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European Urology
|
October 3, 2018
Radiofrequency-induced Thermo-chemotherapy Effect Versus a Second Course of Bacillus Calmette-Guérin or Institutional Standard in Patients with Recurrence of Non-muscle-invasive Bladder Cancer Following Induction or Maintenance Bacillus Calmette-Guérin Therapy (HYMN): A Phase III, Open-label, Randomised Controlled Trial
Wei Shen Tan, Anesh Panchal, Laura Buckley, et al.
Epilepsia
|
January 7, 2021
The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy
Alexandre N Datta, Nadia Bahi-Buisson, Thierry Bienvenu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 7, 2019
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome
Thomas Besnard, Natacha Sloboda, Alice Goldenberg, et al.
Annals of Clinical and Translational Neurology
|
April 26, 2019
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice
Milka Pringsheim, Diana Mitter, Simone Schröder, et al.
Biomedicines
|
October 31, 2020
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood
Jan Henje Döring, Afshin Saffari, Thomas Bast, et al.
Vaccine
|
August 21, 2018
Narcolepsy and adjuvanted pandemic influenza A (H1N1) 2009 vaccines - Multi-country assessment
Daniel Weibel, Miriam Sturkenboom, Steven Black, et al.
Neurology
|
July 5, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in <i>STXBP1</i>
Kim M Thalwitzer, Jan H Driedger, Julie Xian, et al.
Neurology
|
October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>
Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.
Nature Genetics
|
August 13, 2013
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Johannes R Lemke, Dennis Lal, Eva M Reinthaler, et al.
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Showing results (421-430 of 429) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 429 results.
European Urology
|
October 3, 2018
Radiofrequency-induced Thermo-chemotherapy Effect Versus a Second Course of Bacillus Calmette-Guérin or Institutional Standard in Patients with Recurrence of Non-muscle-invasive Bladder Cancer Following Induction or Maintenance Bacillus Calmette-Guérin Therapy (HYMN): A Phase III, Open-label, Randomised Controlled Trial
Wei Shen Tan, Anesh Panchal, Laura Buckley, et al.
Epilepsia
|
January 7, 2021
The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy
Alexandre N Datta, Nadia Bahi-Buisson, Thierry Bienvenu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 7, 2019
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome
Thomas Besnard, Natacha Sloboda, Alice Goldenberg, et al.
Annals of Clinical and Translational Neurology
|
April 26, 2019
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice
Milka Pringsheim, Diana Mitter, Simone Schröder, et al.
Biomedicines
|
October 31, 2020
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood
Jan Henje Döring, Afshin Saffari, Thomas Bast, et al.
Vaccine
|
August 21, 2018
Narcolepsy and adjuvanted pandemic influenza A (H1N1) 2009 vaccines - Multi-country assessment
Daniel Weibel, Miriam Sturkenboom, Steven Black, et al.
Neurology
|
July 5, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in <i>STXBP1</i>
Kim M Thalwitzer, Jan H Driedger, Julie Xian, et al.
Neurology
|
October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>
Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.
Nature Genetics
|
August 13, 2013
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Johannes R Lemke, Dennis Lal, Eva M Reinthaler, et al.
Page
of 43