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Austin Larson

Showing results (1-10 of 61) with videos related to

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Maternal and Child Health Journal|April 12, 2012
Association of head circumference and shoulder dystocia in macrosomic neonatesAustin Larson, David E Mandelbaum
Discovery Medicine|December 4, 2012
Disorders of sex development: clinically relevant genes involved in gonadal differentiationAustin Larson, Natalie J Nokoff, Sharon Travers
Pediatric Emergency Care|March 7, 2013
Seizures and methemoglobinemia in an infant after excessive EMLA applicationAustin Larson, Timothy Stidham, Shireen Banerji, et al.
Discovery Medicine|April 2, 2015
Genetic causes of pituitary hormone deficienciesAustin Larson, Natalie J Nokoff, Naomi J L Meeks
American Journal of Medical Genetics. Part A|August 22, 2019
IRF2BPL gene mutation: Expanding on neurologic phenotypesEmily Shelkowitz, Jasleen K Singh, Austin Larson, et al.
Mitochondrion|January 11, 2020
LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activityArnaud Besse, Daniel Brezavar, Jennifer Hanson, et al.
American Journal of Medical Genetics. Part A|February 27, 2025
Phenotypic Characteristics of a Patient Cohort With Recessive Dystrophic Epidermolysis Bullosa and the Pathogenic Variant c.7485+5G>A in Intron 98 of COL7A1Micah G Pascual, Hannah C Cox, Austin Larson, et al.
Journal of Child Neurology|November 1, 2019
Serial Magnetic Resonance Imaging (MRI) in Pyruvate Dehydrogenase Complex DeficiencyEmily Shelkowitz, Can Ficicioglu, Nicholas Stence, et al.
Pediatric Pulmonology|April 10, 2020
Tracheal and lower airway changes in a patient with mucolipidosis type IIThomas S Poore, Jeremy Prager, Jason P Weinman, et al.
JBMR Plus|November 29, 2023
Skeletal Health in Patients With Mitochondrial Diabetes: Case Series and Review of LiteratureKagan Ege Karakus, Varun Suryadevara, Austin Larson, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Maternal and Child Health Journal|April 12, 2012
Association of head circumference and shoulder dystocia in macrosomic neonatesAustin Larson, David E Mandelbaum
Discovery Medicine|December 4, 2012
Disorders of sex development: clinically relevant genes involved in gonadal differentiationAustin Larson, Natalie J Nokoff, Sharon Travers
Pediatric Emergency Care|March 7, 2013
Seizures and methemoglobinemia in an infant after excessive EMLA applicationAustin Larson, Timothy Stidham, Shireen Banerji, et al.
Discovery Medicine|April 2, 2015
Genetic causes of pituitary hormone deficienciesAustin Larson, Natalie J Nokoff, Naomi J L Meeks
American Journal of Medical Genetics. Part A|August 22, 2019
IRF2BPL gene mutation: Expanding on neurologic phenotypesEmily Shelkowitz, Jasleen K Singh, Austin Larson, et al.
Mitochondrion|January 11, 2020
LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activityArnaud Besse, Daniel Brezavar, Jennifer Hanson, et al.
American Journal of Medical Genetics. Part A|February 27, 2025
Phenotypic Characteristics of a Patient Cohort With Recessive Dystrophic Epidermolysis Bullosa and the Pathogenic Variant c.7485+5G>A in Intron 98 of COL7A1Micah G Pascual, Hannah C Cox, Austin Larson, et al.
Journal of Child Neurology|November 1, 2019
Serial Magnetic Resonance Imaging (MRI) in Pyruvate Dehydrogenase Complex DeficiencyEmily Shelkowitz, Can Ficicioglu, Nicholas Stence, et al.
Pediatric Pulmonology|April 10, 2020
Tracheal and lower airway changes in a patient with mucolipidosis type IIThomas S Poore, Jeremy Prager, Jason P Weinman, et al.
JBMR Plus|November 29, 2023
Skeletal Health in Patients With Mitochondrial Diabetes: Case Series and Review of LiteratureKagan Ege Karakus, Varun Suryadevara, Austin Larson, et al.
Pageof 7