(Q40865002)

24 September 2017

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title

Biology of neuronal dysfunction in storage disorders (English)

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24 September 2017

S U Walkley

1

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PubMed ID

8411982

24 September 2017

P A March

series ordinal

2

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24 September 2017

1 January 1993

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Journal of Inherited Metabolic Disease

24 September 2017

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24 September 2017

16

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24 September 2017

2

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24 September 2017

284-287

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https://scigraph.springernature.com/pub.10.1007/bf00710266

24 September 2017

0 references

cites work

Ectopic dendrites occur only on cortical pyramidal cells containing elevated GM2 ganglioside in alpha-mannosidosis

1 reference

12 December 2020

Pathobiology of neuronal storage disease.

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12 December 2020

Studies of the uptake of3H-GABA and [3H]glycine in slices and homogenates of rat brain and spinal cord by electron microscopic autoradiography

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12 December 2020

Metabolism and nervous system disease: a challenge for our times. Part II.

1 reference

12 December 2020

Neuroaxonal dystrophy in neuronal storage disorders: evidence for major GABAergic neuron involvement.

1 reference

12 December 2020

Ectopic dendritogenesis and associated synapse formation in swainsonine-induced neuronal storage disease

1 reference

12 December 2020

Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinoses.

1 reference

12 December 2020

The cellular pathology of neuronal ceroid-lipofuscinosis. A golgi-electronmicroscopic study.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00710266

1 reference

PubMed ID

8411982

Dimensions Publication ID

24 September 2017

0 references

1 reference

PubMed ID

8411982