Autosomal dominant adult neuronal ceroid lipofuscinosis: parkinsonism due to both striatal and nigral dysfunction (Q48552779)

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scientific article published in May 2002

Language	Label	Description	Also known as
English	Autosomal dominant adult neuronal ceroid lipofuscinosis: parkinsonism due to both striatal and nigral dysfunction	scientific article published in May 2002

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

Autosomal dominant adult neuronal ceroid lipofuscinosis: parkinsonism due to both striatal and nigral dysfunction (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

Parkinson's disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

neuronal ceroid lipofuscinosis

1 reference

based on heuristic

inferred from title

parkinsonian syndrome

1 reference

based on heuristic

inferred from title

Raymund A. C. Roos

6

object named as

Raymund A C Roos

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

2

object named as

Esther Brusse

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

author name string

Peter C G Nijssen

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

Antonius C M Leyten

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

J J Martin

4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

Johannes L J M Teepen

5

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

language of work or name

0 references

publication date

1 May 2002

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

17

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

482-487

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

The adult and a new late adult forms of neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Kufs' disease: a critical reappraisal

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

A dominant form of neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL).

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

The neuronal ceroid-lipofuscinoses. Recent advances.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Immunocytochemical studies in the ceroid-lipofuscinoses (Batten disease) using antibodies to subunit c of mitochondrial ATP synthase

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Batten's disease: eight genes and still counting?

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Classification of the neuronal ceroid-lipofuscinoses: expansion of the atypical forms

1 reference

https://api.crossref.org/works/10.1002%2FMDS.10104

21 January 2018

Identifiers

10.1002/MDS.10104

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12112194

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