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Developmental Medicine & Child Neurology, ISSN 0012-1622, 08/2017, Volume 59, Issue 8, pp. 777 - 778
This commentary is on the original article by Simonati et al. on pages 815–821 of this issue. 
PEDIATRICS | CLINICAL NEUROLOGY | MUTATIONS | Membrane Proteins | Humans | Neuronal Ceroid-Lipofuscinoses | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 07/2012, Volume 79, Issue 2, pp. 183 - 191
Journal Article
2011, 2nd ed., Contemporary neurology series, ISBN 019959001X, Volume 78, xxx, 444
Book
Human Mutation, ISSN 1059-7794, 07/2019
Neuronal ceroid lipofuscinosis type 2 (CLN2 disease) is an autosomal recessive condition caused by variants in the TPP1 gene, leading to deficient activity of... 
Index Medicus
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 8, pp. 749 - 751
  The disease course also seemed to be slower than without the drugs when compared with older untreated siblings and historical studies, especially in terms of... 
Neurology | CLINICAL NEUROLOGY | NEURONAL CEROID-LIPOFUSCINOSIS | Neuronal Ceroid-Lipofuscinoses - drug therapy | Humans | Female | Male | Acetylcysteine - administration & dosage | Neuronal Ceroid-Lipofuscinoses - diagnosis | Cysteamine - administration & dosage | Cells | Mutation | Drug therapy | Stem cells | Colleges & universities | Index Medicus
Journal Article
1999, Biomedical and health research, ISBN 9051994818, Volume 33., xiv, 197
Book
BBA - Molecular Basis of Disease, ISSN 0925-4439, 10/2015, Volume 1852, Issue 10, pp. 2235 - 2236
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2012, Volume 90, Issue 6, pp. 1102 - 1107
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 11/2013, Volume 1832, Issue 11, pp. 1793 - 1794
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S71 - S71
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2011, Volume 89, Issue 2, pp. 241 - 252
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2018, Volume 123, Issue 2, pp. S97 - S97
Journal Article
Molecular Therapy, ISSN 1525-0016, 05/2018, Volume 26, Issue 5, pp. 1343 - 1353
The neuronal ceroid lipofuscinoses (NCLs) are inherited lysosomal storage disorders characterized by general neurodegeneration and premature death. Sight loss... 
photoreceptors | AAV gene therapy | retina | lysosomal storage disorders | neuronal ceroid lipofuscinoses | bipolar cells | Batten disease | Index Medicus | Original
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 2006, Volume 1762, Issue 10, pp. 857 - 864
Journal Article
Journal Article
MOLECULAR THERAPY, ISSN 1525-0016, 05/2018, Volume 26, Issue 5, pp. 1343 - 1353
The neuronal ceroid lipofuscinoses (NCLs) are inherited lysosomal storage disorders characterized by general neurodegeneration and premature death. Sight loss... 
LONG-TERM | MEDICINE, RESEARCH & EXPERIMENTAL | TRANSDUCTION | ADENOASSOCIATED-VIRUS | DELIVERY | LEBER CONGENITAL AMAUROSIS | THERAPY | VISUAL FUNCTION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | RETINITIS-PIGMENTOSA | NEURONAL CEROID-LIPOFUSCINOSIS | STATIONARY NIGHT BLINDNESS
Journal Article