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Tyler Reimschisel

Showing results (1-10 of 17) with videos related to

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Pediatrics|October 24, 2012
You too can teach clinical reasoning!Amy Fleming, William Cutrer, Tyler Reimschisel, et al.
Medical Teacher|July 1, 2017
A systematic review of the published literature on team-based learning in health professions educationTyler Reimschisel, Anna L Herring, Jennifer Huang, et al.
Developmental Medicine and Child Neurology|July 10, 2008
Impact of congenital talipes equinovarus etiology on treatment outcomesChristina A Gurnett, Stephanie Boehm, Anne Connolly, et al.
Journal of Inherited Metabolic Disease|December 1, 2012
Estimating the probability of IQ impairment from blood phenylalanine for phenylketonuria patients: a hierarchical meta-analysisChristopher J Fonnesbeck, Melissa L McPheeters, Shanthi Krishnaswami, et al.
JIMD Reports|February 23, 2013
A Systematic Review of BH4 (Sapropterin) for the Adjuvant Treatment of PhenylketonuriaMary Lou Lindegren, Shanthi Krishnaswami, Tyler Reimschisel, et al.
European Journal of Human Genetics : EJHG|November 25, 2004
A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expressionJennifer A Dunston, Tyler Reimschisel, Yu-Qiang Ding, et al.
The Journal of Pediatrics|January 26, 2010
Four-year prospective clinical trial of agalsidase alfa in children with Fabry diseaseRaphael Schiffmann, Rick A Martin, Tyler Reimschisel, et al.
Molecular Genetics and Metabolism|January 14, 2009
High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGHOleg A Shchelochkov, Fang-Yuan Li, Michael T Geraghty, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2011
Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two femalesMagdalena Bartnik, Katarzyna Derwińska, Monika Gos, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
Phenotypic manifestations of copy number variation in chromosome 16p13.11Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Pediatrics|October 24, 2012
You too can teach clinical reasoning!Amy Fleming, William Cutrer, Tyler Reimschisel, et al.
Medical Teacher|July 1, 2017
A systematic review of the published literature on team-based learning in health professions educationTyler Reimschisel, Anna L Herring, Jennifer Huang, et al.
Developmental Medicine and Child Neurology|July 10, 2008
Impact of congenital talipes equinovarus etiology on treatment outcomesChristina A Gurnett, Stephanie Boehm, Anne Connolly, et al.
Journal of Inherited Metabolic Disease|December 1, 2012
Estimating the probability of IQ impairment from blood phenylalanine for phenylketonuria patients: a hierarchical meta-analysisChristopher J Fonnesbeck, Melissa L McPheeters, Shanthi Krishnaswami, et al.
JIMD Reports|February 23, 2013
A Systematic Review of BH4 (Sapropterin) for the Adjuvant Treatment of PhenylketonuriaMary Lou Lindegren, Shanthi Krishnaswami, Tyler Reimschisel, et al.
European Journal of Human Genetics : EJHG|November 25, 2004
A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expressionJennifer A Dunston, Tyler Reimschisel, Yu-Qiang Ding, et al.
The Journal of Pediatrics|January 26, 2010
Four-year prospective clinical trial of agalsidase alfa in children with Fabry diseaseRaphael Schiffmann, Rick A Martin, Tyler Reimschisel, et al.
Molecular Genetics and Metabolism|January 14, 2009
High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGHOleg A Shchelochkov, Fang-Yuan Li, Michael T Geraghty, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2011
Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two femalesMagdalena Bartnik, Katarzyna Derwińska, Monika Gos, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
Phenotypic manifestations of copy number variation in chromosome 16p13.11Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, et al.
Pageof 2