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J C Stevens

Showing results (201-210 of 247) with videos related to

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Neurology|September 25, 2003
Practice parameter: immunotherapy for Guillain-Barré syndrome: report of the Quality Standards Subcommittee of the American Academy of NeurologyR A C Hughes, E F M Wijdicks, R Barohn, et al.
Molecular Genetics & Genomic Medicine|March 25, 2018
Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 geneVyne van der Schoot, Sonja de Munnik, Hanka Venselaar, et al.
American Journal of Medical Genetics. Part A|September 3, 2009
Identical cryptic partial monosomy 20pter and trisomy 20qter in three adult siblings due to a large maternal pericentric inversion: detection by MLPA and breakpoint mapping by SNP array analysisServi J C Stevens, Eric E J G L Smeets, Eveline Blom, et al.
Neurology|May 9, 2001
Practice parameter: management of dementia (an evidence-based review) [RETIRED]. Report of the Quality Standards Subcommittee of the American Academy of NeurologyR S Doody, J C Stevens, C Beck, et al.
Neurology|April 30, 2008
Invited article: Neurology and quality improvement: an introductionC T Bever, R G Holloway, D J Iverson, et al.
Human Mutation|September 10, 2019
Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculatureChantal Kerkhofs, Servi J C Stevens, Saul N Faust, et al.
The Pediatric Infectious Disease Journal|January 1, 1997
Sequential ciprofloxacin therapy in pediatric cystic fibrosis: comparative study vs. ceftazidime/tobramycin in the treatment of acute pulmonary exacerbations. The Cystic Fibrosis Study GroupD A Church, J F Kanga, R J Kuhn, et al.
American Journal of Medical Genetics. Part A|September 24, 2025
Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16BServi J C Stevens, Wanwisa van Dijk, Nicole Y Souren, et al.
Human Mutation|April 25, 2018
De novo mutations in the SET nuclear proto-oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disabilityServi J C Stevens, Vyne van der Schoot, Magalie S Leduc, et al.
Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
Pageof 25

Showing results (201-210 of 247) with videos related to

Sort By:
Pageof 25
Neurology|September 25, 2003
Practice parameter: immunotherapy for Guillain-Barré syndrome: report of the Quality Standards Subcommittee of the American Academy of NeurologyR A C Hughes, E F M Wijdicks, R Barohn, et al.
Molecular Genetics & Genomic Medicine|March 25, 2018
Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 geneVyne van der Schoot, Sonja de Munnik, Hanka Venselaar, et al.
American Journal of Medical Genetics. Part A|September 3, 2009
Identical cryptic partial monosomy 20pter and trisomy 20qter in three adult siblings due to a large maternal pericentric inversion: detection by MLPA and breakpoint mapping by SNP array analysisServi J C Stevens, Eric E J G L Smeets, Eveline Blom, et al.
Neurology|May 9, 2001
Practice parameter: management of dementia (an evidence-based review) [RETIRED]. Report of the Quality Standards Subcommittee of the American Academy of NeurologyR S Doody, J C Stevens, C Beck, et al.
Neurology|April 30, 2008
Invited article: Neurology and quality improvement: an introductionC T Bever, R G Holloway, D J Iverson, et al.
Human Mutation|September 10, 2019
Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculatureChantal Kerkhofs, Servi J C Stevens, Saul N Faust, et al.
The Pediatric Infectious Disease Journal|January 1, 1997
Sequential ciprofloxacin therapy in pediatric cystic fibrosis: comparative study vs. ceftazidime/tobramycin in the treatment of acute pulmonary exacerbations. The Cystic Fibrosis Study GroupD A Church, J F Kanga, R J Kuhn, et al.
American Journal of Medical Genetics. Part A|September 24, 2025
Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16BServi J C Stevens, Wanwisa van Dijk, Nicole Y Souren, et al.
Human Mutation|April 25, 2018
De novo mutations in the SET nuclear proto-oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disabilityServi J C Stevens, Vyne van der Schoot, Magalie S Leduc, et al.
Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
Pageof 25