Publications by authors named "Alison Yeung"

23Publications

Hyperinsulinaemic hypoglycaemia: A rare association of vanishing white matter disease.

JIMD Rep 2020 Jan 12;51(1):11-16. Epub 2019 Nov 12.

Department of Metabolic Medicine Royal Children's Hospital Melbourne Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/jmd2.12081DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012737PMC
January 2020

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.

Authors:
Przemyslaw Szafranski Tomasz Gambin Avinash V Dharmadhikari Kadir Caner Akdemir Shalini N Jhangiani Jennifer Schuette Nihal Godiwala Svetlana A Yatsenko Jessica Sebastian Suneeta Madan-Khetarpal Urvashi Surti Rosanna G Abellar David A Bateman Ashley L Wilson Melinda H Markham Jill Slamon Fernando Santos-Simarro María Palomares Julián Nevado Pablo Lapunzina Brian Hon-Yin Chung Wai-Lap Wong Yoyo Wing Yiu Chu Gary Tsz Kin Mok Eitan Kerem Joel Reiter Namasivayam Ambalavanan Scott A Anderson David R Kelly Joseph Shieh Taryn C Rosenthal Kristin Scheible Laurie Steiner M Anwar Iqbal Margaret L McKinnon Sara Jane Hamilton Kamilla Schlade-Bartusiak Dawn English Glenda Hendson Elizabeth R Roeder Thomas S DeNapoli Rebecca Okashah Littlejohn Daynna J Wolff Carol L Wagner Alison Yeung David Francis Elizabeth K Fiorino Morris Edelman Joyce Fox Denise A Hayes Sandra Janssens Elfride De Baere Björn Menten Anne Loccufier Lieve Vanwalleghem Philippe Moerman Yves Sznajer Amy S Lay Jennifer L Kussmann Jasneek Chawla Diane J Payton Gael E Phillips Erwin Brosens Dick Tibboel Annelies de Klein Isabelle Maystadt Richard Fisher Neil Sebire Alison Male Maya Chopra Jason Pinner Girvan Malcolm Gregory Peters Susan Arbuckle Melissa Lees Zoe Mead Oliver Quarrell Richard Sayers Martina Owens Charles Shaw-Smith Janet Lioy Eileen McKay Nicole de Leeuw Ilse Feenstra Liesbeth Spruijt Frances Elmslie Timothy Thiruchelvam Carlos A Bacino Claire Langston James R Lupski Partha Sen Edwina Popek Paweł Stankiewicz

Hum Genet 2016 May 12;135(5):569-586. Epub 2016 Apr 12.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-016-1655-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518754PMC
May 2016

SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia.

Am J Med Genet A 2015 Oct 8;167A(10):2319-26. Epub 2015 Jun 8.

Newborn Intensive Care Unit, Royal Children's Hospital, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.37177DOI Listing
October 2015

Letters to the Editor Regarding Dr. Laskin's Perspectives Article.

Authors:
Alison Y Yeung

J Oral Maxillofac Surg 2015 Jun 2;73(6):1025-6. Epub 2015 May 2.

Greenville, NC.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.joms.2015.04.011DOI Listing
June 2015

Neonatal presentation of chromosome 9q33.2-q34.3 duplication.

Gene 2013 Sep 4;527(2):541-4. Epub 2013 Jul 4.

Monash Newborn, Monash Children's, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.gene.2013.06.043DOI Listing
September 2013

Sporadic Burkitt lymphoma of the jaw: case report and review of the literature.

Quintessence Int 2012 Apr;43(4):333-6

Department of Diagnostic Sciences, School of Dental Medicine, University of Pittsburgh, PA 15213, USA.

View Article

Download full-text PDF

Source
April 2012

4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment.

Eur J Med Genet 2009 Nov-Dec;52(6):440-2. Epub 2009 Sep 20.

Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2009.09.004DOI Listing
February 2010

Familial upper eyelid coloboma with ipsilateral anterior hairline abnormality: two new reports of MOTA syndrome.

Am J Med Genet A 2009 Feb;149A(4):767-9

Genetic Health Services Victoria, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.32743DOI Listing
February 2009

Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p.

Am J Med Genet A 2009 Mar;149A(3):505-9

Victorian Clinical Genetics Services, Royal Children's Hospital, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.32664DOI Listing
March 2009

Rebuttal paper to 'Sunflower therapy for children with specific learning difficulties (dyslexia): a randomised, controlled trial'.

Complement Ther Clin Pract 2009 Feb 14;15(1):44-6. Epub 2008 Nov 14.

Sunflower Trust, 10 Guildford Park Road, Guildford, Surrey GU2 7ND, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ctcp.2008.09.006DOI Listing
February 2009