Publications by authors named "Pim Suwannarat"

18Publications

Epigenetics of depression.

Prog Mol Biol Transl Sci 2014 ;128:103-37

Inova Neurosciences Institute, Inova Health System, Falls Church, Virginia, USA; Department of Molecular Neuroscience, The Krasnow Institute for Advanced Study, George Mason University, Fairfax, Virginia, USA.

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http://dx.doi.org/10.1016/B978-0-12-800977-2.00005-XDOI Listing
August 2015

Aortic stenosis and vascular calcifications in alkaptonuria.

Mol Genet Metab 2012 Feb 30;105(2):198-202. Epub 2011 Oct 30.

Cardiovascular and Pulmonary Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD, USA.

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http://dx.doi.org/10.1016/j.ymgme.2011.10.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276068PMC
February 2012

A 3-year randomized therapeutic trial of nitisinone in alkaptonuria.

Mol Genet Metab 2011 Aug 6;103(4):307-14. Epub 2011 May 6.

Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.ymgme.2011.04.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148330PMC
August 2011

A novel mutation of cystathionine beta-synthase gene in a Thai boy with homocystinuria.

J Pediatr Hematol Oncol 2009 Oct;31(10):768-70

Department of Pediatrics, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

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https://insights.ovid.com/crossref?an=00043426-200910000-000
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http://dx.doi.org/10.1097/MPH.0b013e3181a32bb8DOI Listing
October 2009

Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria.

Hum Mutat 2009 Dec;30(12):1611-9

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1002/humu.21120DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830005PMC
December 2009

Musculoskeletal findings and disability in alkaptonuria.

J Rheumatol 2006 Nov 15;33(11):2280-5. Epub 2006 Sep 15.

Rehabilitation Medicine Department, Clinical Center, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA.

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November 2006

Disorders of free sialic acid.

Authors:
Pim Suwannarat

Mol Genet Metab 2005 Jun;85(2):85-7

Clinical Genetics and Biochemical Genetics, Medical Genetics Branch, National Human Genome Reseasrch Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.ymgme.2005.04.005DOI Listing
June 2005

Use of nitisinone in patients with alkaptonuria.

Metabolism 2005 Jun;54(6):719-28

Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-1852, USA.

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http://dx.doi.org/10.1016/j.metabol.2004.12.017DOI Listing
June 2005

Two novel CHS1 (LYST) mutations: clinical correlations in an infant with Chediak-Higashi syndrome.

Mol Genet Metab 2005 Jun 25;85(2):125-32. Epub 2005 Mar 25.

Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671920500074
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http://dx.doi.org/10.1016/j.ymgme.2005.02.011DOI Listing
June 2005

Blue pigmentation and arthritis in an elderly man.

J Am Acad Dermatol 2005 Jan;52(1):122-4

Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892-1908, USA.

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http://dx.doi.org/10.1016/j.jaad.2004.09.011DOI Listing
January 2005

Minocycline-induced hyperpigmentation masquerading as alkaptonuria in individuals with joint pain.

Arthritis Rheum 2004 Nov;50(11):3698-701

Section on Human Biochemical Genetics, National Human Genome Research Institute, NIH Building 10, 10 Center Drive, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1002/art.20606DOI Listing
November 2004