ULC. All rights reserved