(Q40538599)

21 September 2017

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title

The neuronal ceroid-lipofuscinoses (Batten disease): comparative aspects (English)

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21 September 2017

1

Jolly RD

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21 September 2017

2

Palmer DN

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21 September 2017

publication date

1 February 1995

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Neuropathology and Applied Neurobiology

21 September 2017

published in

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21 September 2017

volume

21

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21 September 2017

issue

1

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21 September 2017

page(s)

50-60

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Pathoarchitectonic pattern of iso- and allocortical lesions in juvenile and adult neuronal ceroid-lipofuscinosis

21 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Loss of pigment-laden stellate cells: a severe alteration of the isocortex in juvenile neuronal ceroid-lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Pigmentoarchitectonic pathology of the isocortex in juvenile neuronal ceroid-lipofuscinosis: Axonal enlargements in layer IIIab and cell loss in layer V

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Evidence for processing of dolichol-linked oligosaccharides in patients with neuronal ceroid-lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

DNA sequences of a bovine gene and of two related pseudogenes for the proteolipid subunit of mitochondrial ATP synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Molecular basis of lysosomal accumulation of subunit c of mitochondrial ATP synthase in neuronal ceroid-lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Protracted juvenile neuronal ceroid-lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Stored dolichyl pyrophosphoryl oligosaccharides in Batten disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Survey of amino-terminal proteolytic cleavage sites in mitochondrial precursor proteins: leader peptides cleaved by two matrix proteases share a three-amino acid motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

An animal model of the infantile type of neuronal ceroid-lipofuscinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Molecular genetics of neuronal ceroid lipofuscinoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Sheep and other animals with ceroid-lipofuscinoses: their relevance to Batten disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Human forms of neuronal ceroid-lipofuscinosis (Batten disease): consensus on diagnostic criteria, Hamburg 1992.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Immunolocalization studies of subunit c in late-infantile and juvenile Batten disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Characterization of the expressed genes for subunit c of mitochondrial ATP synthase in sheep with ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Storage bodies in the ceroid-lipofuscinoses (Batten disease): low-molecular-weight components, unusual amino acids and reconstitution of fluorescent bodies from non-fluorescent components

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Biochemical studies on the juvenile form of ceroid-lipofuscinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Infantile neuronal ceroid-lipofuscinosis (INCL): diagnostic criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Identification of the subunits of F1F0-ATPase from bovine heart mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Biology of neuronal dysfunction in storage disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Variability in the clinical and pathological findings in the neuronal ceroid lipofuscinoses: Review of data and observations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

Topographic heterogeneity of amyloid B-protein epitopes in brains with various forms of neuronal ceroid lipofuscinoses suggesting defective processing of amyloid precursor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1995.TB01028.X

10.1111/J.1365-2990.1995.TB01028.X

21 January 2018

Identifiers

DOI

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21 September 2017

1 reference