R A Geerdink - JoVE Visualize

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Human Genetics|July 26, 1977

Phosphoglucose isomerase (PGI) variants in the NetherlandsS G Welch, H A Bartstra, R A Geerdink

European Journal of Clinical Investigation|February 1, 1995

Heterozygous familial hypercholesterolaemia is associated with pathological exercise-induced leakage of muscle proteins, which is not aggravated by simvastatin therapyJ W Smit, P R Bär, R A Geerdink, et al.

Henry Ford Hospital Medical Journal|January 1, 1989

Evolutionary pathways of the calcitonin (CALC) genesC J Lips, R A Geerdink, M G Nieuwenhuis, et al.

Diabetic Medicine : a Journal of the British Diabetic Association|June 19, 1998

Oral magnesium supplementation in insulin-requiring Type 2 diabetic patientsH W de Valk, R Verkaaik, H J van Rijn, et al.

Tropical and Geographical Medicine|September 1, 1975

Serum factors and red cell enzymes in Carib and Arowak Indians from SurinamR A Geerdink, K Okhura, E Li Fo Sjoe, et al.

American Journal of Medical Genetics|December 1, 1989

Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardationR C Hennekam, R A Geerdink, B C Hamel, et al.

Clinical Genetics|November 1, 1979

Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysisA J Vermorken, G T Spierenburg, C A van Bennekom, et al.

Gastroenterology|September 1, 1992

Successful dissolution of cholesterol gallstone during treatment with pravastatinJ W Smit, K J van Erpecum, M F Stolk, et al.

Henry Ford Hospital Medical Journal|January 1, 1992

Long-term follow-up in four large MEN 2 families in The NetherlandsC J Lips, M J Berends, J Brouwers-Smalbraak, et al.

American Journal of Human Genetics|February 1, 1993

The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindredR M Landsvater, A G Rombouts, G J te Meerman, et al.

Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:

Pageof 2

Human Genetics|July 26, 1977

Phosphoglucose isomerase (PGI) variants in the NetherlandsS G Welch, H A Bartstra, R A Geerdink

European Journal of Clinical Investigation|February 1, 1995

Heterozygous familial hypercholesterolaemia is associated with pathological exercise-induced leakage of muscle proteins, which is not aggravated by simvastatin therapyJ W Smit, P R Bär, R A Geerdink, et al.

Henry Ford Hospital Medical Journal|January 1, 1989

Evolutionary pathways of the calcitonin (CALC) genesC J Lips, R A Geerdink, M G Nieuwenhuis, et al.

Diabetic Medicine : a Journal of the British Diabetic Association|June 19, 1998

Oral magnesium supplementation in insulin-requiring Type 2 diabetic patientsH W de Valk, R Verkaaik, H J van Rijn, et al.

Tropical and Geographical Medicine|September 1, 1975

Serum factors and red cell enzymes in Carib and Arowak Indians from SurinamR A Geerdink, K Okhura, E Li Fo Sjoe, et al.

American Journal of Medical Genetics|December 1, 1989

Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardationR C Hennekam, R A Geerdink, B C Hamel, et al.

Clinical Genetics|November 1, 1979

Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysisA J Vermorken, G T Spierenburg, C A van Bennekom, et al.

Gastroenterology|September 1, 1992

Successful dissolution of cholesterol gallstone during treatment with pravastatinJ W Smit, K J van Erpecum, M F Stolk, et al.

Henry Ford Hospital Medical Journal|January 1, 1992

Long-term follow-up in four large MEN 2 families in The NetherlandsC J Lips, M J Berends, J Brouwers-Smalbraak, et al.

American Journal of Human Genetics|February 1, 1993

The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindredR M Landsvater, A G Rombouts, G J te Meerman, et al.

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