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JE Deane, SC Graham, NN Kim… - Proceedings of the …, 2011 - National Acad Sciences
Krabbe disease is a devastating neurodegenerative disease characterized by widespread demyelination
that is caused by defects in the enzyme galactocerebrosidase (GALC). Disease-causing mutations
have been identified throughout the GALC gene. However, a molecular understanding of ...
Cited by 1
H Yagasaki, M Kato, M Ishige, H Shichino… - International journal of …, 2011 - Springer
Krabbe disease is a type of inborn metabolic diseases (IMDs) caused by galactosylceramidase
deficiency [1]. It is an autosomal recessive neurodegenerative disorder char- acterized by demyelination
in both the central nervous system (CNS) and peripheral nervous system. Because ...
Related articles - All 3 versions
Y Wang, A Gupta, Z Liu, H Zhang, ML Escolar… - NeuroImage, 2011 - Elsevier
In recent years, diffusion tensor imaging (DTI) has become the modality of choice to investigate
white matter pathology in the developing brain. To study neonate Krabbe disease with DTI, we
evaluate the performance of linear and non-linear DTI registration algorithms for atlas ...
All 7 versions
[PDF] from uic.eduAB White, F Galbiati, MI Givogri… - Journal of …, 2011 - Wiley Online Library
AB White,1 F. Galbiati,1 MI Givogri,1 A. Lopez Rosas,1 X. Qiu,2 R. van Breemen,2 and ER
Bongarzone1* 1Department of Anatomy and Cell Biology, University of Illinois, Chicago, Illinois
2Department of Medicinal Chemistry and Pharmacognosy, University of Illinois, Chicago, ...
Cited by 2 - Related articles - All 5 versions
PK Duffner, A Barczykowski, K Jalal, L Yan… - Pediatric Neurology, 2011 - Elsevier
New York State began screening for Krabbe disease in 2006 to identify infants with Krabbe disease
before symptom onset. Because neither galactocerebrosidase activity nor most genotypes reliably
predict phenotype, the World Wide Registry was developed to determine whether other ...

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