M A Kroos - JoVE Visualize

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European Journal of Human Genetics : EJHG|September 14, 1999

Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counsellingM G Ausems, J Verbiest, M P Hermans, et al.

Human Molecular Genetics|September 16, 1998

Recombinant human acid alpha-glucosidase: high level production in mouse milk, biochemical characteristics, correction of enzyme deficiency in GSDII KO miceA G Bijvoet, M A Kroos, F R Pieper, et al.

Biochemical and Biophysical Research Communications|February 15, 1993

Biochemical genetics of glycogenosis type II in Brahman cattleH A Wisselaar, M M Hermans, W J Visser, et al.

Annals of Neurology|September 1, 1995

Genotype-phenotype correlation in adult-onset acid maltase deficiencyJ H Wokke, M G Ausems, M J van den Boogaard, et al.

Journal of Inherited Metabolic Disease|April 24, 2009

Enzyme analysis for Pompe disease in leukocytes; superior results with natural substrate compared with artificial substratesO P van Diggelen, L F Oemardien, N A M E van der Beek, et al.

Human Molecular Genetics|November 5, 1999

Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type IIA G Bijvoet, H Van Hirtum, M A Kroos, et al.

Human Molecular Genetics|February 28, 1998

Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe diseaseA G Bijvoet, E H van de Kamp, M A Kroos, et al.

Community Genetics|June 8, 2004

Glycogen storage disease type II: birth prevalence agrees with predicted genotype frequencyM G Ausems, K ten Berg, M A Kroos, et al.

Journal of the Neurological Sciences|September 2, 2008

Cardiac evaluation in children and adults with Pompe disease sharing the common c.-32-13T>G genotype rarely reveals abnormalitiesN A M E van der Beek, O I I Soliman, C I van Capelle, et al.

Journal of Medical Genetics|June 1, 1996

Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeJ L Keulemans, A J Reuser, M A Kroos, et al.

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Showing results (31-40 of 42) with videos related to

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European Journal of Human Genetics : EJHG|September 14, 1999

Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counsellingM G Ausems, J Verbiest, M P Hermans, et al.

Human Molecular Genetics|September 16, 1998

Recombinant human acid alpha-glucosidase: high level production in mouse milk, biochemical characteristics, correction of enzyme deficiency in GSDII KO miceA G Bijvoet, M A Kroos, F R Pieper, et al.

Biochemical and Biophysical Research Communications|February 15, 1993

Biochemical genetics of glycogenosis type II in Brahman cattleH A Wisselaar, M M Hermans, W J Visser, et al.

Annals of Neurology|September 1, 1995

Genotype-phenotype correlation in adult-onset acid maltase deficiencyJ H Wokke, M G Ausems, M J van den Boogaard, et al.

Journal of Inherited Metabolic Disease|April 24, 2009

Enzyme analysis for Pompe disease in leukocytes; superior results with natural substrate compared with artificial substratesO P van Diggelen, L F Oemardien, N A M E van der Beek, et al.

Human Molecular Genetics|November 5, 1999

Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type IIA G Bijvoet, H Van Hirtum, M A Kroos, et al.

Human Molecular Genetics|February 28, 1998

Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe diseaseA G Bijvoet, E H van de Kamp, M A Kroos, et al.

Community Genetics|June 8, 2004

Glycogen storage disease type II: birth prevalence agrees with predicted genotype frequencyM G Ausems, K ten Berg, M A Kroos, et al.

Journal of the Neurological Sciences|September 2, 2008

Cardiac evaluation in children and adults with Pompe disease sharing the common c.-32-13T>G genotype rarely reveals abnormalitiesN A M E van der Beek, O I I Soliman, C I van Capelle, et al.

Journal of Medical Genetics|June 1, 1996

Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeJ L Keulemans, A J Reuser, M A Kroos, et al.

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