(Q44558820)

4 December 2017

title

Analysis of EEG patterns and genotypes in patients with Angelman syndrome (English)

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2

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13

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Marcin Zarowski

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Matt Gregas

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Dean P Sarco

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1

Martina Vendrame

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Hans Shuhaiber

5

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Augusto Morales

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Mark Nespeca

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Cia Sharpe

9

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Kevin Haas

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Gregory Barnes

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Daniel Glaze

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language of work or name

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16 February 2012

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4 December 2017

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4 December 2017

volume

23

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4 December 2017

issue

3

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4 December 2017

page(s)

261-265

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Clinical and genetic aspects of Angelman syndrome

4 December 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Angelman syndrome: Mutations influence features in early childhood

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Notched delta, phenotype, and Angelman syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Angelman syndrome reviewed from a neurophysiological perspective. The UBE3A-GABRB3 hypothesis

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Angelman syndrome: correlations between epilepsy phenotypes and genotypes

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Epilepsy in Angelman syndrome associated with chromosome 15q deletion

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Seizure and EEG patterns in Angelman's syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

The EEG in early diagnosis of the Angelman (happy puppet) syndrome.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Angelman syndrome: is there a characteristic EEG?

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Diagnosis of Angelman syndrome: clinical and EEG criteria

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Myoclonic status in nonprogressive encephalopathies: an update

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.11.027

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

7 January 2021

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10.1016/J.YEBEH.2011.11.027

7 January 2021

Identifiers

DOI

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4 December 2017

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