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Alison Gardner

Showing results (21-30 of 54) with videos related to

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Journal of Public Health (Oxford, England)|October 2, 2024
Cognitive impairment and exploitation: connecting fragments of a bigger picture through dataAisha M Abubakar, Rowland G Seymour, Alison Gardner, et al.
Veterinary Surgery : VS|June 7, 2023
Assessment and comparison of microcirculation and macrocirculation in horses undergoing emergency exploratory celiotomy versus elective surgical proceduresPatrick W Foth, Alison Gardner, Carolina Ricco Pereira, et al.
Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology|November 28, 2017
Double outlet right ventricle with subpulmonary ventricular septal defect (Taussig-Bing anomaly) and other complex congenital cardiac malformations in an American Quarter Horse foalRebecca Kohnken, Karsten Schober, Jennifer Godman, et al.
Molecular Pharmacology|July 15, 2017
Molecular Basis of Altered hERG1 Channel Gating Induced by Ginsenoside Rg3Alison Gardner, Wei Wu, Steven Thomson, et al.
The American Surgeon|May 30, 2023
Storage Practices, Devices, and Presence of Children Among Owners of Firearms: Informing Pediatric Firearm SafetyMichaela Gaffley, Jessica L Rauh, Alison Gardner, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 29, 2008
Randomized comparison of cooked and noncooked diets in patients undergoing remission induction therapy for acute myeloid leukemiaAlison Gardner, Gloria Mattiuzzi, Stefan Faderl, et al.
Clinical Endocrinology|May 6, 2016
Identification of an IGSF1-specific deletion in a five-generation pedigree with X-linked Central Hypothyroidism without macroorchidismJames N Hughes, Matthew Aubert, Jessica Heatlie, et al.
European Journal of Medical Genetics|July 21, 2020
Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansionRenee Carroll, Marie Shaw, Maria Arvio, et al.
European Journal of Medical Genetics|August 6, 2013
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyGai McMichael, Eric Haan, Alison Gardner, et al.
European Journal of Medical Genetics|May 3, 2015
Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndromeMarie Shaw, Tzu Ying Yap, Lyndal Henden, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Journal of Public Health (Oxford, England)|October 2, 2024
Cognitive impairment and exploitation: connecting fragments of a bigger picture through dataAisha M Abubakar, Rowland G Seymour, Alison Gardner, et al.
Veterinary Surgery : VS|June 7, 2023
Assessment and comparison of microcirculation and macrocirculation in horses undergoing emergency exploratory celiotomy versus elective surgical proceduresPatrick W Foth, Alison Gardner, Carolina Ricco Pereira, et al.
Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology|November 28, 2017
Double outlet right ventricle with subpulmonary ventricular septal defect (Taussig-Bing anomaly) and other complex congenital cardiac malformations in an American Quarter Horse foalRebecca Kohnken, Karsten Schober, Jennifer Godman, et al.
Molecular Pharmacology|July 15, 2017
Molecular Basis of Altered hERG1 Channel Gating Induced by Ginsenoside Rg3Alison Gardner, Wei Wu, Steven Thomson, et al.
The American Surgeon|May 30, 2023
Storage Practices, Devices, and Presence of Children Among Owners of Firearms: Informing Pediatric Firearm SafetyMichaela Gaffley, Jessica L Rauh, Alison Gardner, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 29, 2008
Randomized comparison of cooked and noncooked diets in patients undergoing remission induction therapy for acute myeloid leukemiaAlison Gardner, Gloria Mattiuzzi, Stefan Faderl, et al.
Clinical Endocrinology|May 6, 2016
Identification of an IGSF1-specific deletion in a five-generation pedigree with X-linked Central Hypothyroidism without macroorchidismJames N Hughes, Matthew Aubert, Jessica Heatlie, et al.
European Journal of Medical Genetics|July 21, 2020
Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansionRenee Carroll, Marie Shaw, Maria Arvio, et al.
European Journal of Medical Genetics|August 6, 2013
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyGai McMichael, Eric Haan, Alison Gardner, et al.
European Journal of Medical Genetics|May 3, 2015
Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndromeMarie Shaw, Tzu Ying Yap, Lyndal Henden, et al.
Pageof 6