Danijela Petkovic Ramadža

Danijela Petkovic Ramadža

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Danijela Petkovic Ramadža

Danijela Petkovic Ramadža

Publications by authors named "Danijela Petkovic Ramadža"

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Molecular basis and clinical presentation of classic galactosemia in a Croatian population.

J Pediatr Endocrinol Metab 2018 Jan;31(1):71-75

Metabolism and Genetics Group, Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.

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http://dx.doi.org/10.1515/jpem-2017-0302DOI Listing
January 2018

Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.

J Inherit Metab Dis 2017 01 26;40(1):5-20. Epub 2016 Sep 26.

Laboratory of Clinical Biochemistry and Metabolism, Department of General Pediatrics Adolescent Medicine and Neonatology, University Medical Centre Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.1007/s10545-016-9972-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203850PMC
January 2017

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

Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene.

Coll Antropol 2009 Dec;33(4):1255-8

Department of Pediatrics, University Hospital Center Zagreb, Zagreb, Croatia.

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December 2009