M M Hermans - JoVE Visualize

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Journal of Internal Medicine|January 13, 2001

Growth hormone overproduction in a patient with multiple endocrine neoplasia type IM M Hermans, C J Lips, B Bravenboer

The Netherlands Journal of Medicine|May 4, 2001

Malabsorption syndrome in a patient of Mediterranean origin; immunoproliferative small intestinal diseaseM M Hermans, P Klinkhamer, A Stronkhorst, et al.

Pflugers Archiv : European Journal of Physiology|November 1, 1995

pH sensitivity of the cardiac gap junction proteins, connexin 45 and 43M M Hermans, P Kortekaas, H J Jongsma, et al.

The American Journal of Gastroenterology|June 1, 1997

The relationship between lactose tolerance test results and symptoms of lactose intoleranceM M Hermans, R J Brummer, A M Ruijgers, et al.

Biochemical and Biophysical Research Communications|January 13, 1998

Mutation detection in glycogen storage-disease type II by RT-PCR and automated sequencingM M Hermans, D van Leenen, M A Kroos, et al.

Clinical Genetics|July 11, 1998

Glycogen storage disease type II: identification of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase geneM A Kroos, D van Leenen, J Verbiest, et al.

Cardiovascular Research|March 23, 2000

Human connexin40 gap junction channels are modulated by cAMPH V van Rijen, T A van Veen, M M Hermans, et al.

European Journal of Immunology|March 1, 1993

Diversity of immunoglobulin kappa light chain gene rearrangements and evidence for somatic mutation in V kappa IV family gene segments in X-linked agammaglobulinemiaE Timmers, M M Hermans, M E Kraakman, et al.

Expert Review of Molecular Diagnostics|June 8, 2022

Impact of the new European Union In Vitro Diagnostics Regulation on the practice of hospital diagnostic laboratoriesAudrey M M Hermans, Marc Maliepaard, Wouter P C Boon, et al.

Human Mutation|January 1, 1993

Two mutations affecting the transport and maturation of lysosomal alpha-glucosidase in an adult case of glycogen storage disease type IIM M Hermans, M A Kroos, E de Graaff, et al.

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Showing results (1-10 of 45) with videos related to

Sort By:

Pageof 5

Journal of Internal Medicine|January 13, 2001

Growth hormone overproduction in a patient with multiple endocrine neoplasia type IM M Hermans, C J Lips, B Bravenboer

The Netherlands Journal of Medicine|May 4, 2001

Malabsorption syndrome in a patient of Mediterranean origin; immunoproliferative small intestinal diseaseM M Hermans, P Klinkhamer, A Stronkhorst, et al.

Pflugers Archiv : European Journal of Physiology|November 1, 1995

pH sensitivity of the cardiac gap junction proteins, connexin 45 and 43M M Hermans, P Kortekaas, H J Jongsma, et al.

The American Journal of Gastroenterology|June 1, 1997

The relationship between lactose tolerance test results and symptoms of lactose intoleranceM M Hermans, R J Brummer, A M Ruijgers, et al.

Biochemical and Biophysical Research Communications|January 13, 1998

Mutation detection in glycogen storage-disease type II by RT-PCR and automated sequencingM M Hermans, D van Leenen, M A Kroos, et al.

Clinical Genetics|July 11, 1998

Glycogen storage disease type II: identification of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase geneM A Kroos, D van Leenen, J Verbiest, et al.

Cardiovascular Research|March 23, 2000

Human connexin40 gap junction channels are modulated by cAMPH V van Rijen, T A van Veen, M M Hermans, et al.

European Journal of Immunology|March 1, 1993

Diversity of immunoglobulin kappa light chain gene rearrangements and evidence for somatic mutation in V kappa IV family gene segments in X-linked agammaglobulinemiaE Timmers, M M Hermans, M E Kraakman, et al.

Expert Review of Molecular Diagnostics|June 8, 2022

Impact of the new European Union In Vitro Diagnostics Regulation on the practice of hospital diagnostic laboratoriesAudrey M M Hermans, Marc Maliepaard, Wouter P C Boon, et al.

Human Mutation|January 1, 1993

Two mutations affecting the transport and maturation of lysosomal alpha-glucosidase in an adult case of glycogen storage disease type IIM M Hermans, M A Kroos, E de Graaff, et al.

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