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American Journal of Human Genetics
|
October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)
C Donger, E Krejci, A P Serradell, et al.
Neurosurgery
|
April 27, 2020
Letter: Maintaining Neurosurgical Resident Education and Safety During the COVID-19 Pandemic
David P Bray, Geoffrey P Stricsek, James Malcolm, et al.
World Neurosurgery
|
February 21, 2022
Telemedicine in Spine Surgery: Outcomes for 138 Patients With Virtual Preoperative Assessment Compared to Historical Controls
Alexander C M Greven, Beau M McGinley, Anudeep S Nakirikanti, et al.
Nature Genetics
|
February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
N Neyroud, F Tesson, I Denjoy, et al.
Diabetes & Metabolism
|
November 2, 2019
Performance of a selective screening strategy for diagnosis of hyperglycaemia in pregnancy as defined by IADPSG/WHO criteria
E Cosson, E Vicaut, D Sandre-Banon, et al.
Cureus
|
September 11, 2023
Comparing Cortical Bone Trajectory and Traditional Pedicle Screws in Transforaminal Lumbar Interbody Fusion: A Retrospective Cohort Study of One-Year Outcomes
Juanmarco Gutierrez, Andrew M Erwood, James G Malcolm, et al.
Journal of Medical Genetics
|
July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy
P Richard, R Isnard, L Carrier, et al.
American Journal of Obstetrics and Gynecology
|
June 13, 2017
Frequency and consequences of ventricular hypertrophy in pregnant women with treated chronic hypertension
Anne M Ambia, Jamie L Morgan, Karen L Wilson, et al.
Spine
|
November 13, 2020
Telemedicine in the Evaluation and Management of Neurosurgical Spine Patients: Questionnaire Assessment of 346 Consecutive Patients
Alexander C M Greven, Beau M McGinley, Ndeye F Guisse, et al.
Heart (British Cardiac Society)
|
March 8, 2011
Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy
E Gandjbakhch, P Charron, V Fressart, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 145) with videos related to
Sort By:
Page
of 15
American Journal of Human Genetics
|
October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)
C Donger, E Krejci, A P Serradell, et al.
Neurosurgery
|
April 27, 2020
Letter: Maintaining Neurosurgical Resident Education and Safety During the COVID-19 Pandemic
David P Bray, Geoffrey P Stricsek, James Malcolm, et al.
World Neurosurgery
|
February 21, 2022
Telemedicine in Spine Surgery: Outcomes for 138 Patients With Virtual Preoperative Assessment Compared to Historical Controls
Alexander C M Greven, Beau M McGinley, Anudeep S Nakirikanti, et al.
Nature Genetics
|
February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
N Neyroud, F Tesson, I Denjoy, et al.
Diabetes & Metabolism
|
November 2, 2019
Performance of a selective screening strategy for diagnosis of hyperglycaemia in pregnancy as defined by IADPSG/WHO criteria
E Cosson, E Vicaut, D Sandre-Banon, et al.
Cureus
|
September 11, 2023
Comparing Cortical Bone Trajectory and Traditional Pedicle Screws in Transforaminal Lumbar Interbody Fusion: A Retrospective Cohort Study of One-Year Outcomes
Juanmarco Gutierrez, Andrew M Erwood, James G Malcolm, et al.
Journal of Medical Genetics
|
July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy
P Richard, R Isnard, L Carrier, et al.
American Journal of Obstetrics and Gynecology
|
June 13, 2017
Frequency and consequences of ventricular hypertrophy in pregnant women with treated chronic hypertension
Anne M Ambia, Jamie L Morgan, Karen L Wilson, et al.
Spine
|
November 13, 2020
Telemedicine in the Evaluation and Management of Neurosurgical Spine Patients: Questionnaire Assessment of 346 Consecutive Patients
Alexander C M Greven, Beau M McGinley, Ndeye F Guisse, et al.
Heart (British Cardiac Society)
|
March 8, 2011
Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy
E Gandjbakhch, P Charron, V Fressart, et al.
Page
of 15