(Q48343528)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

title

Unusual diagnosis in a child suffering from juvenile Alexander disease: clinical and imaging report (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Caterina Garone

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

author name string

Marjo S Van der Knaap

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Alessandra Errani

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Maria Chiara Colonnelli

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Roberta Bracceschi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Elisabetta Malaspina

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Filomena Caterina Moscano

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Jasenka Sarajlija

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Robert A Zimmerman

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Gajja S Salomons

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

Bruno Bernardi

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

publication date

1 December 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

Journal of Child Neurology

22 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

page(s)

1075-1080

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant.

22 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Alexander disease--classification revisited and isolation of a neonatal form

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Unusual variants of Alexander's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Benign course of central pontine myelinolysis in a patient with anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Central pontine myelinolysis associated with hypokalaemia in anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Atypical focal MRI lesions in a case of juvenile Alexander's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

MR imaging and 1H-MR spectroscopy in a case of juvenile Alexander disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Rosenthal fibers in Alexander's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

The clinicopathological spectrum of Rosenthal fibre encephalopathy and Alexander's disease: a case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Dysmyelinogenic leukodystrophy; report of a case of a new, presumably familial type of leukodystrophy with megalobarencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Fluctuation of computed tomographic findings in white matter in Alexander's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F7010.2006.00235

21 January 2018

Identifiers

DOI

10.1177/7010.2006.00235

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17156703%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

1 reference