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Sanmati R Cuddapah

Showing results (1-10 of 7) with videos related to

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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 20, 2015
IRF6 Sequencing in Interrupted CleftingSanmati R Cuddapah, Selma Kominek, John H Grant, et al.
Molecular Genetics and Metabolism|March 13, 2023
2-Methylglutaconic acid as a biomarker in routine urine organic acids leading to the diagnosis of glutaric acidemia type I in a low excretorParith Wongkittichote, Xinying Hong, Stephen R Master, et al.
JIMD Reports|September 13, 2023
Biochemical characterization of patients with dihydrolipoamide dehydrogenase deficiencyParith Wongkittichote, Sanmati R Cuddapah, Stephen R Master, et al.
International Journal of Neonatal Screening|November 18, 2020
Newborn Screening for Pompe Disease: Pennsylvania ExperienceCan Ficicioglu, Rebecca C Ahrens-Nicklas, Joshua Barch, et al.
JIMD Reports|January 13, 2025
Liver Transplant From a Deceased Donor With Cystinosis: A Case ReportRaeda Taj, Kim Ng, Sanmati R Cuddapah, et al.
Molecular Genetics and Metabolism Reports|November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signatureJessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Pediatrics|June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics CareKatherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 20, 2015
IRF6 Sequencing in Interrupted CleftingSanmati R Cuddapah, Selma Kominek, John H Grant, et al.
Molecular Genetics and Metabolism|March 13, 2023
2-Methylglutaconic acid as a biomarker in routine urine organic acids leading to the diagnosis of glutaric acidemia type I in a low excretorParith Wongkittichote, Xinying Hong, Stephen R Master, et al.
JIMD Reports|September 13, 2023
Biochemical characterization of patients with dihydrolipoamide dehydrogenase deficiencyParith Wongkittichote, Sanmati R Cuddapah, Stephen R Master, et al.
International Journal of Neonatal Screening|November 18, 2020
Newborn Screening for Pompe Disease: Pennsylvania ExperienceCan Ficicioglu, Rebecca C Ahrens-Nicklas, Joshua Barch, et al.
JIMD Reports|January 13, 2025
Liver Transplant From a Deceased Donor With Cystinosis: A Case ReportRaeda Taj, Kim Ng, Sanmati R Cuddapah, et al.
Molecular Genetics and Metabolism Reports|November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signatureJessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Pediatrics|June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics CareKatherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Pageof 1