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Tarja Linnankivi

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American Journal of Medical Genetics. Part A|November 21, 2012
Neuroimaging and neurological findings in patients with hypochondroplasia and FGFR3 N540K mutationTarja Linnankivi, Outi Mäkitie, Leena Valanne, et al.
Developmental Medicine and Child Neurology|October 30, 2021
Visual field defects after vigabatrin treatment during infancy: retrospective population-based studyHenna Jonsson, Mikko Lehto, Sampsa Vanhatalo, et al.
Human Mutation|June 10, 2016
Splicing Defect in Mitochondrial Seryl-tRNA Synthetase Gene Causes Progressive Spastic Paresis Instead of HUPRA SyndromeTarja Linnankivi, Nirajan Neupane, Uwe Richter, et al.
Brain Communications|November 30, 2022
Networks of cortical activity in infants with epilepsySami Auno, Henna Jonsson, Tarja Linnankivi, et al.
Epilepsy & Behavior : E&B|April 2, 2025
Gaze behavior in infancy associates with developmental outcome at the age of two years in early-onset epilepsiesHenna Jonsson, Sofie de Sena, Tarja Linnankivi, et al.
American Journal of Medical Genetics. Part A|April 28, 2011
Cerebroretinal microangiopathy with calcifications and cysts: characterization of the skeletal phenotypeSanna Toiviainen-Salo, Tarja Linnankivi, Anne Saarinen, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
18q deletions: clinical, molecular, and brain MRI findings of 14 individualsTarja Linnankivi, Pentti Tienari, Mirja Somer, et al.
Epilepsia Open|May 24, 2024
Epilepsies with onset during the first year of life: A prospective study on syndromes, etiologies, and outcomesHenna Jonsson, Eija Gaily, Susanna Stjerna, et al.
American Journal of Human Genetics|March 6, 2012
Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cystsAnne Polvi, Tarja Linnankivi, Tero Kivelä, et al.
Neurology|June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactateAnna-Kaisa Anttonen, Taru Hilander, Tarja Linnankivi, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|November 21, 2012
Neuroimaging and neurological findings in patients with hypochondroplasia and FGFR3 N540K mutationTarja Linnankivi, Outi Mäkitie, Leena Valanne, et al.
Developmental Medicine and Child Neurology|October 30, 2021
Visual field defects after vigabatrin treatment during infancy: retrospective population-based studyHenna Jonsson, Mikko Lehto, Sampsa Vanhatalo, et al.
Human Mutation|June 10, 2016
Splicing Defect in Mitochondrial Seryl-tRNA Synthetase Gene Causes Progressive Spastic Paresis Instead of HUPRA SyndromeTarja Linnankivi, Nirajan Neupane, Uwe Richter, et al.
Brain Communications|November 30, 2022
Networks of cortical activity in infants with epilepsySami Auno, Henna Jonsson, Tarja Linnankivi, et al.
Epilepsy & Behavior : E&B|April 2, 2025
Gaze behavior in infancy associates with developmental outcome at the age of two years in early-onset epilepsiesHenna Jonsson, Sofie de Sena, Tarja Linnankivi, et al.
American Journal of Medical Genetics. Part A|April 28, 2011
Cerebroretinal microangiopathy with calcifications and cysts: characterization of the skeletal phenotypeSanna Toiviainen-Salo, Tarja Linnankivi, Anne Saarinen, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
18q deletions: clinical, molecular, and brain MRI findings of 14 individualsTarja Linnankivi, Pentti Tienari, Mirja Somer, et al.
Epilepsia Open|May 24, 2024
Epilepsies with onset during the first year of life: A prospective study on syndromes, etiologies, and outcomesHenna Jonsson, Eija Gaily, Susanna Stjerna, et al.
American Journal of Human Genetics|March 6, 2012
Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cystsAnne Polvi, Tarja Linnankivi, Tero Kivelä, et al.
Neurology|June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactateAnna-Kaisa Anttonen, Taru Hilander, Tarja Linnankivi, et al.
Pageof 3