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John Pappas

Showing results (1-10 of 59) with videos related to

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Immunology Letters|September 7, 2005
A single-step enrichment of Th2 lymphocytes using CCR4 microbeadsJohn Pappas, Nancy Quan, Namit Ghildyal
Cutis|February 18, 2022
Severe Acute Systemic Reaction After the First Injections of IxekizumabJohn Pappas, Maryam Liaqat, Analisa V Halpern
American Journal of Medical Genetics. Part A|October 23, 2018
Intellectual disability due to monoallelic variant in GATAD2B and mosaicism in unaffected parentRachel Rabin, Francisca Millan, Juan Cabrera-Luque, et al.
Case Reports in Endocrinology|June 17, 2017
Clinical Phenotype in a Toddler with a Novel Heterozygous Mutation of the Vitamin D ReceptorPreneet Cheema Brar, Elena Dingle, John Pappas, et al.
Journal of Pediatric and Adolescent Gynecology|June 11, 2025
A Case Report of Primary Ovarian Failure in an Adolescent Associated with a Homozygous Pathogenic Variant in the Mitochondrial Poly-A-Polymerase Gene (MTPAP)Jessy Epstein, Simrat Veera, John Pappas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 5, 2013
Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomyPayal R Patel, John Pappas, Nicoleta C Arva, et al.
American Journal of Medical Genetics. Part A|March 8, 2021
Severe epileptic encephalopathy associated with compound heterozygosity of THG1L variants in the Ashkenazi Jewish populationRachel Rabin, Yoel Hirsch, Martin M Johansson, et al.
Journal of Medical Internet Research|August 24, 2019
Comparing Characteristics of Patients Who Connect Their iPhones to an Electronic Health Records System Versus Patients Who Connect Without Personal Devices: Cohort StudyWilliam J Gordon, David W Bates, Daniel Fuchs, et al.
Molecular Genetics & Genomic Medicine|July 22, 2020
Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosisOdelia Chorin, Naomi Yachelevich, Khaled Mohamed, et al.
Pain Practice : the Official Journal of World Institute of Pain|March 17, 2010
Aprepitant vs. multimodal prophylaxis in the prevention of nausea and vomiting following extended-release epidural morphineCraig T Hartrick, Yeong-Shiuh Tang, David Hunstad, et al.
Pageof 6

Showing results (1-10 of 59) with videos related to

Sort By:
Pageof 6
Immunology Letters|September 7, 2005
A single-step enrichment of Th2 lymphocytes using CCR4 microbeadsJohn Pappas, Nancy Quan, Namit Ghildyal
Cutis|February 18, 2022
Severe Acute Systemic Reaction After the First Injections of IxekizumabJohn Pappas, Maryam Liaqat, Analisa V Halpern
American Journal of Medical Genetics. Part A|October 23, 2018
Intellectual disability due to monoallelic variant in GATAD2B and mosaicism in unaffected parentRachel Rabin, Francisca Millan, Juan Cabrera-Luque, et al.
Case Reports in Endocrinology|June 17, 2017
Clinical Phenotype in a Toddler with a Novel Heterozygous Mutation of the Vitamin D ReceptorPreneet Cheema Brar, Elena Dingle, John Pappas, et al.
Journal of Pediatric and Adolescent Gynecology|June 11, 2025
A Case Report of Primary Ovarian Failure in an Adolescent Associated with a Homozygous Pathogenic Variant in the Mitochondrial Poly-A-Polymerase Gene (MTPAP)Jessy Epstein, Simrat Veera, John Pappas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 5, 2013
Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomyPayal R Patel, John Pappas, Nicoleta C Arva, et al.
American Journal of Medical Genetics. Part A|March 8, 2021
Severe epileptic encephalopathy associated with compound heterozygosity of THG1L variants in the Ashkenazi Jewish populationRachel Rabin, Yoel Hirsch, Martin M Johansson, et al.
Journal of Medical Internet Research|August 24, 2019
Comparing Characteristics of Patients Who Connect Their iPhones to an Electronic Health Records System Versus Patients Who Connect Without Personal Devices: Cohort StudyWilliam J Gordon, David W Bates, Daniel Fuchs, et al.
Molecular Genetics & Genomic Medicine|July 22, 2020
Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosisOdelia Chorin, Naomi Yachelevich, Khaled Mohamed, et al.
Pain Practice : the Official Journal of World Institute of Pain|March 17, 2010
Aprepitant vs. multimodal prophylaxis in the prevention of nausea and vomiting following extended-release epidural morphineCraig T Hartrick, Yeong-Shiuh Tang, David Hunstad, et al.
Pageof 6