Perinatal dyskinesia as a presenting feature in Prader Willi Syndrome-Reference-Cited by-同舟云学术

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Perinatal dyskinesia as a presenting feature in Prader Willi Syndrome

Published:2009-07 Issue:4 Volume:13 Page:350-355
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

McSweeney Niamh,Cowan Frances,Manzur Adnan,Robb Stephanie,Muntoni Francesco

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference34 articles.

1. Prader Willi syndrome: advances in genetics, pathophysiology and treatment;Goldstone;Trends Endocrinol Metabol,2004

2. Prader Willi syndrome: a neonatology success story;McCandless;Neoreviews,2005

3. Deletion of chromosome 15 as a cause of Prader Willi Syndrome;Ledbetter;N Engl J Med,1981

4. The frequency of uniparental disomy in Prader Willi Syndrome: implications for molecular diagnosis;Mascari;N Engl J Med,1992

5. Imprinting mutations suggested by abnormal methylation patterns in familial Angelman and Prader Willi Syndrome;Reiss;Am J Hum Genet,1994

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hypotonia in the Newborn;Common Problems in the Newborn Nursery;2018-10-10

2. Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome;Journal of Medical Genetics;2018-05-18

3. Current World Literature;Current Opinion in Pulmonary Medicine;2010-11

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