Literature DB >> 19533781

Characteristics and frequency of seizure disorder in 56 patients with Prader-Willi syndrome.

Zheng Fan, Robert Greenwood, Amy Fisher, Surekha Pendyal, Cynthia M Powell.   

Abstract

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Year:  2009        PMID： 19533781     DOI： 10.1002/ajmg.a.32934

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  10 in total

Review 1.  Genetic and biologic classification of infantile spasms.

Authors:  Alex R Paciorkowski; Liu Lin Thio; William B Dobyns
Journal:  Pediatr Neurol       Date:  2011-12       Impact factor: 3.372

2.  Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Authors:  Alberto Verrotti; Raffaella Cusmai; Daniela Laino; Marco Carotenuto; Maria Esposito; Raffaele Falsaperla; Lucia Margari; Renata Rizzo; Salvatore Savasta; Salvatore Grosso; Pasquale Striano; Vincenzo Belcastro; Emilio Franzoni; Paolo Curatolo; Lucio Giordano; Elena Freri; Sara Matricardi; Dario Pruna; Irene Toldo; Elisabetta Tozzi; Lucio Lobefalo; Francesca Operto; Emma Altobelli; Francesco Chiarelli; Alberto Spalice
Journal:  J Neurol       Date:  2014-10-18       Impact factor: 4.849

3.  Electrical status epilepticus during sleep in a child with Prader-Willi syndrome: a case report.

Authors:  Berrin Ergun-Longmire; Minh H N Nguyen; Gulnur Com
Journal:  AME Case Rep       Date:  2022-01-25

Review 4.  Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects.

Authors:  Alberto Verrotti; Claudia Soldani; Daniela Laino; Renato d'Alonzo; Salvatore Grosso
Journal:  World J Pediatr       Date:  2014-05-07       Impact factor: 2.764

5.  Prader-Willi syndrome: A primer for clinicians.

Authors:  Mary Cataletto; Moris Angulo; Gila Hertz; Barbara Whitman
Journal:  Int J Pediatr Endocrinol       Date:  2011-10-18

Review 6.  Genetics of bipolar disorder.

Authors:  Berit Kerner
Journal:  Appl Clin Genet       Date:  2014-02-12

Review 7.  Puzzle Pieces: Neural Structure and Function in Prader-Willi Syndrome.

Authors:  Katherine E Manning; Anthony J Holland
Journal:  Diseases       Date:  2015-12-17

8.  ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison.

Authors:  Sarah F Barclay; Casey M Rand; Lisa Nguyen; Richard J A Wilson; Rachel Wevrick; William T Gibson; N Torben Bech-Hansen; Debra E Weese-Mayer
Journal:  Orphanet J Rare Dis       Date:  2018-07-20       Impact factor: 4.123

9.  Treatment of Epilepsy Associated with Common Chromosomal Developmental Diseases.

Authors:  Magdalena Budisteanu; Claudia Jurca; Sorina Mihaela Papuc; Ina Focsa; Dan Riga; Sorin Riga; Alexandru Jurca; Aurora Arghir
Journal:  Open Life Sci       Date:  2020-02-28       Impact factor: 0.938

Review 10.  Clinical characteristics and epilepsy in genomic imprinting disorders: Angelman syndrome and Prader-Willi syndrome.

Authors:  Tzong-Shi Wang; Wen-Hsin Tsai; Li-Ping Tsai; Shi-Bing Wong
Journal:  Ci Ji Yi Xue Za Zhi       Date:  2019-10-31
  10 in total

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