Familial encephalopathy with neuroserpin inclusion bodies (Q35750194)

10 August 2017

title

Familial encephalopathy with neuroserpin inclusion bodies (English)

1 reference

familial encephalopathy with neuroserpin inclusion bodies

10 August 2017

main subject

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14

F Lacbawan

1 reference

10 August 2017

R L Davis

1

1 reference

10 August 2017

P D Holohan

2

1 reference

10 August 2017

A E Shrimpton

3

1 reference

10 August 2017

A H Tatum

4

1 reference

10 August 2017

J Daucher

5

1 reference

10 August 2017

G H Collins

6

1 reference

10 August 2017

R Todd

7

1 reference

10 August 2017

C Bradshaw

8

1 reference

10 August 2017

P Kent

9

1 reference

10 August 2017

D Feiglin

10

1 reference

10 August 2017

A Rosenbaum

11

1 reference

10 August 2017

M S Yerby

12

1 reference

10 August 2017

C M Shaw

13

1 reference

10 August 2017

D A Lawrence

15

1 reference

10 August 2017

language of work or name

English

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publication date

1 December 1999

1 reference

The American Journal of Pathology

10 August 2017

published in

1 reference

10 August 2017

volume

155

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10 August 2017

issue

6

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10 August 2017

page(s)

1901-1913

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The brain-stem lesions in Parkinsonism

10 August 2017

cites work

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Familial dementia caused by polymerization of mutant neuroserpin

12 July 2018

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12 July 2018

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Conformational changes and disease--serpins, prions and Alzheimer's.

12 July 2018

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Protein precipitation: a common etiology in neurodegenerative disorders?

12 July 2018

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12 July 2018

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The axonally secreted serine proteinase inhibitor, neuroserpin, inhibits plasminogen activators and plasmin but not thrombin

12 July 2018

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Neuroserpin, a brain-associated inhibitor of tissue plasminogen activator is localized primarily in neurons. Implications for the regulation of motor learning and neuronal survival

12 July 2018

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12 July 2018

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12 July 2018

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Human neuroserpin (PI12): cDNA cloning and chromosomal localization to 3q26

12 July 2018

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12 July 2018

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12 July 2018

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Inhibitory conformation of the reactive loop of alpha 1-antitrypsin

12 July 2018

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Early-onset dementias: clinical, neuropathological and genetic characteristics

12 July 2018

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The serpin superfamily of proteinase inhibitors: structure, function, and regulation

12 July 2018

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Extravascular proteolysis and the nervous system: serine protease/serpin balance

12 July 2018

1 reference

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What do dysfunctional serpins tell us about molecular mobility and disease?

12 July 2018

1 reference

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Dense microspheres in normal human brain

12 July 2018

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A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes: a report of four cases and a review of the occurrence of polyglucosan bodies in other conditions such as Lafora'

12 July 2018

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Atypical inclusion bodies with myoclonic epilepsy

12 July 2018

1 reference

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[Myoclonic bodies and progressive myoclonic epilepsy]

12 July 2018

1 reference

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Studies of corpora amylacea. I. Isolation and preliminary characterization by chemical and histochemical techniques

12 July 2018

1 reference

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Myoclonus epilepsy with Lafora bodies. An ultrastruc- tural and cytochemical study

12 July 2018

1 reference

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Histochemistry and ultrastructure of atypical myoclonus body (type II).

12 July 2018

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Studies in myoclonus epilepsy (Lafora body form). II. Polyglucosans in the systemic deposits of myoclonus epilepsy and in corpora amylacea

12 July 2018

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Studies in myoclonus epilepsy (Lafora body form). I. Isolation and preliminary characterization of Lafora bodies in two cases

12 July 2018

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12 July 2018

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Progressive dementia and epilepsy in a young adult: unusual intraneuronal inclusions

12 July 2018

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Diffuse Lewy body disease: correlative neuropathology using anti-ubiquitin immunocytochemistry

12 July 2018

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Saturation mutagenesis of the plasminogen activator inhibitor-1 reactive center

12 July 2018

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12 July 2018

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12 July 2018

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25 September 2018

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Specific pathological Tau protein variants characterize Pick's disease.

25 September 2018

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New aspects of the pathology of neurodegenerative disorders as revealed by ubiquitin antibodies

25 September 2018

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Tau, ubiquitin, and alpha B-crystallin immunohistochemistry define the principal causes of degenerative frontotemporal dementia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965510-1

Dimedone as an aldehyde blocking reagent to facilitate the histochemical demonstration of glycogen

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965510-1

Corpora-amylacea and the family of polyglucosan diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965510-1

Atypical inclusion body progressive myoclonus epilepsy: a fifth case?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965510-1

Structural explanation for the deficiency of S alpha 1-antitrypsin

7 January 2021

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Alpha 1 -antitrypsin (A1AT) accumulation in livers of emphysematous patients with A1AT deficiency

7 January 2021

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The role of thrombin-like (serine) proteases in the development, plasticity and pathology of the nervous system

7 January 2021

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Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10595921

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Immunohistochemistry of neuronal inclusions in the cerebral cortex and brain-stem in Lewy body disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10595921

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)65510-1

1 reference

10 August 2017

1 reference

10 August 2017

1 reference