Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E W Naylor

Showing results (41-50 of 60) with videos related to

Pageof 6
Sort By:
Journal of Medical Screening|June 7, 2003
Assays for thyroid-stimulating hormone using dried blood spotted filter paper specimens to screen for hypothyroidism in older children and adultsL F Hofman, T P Foley, J J Henry, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|June 13, 2001
Inherited metabolic disorders in Thailand--Siriraj experienceP Wasant, J Svasti, C Srisomsap, et al.
Clinical Chemistry|November 20, 1997
Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometryD H Chace, S L Hillman, J L Van Hove, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
DNA microarray technology for neonatal screeningS F Dobrowolski, R A Banas, E W Naylor, et al.
The Journal of Pediatrics|February 1, 1981
A simple screening test for reduced glutathione in filter paper spots of bloodM D Garrick, A P Orfanos, L Rogers, et al.
Archives of Pathology & Laboratory Medicine|December 3, 1999
Optimization of an automated DNA purification protocol for neonatal screeningE M Heath, D P O'Brien, R Banas, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Intermittent non-ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: an apparent defect in beta-oxidation of fatty acidsE W Naylor, L L Mosovich, R Guthrie, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 21, 1980
Enzymatic studies of urinary isomeric chondroitin sulfates from patients with mucopolysaccharidoses. The application of high performance liquid chromatographyG J Lee, J E Evans, H Tieckelmann, et al.
Clinical Chemistry|October 24, 2001
Rapid diagnosis of methylmalonic and propionic acidemias: quantitative tandem mass spectrometric analysis of propionylcarnitine in filter-paper blood specimens obtained from newbornsD H Chace, J C DiPerna, T A Kalas, et al.
Pediatrics|March 1, 1987
Guanosine triphosphate cyclohydrolase I deficiency: early diagnosis by routine urine pteridine screeningE W Naylor, D Ennis, A G Davidson, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Journal of Medical Screening|June 7, 2003
Assays for thyroid-stimulating hormone using dried blood spotted filter paper specimens to screen for hypothyroidism in older children and adultsL F Hofman, T P Foley, J J Henry, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|June 13, 2001
Inherited metabolic disorders in Thailand--Siriraj experienceP Wasant, J Svasti, C Srisomsap, et al.
Clinical Chemistry|November 20, 1997
Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometryD H Chace, S L Hillman, J L Van Hove, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
DNA microarray technology for neonatal screeningS F Dobrowolski, R A Banas, E W Naylor, et al.
The Journal of Pediatrics|February 1, 1981
A simple screening test for reduced glutathione in filter paper spots of bloodM D Garrick, A P Orfanos, L Rogers, et al.
Archives of Pathology & Laboratory Medicine|December 3, 1999
Optimization of an automated DNA purification protocol for neonatal screeningE M Heath, D P O'Brien, R Banas, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Intermittent non-ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: an apparent defect in beta-oxidation of fatty acidsE W Naylor, L L Mosovich, R Guthrie, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 21, 1980
Enzymatic studies of urinary isomeric chondroitin sulfates from patients with mucopolysaccharidoses. The application of high performance liquid chromatographyG J Lee, J E Evans, H Tieckelmann, et al.
Clinical Chemistry|October 24, 2001
Rapid diagnosis of methylmalonic and propionic acidemias: quantitative tandem mass spectrometric analysis of propionylcarnitine in filter-paper blood specimens obtained from newbornsD H Chace, J C DiPerna, T A Kalas, et al.
Pediatrics|March 1, 1987
Guanosine triphosphate cyclohydrolase I deficiency: early diagnosis by routine urine pteridine screeningE W Naylor, D Ennis, A G Davidson, et al.
Pageof 6