(Q48867761)

English

Four siblings with Hallervorden-Spatz disease.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Four siblings with Hallervorden-Spatz disease. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

1 reference

based on heuristic

inferred from title

author name string

Vaher U

1

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Napa A

2

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Nurmiste A

3

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Piirsoo A

4

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Sibul H

5

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Talvik T

6

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

publication date

1 July 2001

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Brain and Development

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

23

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

4

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

236-239

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

Naming of syndromes and unethical activities: the case of Hallervorden and Spatz.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Hallervorden-Spatz Syndrome and Brain Iron Metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Stereotactic pallidotomy in a child with Hallervorden-Spatz disease. Case report

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Optic atrophy as the first symptom in Hallervorden-Spatz syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatosensory evoked potentials in Hallervorden-Spatz-neuroaxonal-dystrophy complex with dorsal column involvement.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Infantile neuroaxonal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuroaxonal dystrophy with dystonia and pallidal involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900184-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0387-7604(01)00184-X

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/11377002

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