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N J BRANDT

Showing results (1-10 of 52) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1984
Symptoms and signs in organic aciduriasN J Brandt
Journal of Inherited Metabolic Disease|January 1, 1978
Prenatal and postnatal diagnostic difficulties in a family with rare alleles of the galactose-1-phosphate uridyl transferase locusE Christensen, N J Brandt
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduriaE Christensen, N J Brandt
Prenatal Diagnosis|March 1, 1985
Disaccharidase deficiency in amniotic fluid from cases of cystic fibrosisM Schwartz, N J Brandt
Archives of Disease in Childhood|February 1, 1981
Congenital hypothyroidism in DenmarkB B Jacobsen, N J Brandt
Ugeskrift for Laeger|June 20, 1994
[Screening for carriers of cystic fibrosis. Result of a pilot study among pregnant women]N J Brandt, M Schwartz, F Skovby
European Journal of Human Genetics : EJHG|January 1, 1993
Screening for carriers of cystic fibrosis among pregnant women: a pilot studyM Schwartz, N J Brandt, F Skovby
Journal of Inherited Metabolic Disease|January 1, 1983
Normal glycine transport in cultured diploid fibroblasts from hyperglycinaemic subjectsS Kølvraa, F Rosleff, N J Brandt
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 25, 1980
Excretion of short-chain N-acylglycines in the urine of a patient with D-glyceric acidemiaS Kølvraa, N Gregersen, N J Brandt
Ugeskrift for Laeger|February 6, 1989
[Refsum's disease. Hereditary atactic polyneuritis]N J Brandt, E Christensen, T Rosenberg
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1984
Symptoms and signs in organic aciduriasN J Brandt
Journal of Inherited Metabolic Disease|January 1, 1978
Prenatal and postnatal diagnostic difficulties in a family with rare alleles of the galactose-1-phosphate uridyl transferase locusE Christensen, N J Brandt
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduriaE Christensen, N J Brandt
Prenatal Diagnosis|March 1, 1985
Disaccharidase deficiency in amniotic fluid from cases of cystic fibrosisM Schwartz, N J Brandt
Archives of Disease in Childhood|February 1, 1981
Congenital hypothyroidism in DenmarkB B Jacobsen, N J Brandt
Ugeskrift for Laeger|June 20, 1994
[Screening for carriers of cystic fibrosis. Result of a pilot study among pregnant women]N J Brandt, M Schwartz, F Skovby
European Journal of Human Genetics : EJHG|January 1, 1993
Screening for carriers of cystic fibrosis among pregnant women: a pilot studyM Schwartz, N J Brandt, F Skovby
Journal of Inherited Metabolic Disease|January 1, 1983
Normal glycine transport in cultured diploid fibroblasts from hyperglycinaemic subjectsS Kølvraa, F Rosleff, N J Brandt
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 25, 1980
Excretion of short-chain N-acylglycines in the urine of a patient with D-glyceric acidemiaS Kølvraa, N Gregersen, N J Brandt
Ugeskrift for Laeger|February 6, 1989
[Refsum's disease. Hereditary atactic polyneuritis]N J Brandt, E Christensen, T Rosenberg
Pageof 6