Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment (Q56350599)

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27 December 2019

title

Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment (English)

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27 December 2019

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Adriano Yacubian Fernandes

1

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27 December 2019

A Palhares

2

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27 December 2019

author name string

A Giglio

3

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27 December 2019

R C Gabarra

4

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27 December 2019

S Zanini

5

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27 December 2019

L Portela

6

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27 December 2019

J P P Plese

7

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27 December 2019

language of work or name

English

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publication date

1 March 2004

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Journal of neuroradiology. Journal de neuroradiologie

27 December 2019

published in

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27 December 2019

volume

31

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27 December 2019

issue

2

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27 December 2019

page(s)

116-122

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Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

27 December 2019

cites work

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The central nervous system in the Apert syndrome

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Birth prevalence study of the Apert syndrome

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Acrocephalosyndactylia associated with a chromosomal translocation. 46,XX, t (2p-; Cq+)

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Morbidity associated with increased intracranial pressure in Apert and Pfeiffer syndromes: the need for long-term evaluation.

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Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes

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7 January 2021

Prenatal diagnosis of Apert syndrome with widely separated cranial sutures

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7 January 2021

Apert's syndrome with central nervous system anomalies

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7 January 2021

Timing of treatment for craniosynostosis and facio-craniosynostosis: a 20-year experience

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7 January 2021

Exclusive paternal origin of new mutations in Apert syndrome

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7 January 2021

Cranial suture disease in the Apert's syndrome infant

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7 January 2021

[Mental prognosis of Apert syndrome]

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7 January 2021

Prognosis for mental function in Apert's syndrome

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7 January 2021

Male transmission of Apert syndrome

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7 January 2021

Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome

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7 January 2021

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

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7 January 2021

10.1016/S0150-9861(04)96978-7

Identifiers

DOI

1 reference

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27 December 2019

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