Wanda Gradowska

Wanda Gradowska

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Wanda Gradowska

Wanda Gradowska

Publications by authors named "Wanda Gradowska"

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Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.

J Inherit Metab Dis 2015 Nov;38(6):1157-8

Hospital San Joan de Deu, Servicio de Neurologia and CIBERER, ISCIII, Barcelona, Spain.

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http://link.springer.com/content/pdf/10.1007%2Fs10545-015-98
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http://link.springer.com/10.1007/s10545-015-9868-y
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http://dx.doi.org/10.1007/s10545-015-9868-yDOI Listing
November 2015

Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient.

J Inherit Metab Dis 2010 Dec 14;33 Suppl 3:S21-4. Epub 2010 Jan 14.

Department of Metabolic Diseases, Endocrinology and Diabetology, The Children's Memorial Health Institute, Al Dzieci Polskich 20, 04-730 Warsaw, Poland.

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http://dx.doi.org/10.1007/s10545-009-9011-zDOI Listing
December 2010

Aminoacylase 1 deficiency associated with autistic behavior.

J Inherit Metab Dis 2010 Dec 18;33 Suppl 3:S211-4. Epub 2010 May 18.

Department of Metabolic Diseases, Endocrinology and Diabetology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.

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http://dx.doi.org/10.1007/s10545-010-9089-3DOI Listing
December 2010

Evaluation of somatic development in adult patients with previously undiagnosed and/or untreated phenylketonuria.

Med Princ Pract 2010 9;19(1):46-50. Epub 2009 Dec 9.

Department of Physiotherapy, Faculty of Medicine, University of Rzeszów, Rzeszów, Poland.

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http://dx.doi.org/10.1159/000252834DOI Listing
April 2010

Investigation of a wide spectrum of inherited metabolic disorders by 13C NMR spectroscopy.

Acta Biochim Pol 2008 23;55(1):107-18. Epub 2008 Jan 23.

Faculty of Chemistry, Warsaw University of Technology, Warszawa, Poland.

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September 2008

Clinical, biochemical and molecular findings in seven Polish patients with adenylosuccinate lyase deficiency.

Mol Genet Metab 2008 Aug 3;94(4):435-42. Epub 2008 Jun 3.

Department of Metabolic Diseases, Endocrinology and Diabetology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.

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http://dx.doi.org/10.1016/j.ymgme.2008.04.013DOI Listing
August 2008

Biochemical and clinical characteristics of creatine deficiency syndromes.

Acta Biochim Pol 2004 ;51(4):875-82

Division of Metabolic Diseases, Department of Pedatrics, Children's Memorial Health Institute, Warsaw, Poland.

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http://dx.doi.org/045104875DOI Listing
August 2005

Characterisation of the 1H and 13C NMR spectra of N-acetylaspartylglutamate and its detection in urine from patients with Canavan disease.

J Pharm Biomed Anal 2003 Mar;31(3):455-63

Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw, Poland.

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http://dx.doi.org/10.1016/s0731-7085(02)00691-xDOI Listing
March 2003

Determination of the absolute configuration of 2-hydroxyglutaric acid and 5-oxoproline in urine samples by high-resolution NMR spectroscopy in the presence of chiral lanthanide complexes.

J Pharm Biomed Anal 2002 Jun;28(6):1061-71

Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, Warsaw, Poland.

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http://dx.doi.org/10.1016/s0731-7085(02)00032-8DOI Listing
June 2002