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Maria Dahlin

Showing results (21-30 of 42) with videos related to

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Jvs-Vascular Science|October 7, 2021
Resolving the biological paradox of aneurysm formation in children with tuberous sclerosis complexUlf Hedin, Hans Brunnström, Maria Dahlin, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Copy number variations in children with brain malformations and refractory epilepsyJosephine Wincent, Sintia Kolbjer, Daniel Martin, et al.
Ebiomedicine|May 22, 2022
Higher levels of Bifidobacteria and tumor necrosis factor in children with drug-resistant epilepsy are associated with anti-seizure response to the ketogenic dietMaria Dahlin, Stephanie S Singleton, John A David, et al.
Brain Communications|August 24, 2023
Polymicrogyria: epidemiology, imaging, and clinical aspects in a population-based cohortSintia Kolbjer, Daniel A Martín Muñoz, Anne K Örtqvist, et al.
Journal of Inherited Metabolic Disease|December 7, 2021
Novel imaging findings in pyruvate dehydrogenase complex (PDHc) deficiency-Results from a nationwide population-based studyAntri Savvidou, Liz Ivarsson, Karin Naess, et al.
Cell Metabolism|August 6, 2008
The circulating metabolic regulator FGF21 is induced by prolonged fasting and PPARalpha activation in manCecilia Gälman, Tomas Lundåsen, Alexei Kharitonenkov, et al.
NPJ Biofilms and Microbiomes|February 1, 2019
The ketogenic diet influences taxonomic and functional composition of the gut microbiota in children with severe epilepsyMarie Lindefeldt, Alexander Eng, Hamid Darban, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 2, 2010
Circulating proprotein convertase subtilisin kexin type 9 has a diurnal rhythm synchronous with cholesterol synthesis and is reduced by fasting in humansLena Persson, Guoqing Cao, Lars Ståhle, et al.
Orphanet Journal of Rare Diseases|November 27, 2014
TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complexJohn C Kingswood, Paolo Bruzzi, Paolo Curatolo, et al.
Orphanet Journal of Rare Diseases|July 7, 2021
Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)Matthias Sauter, Elena Belousova, Mirjana P Benedik, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Jvs-Vascular Science|October 7, 2021
Resolving the biological paradox of aneurysm formation in children with tuberous sclerosis complexUlf Hedin, Hans Brunnström, Maria Dahlin, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Copy number variations in children with brain malformations and refractory epilepsyJosephine Wincent, Sintia Kolbjer, Daniel Martin, et al.
Ebiomedicine|May 22, 2022
Higher levels of Bifidobacteria and tumor necrosis factor in children with drug-resistant epilepsy are associated with anti-seizure response to the ketogenic dietMaria Dahlin, Stephanie S Singleton, John A David, et al.
Brain Communications|August 24, 2023
Polymicrogyria: epidemiology, imaging, and clinical aspects in a population-based cohortSintia Kolbjer, Daniel A Martín Muñoz, Anne K Örtqvist, et al.
Journal of Inherited Metabolic Disease|December 7, 2021
Novel imaging findings in pyruvate dehydrogenase complex (PDHc) deficiency-Results from a nationwide population-based studyAntri Savvidou, Liz Ivarsson, Karin Naess, et al.
Cell Metabolism|August 6, 2008
The circulating metabolic regulator FGF21 is induced by prolonged fasting and PPARalpha activation in manCecilia Gälman, Tomas Lundåsen, Alexei Kharitonenkov, et al.
NPJ Biofilms and Microbiomes|February 1, 2019
The ketogenic diet influences taxonomic and functional composition of the gut microbiota in children with severe epilepsyMarie Lindefeldt, Alexander Eng, Hamid Darban, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 2, 2010
Circulating proprotein convertase subtilisin kexin type 9 has a diurnal rhythm synchronous with cholesterol synthesis and is reduced by fasting in humansLena Persson, Guoqing Cao, Lars Ståhle, et al.
Orphanet Journal of Rare Diseases|November 27, 2014
TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complexJohn C Kingswood, Paolo Bruzzi, Paolo Curatolo, et al.
Orphanet Journal of Rare Diseases|July 7, 2021
Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)Matthias Sauter, Elena Belousova, Mirjana P Benedik, et al.
Pageof 5