Mowat-Wilson syndrome: the first report of an association with central nervous system tumors. (Q41931367)

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26 February 2020

title

Mowat-Wilson syndrome: the first report of an association with central nervous system tumors (English)

1 reference

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26 February 2020

main subject

Mowat-Wilson syndrome

1 reference

1

1 reference

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26 February 2020

María S Brassesco

3

1 reference

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26 February 2020

Carlos Scrideli

9

1 reference

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26 February 2020

Luiz Gonzaga Tone

10

1 reference

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7

Luciano Neder

1 reference

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26 February 2020

Sabrine Teixeira Ferraz

2

object named as

Sabrine Teixeira Ferraz

1 reference

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26 February 2020

author name string

Xiumei Zhen

4

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26 February 2020

Yiping Shen

5

1 reference

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26 February 2020

Antonio Carlos dos Santos

6

1 reference

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26 February 2020

Ricardo Santos Oliveira

8

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26 February 2020

publication date

3 October 2013

1 reference

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26 February 2020

published in

Child's Nervous System

1 reference

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26 February 2020

volume

29

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issue

12

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26 February 2020

page(s)

2151-2155

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https://scigraph.springernature.com/pub.10.1007/s00381-013-2283-5

26 February 2020

exact match

0 references

cites work

Hirschsprung disease, associated syndromes, and genetics: a review

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

Favorable outcomes of pediatric patients treated with radiotherapy to the central nervous system who develop radiation-induced meningiomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

21 January 2018

Mowat-Wilson syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

The contribution of associated congenital anomalies in understanding Hirschsprung's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

Hirschsprung's disease and the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-013-2283-5

The behavioral phenotype of Mowat-Wilson syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24092421

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mowat-Wilson syndrome: the first two Malaysian cases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24092421

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00381-013-2283-5

1 reference

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Dimensions Publication ID

26 February 2020

0 references

1 reference

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