Search research articles
Contact Us
Filters
Showing results (371-380 of 379) with videos related to
Page
of 38
Sort By:
You have reached the last page of results.
This site can display upto 379 results.
Neurology
|
March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants
Niklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
European Journal of Cancer (Oxford, England : 1990)
|
June 5, 2023
Long-term survival with IDH wildtype glioblastoma: first results from the ETERNITY Brain Tumor Funders' Collaborative Consortium (EORTC 1419)
Caroline Hertler, Jörg Felsberg, Dorothee Gramatzki, et al.
Neurology
|
December 31, 2017
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
Mark McCormack, Hongsheng Gui, Andrés Ingason, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Structural mapping of GABRB3 variants reveals genotype-phenotype correlations
Katrine M Johannesen, Sumaiya Iqbal, Milena Guazzi, et al.
Nature Communications
|
October 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
Rahel T Florian, Florian Kraft, Elsa Leitão, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
March 28, 2016
Moving the mandible in orthognathic surgery - A multicenter analysis
Oliver C Thiele, Matthias Kreppel, Gido Bittermann, et al.
Nature Communications
|
October 31, 2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Mark A Corbett, Thessa Kroes, Liana Veneziano, et al.
Brain : a Journal of Neurology
|
August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Katrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Page
of 38
Search research articles
Search
Showing results (371-380 of 379) with videos related to
Sort By:
Page
of 38
You have reached the last page of results.
This site can display upto 379 results.
Neurology
|
March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants
Niklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
European Journal of Cancer (Oxford, England : 1990)
|
June 5, 2023
Long-term survival with IDH wildtype glioblastoma: first results from the ETERNITY Brain Tumor Funders' Collaborative Consortium (EORTC 1419)
Caroline Hertler, Jörg Felsberg, Dorothee Gramatzki, et al.
Neurology
|
December 31, 2017
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
Mark McCormack, Hongsheng Gui, Andrés Ingason, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Structural mapping of GABRB3 variants reveals genotype-phenotype correlations
Katrine M Johannesen, Sumaiya Iqbal, Milena Guazzi, et al.
Nature Communications
|
October 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
Rahel T Florian, Florian Kraft, Elsa Leitão, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
March 28, 2016
Moving the mandible in orthognathic surgery - A multicenter analysis
Oliver C Thiele, Matthias Kreppel, Gido Bittermann, et al.
Nature Communications
|
October 31, 2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Mark A Corbett, Thessa Kroes, Liana Veneziano, et al.
Brain : a Journal of Neurology
|
August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Katrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Page
of 38