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Hope Northrup

Showing results (51-60 of 157) with videos related to

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Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|February 27, 2010
Obstetrics/gynecology residents' knowledge of hereditary breast and ovarian cancer and Lynch syndromeKaylene J Ready, Molly S Daniels, Charlotte C Sun, et al.
American Journal of Medical Genetics. Part A|September 2, 2021
The youngest pair of siblings with Mucopolysaccharidosis type IVA to receive enzyme replacement therapy to date: A case reportMarta Frigeni, David F Rodriguez-Buritica, Heather Saavedra, et al.
Pediatrics|September 9, 2006
Introduction to the newborn screening fact sheetsCelia I Kaye, , Frank Accurso, et al.
Pediatric Neurology|December 12, 2018
The Impact of Psychiatric Symptoms on Tuberous Sclerosis Complex and Utilization of Mental Health TreatmentKate E Mowrey, Myla Ashfaq, Deborah A Pearson, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|January 24, 2008
Genes in glucose metabolism and association with spina bifidaChristina M Davidson, Hope Northrup, Terri M King, et al.
Chronobiology International|August 17, 2002
Circadian pattern of blood pressure, heart rate, and double product in liver glycogen storage diseaseRobert J Yetman, Melanie Andrew-Casal, Ramón C Hermida, et al.
American Journal of Medical Genetics. Part A|September 27, 2017
Mutations in folate transporter genes and risk for human myelomeningoceleTina O Findley, Joy C Tenpenny, Michelle R O'Byrne, et al.
American Journal of Obstetrics and Gynecology|August 18, 2009
Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifidaCarla A Martinez, Hope Northrup, Jone-Ing Lin, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 22, 2011
Association of retinoic acid receptor genes with meningomyelocelePhong X Tran, Kit Sing Au, Alanna C Morrison, et al.
JIMD Reports|November 6, 2023
Arginase deficiency masked by cerebral palsy and coagulopathy-Three varied presentations of Latin American originShelby L Mills, Paige Roberts, Myla Ashfaq, et al.
Pageof 16

Showing results (51-60 of 157) with videos related to

Sort By:
Pageof 16
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|February 27, 2010
Obstetrics/gynecology residents' knowledge of hereditary breast and ovarian cancer and Lynch syndromeKaylene J Ready, Molly S Daniels, Charlotte C Sun, et al.
American Journal of Medical Genetics. Part A|September 2, 2021
The youngest pair of siblings with Mucopolysaccharidosis type IVA to receive enzyme replacement therapy to date: A case reportMarta Frigeni, David F Rodriguez-Buritica, Heather Saavedra, et al.
Pediatrics|September 9, 2006
Introduction to the newborn screening fact sheetsCelia I Kaye, , Frank Accurso, et al.
Pediatric Neurology|December 12, 2018
The Impact of Psychiatric Symptoms on Tuberous Sclerosis Complex and Utilization of Mental Health TreatmentKate E Mowrey, Myla Ashfaq, Deborah A Pearson, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|January 24, 2008
Genes in glucose metabolism and association with spina bifidaChristina M Davidson, Hope Northrup, Terri M King, et al.
Chronobiology International|August 17, 2002
Circadian pattern of blood pressure, heart rate, and double product in liver glycogen storage diseaseRobert J Yetman, Melanie Andrew-Casal, Ramón C Hermida, et al.
American Journal of Medical Genetics. Part A|September 27, 2017
Mutations in folate transporter genes and risk for human myelomeningoceleTina O Findley, Joy C Tenpenny, Michelle R O'Byrne, et al.
American Journal of Obstetrics and Gynecology|August 18, 2009
Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifidaCarla A Martinez, Hope Northrup, Jone-Ing Lin, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 22, 2011
Association of retinoic acid receptor genes with meningomyelocelePhong X Tran, Kit Sing Au, Alanna C Morrison, et al.
JIMD Reports|November 6, 2023
Arginase deficiency masked by cerebral palsy and coagulopathy-Three varied presentations of Latin American originShelby L Mills, Paige Roberts, Myla Ashfaq, et al.
Pageof 16