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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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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Discovery and Biosynthesis of the Novel Glycotetrapeptide Antibiotic Biffamycin A. [PDF]
Brigham MW +11 more
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Adult-onset neuronal ceroid lipofuscinosis misdiagnosed as autoimmune encephalitis and normal-pressure hydrocephalus: A 10-year case report and case-based review. [PDF]
Huang H +5 more
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Editorial: Neuronal ceroid lipofuscinosis: molecular genetics and epigenetics. [PDF]
Nicolaou P.
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Loss of the ER-cargo protein CLN8 increases severity of acute pancreatitis and upregulates ER-stress and ER-phagy. [PDF]
Zierke L +9 more
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High Diagnostic Yield and Clinical Utility of Next-Generation Sequencing in Children with Epilepsy and Neurodevelopmental Delays: A Retrospective Study. [PDF]
Charouf D +5 more
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