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PPARα and RXRα in the regulation of neuronal ceroid lipofuscinosis genes: implications for Batten disease therapy. [PDF]
Chandra S, Pahan K.
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Topiramate-Responsive Myoclonic Status Epilepticus in a Child with Progressive Myoclonus Epilepsy Due to Neuronal Ceroid Lipofuscinosis Type 8: A Case Report. [PDF]
Tsuchie H +4 more
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Pilot Study of Fingolimod Treatment in Neuronal Ceroid Lipofuscinosis Type 1. [PDF]
Messina M +11 more
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Neurodegenerative Diseases in Children: A Comprehensive Review. [PDF]
Ailioaie C +4 more
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Neuronal Ceroid Lipofuscinosis-like Disorder in a Dachshund with Sequence Variants in Lysosome-Related Genes. [PDF]
Coates JR +7 more
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The neuronal ceroid‐lipofuscinoses
Developmental Disabilities Research Reviews, 2013The neuronal ceroid‐lipofuscinoses (NCL's, Batten disease) represent a group of severe neurodegenerative diseases, which mostly present in childhood. The phenotypes are similar and include visual loss, seizures, loss of motor and cognitive function, and early death.
Dinesh Rakheja
exaly +3 more sources
Progress in Neuropathology of the Neuronal Ceroid Lipofuscinoses
Molecular Genetics and Metabolism, 1999Since the last, 6th, International Congress on Neuronal Ceroid-Lipofuscinoses, neuropathological advances in neuronal ceroid lipofuscinoses (NCL) have been made in several areas: (1) In adult NCL (ANCL) lipopigments have now been repeatedly confirmed to contain subunit c of mitochondrial ATP synthase and even sphingolipid activators (saposins).
Alfried Kohlschütter +2 more
exaly +3 more sources

