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

S Pitkänen

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Biochemical and Molecular Medicine|December 1, 1996
Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast culturesS Pitkänen, S Raha, B H Robinson
Journal of Inherited Metabolic Disease|January 1, 1996
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findingsS Pitkänen, A Feigenbaum, R Laframboise, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 26, 2000
Serum tumor marker CA 125 is an early and sensitive indicator of veno-occlusive disease in children undergoing bone marrow transplantationJ Petäjä, S Pitkänen, K Vettenranta, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 19, 2000
Mitochondrial dysfunction in congenital nephrotic syndromeM L Solin, S Pitkänen, J W Taanman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 31, 2003
Association between serum oncofetal antigens CA 19-9 and CA 125 and clinical status in patients with cystic fibrosisE Gronowitz, S Pitkänen, I Kjellmer, et al.
Genomics|November 1, 1996
Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13S J Hyslop, A M Duncan, S Pitkänen, et al.
British Journal of Cancer|July 2, 1999
Generation of reactive oxygen species by human mesothelioma cellsK Kahlos, S Pitkänen, I Hassinen, et al.
Journal of the Neurological Sciences|June 1, 1986
Cholesterol esterase activity in cerebrospinal fluid of multiple sclerosis patientsA S Pitkänen, T O Halonen, H O Kilpeläinen, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 10, 1999
Serum type III procollagen in children with type I hereditary tyrosinemiaS Pitkänen, M K Salo, K Vettenranta, et al.
Pediatric Research|February 1, 1994
Serum levels of oncofetal markers CA 125, CA 19-9, and alpha-fetoprotein in children with hereditary tyrosinemia type IS Pitkänen, M K Salo, P Kuusela, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Biochemical and Molecular Medicine|December 1, 1996
Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast culturesS Pitkänen, S Raha, B H Robinson
Journal of Inherited Metabolic Disease|January 1, 1996
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findingsS Pitkänen, A Feigenbaum, R Laframboise, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 26, 2000
Serum tumor marker CA 125 is an early and sensitive indicator of veno-occlusive disease in children undergoing bone marrow transplantationJ Petäjä, S Pitkänen, K Vettenranta, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 19, 2000
Mitochondrial dysfunction in congenital nephrotic syndromeM L Solin, S Pitkänen, J W Taanman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 31, 2003
Association between serum oncofetal antigens CA 19-9 and CA 125 and clinical status in patients with cystic fibrosisE Gronowitz, S Pitkänen, I Kjellmer, et al.
Genomics|November 1, 1996
Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13S J Hyslop, A M Duncan, S Pitkänen, et al.
British Journal of Cancer|July 2, 1999
Generation of reactive oxygen species by human mesothelioma cellsK Kahlos, S Pitkänen, I Hassinen, et al.
Journal of the Neurological Sciences|June 1, 1986
Cholesterol esterase activity in cerebrospinal fluid of multiple sclerosis patientsA S Pitkänen, T O Halonen, H O Kilpeläinen, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 10, 1999
Serum type III procollagen in children with type I hereditary tyrosinemiaS Pitkänen, M K Salo, K Vettenranta, et al.
Pediatric Research|February 1, 1994
Serum levels of oncofetal markers CA 125, CA 19-9, and alpha-fetoprotein in children with hereditary tyrosinemia type IS Pitkänen, M K Salo, P Kuusela, et al.
Pageof 2