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Inga Talvik

Showing results (31-40 of 51) with videos related to

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Neuromuscular Disorders : NMD|October 26, 2002
Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophyUlvi Astra Talkop, Inga Talvik, Margit Sõnajalg, et al.
Neural Plasticity|January 12, 2017
Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal StrokeNigul Ilves, Pilvi Ilves, Rael Laugesaar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 18, 2014
Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalitiesEve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, et al.
Epilepsy Research|March 30, 2013
Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipinKadi Veri, Oivi Uibo, Tiina Talvik, et al.
Frontiers in Genetics|January 10, 2022
The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in EstoniaSiiri Sarv, Tiina Kahre, Eve Vaidla, et al.
Journal of Child Neurology|December 20, 2013
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disordersUlvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.
Journal of Child Neurology|June 5, 2018
Incidence of Childhood Epilepsy in EstoniaKadi Veri, Inga Talvik, Ulvi Vaher, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophyKarit Reinson, Eve Õiglane-Shlik, Inga Talvik, et al.
Neuromuscular Disorders : NMD|January 20, 2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportionSander Pajusalu, Inga Talvik, Klari Noormets, et al.
European Journal of Human Genetics : EJHG|January 19, 2018
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiencySanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|October 26, 2002
Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophyUlvi Astra Talkop, Inga Talvik, Margit Sõnajalg, et al.
Neural Plasticity|January 12, 2017
Resting-State Functional Connectivity and Cognitive Impairment in Children with Perinatal StrokeNigul Ilves, Pilvi Ilves, Rael Laugesaar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 18, 2014
Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalitiesEve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, et al.
Epilepsy Research|March 30, 2013
Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipinKadi Veri, Oivi Uibo, Tiina Talvik, et al.
Frontiers in Genetics|January 10, 2022
The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in EstoniaSiiri Sarv, Tiina Kahre, Eve Vaidla, et al.
Journal of Child Neurology|December 20, 2013
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disordersUlvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.
Journal of Child Neurology|June 5, 2018
Incidence of Childhood Epilepsy in EstoniaKadi Veri, Inga Talvik, Ulvi Vaher, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophyKarit Reinson, Eve Õiglane-Shlik, Inga Talvik, et al.
Neuromuscular Disorders : NMD|January 20, 2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportionSander Pajusalu, Inga Talvik, Klari Noormets, et al.
European Journal of Human Genetics : EJHG|January 19, 2018
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiencySanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Pageof 6