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Brain and Development, ISSN 0387-7604, 06/2019, Volume 41, Issue 6, pp. 542 - 545
Neuronal ceroid lipofuscinosis (NCL) is a group of progressive neurodegenerative disorders characterized by intracellular accumulation of ceroid lipopigments.... 
Cerebellar atrophy | Progranulin | Neuronal ceroid lipofuscinosis | CLN11 | CLINICAL NEUROLOGY | FRONTOTEMPORAL DEMENTIA | Proteins | Medical research | Medical colleges | Nervous system diseases | Gene mutations | Neurons | Medicine, Experimental | Eye diseases | Seizures (Medicine) | Dementia
Journal Article
Journal Article
The Indian Journal of Pediatrics, ISSN 0019-5456, 11/2017, Volume 84, Issue 11, pp. 865 - 866
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s12098-017-2385-2 
Medicine & Public Health | Pediatrics | Gynecology | PEDIATRICS | WHITE-MATTER INJURY | Infants (Newborn) | Encephalitis
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 10/2016, Volume 19, Issue 4, pp. 528 - 530
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2011, Volume 44, Issue 5, pp. 374 - 376
Journal Article
Journal Article
The Indian Journal of Pediatrics, ISSN 0019-5456, 3/2014, Volume 81, Issue 3, pp. 296 - 298
L-2-Hydroxyglutaric aciduria (L-2-HGA) is a rare type of organic acidemia that has characteristic neurological manifestations including macrocephaly,... 
Pediatrics | Medicine & Public Health | Gynecology | Children | Amino acid metabolism | L-2-Hydroxyglutaric aciduria | India | L-2-hydroxyglutaric aciduria | PEDIATRICS | PATIENT | Amino acidmetabolism | Female | Male | Brain Diseases, Metabolic, Inborn | Child | Humans | Adolescent | Medical colleges | Family | Seizures (Medicine) | Epilepsy | Index Medicus
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 12/2010, Volume 13, Issue 4, pp. 289 - 292
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 01/2012, Volume 15, Issue 1, pp. 31 - 34
Background and Objectives: Glutaric aciduria Type-I (GA-I) has characteristic clinical and neuroimaging features, which clinches the diagnosis in a majority of... 
Encephalitis | macrocephaly | glutaric aciduria type 1 | neuroimaging | DIAGNOSIS | MANAGEMENT | COA DEHYDROGENASE-DEFICIENCY | NATURAL-HISTORY | CLINICAL NEUROLOGY | Metabolism, Inborn errors of | Care and treatment | Diagnosis | Neurology | Metabolic disorders | Short Communication
Journal Article
Canadian Journal of Neurological Sciences, ISSN 0317-1671, 11/2014, Volume 41, Issue 6, pp. 777 - 779
An 8-year-old boy, born to a third-degree consanguineous couple with no adverse perinatal events, presented with complaints of delayed development and gait... 
SPECTROSCOPY | CLINICAL NEUROLOGY | Neuroimaging - methods | Male | Giant Axonal Neuropathy - physiopathology | Child | Humans | Giant Axonal Neuropathy - diagnosis | Index Medicus
Journal Article
Neurology India, ISSN 0028-3886, 2009, Volume 57, Issue 2, p. 225
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 07/2011, Volume 14, Issue 3, p. 222
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 07/2011, Volume 14, Issue 3, p. 222
Coming to inclusion of one patient with HIV and ADEM in our series, we agree that progressive multifocal leucoencephalopathy (PML) was a possibility, although... 
Medical research | Human immunodeficiency virus--HIV
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 07/2011, Volume 14, Issue 3, pp. 222 - 223
Journal Article
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