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Martin Smitka

Showing results (11-20 of 40) with videos related to

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Clinical and Experimental Rheumatology|April 5, 2017
Childhood primary large vessel CNS vasculitis: single-centre experience and review of the literatureSonja Walsh, Ralf Knöfler, Gabriele Hahn, et al.
Annals of the Rheumatic Diseases|November 5, 2016
Response to: 'JAK inhibition in STING-associated interferonopathy' by Crow et alVictoria Tüngler, Nadja König, Claudia Günther, et al.
The Journal of Pediatrics|November 26, 2019
The Clinical and Molecular Spectrum of GM1 GangliosidosisLaila Arash-Kaps, Katalin Komlosi, Marlene Seegräber, et al.
Frontiers in Pediatrics|October 29, 2021
Diagnosis and Treatment of Small Vessel Childhood Primary Angiitis of the Central Nervous System (sv-cPACNS): An International SurveyPaul Keenan, Jürgen Brunner, Angela S Quan, et al.
Annals of Neurology|November 11, 2008
Sedative and anticonvulsant drugs suppress postnatal neurogenesisVanya G Stefovska, Ortrud Uckermann, Miroslaw Czuczwar, et al.
Frontiers in Pediatrics|April 12, 2021
Diagnosis and Treatment of Angiography Positive Medium to Large Vessel Childhood Primary Angiitis of Central Nervous System (p-cPACNS): An International SurveyAngela S Quan, Jürgen Brunner, Benjamin Rose, et al.
Neuropediatrics|October 19, 2019
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular DisordersMaja von der Hagen, Lena-Luise Becker, Thomas F Wienker, et al.
Brain & Development|March 1, 2016
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutationKatharina Sell, Katja Storch, Gabriele Hahn, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 10, 2017
Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR geneLisa Schmelzer, Martin Smitka, Christine Wolf, et al.
Rheumatology (Oxford, England)|November 17, 2020
Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?André Heinen, Anja Schnabel, Normi Brück, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Clinical and Experimental Rheumatology|April 5, 2017
Childhood primary large vessel CNS vasculitis: single-centre experience and review of the literatureSonja Walsh, Ralf Knöfler, Gabriele Hahn, et al.
Annals of the Rheumatic Diseases|November 5, 2016
Response to: 'JAK inhibition in STING-associated interferonopathy' by Crow et alVictoria Tüngler, Nadja König, Claudia Günther, et al.
The Journal of Pediatrics|November 26, 2019
The Clinical and Molecular Spectrum of GM1 GangliosidosisLaila Arash-Kaps, Katalin Komlosi, Marlene Seegräber, et al.
Frontiers in Pediatrics|October 29, 2021
Diagnosis and Treatment of Small Vessel Childhood Primary Angiitis of the Central Nervous System (sv-cPACNS): An International SurveyPaul Keenan, Jürgen Brunner, Angela S Quan, et al.
Annals of Neurology|November 11, 2008
Sedative and anticonvulsant drugs suppress postnatal neurogenesisVanya G Stefovska, Ortrud Uckermann, Miroslaw Czuczwar, et al.
Frontiers in Pediatrics|April 12, 2021
Diagnosis and Treatment of Angiography Positive Medium to Large Vessel Childhood Primary Angiitis of Central Nervous System (p-cPACNS): An International SurveyAngela S Quan, Jürgen Brunner, Benjamin Rose, et al.
Neuropediatrics|October 19, 2019
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular DisordersMaja von der Hagen, Lena-Luise Becker, Thomas F Wienker, et al.
Brain & Development|March 1, 2016
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutationKatharina Sell, Katja Storch, Gabriele Hahn, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 10, 2017
Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR geneLisa Schmelzer, Martin Smitka, Christine Wolf, et al.
Rheumatology (Oxford, England)|November 17, 2020
Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?André Heinen, Anja Schnabel, Normi Brück, et al.
Pageof 4