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N J BRANDT

Showing results (11-20 of 52) with videos related to

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Acta Paediatrica Scandinavica|July 1, 1979
Nonketotic hyperglycinemia. Clinical, biochemical and therapeutic aspectsS Kølvraa, N J Brandt, E Christensen
Journal of Inherited Metabolic Disease|January 1, 1987
Adenine phosphoribosyltransferase deficiency: a case diagnosed by GC-MS identification of 2,8-dihydroxyadenine in urinary crystalsE Christensen, N J Brandt, T Laxdal
Pediatric Research|September 1, 1980
Studies of the glycine metabolism in a patient with D-glyceric acidemia and hyperglycinemiaS Kølvraa, E Christensen, N J Brandt
Pediatric Research|October 1, 1976
D-glyceric acidemia: biohcemical studies of a new syndromeS Kolvraa, K Rasmussen, N J Brandt
Acta Paediatrica Scandinavica|November 1, 1982
Congenital primary hypothyroidism and HLAB B Jacobsen, N J Brandt, A Svejgaard
Acta Paediatrica Scandinavica|September 1, 1983
Prolidase deficiencyP S Pedersen, E Christensen, N J Brandt
Human Heredity|January 1, 1977
Congenital hypomegakaryocytic thrombocytopenia associated with bilateral absence of the radius - the TAR syndromeS B Edelberg, J Cohn, N J Brandt
Acta Paediatrica Scandinavica|March 1, 1982
Studies on pyruvate carboxylase, pyruvate decarboxylase and lipoamide dehydrogenase in subacute necrotizing encephalomyelopathyT L Hansen, E Christensen, N J Brandt
Ugeskrift for Laeger|July 10, 1998
[Gaucher disease type 1--therapeutic results of enzyme substitution]J Steensberg, K G Nielsen, N J Brandt
Ugeskrift for Laeger|July 10, 1998
[Enzyme substitution in Gauscher disease]J Steensberg, K G Nielsen, N J Brandt
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Acta Paediatrica Scandinavica|July 1, 1979
Nonketotic hyperglycinemia. Clinical, biochemical and therapeutic aspectsS Kølvraa, N J Brandt, E Christensen
Journal of Inherited Metabolic Disease|January 1, 1987
Adenine phosphoribosyltransferase deficiency: a case diagnosed by GC-MS identification of 2,8-dihydroxyadenine in urinary crystalsE Christensen, N J Brandt, T Laxdal
Pediatric Research|September 1, 1980
Studies of the glycine metabolism in a patient with D-glyceric acidemia and hyperglycinemiaS Kølvraa, E Christensen, N J Brandt
Pediatric Research|October 1, 1976
D-glyceric acidemia: biohcemical studies of a new syndromeS Kolvraa, K Rasmussen, N J Brandt
Acta Paediatrica Scandinavica|November 1, 1982
Congenital primary hypothyroidism and HLAB B Jacobsen, N J Brandt, A Svejgaard
Acta Paediatrica Scandinavica|September 1, 1983
Prolidase deficiencyP S Pedersen, E Christensen, N J Brandt
Human Heredity|January 1, 1977
Congenital hypomegakaryocytic thrombocytopenia associated with bilateral absence of the radius - the TAR syndromeS B Edelberg, J Cohn, N J Brandt
Acta Paediatrica Scandinavica|March 1, 1982
Studies on pyruvate carboxylase, pyruvate decarboxylase and lipoamide dehydrogenase in subacute necrotizing encephalomyelopathyT L Hansen, E Christensen, N J Brandt
Ugeskrift for Laeger|July 10, 1998
[Gaucher disease type 1--therapeutic results of enzyme substitution]J Steensberg, K G Nielsen, N J Brandt
Ugeskrift for Laeger|July 10, 1998
[Enzyme substitution in Gauscher disease]J Steensberg, K G Nielsen, N J Brandt
Pageof 6