David A Whiteman

David A H Whiteman

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David A Whiteman

David A H Whiteman

Publications by authors named "David A H Whiteman"

15Publications

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1PubMed Central Citations

Development of a mnemonic screening tool for identifying subjects with Hunter syndrome.

Eur J Pediatr 2013 Jul 7;172(7):965-70. Epub 2013 Mar 7.

Global Medical Affairs Shire Human Genetic Therapies, Inc, 300 Shire Way, Lexington, MA 02421, USA.

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http://dx.doi.org/10.1007/s00431-013-1967-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701787PMC
July 2013

The Hunter syndrome-functional outcomes for clinical understanding scale (HS-FOCUS) questionnaire: evaluation of measurement properties.

Qual Life Res 2013 May 19;22(4):875-84. Epub 2012 May 19.

United BioSource Corporation, 26-28 Hammersmith Grove, London, W6 7HA, UK.

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http://dx.doi.org/10.1007/s11136-012-0196-5DOI Listing
May 2013

Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS).

Mol Genet Metab 2011 Jun 4;103(2):113-20. Epub 2011 Mar 4.

Dept. of Pediatrics, Northwestern University Feinberg School of Medicine, Children's Memorial Hospital, 2300 Children's Plaza, Chicago, IL 60614, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671921100061
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http://dx.doi.org/10.1016/j.ymgme.2011.02.018DOI Listing
June 2011

Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.

Genet Med 2006 Oct;8(10):641-52

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://dx.doi.org/10.109701.gim.0000237781.10594.d1DOI Listing
October 2006

Diagnosis and management of defects of mitochondrial beta-oxidation.

Curr Opin Clin Nutr Metab Care 2002 Nov;5(6):601-9

Department of Medical Genetics and Department of Biochemistry and Molecular Biology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1097/01.mco.0000038807.16540.9bDOI Listing
November 2002

Primer on medical genomics part I: History of genetics and sequencing of the human genome.

Mayo Clin Proc 2002 Aug;77(8):773-82

Division of Laboratory Genetics, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.8.773DOI Listing
August 2002

Primer on medical genomics part II: Background principles and methods in molecular genetics.

Mayo Clin Proc 2002 Aug;77(8):785-808

Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.8.785DOI Listing
August 2002

Ehlers-Danlos syndrome type IV and a novel mutation of the type III procollagen gene as a cause of abdominal apoplexy.

Mayo Clin Proc 2002 Aug;77(8):861-3

Division of Vascular Surgery, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.8.861DOI Listing
August 2002

Defects of mitochondrial beta-oxidation: a growing group of disorders.

Neuromuscul Disord 2002 Mar;12(3):235-46

Department of Medical Genetics, Mayo Clinic and Foundation, 200 First Street, SW, Rochester, MN 55905, USA.

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March 2002