Terkko Navigator / Lonka, L.

Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6

The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy

Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells

Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8

The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

18 children with slight glomerular proteinuria demonstrated incidentally

Rhabdomyolysis and acute kidney insufficiency

Benzodiazepine intoxication treated with flumazenil (Anexate, RO 15-1788)

Rhabdomyolysis

Fatal non-traumatic rhabdomyolysis developing during training for running

Ciprofloxacin for cholangitis

Cocaine poisoning

Fatal rhabdomyolysis in marathon runner

Acute cannabis poisoning

Acute renal failure caused by polymyxin B containing ointment

Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6.

The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy.

Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells.

Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8.

The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum.