Publications by authors named "Haide Poder"

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Clinical severity and cardiac phenotype in phosphomannomutase 2-congenital disorders of glycosylation : Insights into genetics and management recommendations.
Veronika Holubova, Rita Barone, Stephanie Grunewald, Markéta Tesařová, Hana Hansíková

J Inherit Metab Dis· January 2025

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The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia.
Siiri Sarv, Tiina Kahre, Eve Vaidla, Sander Pajusalu, Kai Muru

Front Genet· December 2021

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De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion.
Sander Pajusalu, Inga Talvik, Klari Noormets, Tiina Talvik, Haide Põder

Neuromuscul Disord· March 2016

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Outcome of infants with inflicted traumatic brain injury (shaken baby syndrome) in Estonia.
Inga Talvik, Mairi Männamaa, Piret Jüri, Kaja Leito, Haide Põder

Acta Paediatr· August 2007

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Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented.
Eve Oiglane-Shlik, Tiina Talvik, Riina Zordania, Haide Põder, Tiina Kahre

Am J Med Genet A· September 2006

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Inflicted traumatic brain injury (ITBI) or shaken baby syndrome (SBS) in Estonia.
Inga Talvik, Tuuli Metsvaht, Kaja Leito, Haide Põder, Pille Kool

Acta Paediatr· July 2006

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