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A C Muntau

Showing results (1-10 of 30) with videos related to

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Fortschritte Der Medizin|August 10, 1990
[Alcohol embryopathy. Review and case example]A C Muntau, O Butenandt
Molecular Genetics and Metabolism|April 18, 2000
Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examinationW Röschinger, A C Muntau, G Rudolph, et al.
American Journal of Human Genetics|August 26, 2000
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GA C Muntau, P U Mayerhofer, B C Paton, et al.
Biochemical and Biophysical Research Communications|February 19, 2000
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypesA C Muntau, A Holzinger, P U Mayerhofer, et al.
Neurology|October 24, 2001
Fish oil supplementation improves visual evoked potentials in children with phenylketonuriaS Beblo, H Reinhardt, A C Muntau, et al.
European Journal of Pediatrics|June 5, 2001
Molecular analysis and long-term follow-up of patients with different forms of 6-pyruvoyl-tetrahydropterin synthase deficiencyA Dudesek, W Röschinger, A C Muntau, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: two novel casesM Linnebank, F Lagler, A C Muntau, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 6, 2000
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycleW Röschinger, A C Muntau, M Duran, et al.
Biological Chemistry|June 6, 2000
Genomic organization, expression analysis, and chromosomal localization of the mouse PEX3 gene encoding a peroxisomal assembly proteinA C Muntau, P U Mayerhofer, S Albet, et al.
Prenatal Diagnosis|February 20, 2004
First-trimester increased nuchal translucency as a prenatal sign of Zellweger syndromeS Strenge, U G Froster, R J A Wanders, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Fortschritte Der Medizin|August 10, 1990
[Alcohol embryopathy. Review and case example]A C Muntau, O Butenandt
Molecular Genetics and Metabolism|April 18, 2000
Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examinationW Röschinger, A C Muntau, G Rudolph, et al.
American Journal of Human Genetics|August 26, 2000
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GA C Muntau, P U Mayerhofer, B C Paton, et al.
Biochemical and Biophysical Research Communications|February 19, 2000
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypesA C Muntau, A Holzinger, P U Mayerhofer, et al.
Neurology|October 24, 2001
Fish oil supplementation improves visual evoked potentials in children with phenylketonuriaS Beblo, H Reinhardt, A C Muntau, et al.
European Journal of Pediatrics|June 5, 2001
Molecular analysis and long-term follow-up of patients with different forms of 6-pyruvoyl-tetrahydropterin synthase deficiencyA Dudesek, W Röschinger, A C Muntau, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: two novel casesM Linnebank, F Lagler, A C Muntau, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 6, 2000
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycleW Röschinger, A C Muntau, M Duran, et al.
Biological Chemistry|June 6, 2000
Genomic organization, expression analysis, and chromosomal localization of the mouse PEX3 gene encoding a peroxisomal assembly proteinA C Muntau, P U Mayerhofer, S Albet, et al.
Prenatal Diagnosis|February 20, 2004
First-trimester increased nuchal translucency as a prenatal sign of Zellweger syndromeS Strenge, U G Froster, R J A Wanders, et al.
Pageof 3