Neuropsychiatric manifestations of Kufs disease. [PDF]
Vijayan S, Selvaraj A.
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Lysosomal dysfunction, autophagic defects, and CLN5 accumulation underlie the pathogenesis of KCTD7-mutated neuronal ceroid lipofuscinoses. [PDF]
Wang Y, Wang H, Wang C.
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Neuronal Ceroid Lipofuscinosis-Concepts, Classification, and Avenues for Therapy. [PDF]
Zhang Y, Du B, Zou M, Peng B, Rao Y.
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Neuronal ceroid lipofuscinosis: underlying mechanisms and emerging therapeutic targets. [PDF]
Ziółkowska EA +5 more
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Iatrogenic cerebral amyloid angiopathy 30 years after childhood cadaveric dura mater transplantation: a case report. [PDF]
Takai I +13 more
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Pediatric onset neuronal ceroid lipofuscinoses: Unraveling clinical and genetic specifications. [PDF]
Ahdi SG, Alvi JR, Ashfaq A, Sultan T.
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(<i>E</i>)-2,4-Di-amino-5-{7-[(4-chloro-phen-yl)diazen-yl]-3,3-dimethyl-1-oxo-2,3,4,9-tetra-hydro-1<i>H</i>-xanthen-9-yl}-6-oxo-1,6-di-hydro-pyridine-3-carbo-nitrile di-methyl-formamide monosolvate. [PDF]
Elgemeie GH +3 more
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Losartan API and Nitrosamines Impurities-Stability Profile Investigation Using HPLC, LC-MS, and In Silico Assessment. [PDF]
Martini PRR +6 more
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Genetic Reasons for Phenotypic Diversity in Neuronal Ceroid Lipofuscinoses and High-Resolution Imaging as a Marker of Retinal Disease. [PDF]
Huey J +11 more
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