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P Adam

Showing results (331-340 of 555) with videos related to

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Journal of Magnetic Resonance (San Diego, Calif. : 1997)|February 24, 2009
Improving the accuracy of pulsed field gradient NMR diffusion experiments: Correction for gradient non-uniformityMark A Connell, Paul J Bowyer, P Adam Bone, et al.
American Journal of Medical Genetics. Part A|January 8, 2013
Four new patients with Gomez-Lopez-Hernandez syndrome and proposed diagnostic criteriaEric T Rush, Margaret P Adam, Robin D Clark, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 7, 2021
MEF2 (Myocyte Enhancer Factor 2) Is Essential for Endothelial Homeostasis and the Atheroprotective Gene Expression ProgramYao Wei Lu, Nina Martino, Brennan D Gerlach, et al.
American Journal of Medical Genetics. Part A|October 14, 2016
Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22Heather M Byers, Margaret P Adam, Amy LaCroix, et al.
Annals of Internal Medicine|January 17, 2022
Diagnostic Imaging and Medical Management of Acute Left-Sided Colonic Diverticulitis : A Systematic ReviewEthan M Balk, Gaelen P Adam, Monika Reddy Bhuma, et al.
Cytogenetic and Genome Research|September 7, 2006
Characterization of chromosomal aberrations in diffuse large B-cell lymphoma (DLBL) by G-banding and spectral karyotyping (SKY)P Adam, C Steinlein, M Schmid, et al.
Annals of Internal Medicine|September 23, 2018
Treatments of Primary Basal Cell Carcinoma of the Skin: A Systematic Review and Network Meta-analysisAaron M Drucker, Gaelen P Adam, Valerie Rofeberg, et al.
Cytogenetic and Genome Research|November 15, 2007
Cell migration patterns and ongoing somatic mutations in the progression of follicular lymphomaP Adam, J Schoof, M Hartmann, et al.
American Journal of Medical Genetics. Part A|November 18, 2014
Increased body mass in infancy and early toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center defectsMarie-Luise Brennan, Margaret P Adam, Laurie H Seaver, et al.
Frontiers in Nephrology|April 16, 2025
Case Report: a novel variant in <i>WT1</i> leads to focal segmental glomerulosclerosis and uterovaginal anomalies through exon skippingJonathan Marquez, Lauren O'Sullivan, Audrey E Squire, et al.
Pageof 56

Showing results (331-340 of 555) with videos related to

Sort By:
Pageof 56
Journal of Magnetic Resonance (San Diego, Calif. : 1997)|February 24, 2009
Improving the accuracy of pulsed field gradient NMR diffusion experiments: Correction for gradient non-uniformityMark A Connell, Paul J Bowyer, P Adam Bone, et al.
American Journal of Medical Genetics. Part A|January 8, 2013
Four new patients with Gomez-Lopez-Hernandez syndrome and proposed diagnostic criteriaEric T Rush, Margaret P Adam, Robin D Clark, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 7, 2021
MEF2 (Myocyte Enhancer Factor 2) Is Essential for Endothelial Homeostasis and the Atheroprotective Gene Expression ProgramYao Wei Lu, Nina Martino, Brennan D Gerlach, et al.
American Journal of Medical Genetics. Part A|October 14, 2016
Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22Heather M Byers, Margaret P Adam, Amy LaCroix, et al.
Annals of Internal Medicine|January 17, 2022
Diagnostic Imaging and Medical Management of Acute Left-Sided Colonic Diverticulitis : A Systematic ReviewEthan M Balk, Gaelen P Adam, Monika Reddy Bhuma, et al.
Cytogenetic and Genome Research|September 7, 2006
Characterization of chromosomal aberrations in diffuse large B-cell lymphoma (DLBL) by G-banding and spectral karyotyping (SKY)P Adam, C Steinlein, M Schmid, et al.
Annals of Internal Medicine|September 23, 2018
Treatments of Primary Basal Cell Carcinoma of the Skin: A Systematic Review and Network Meta-analysisAaron M Drucker, Gaelen P Adam, Valerie Rofeberg, et al.
Cytogenetic and Genome Research|November 15, 2007
Cell migration patterns and ongoing somatic mutations in the progression of follicular lymphomaP Adam, J Schoof, M Hartmann, et al.
American Journal of Medical Genetics. Part A|November 18, 2014
Increased body mass in infancy and early toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center defectsMarie-Luise Brennan, Margaret P Adam, Laurie H Seaver, et al.
Frontiers in Nephrology|April 16, 2025
Case Report: a novel variant in <i>WT1</i> leads to focal segmental glomerulosclerosis and uterovaginal anomalies through exon skippingJonathan Marquez, Lauren O'Sullivan, Audrey E Squire, et al.
Pageof 56