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Brian Kirmse

Showing results (11-20 of 40) with videos related to

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Molecular Genetics and Metabolism|September 22, 2009
High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuriaLaurie E Profitlich, Brian Kirmse, Melissa P Wasserstein, et al.
The Journal of Infectious Diseases|November 27, 2008
HIV protease inhibitors inhibit the development of preerythrocytic-stage plasmodium parasitesCharlotte V Hobbs, Tatiana Voza, Alida Coppi, et al.
Molecular Genetics and Metabolism|August 27, 2013
The incidence of urea cycle disordersMarshall L Summar, Stefan Koelker, Debra Freedenberg, et al.
Molecular Genetics and Metabolism|May 21, 2024
A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduriaYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatmentYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
The Pediatric Infectious Disease Journal|September 1, 2012
Abnormal newborn screens and acylcarnitines in HIV-exposed and ARV-exposed infantsBrian Kirmse, Charlotte V Hobbs, Inga Peter, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Concurrent non-ketotic hyperglycinemia and propionic acidemia in an eight year old boyPaul S Kruszka, Brian Kirmse, Dina J Zand, et al.
The American Journal of Tropical Medicine and Hygiene|March 13, 2019
Case Report: Ocular Toxocariasis: A Report of Three Cases from the Mississippi DeltaKengo Inagaki, Brian Kirmse, Richard S Bradbury, et al.
O&G Open|February 23, 2026
Acute Fatty Liver of Pregnancy and Fetal Fatty Acid Oxidation Disorders: A Systematic ReviewDante Varotsis, Sarah Araji, Rebecca Horgan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 4, 2015
Novel first-dose adverse drug reactions during a phase I trial of olipudase alfa (recombinant human acid sphingomyelinase) in adults with Niemann-Pick disease type B (acid sphingomyelinase deficiency)Margaret M McGovern, Melissa P Wasserstein, Brian Kirmse, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Molecular Genetics and Metabolism|September 22, 2009
High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuriaLaurie E Profitlich, Brian Kirmse, Melissa P Wasserstein, et al.
The Journal of Infectious Diseases|November 27, 2008
HIV protease inhibitors inhibit the development of preerythrocytic-stage plasmodium parasitesCharlotte V Hobbs, Tatiana Voza, Alida Coppi, et al.
Molecular Genetics and Metabolism|August 27, 2013
The incidence of urea cycle disordersMarshall L Summar, Stefan Koelker, Debra Freedenberg, et al.
Molecular Genetics and Metabolism|May 21, 2024
A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduriaYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatmentYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
The Pediatric Infectious Disease Journal|September 1, 2012
Abnormal newborn screens and acylcarnitines in HIV-exposed and ARV-exposed infantsBrian Kirmse, Charlotte V Hobbs, Inga Peter, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Concurrent non-ketotic hyperglycinemia and propionic acidemia in an eight year old boyPaul S Kruszka, Brian Kirmse, Dina J Zand, et al.
The American Journal of Tropical Medicine and Hygiene|March 13, 2019
Case Report: Ocular Toxocariasis: A Report of Three Cases from the Mississippi DeltaKengo Inagaki, Brian Kirmse, Richard S Bradbury, et al.
O&G Open|February 23, 2026
Acute Fatty Liver of Pregnancy and Fetal Fatty Acid Oxidation Disorders: A Systematic ReviewDante Varotsis, Sarah Araji, Rebecca Horgan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 4, 2015
Novel first-dose adverse drug reactions during a phase I trial of olipudase alfa (recombinant human acid sphingomyelinase) in adults with Niemann-Pick disease type B (acid sphingomyelinase deficiency)Margaret M McGovern, Melissa P Wasserstein, Brian Kirmse, et al.
Pageof 4