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

D Krasnewich

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Blood|May 16, 1998
Splenectomy in Gaucher disease: new management dilemmasD Krasnewich, K Dietrich, L Bauer, et al.
Analytical Biochemistry|May 6, 2003
Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detectionE Orvisky, B Stubblefield, R T Long, et al.
Ophthalmology|March 1, 1993
Ophthalmologic examination in the diagnosis of Proteus syndromeE A Bouzas, D Krasnewich, M Koutroumanidis, et al.
Molecular Genetics and Metabolism|August 18, 2001
Gaucher disease and parkinsonism: a phenotypic and genotypic characterizationN Tayebi, M Callahan, V Madike, et al.
The Journal of Biological Chemistry|April 25, 1991
Sialic acid metabolism in sialuria fibroblastsR Seppala, F Tietze, D Krasnewich, et al.
Pediatric Research|August 6, 2000
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestationE Orvisky, E Sidransky, C E McKinney, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|March 31, 1998
Brief report: association of sex chromosome anomalies with childhood-onset psychotic disordersS Kumra, E Wiggs, D Krasnewich, et al.
Nature|October 12, 1999
Familial dementia caused by polymerization of mutant neuroserpinR L Davis, A E Shrimpton, P D Holohan, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Blood|May 16, 1998
Splenectomy in Gaucher disease: new management dilemmasD Krasnewich, K Dietrich, L Bauer, et al.
Analytical Biochemistry|May 6, 2003
Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detectionE Orvisky, B Stubblefield, R T Long, et al.
Ophthalmology|March 1, 1993
Ophthalmologic examination in the diagnosis of Proteus syndromeE A Bouzas, D Krasnewich, M Koutroumanidis, et al.
Molecular Genetics and Metabolism|August 18, 2001
Gaucher disease and parkinsonism: a phenotypic and genotypic characterizationN Tayebi, M Callahan, V Madike, et al.
The Journal of Biological Chemistry|April 25, 1991
Sialic acid metabolism in sialuria fibroblastsR Seppala, F Tietze, D Krasnewich, et al.
Pediatric Research|August 6, 2000
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestationE Orvisky, E Sidransky, C E McKinney, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|March 31, 1998
Brief report: association of sex chromosome anomalies with childhood-onset psychotic disordersS Kumra, E Wiggs, D Krasnewich, et al.
Nature|October 12, 1999
Familial dementia caused by polymerization of mutant neuroserpinR L Davis, A E Shrimpton, P D Holohan, et al.
Pageof 2