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E W Naylor

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Archives of Surgery (Chicago, Ill. : 1960)|October 1, 1979
Desmoid tumors and mesenteric fibromatosis in Gardner's syndrome: report of kindred 109E W Naylor, E J Gardner, R C Richards
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Laboratory integration and utilization of tandem mass spectrometry in neonatal screening: a model for clinical mass spectrometry in the next millenniumD H Chace, J C DiPerna, E W Naylor
The Journal of Pediatrics|October 1, 1989
False positive alanine tolerance test results in heterozygote detection of urea cycle disordersM L Batshaw, E W Naylor, G H Thomas
Journal of Chromatography|May 1, 1979
Measurement of urinary pyrimidine bases and nucleosides by high-performance liquid chromatographyJ E Evans, H Tieckelmann, E W Naylor, et al.
Pediatrics|October 1, 1982
A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disordersH W Talbot, A B Sumlin, E W Naylor, et al.
Archives of Pediatrics & Adolescent Medicine|September 1, 1994
Diagnosis of cystic fibrosis in a premature infant via neonatal screeningJ L Allen, R Stavis, G S Kaplan, et al.
Journal of Medical Genetics|April 1, 1978
Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicismE W Naylor, W H Murphey, E I Domoszlai, et al.
Biochemical Medicine and Metabolic Biology|April 1, 1993
Neonatal screening for cystic fibrosis: addition of molecular diagnostics to increase specificityW C Spence, J Paulus-Thomas, D M Orenstein, et al.
The Journal of Pediatrics|April 17, 1998
3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their childrenK M Gibson, M J Bennett, E W Naylor, et al.
Psychiatry Research|June 1, 1985
Dihydropteridine reductase in schizophrenic patientsH V Szymanski, A Orfanos, K Narisawa, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Archives of Surgery (Chicago, Ill. : 1960)|October 1, 1979
Desmoid tumors and mesenteric fibromatosis in Gardner's syndrome: report of kindred 109E W Naylor, E J Gardner, R C Richards
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Laboratory integration and utilization of tandem mass spectrometry in neonatal screening: a model for clinical mass spectrometry in the next millenniumD H Chace, J C DiPerna, E W Naylor
The Journal of Pediatrics|October 1, 1989
False positive alanine tolerance test results in heterozygote detection of urea cycle disordersM L Batshaw, E W Naylor, G H Thomas
Journal of Chromatography|May 1, 1979
Measurement of urinary pyrimidine bases and nucleosides by high-performance liquid chromatographyJ E Evans, H Tieckelmann, E W Naylor, et al.
Pediatrics|October 1, 1982
A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disordersH W Talbot, A B Sumlin, E W Naylor, et al.
Archives of Pediatrics & Adolescent Medicine|September 1, 1994
Diagnosis of cystic fibrosis in a premature infant via neonatal screeningJ L Allen, R Stavis, G S Kaplan, et al.
Journal of Medical Genetics|April 1, 1978
Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicismE W Naylor, W H Murphey, E I Domoszlai, et al.
Biochemical Medicine and Metabolic Biology|April 1, 1993
Neonatal screening for cystic fibrosis: addition of molecular diagnostics to increase specificityW C Spence, J Paulus-Thomas, D M Orenstein, et al.
The Journal of Pediatrics|April 17, 1998
3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their childrenK M Gibson, M J Bennett, E W Naylor, et al.
Psychiatry Research|June 1, 1985
Dihydropteridine reductase in schizophrenic patientsH V Szymanski, A Orfanos, K Narisawa, et al.
Pageof 6