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

U Langenbeck

Showing results (1-10 of 68) with videos related to

Pageof 7
Sort By:
Developments in Ophthalmology|July 25, 2003
A glimpse into genomelandU Langenbeck
Journal of Inherited Metabolic Disease|January 23, 2008
Classifying tetrahydrobiopterin responsiveness in the hyperphenylalaninaemiasU Langenbeck
Biochemical Medicine|June 1, 1984
Intracellular levels and metabolism of leucine and alpha-ketoisocaproate in normal and maple syrup urine disease fibroblastsU Wendel, U Langenbeck
European Journal of Pediatrics|July 1, 1996
Towards self-monitoring and self-treatment in phenylketonuria--a way to better diet complianceU Wendel, U Langenbeck
HNO|April 1, 1978
[Studies on the genetics of otosclerosis (author's transl)]M Schröder, U Langenbeck
Human Genetics|March 17, 1978
Lack of association between psoriasis vulgaris and red cell acid phosphatase polymorphismG Matthaei, U Langenbeck
Annals of Nutrition & Metabolism|January 1, 1984
Serum branched-chain amino and keto acid response to a protein-rich meal in manP Schauder, K Schröder, U Langenbeck
American Journal of Medical Genetics|May 1, 1988
The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS)U Langenbeck, I Varga, I Hansmann
Journal of Inherited Metabolic Disease|January 1, 1981
Renal transport of aromatic acids in patients with phenylketonuriaU Langenbeck, A Behbehani, H Luthe
Biomedical Mass Spectrometry|September 1, 1985
Keto acids in tissues and biological fluids: O-t-butyldimethylsilyl quinoxalinols as derivatives for sensitive gas chromatographic/mass spectrometric determinationU Langenbeck, H Luthe, G Schaper
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Developments in Ophthalmology|July 25, 2003
A glimpse into genomelandU Langenbeck
Journal of Inherited Metabolic Disease|January 23, 2008
Classifying tetrahydrobiopterin responsiveness in the hyperphenylalaninaemiasU Langenbeck
Biochemical Medicine|June 1, 1984
Intracellular levels and metabolism of leucine and alpha-ketoisocaproate in normal and maple syrup urine disease fibroblastsU Wendel, U Langenbeck
European Journal of Pediatrics|July 1, 1996
Towards self-monitoring and self-treatment in phenylketonuria--a way to better diet complianceU Wendel, U Langenbeck
HNO|April 1, 1978
[Studies on the genetics of otosclerosis (author's transl)]M Schröder, U Langenbeck
Human Genetics|March 17, 1978
Lack of association between psoriasis vulgaris and red cell acid phosphatase polymorphismG Matthaei, U Langenbeck
Annals of Nutrition & Metabolism|January 1, 1984
Serum branched-chain amino and keto acid response to a protein-rich meal in manP Schauder, K Schröder, U Langenbeck
American Journal of Medical Genetics|May 1, 1988
The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS)U Langenbeck, I Varga, I Hansmann
Journal of Inherited Metabolic Disease|January 1, 1981
Renal transport of aromatic acids in patients with phenylketonuriaU Langenbeck, A Behbehani, H Luthe
Biomedical Mass Spectrometry|September 1, 1985
Keto acids in tissues and biological fluids: O-t-butyldimethylsilyl quinoxalinols as derivatives for sensitive gas chromatographic/mass spectrometric determinationU Langenbeck, H Luthe, G Schaper
Pageof 7