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Pranesh Chakraborty

Showing results (121-130 of 154) with videos related to

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Plos One|July 5, 2013
Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERTSuhrad G Banugaria, Sean N Prater, Trusha T Patel, et al.
Trials|November 18, 2021
Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveysAlison H Howie, Kylie Tingley, Michal Inbar-Feigenberg, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|June 1, 2016
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unitHussein Daoud, Stephanie M Luco, Rui Li, et al.
Journal of Inherited Metabolic Disease|July 26, 2015
Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groupsSara D Khangura, Kylie Tingley, Pranesh Chakraborty, et al.
American Journal of Medical Genetics. Part A|December 23, 2015
Genotype-phenotype characterization in 13 individuals with chromosome Xp11.22 duplicationsSarah E Grams, Bob Argiropoulos, Matthew Lines, et al.
Journal of the Pediatric Infectious Diseases Society|June 19, 2023
Estimating the Incidence of First RSV Hospitalization in Children Born in Ontario, CanadaSarah A Buchan, Hannah Chung, Teresa To, et al.
Trials|December 21, 2017
Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveysBeth K Potter, Brian Hutton, Tammy J Clifford, et al.
Blood|April 5, 2013
A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)Daniel H Wiseman, Alison May, Stephen Jolles, et al.
BMC Pediatrics|April 18, 2015
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric diseaseSara D Khangura, Maria D Karaceper, Yannis Trakadis, et al.
Plos One|December 7, 2021
Dried blood spot specimens for SARS-CoV-2 antibody testing: A multi-site, multi-assay comparisonFrançois Cholette, Christine Mesa, Angela Harris, et al.
Pageof 16

Showing results (121-130 of 154) with videos related to

Sort By:
Pageof 16
Plos One|July 5, 2013
Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERTSuhrad G Banugaria, Sean N Prater, Trusha T Patel, et al.
Trials|November 18, 2021
Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveysAlison H Howie, Kylie Tingley, Michal Inbar-Feigenberg, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|June 1, 2016
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unitHussein Daoud, Stephanie M Luco, Rui Li, et al.
Journal of Inherited Metabolic Disease|July 26, 2015
Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groupsSara D Khangura, Kylie Tingley, Pranesh Chakraborty, et al.
American Journal of Medical Genetics. Part A|December 23, 2015
Genotype-phenotype characterization in 13 individuals with chromosome Xp11.22 duplicationsSarah E Grams, Bob Argiropoulos, Matthew Lines, et al.
Journal of the Pediatric Infectious Diseases Society|June 19, 2023
Estimating the Incidence of First RSV Hospitalization in Children Born in Ontario, CanadaSarah A Buchan, Hannah Chung, Teresa To, et al.
Trials|December 21, 2017
Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveysBeth K Potter, Brian Hutton, Tammy J Clifford, et al.
Blood|April 5, 2013
A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)Daniel H Wiseman, Alison May, Stephen Jolles, et al.
BMC Pediatrics|April 18, 2015
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric diseaseSara D Khangura, Maria D Karaceper, Yannis Trakadis, et al.
Plos One|December 7, 2021
Dried blood spot specimens for SARS-CoV-2 antibody testing: A multi-site, multi-assay comparisonFrançois Cholette, Christine Mesa, Angela Harris, et al.
Pageof 16