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

T Tønnesen

Showing results (1-10 of 57) with videos related to

Pageof 6
Sort By:
Cytobiologie|April 1, 1978
The genes for 5 S ribosomal RNA and transfer RNA in Tetrahymena pyriformisT Tønnesen
Human Genetics|January 1, 1984
The use of fructose 1-phosphate to detect Hunter heterozygotes in fibroblast cultures from high-risk carriersT Tønnesen
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 30, 1986
[Hemorrhagic cystitis in peroral treatment with cyclophosphamide]R Lilleng, T Tønnesen
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal and postnatal diagnosis of Menkes disease, an inherited disorder of copper metabolismT Tønnesen, N Horn
Acta Neurologica Scandinavica|January 1, 1985
A variant form of metachromatic leucodystrophy in a patient suffering from another congenital degenerative neurological diseaseA M Nordenbo, T Tønnesen
Human Genetics|January 1, 1983
Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndromeT Tønnesen, F Güttler, C Lykkelund
Journal of Inherited Metabolic Disease|January 1, 1994
Detection of genetic defects in Menkes disease by direct mutation analysis and its implications in carrier diagnosisZ Tümer, T Tønnesen, N Horn
Brain Pathology (Zurich, Switzerland)|October 1, 1992
Menkes disease: an X-linked neurological disorder of the copper metabolismN Horn, T Tønnesen, Z Tümer
Journal of Inherited Metabolic Disease|January 1, 1988
Highly increased levels of serum beta-hexosaminidase, arylsulphatase A and beta-galactosidase in a patient with sepsisT Tønnesen, P Andersen, F Güttler
Human Genetics|January 1, 1982
Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphateT Tønnesen, C Lykkelund, F Güttler
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Cytobiologie|April 1, 1978
The genes for 5 S ribosomal RNA and transfer RNA in Tetrahymena pyriformisT Tønnesen
Human Genetics|January 1, 1984
The use of fructose 1-phosphate to detect Hunter heterozygotes in fibroblast cultures from high-risk carriersT Tønnesen
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 30, 1986
[Hemorrhagic cystitis in peroral treatment with cyclophosphamide]R Lilleng, T Tønnesen
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal and postnatal diagnosis of Menkes disease, an inherited disorder of copper metabolismT Tønnesen, N Horn
Acta Neurologica Scandinavica|January 1, 1985
A variant form of metachromatic leucodystrophy in a patient suffering from another congenital degenerative neurological diseaseA M Nordenbo, T Tønnesen
Human Genetics|January 1, 1983
Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndromeT Tønnesen, F Güttler, C Lykkelund
Journal of Inherited Metabolic Disease|January 1, 1994
Detection of genetic defects in Menkes disease by direct mutation analysis and its implications in carrier diagnosisZ Tümer, T Tønnesen, N Horn
Brain Pathology (Zurich, Switzerland)|October 1, 1992
Menkes disease: an X-linked neurological disorder of the copper metabolismN Horn, T Tønnesen, Z Tümer
Journal of Inherited Metabolic Disease|January 1, 1988
Highly increased levels of serum beta-hexosaminidase, arylsulphatase A and beta-galactosidase in a patient with sepsisT Tønnesen, P Andersen, F Güttler
Human Genetics|January 1, 1982
Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphateT Tønnesen, C Lykkelund, F Güttler
Pageof 6