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Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
January 22, 2008
Developmental changes in cerebral and visceral blood flow velocity in healthy neonates and infants
Pilvi Ilves, Mare Lintrop, Inga Talvik, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
November 20, 2008
Low cerebral blood flow velocity and head circumference in infants with severe hypoxic ischemic encephalopathy and poor outcome
Pilvi Ilves, Mare Lintrop, Inga Talvik, et al.
European Journal of Medical Genetics
|
April 8, 2014
Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome
Olga Zilina, Tiina Kahre, Inga Talvik, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 21, 2007
Outcome of infants with inflicted traumatic brain injury (shaken baby syndrome) in Estonia
Inga Talvik, Mairi Männamaa, Piret Jüri, et al.
European Journal of Medical Genetics
|
April 25, 2015
De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis
Sander Pajusalu, Tiia Reimand, Oivi Uibo, et al.
Journal of Child Neurology
|
July 5, 2007
Neonatal spinal muscular atrophy type 1 with bone fractures and heart defect
Eve Vaidla, Inga Talvik, Andres Kulla, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 27, 2003
A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia
Ulvi-Astra Talkop, Tiina Kahre, Aita Napa, et al.
Neuroepidemiology
|
October 13, 2006
Descriptive epidemiology of spinal muscular atrophy type I in Estonia
Eve Vaidla, Inga Talvik, Andres Kulla, et al.
Neuropediatrics
|
September 7, 2016
CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature
Stella Lilles, Inga Talvik, Klari Noormets, et al.
Journal of Child Neurology
|
October 9, 2015
Presumed Perinatal Stroke: Risk Factors, Clinical and Radiological Findings
Pilvi Ilves, Rael Laugesaar, Dagmar Loorits, et al.
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of 6
Search research articles
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Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
January 22, 2008
Developmental changes in cerebral and visceral blood flow velocity in healthy neonates and infants
Pilvi Ilves, Mare Lintrop, Inga Talvik, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
November 20, 2008
Low cerebral blood flow velocity and head circumference in infants with severe hypoxic ischemic encephalopathy and poor outcome
Pilvi Ilves, Mare Lintrop, Inga Talvik, et al.
European Journal of Medical Genetics
|
April 8, 2014
Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome
Olga Zilina, Tiina Kahre, Inga Talvik, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 21, 2007
Outcome of infants with inflicted traumatic brain injury (shaken baby syndrome) in Estonia
Inga Talvik, Mairi Männamaa, Piret Jüri, et al.
European Journal of Medical Genetics
|
April 25, 2015
De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis
Sander Pajusalu, Tiia Reimand, Oivi Uibo, et al.
Journal of Child Neurology
|
July 5, 2007
Neonatal spinal muscular atrophy type 1 with bone fractures and heart defect
Eve Vaidla, Inga Talvik, Andres Kulla, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 27, 2003
A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia
Ulvi-Astra Talkop, Tiina Kahre, Aita Napa, et al.
Neuroepidemiology
|
October 13, 2006
Descriptive epidemiology of spinal muscular atrophy type I in Estonia
Eve Vaidla, Inga Talvik, Andres Kulla, et al.
Neuropediatrics
|
September 7, 2016
CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature
Stella Lilles, Inga Talvik, Klari Noormets, et al.
Journal of Child Neurology
|
October 9, 2015
Presumed Perinatal Stroke: Risk Factors, Clinical and Radiological Findings
Pilvi Ilves, Rael Laugesaar, Dagmar Loorits, et al.
Page
of 6