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Human Molecular Genetics
|
August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly
Muhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
Bone Marrow Transplantation
|
April 25, 2017
High-dose thiotepa-based chemotherapy with autologous stem cell support in elderly patients with primary central nervous system lymphoma: a European retrospective study
E Schorb, C P Fox, K Fritsch, et al.
Epilepsia
|
October 17, 2023
Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany
Margarita Maltseva, Felix Rosenow, Susanne Schubert-Bast, et al.
Orphanet Journal of Rare Diseases
|
April 29, 2023
Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany
Margarita Maltseva, Susanne Schubert-Bast, Johann Philipp Zöllner, et al.
Molecular Cancer
|
March 28, 2026
[<sup>18</sup>F]FDG PET/CT multiomics identifies Hedgehog-driven HPV-negative head and neck squamous cell carcinoma
Stefan Stoiber, Daniel Pölöske, Clemens P Spielvogel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 16, 2019
Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany
Adam Strzelczyk, Malin Kalski, Thomas Bast, et al.
Journal of Clinical Medicine
|
August 12, 2023
Implementation and Assessment of a Laparotomy-Assisted Three-Port Fetoscopic Spina Bifida Repair Program
Corinna Keil, Siegmund Köhler, Benjamin Sass, et al.
Annals of Neurology
|
March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood
Dennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Epilepsy Research
|
July 30, 2015
Investigation of GRIN2A in common epilepsy phenotypes
Dennis Lal, Sandra Steinbrücker, Julian Schubert, et al.
Epilepsia
|
January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
Dennis Lal, Holger Trucks, Rikke S Møller, et al.
Page
of 56
Search research articles
Search
Showing results (491-500 of 554) with videos related to
Sort By:
Page
of 56
Human Molecular Genetics
|
August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly
Muhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
Bone Marrow Transplantation
|
April 25, 2017
High-dose thiotepa-based chemotherapy with autologous stem cell support in elderly patients with primary central nervous system lymphoma: a European retrospective study
E Schorb, C P Fox, K Fritsch, et al.
Epilepsia
|
October 17, 2023
Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany
Margarita Maltseva, Felix Rosenow, Susanne Schubert-Bast, et al.
Orphanet Journal of Rare Diseases
|
April 29, 2023
Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany
Margarita Maltseva, Susanne Schubert-Bast, Johann Philipp Zöllner, et al.
Molecular Cancer
|
March 28, 2026
[<sup>18</sup>F]FDG PET/CT multiomics identifies Hedgehog-driven HPV-negative head and neck squamous cell carcinoma
Stefan Stoiber, Daniel Pölöske, Clemens P Spielvogel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 16, 2019
Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany
Adam Strzelczyk, Malin Kalski, Thomas Bast, et al.
Journal of Clinical Medicine
|
August 12, 2023
Implementation and Assessment of a Laparotomy-Assisted Three-Port Fetoscopic Spina Bifida Repair Program
Corinna Keil, Siegmund Köhler, Benjamin Sass, et al.
Annals of Neurology
|
March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood
Dennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Epilepsy Research
|
July 30, 2015
Investigation of GRIN2A in common epilepsy phenotypes
Dennis Lal, Sandra Steinbrücker, Julian Schubert, et al.
Epilepsia
|
January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
Dennis Lal, Holger Trucks, Rikke S Møller, et al.
Page
of 56