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Brain : a Journal of Neurology
|
November 17, 2021
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies
Sathiya N Manivannan, Jolien Roovers, Noor Smal, et al.
Journal of Investigational Allergology & Clinical Immunology
|
September 22, 2020
Cumulative Pollen Concentration Curves for Pollen Allergy Diagnosis
T M Hoffmann, A Travaglini, M A Brighetti, et al.
American Journal of Human Genetics
|
November 12, 2013
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
Arvid Suls, Johanna A Jaehn, Angela Kecskés, et al.
Brain : a Journal of Neurology
|
October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies
Silvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.
Molecular Genetics & Genomic Medicine
|
July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutations
Tania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Nature Genetics
|
March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
January 24, 2026
Early Detection of Lower Adherence to Long-Term e-Diary Recording: A Checkpoint to Target Early Educational Intervention in Seasonal Allergic Rhinitis?
S Dramburg, C J Hernandez Toro, U Grittner, et al.
Allergy
|
February 5, 2024
Heterogeneity of sensitization profiles and clinical phenotypes among patients with seasonal allergic rhinitis in Southern European countries-The @IT.2020 multicenter study
S Dramburg, U Grittner, E Potapova, et al.
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Search research articles
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Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Brain : a Journal of Neurology
|
November 17, 2021
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies
Sathiya N Manivannan, Jolien Roovers, Noor Smal, et al.
Journal of Investigational Allergology & Clinical Immunology
|
September 22, 2020
Cumulative Pollen Concentration Curves for Pollen Allergy Diagnosis
T M Hoffmann, A Travaglini, M A Brighetti, et al.
American Journal of Human Genetics
|
November 12, 2013
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
Arvid Suls, Johanna A Jaehn, Angela Kecskés, et al.
Brain : a Journal of Neurology
|
October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies
Silvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.
Molecular Genetics & Genomic Medicine
|
July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutations
Tania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Nature Genetics
|
March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
January 24, 2026
Early Detection of Lower Adherence to Long-Term e-Diary Recording: A Checkpoint to Target Early Educational Intervention in Seasonal Allergic Rhinitis?
S Dramburg, C J Hernandez Toro, U Grittner, et al.
Allergy
|
February 5, 2024
Heterogeneity of sensitization profiles and clinical phenotypes among patients with seasonal allergic rhinitis in Southern European countries-The @IT.2020 multicenter study
S Dramburg, U Grittner, E Potapova, et al.
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