Neuronal ceroid lipofuscinoses: classification and diagnosis.
about
An over-expression system for characterizing Ppt1 function in DrosophilaLate infantile neuronal ceroid lipofuscinosis: A case report with review of literatureAtypical CLN2 with later onset and prolonged course: a neuropathologic study showing different sensitivity of neuronal subpopulations to TPP1 deficiency.A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis.Palmitoyl-protein thioesterase 1 deficiency in Drosophila melanogaster causes accumulation of abnormal storage material and reduced life spanWhen ethics constrains clinical research: trial design of control arms in "greater than minimal risk" pediatric trialsA reversal learning task detects cognitive deficits in a Dachshund model of late-infantile neuronal ceroid lipofuscinosis.Genetic modifiers of Drosophila palmitoyl-protein thioesterase 1-induced degeneration.Embryonic stem cell-derived neural progenitors incorporate into degenerating retina and enhance survival of host photoreceptors.Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosisPhenotypic characterization of a mouse model of juvenile neuronal ceroid lipofuscinosis.Tripeptidyl-peptidase I in health and disease.Lysosomal Storage Diseases-Regulating Neurodegeneration.Brain Region-Specific Degeneration with Disease Progression in Late Infantile Neuronal Ceroid Lipofuscinosis (CLN2 Disease).Drosophila melanogaster as a model organism of brain diseasesLong-term expression and safety of administration of AAVrh.10hCLN2 to the brain of rats and nonhuman primates for the treatment of late infantile neuronal ceroid lipofuscinosis.Neuronal ceroid lipofuscinosis type CLN2: a new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America.Analysis of NCL Proteins from an Evolutionary Standpoint.The neuropsychiatry of inborn errors of metabolism.Biosynthesis, glycosylation, and enzymatic processing in vivo of human tripeptidyl-peptidase I.Interactions between the juvenile Batten disease gene, CLN3, and the Notch and JNK signalling pathways.Prospects for stem cell therapy in neuronal ceroid lipofuscinosis.
P2860
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P2860
Neuronal ceroid lipofuscinoses: classification and diagnosis.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@ast
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@en
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@nl
type
label
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@ast
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@en
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@nl
prefLabel
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@ast
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@en
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@nl
P2093
P1433
P1476
Neuronal ceroid lipofuscinoses: classification and diagnosis.
@en
P2093
P356
10.1016/S0065-2660(01)45002-4
P577
2001-01-01T00:00:00Z