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Patricia Ward

Showing results (21-30 of 35) with videos related to

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Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|March 12, 2014
Calibration of the brief food frequency questionnaire among patients on dialysisCynthia Delgado, Patricia Ward, Glenn M Chertow, et al.
Journal of Neurodevelopmental Disorders|May 23, 2024
Rescue of impaired blood-brain barrier in tuberous sclerosis complex patient derived neurovascular unitJacquelyn A Brown, Shannon L Faley, Monika Judge, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular UnitJacquelyn A Brown, Shannon L Faley, Monika Judge, et al.
Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemiaDavid P Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 13, 2003
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisisLeah Rae Donahue, Bo Chang, Subburaman Mohan, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Disruption of G3BP1 Granules Promotes Mammalian CNS and PNS Axon RegenerationPabitra K Sahoo, Manasi Agrawal, Nicholas Hanovice, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardizationCeleste Eno, Pinar Bayrak-Toydemir, Lora Bean, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|March 12, 2014
Calibration of the brief food frequency questionnaire among patients on dialysisCynthia Delgado, Patricia Ward, Glenn M Chertow, et al.
Journal of Neurodevelopmental Disorders|May 23, 2024
Rescue of impaired blood-brain barrier in tuberous sclerosis complex patient derived neurovascular unitJacquelyn A Brown, Shannon L Faley, Monika Judge, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular UnitJacquelyn A Brown, Shannon L Faley, Monika Judge, et al.
Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemiaDavid P Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 13, 2003
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisisLeah Rae Donahue, Bo Chang, Subburaman Mohan, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Disruption of G3BP1 Granules Promotes Mammalian CNS and PNS Axon RegenerationPabitra K Sahoo, Manasi Agrawal, Nicholas Hanovice, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardizationCeleste Eno, Pinar Bayrak-Toydemir, Lora Bean, et al.
Pageof 4