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David Miller

Showing results (561-570 of 607) with videos related to

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Cancer & Metabolism|February 7, 2017
Mitochondrial mutations and metabolic adaptation in pancreatic cancerRae-Anne Hardie, Ellen van Dam, Mark Cowley, et al.
The Journal of Allergy and Clinical Immunology|August 14, 2013
Environmental assessment and exposure reduction of cockroaches: a practice parameterJay Portnoy, Ginger L Chew, Wanda Phipatanakul, et al.
Annals of Vascular Surgery|December 29, 2020
Higher Risk for Reintervention in Patients after Stenting for Radiation-Induced Internal Carotid Artery Stenosis: A Single-Center Analysis and Systematic ReviewYoung Erben, Camila Franco-Mesa, David Miller, et al.
Neurosurgery|January 8, 2024
Trends in the Utilization of Surgical Modalities for the Treatment of Drug-Resistant Epilepsy: A Comprehensive 10-Year Analysis Using the National Inpatient SampleAbdul Karim Ghaith, Victor Gabriel El-Hajj, Jesus E Sanchez-Garavito, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Nature Genetics|February 26, 2015
Corrigendum: Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|November 26, 2013
Environmental assessment and exposure control of dust mites: a practice parameterJay Portnoy, Jeffrey D Miller, P Brock Williams, et al.
Neurology|November 11, 2018
<i>PCNT</i> point mutations and familial intracranial aneurysmsOswaldo Lorenzo-Betancor, Patrick R Blackburn, Emily Edwards, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2018
Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disordersLisa J Ewans, Deborah Schofield, Rupendra Shrestha, et al.
American Journal of Human Genetics|April 16, 2013
A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellumCas Simons, Nicole I Wolf, Nathan McNeil, et al.
Pageof 61

Showing results (561-570 of 607) with videos related to

Sort By:
Pageof 61
Cancer & Metabolism|February 7, 2017
Mitochondrial mutations and metabolic adaptation in pancreatic cancerRae-Anne Hardie, Ellen van Dam, Mark Cowley, et al.
The Journal of Allergy and Clinical Immunology|August 14, 2013
Environmental assessment and exposure reduction of cockroaches: a practice parameterJay Portnoy, Ginger L Chew, Wanda Phipatanakul, et al.
Annals of Vascular Surgery|December 29, 2020
Higher Risk for Reintervention in Patients after Stenting for Radiation-Induced Internal Carotid Artery Stenosis: A Single-Center Analysis and Systematic ReviewYoung Erben, Camila Franco-Mesa, David Miller, et al.
Neurosurgery|January 8, 2024
Trends in the Utilization of Surgical Modalities for the Treatment of Drug-Resistant Epilepsy: A Comprehensive 10-Year Analysis Using the National Inpatient SampleAbdul Karim Ghaith, Victor Gabriel El-Hajj, Jesus E Sanchez-Garavito, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Nature Genetics|February 26, 2015
Corrigendum: Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|November 26, 2013
Environmental assessment and exposure control of dust mites: a practice parameterJay Portnoy, Jeffrey D Miller, P Brock Williams, et al.
Neurology|November 11, 2018
<i>PCNT</i> point mutations and familial intracranial aneurysmsOswaldo Lorenzo-Betancor, Patrick R Blackburn, Emily Edwards, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2018
Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disordersLisa J Ewans, Deborah Schofield, Rupendra Shrestha, et al.
American Journal of Human Genetics|April 16, 2013
A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellumCas Simons, Nicole I Wolf, Nathan McNeil, et al.
Pageof 61