Sage Journals: Discover world-class research

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First published 2007-09

Prader-Willi Syndrome: An Update and Review for the Primary Pediatrician

Christina Chen, Jeannie Visootsak, Shelley Dills [...]

Clinical Pediatrics

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Research article

First published 2010-8

Eventration of the diaphragm in a newborn with Prader Willi Syndrome

I. Shareena, J. Rohana, C.Y. Wong [...]

Journal of Neonatal-Perinatal Medicine

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Case report

First published 2021-11

Comprehensive Orthodontic Treatment of a Patient With Prader–Willi Syndrome

Yume Uemura, Ayaka Oka, Hiroshi Kurosaka [...]

The Cleft Palate Craniofacial Journal

Open access

Case report

First published 2013

Molecular Characterization of a Patient Presumed to Have Prader-Willi Syndrome

Marina Falaleeva, Carlos R. Sulsona, Horst R. Zielke [...]

Clinical Medicine Insights: Case Reports

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Research article

First published 2015-3

A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene ( MTCYB ) in a Patient with Prader Willi Syndrome

Uluç Yiş, Fatih Süheyl Ezgü, Pakize Karakaya [...]

Journal of Child Neurology

Open access

Case report

First published 2019

Malignant otitis externa in a 21-year-old male patient with Prader–Willi syndrome

Marcos Frata Rihl, Felipe Marchiori Bau, Igor de Oliveira [...]

Sage Open Medical Case Reports

Open access

Case report

First published 2020

Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report

Kyung Woo Kim, Seung Hwan Kim, Eun Jin Ahn [...]

Sage Open Medical Case Reports

Retricted access

Case report

First published 2019-3

Orthognathic Correction in Prader-Willi Syndrome: Occlusion and Sleep Restored

Keliang Kevin Xiao, Shikhar Tomur, Robert Beckerman [...]

The Cleft Palate Craniofacial Journal

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Other

First published 2007-06

Cardiac tamponade due to systemic lupus erythematosus in patient with Prader-Willi syndrome after growth hormone therapy

Y. Kuramochi, T. Kato, M. Sudou [...]

Lupus

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Other

First published 2008-01

Persistent Growth Failure in Prader-Willi Syndrome Associated With Short-Chain Acyl-CoA Dehydrogenase Gene Variant

Dan-Victor Giurgiutiu, Lesby M. Espinoza, Tim C. Wood [...]

Journal of Child Neurology

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