Publications by authors named "Arabella Smith"

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The dilemma of diagnostic testing for Prader-Willi syndrome.
Arabella Smith, Dorothy Hung

Transl Pediatr· January 2017

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Erratum: Postprandial metabolism in adults with prader-willi syndrome.
Louise Purtell, Alexander Viardot, Lisa Sze, Georgina Loughnan, Katharine Steinbeck, Arabella Smith

Obesity (Silver Spring)· August 2016

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Postprandial metabolism in adults with Prader-Willi syndrome.
Louise Purtell, Alexander Viardot, Lisa Sze, Georgina Loughnan, Katharine Steinbeck, Arabella Smith

Obesity (Silver Spring)· June 2015

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Postprandial cardiac autonomic function in Prader-Willi syndrome.
Louise Purtell, Arthur Jenkins, Alexander Viardot, Herbert Herzog, Amanda Sainsbury, Arabella Smith

Clin Endocrinol (Oxf)· July 2013

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Chimerism and tolerance in a recipient of a deceased-donor liver transplant.
Stephen I Alexander, Neil Smith, Min Hu, Deborah Verran, Albert Shun, Arabella Smith

N Engl J Med· January 2008

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Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma.
Jothy Kandasamy, Arabella Smith, Sara Diaz, Barbara Rose, Christopher O'Brien

Cancer Genet Cytogenet· August 2007

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Mortality in Prader-Willi syndrome.
Stewart L Einfeld, Sophie J Kavanagh, Arabella Smith, Elizabeth J Evans, Bruce J Tonge

Am J Ment Retard· May 2006

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Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11).
Arabella Smith, Praboth Das, John O'Reilly, Crisoula Patsouris, Lynda J Campbell

Cancer Genet Cytogenet· April 2006

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MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.
Clelia Tiziana Storlazzi, Thoas Fioretos, Cecilia Surace, Angelo Lonoce, Angela Mastrorilli, Arabella Smith

Hum Mol Genet· March 2006

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Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader-Willi and Angelman syndrome.
Arabella Smith, Lisa Robson, Luke St Heaps

Ann Genet· November 2003

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Use of FISH in an aggressive diffuse large B cell lymphoma.
Arabella Smith, Philippa Kirkpatrick, Luke St Heaps, Praveen Sharma, Marcella Roman

Pathology· February 2003

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Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome.
Arabella Smith, Peter J Shaw, Boyd Webster, Ahti Lammi, Kevin Gaskin

Pediatr Hematol Oncol· January 2003

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Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH.
Arabella Smith, Luke St Heaps, Lisa Robson

Am J Med Genet· December 2002

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Mucoepidermoid carcinoma of the bronchus in a 15-year-old girl with complex cytogenetic rearrangement involving 11q and over-expression of cyclin D1.
Wade Barrett, Luke St Heaps, Sara Diaz, Praveen Sharma, Susan Arbuckle, Arabella Smith

Med Pediatr Oncol· July 2002

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