Publications by authors named "Haide Põder"

4Publications

De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion.

Neuromuscul Disord 2016 Mar 3;26(3):236-9. Epub 2015 Dec 3.

Department of Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia; Institute of Biomedicine and Translational Medicine, Department of Biomedicine, University of Tartu, Tartu, Estonia; Department of Pediatrics, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.nmd.2015.11.011DOI Listing
March 2016

Outcome of infants with inflicted traumatic brain injury (shaken baby syndrome) in Estonia.

Acta Paediatr 2007 Aug 18;96(8):1164-8. Epub 2007 Jun 18.

Children's Clinic of Tartu University Hospital, Tartu, Estonia.

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http://dx.doi.org/10.1111/j.1651-2227.2007.00362.xDOI Listing
August 2007