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H Scheffer

Showing results (81-90 of 154) with videos related to

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Neurogastroenterology and Motility|December 5, 2002
Elicitation of transient lower oesophageal sphincter relaxations in response to gastric distension and meal ingestionR C H Scheffer, L M A Akkermans, J E Bais, et al.
European Journal of Pediatrics|June 2, 2000
Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chartJ P Rake, A M ten Berge, G Visser, et al.
Human Mutation|March 29, 2000
Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypesJ P Rake, A M ten Berge, G Visser, et al.
Human Mutation|March 27, 1999
Glycogen storage disease type Ia: four novel mutations (175delGG, R170X, G266V and V338F) identified. Mutations in brief no. 220. OnlineJ P Rake, A M ten Berge, E Verlind, et al.
Human Genetics|June 1, 1991
Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28A J van Essen, K Kok, A van den Berg, et al.
Genes, Chromosomes & Cancer|April 1, 1992
Chromosomal sublocalization of the 2;13 translocation breakpoint in alveolar rhabdomyosarcomaD N Shapiro, M B Valentine, J E Sublett, et al.
Endoscopy|October 1, 2014
A new fully covered metal stent with anti-migration features for the treatment of malignant dysphagiaDaisy Walter, Maarten W van den Berg, Jeanin E van Hooft, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1997
ACE polymorphism does not determine short-term renal response to ACE-inhibition in proteinuric patientsF G van der Kleij, G J Navis, R T Gansevoort, et al.
Lancet (London, England)|April 15, 1995
PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophyG van der Steege, P M Grootscholten, P van der Vlies, et al.
Neurology|September 19, 2008
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromesF Brugman, H Scheffer, J H J Wokke, et al.
Pageof 16

Showing results (81-90 of 154) with videos related to

Sort By:
Pageof 16
Neurogastroenterology and Motility|December 5, 2002
Elicitation of transient lower oesophageal sphincter relaxations in response to gastric distension and meal ingestionR C H Scheffer, L M A Akkermans, J E Bais, et al.
European Journal of Pediatrics|June 2, 2000
Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chartJ P Rake, A M ten Berge, G Visser, et al.
Human Mutation|March 29, 2000
Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypesJ P Rake, A M ten Berge, G Visser, et al.
Human Mutation|March 27, 1999
Glycogen storage disease type Ia: four novel mutations (175delGG, R170X, G266V and V338F) identified. Mutations in brief no. 220. OnlineJ P Rake, A M ten Berge, E Verlind, et al.
Human Genetics|June 1, 1991
Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28A J van Essen, K Kok, A van den Berg, et al.
Genes, Chromosomes & Cancer|April 1, 1992
Chromosomal sublocalization of the 2;13 translocation breakpoint in alveolar rhabdomyosarcomaD N Shapiro, M B Valentine, J E Sublett, et al.
Endoscopy|October 1, 2014
A new fully covered metal stent with anti-migration features for the treatment of malignant dysphagiaDaisy Walter, Maarten W van den Berg, Jeanin E van Hooft, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1997
ACE polymorphism does not determine short-term renal response to ACE-inhibition in proteinuric patientsF G van der Kleij, G J Navis, R T Gansevoort, et al.
Lancet (London, England)|April 15, 1995
PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophyG van der Steege, P M Grootscholten, P van der Vlies, et al.
Neurology|September 19, 2008
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromesF Brugman, H Scheffer, J H J Wokke, et al.
Pageof 16