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J Barranger

Showing results (1-10 of 12) with videos related to

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Annals of Clinical Biochemistry|May 1, 1977
The isoenzymes of phenylalanine hydroxylase in humansC E Parker, J Barranger, R Newhouse, et al.
Biochemical Medicine|February 1, 1977
Studies of the isoenzymes of phenylalanine hydroxylase in humansC E Parker, J Barranger, R Newhouse, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1981
Ocular motor signs in some metabolic diseasesD G Cogan, F C Chu, D Reingold, et al.
Transactions of the American Ophthalmological Society|January 1, 1982
Macula halo syndromeD G Cogan, F C Chu, J Barranger, et al.
Neurosurgery|January 1, 1983
Inability of dimethyl sulfoxide and 5-fluorouracil to open the blood-brain barrierE A Neuwelt, P Barnett, J Barranger, et al.
Minnesota Medicine|April 1, 1979
An adult phenylketonuric with schizophrenia. Clinical and biochemical similarities and possible genetic connection between the two diseasesR O Fisch, W B Hosfield, P N Chang, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Biochemical phenotyping of a single sibship with both cystinosis and Fabry diseaseW A Gahl, M Adamson, I Kaiser-Kupfer, et al.
Journal of Neurochemistry|November 1, 1990
Saposins (sphingolipid activator proteins) in the twitcher mutant mouseH Shigematsu, S Morimoto, Y Kishimoto, et al.
Clinical Genetics|June 2, 2007
Imiglucerase (Cerezyme) improves quality of life in patients with skeletal manifestations of Gaucher diseaseN Weinreb, J Barranger, S Packman, et al.
The Journal of Bone and Joint Surgery. American Volume|July 1, 1986
Evaluation of Gaucher disease using magnetic resonance imagingD I Rosenthal, J A Scott, J Barranger, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Annals of Clinical Biochemistry|May 1, 1977
The isoenzymes of phenylalanine hydroxylase in humansC E Parker, J Barranger, R Newhouse, et al.
Biochemical Medicine|February 1, 1977
Studies of the isoenzymes of phenylalanine hydroxylase in humansC E Parker, J Barranger, R Newhouse, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1981
Ocular motor signs in some metabolic diseasesD G Cogan, F C Chu, D Reingold, et al.
Transactions of the American Ophthalmological Society|January 1, 1982
Macula halo syndromeD G Cogan, F C Chu, J Barranger, et al.
Neurosurgery|January 1, 1983
Inability of dimethyl sulfoxide and 5-fluorouracil to open the blood-brain barrierE A Neuwelt, P Barnett, J Barranger, et al.
Minnesota Medicine|April 1, 1979
An adult phenylketonuric with schizophrenia. Clinical and biochemical similarities and possible genetic connection between the two diseasesR O Fisch, W B Hosfield, P N Chang, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Biochemical phenotyping of a single sibship with both cystinosis and Fabry diseaseW A Gahl, M Adamson, I Kaiser-Kupfer, et al.
Journal of Neurochemistry|November 1, 1990
Saposins (sphingolipid activator proteins) in the twitcher mutant mouseH Shigematsu, S Morimoto, Y Kishimoto, et al.
Clinical Genetics|June 2, 2007
Imiglucerase (Cerezyme) improves quality of life in patients with skeletal manifestations of Gaucher diseaseN Weinreb, J Barranger, S Packman, et al.
The Journal of Bone and Joint Surgery. American Volume|July 1, 1986
Evaluation of Gaucher disease using magnetic resonance imagingD I Rosenthal, J A Scott, J Barranger, et al.
Pageof 2