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Annals of Neurology
|
March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood
Dennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Ecological Applications : a Publication of the Ecological Society of America
|
May 22, 2023
Trait-mediated responses of caterpillar communities to spongy moth outbreaks and subsequent tebufenozide treatments
Benjamin M L Leroy, Dominik Rabl, Marcel Püls, et al.
Brain & Development
|
October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs
Saskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Human Mutation
|
July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease
Julia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
Human Mutation
|
May 26, 2020
ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsy
Sarah H Elsea, Alexander Solyom, Kirt Martin, et al.
Orphanet Journal of Rare Diseases
|
October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopia
Max Lange, Burkhard Kasper, Axel Bohring, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
April 2, 2022
Red blood cell fatty acid patterns from 7 countries: Focus on the Omega-3 index
Jan Philipp Schuchardt, Marianna Cerrato, Martina Ceseri, et al.
Nature Communications
|
September 8, 2024
Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in late-onset Pompe disease
Lina Tan, Jana Zschüntzsch, Stefanie Meyer, et al.
Orphanet Journal of Rare Diseases
|
May 5, 2019
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age - a multicenter retrospective study
Afshin Saffari, Ines Brösse, Adelheid Wiemer-Kruel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 22, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
Karim Kouz, Christina Lissewski, Stephanie Spranger, et al.
Page
of 56
Search research articles
Search
Showing results (501-510 of 559) with videos related to
Sort By:
Page
of 56
Annals of Neurology
|
March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood
Dennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Ecological Applications : a Publication of the Ecological Society of America
|
May 22, 2023
Trait-mediated responses of caterpillar communities to spongy moth outbreaks and subsequent tebufenozide treatments
Benjamin M L Leroy, Dominik Rabl, Marcel Püls, et al.
Brain & Development
|
October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs
Saskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Human Mutation
|
July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease
Julia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
Human Mutation
|
May 26, 2020
ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsy
Sarah H Elsea, Alexander Solyom, Kirt Martin, et al.
Orphanet Journal of Rare Diseases
|
October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopia
Max Lange, Burkhard Kasper, Axel Bohring, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
April 2, 2022
Red blood cell fatty acid patterns from 7 countries: Focus on the Omega-3 index
Jan Philipp Schuchardt, Marianna Cerrato, Martina Ceseri, et al.
Nature Communications
|
September 8, 2024
Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in late-onset Pompe disease
Lina Tan, Jana Zschüntzsch, Stefanie Meyer, et al.
Orphanet Journal of Rare Diseases
|
May 5, 2019
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age - a multicenter retrospective study
Afshin Saffari, Ines Brösse, Adelheid Wiemer-Kruel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 22, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
Karim Kouz, Christina Lissewski, Stephanie Spranger, et al.
Page
of 56