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G Matthijs

Showing results (141-150 of 157) with videos related to

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British Journal of Cancer|June 13, 2015
Microsatellite instable vs stable colon carcinomas: analysis of tumour heterogeneity, inflammation and angiogenesisL De Smedt, J Lemahieu, S Palmans, et al.
Human Mutation|September 12, 2000
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)E Schollen, L Dorland, T J de Koning, et al.
British Journal of Cancer|March 15, 2012
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer familiesD J Osher, K De Leeneer, G Michils, et al.
Diagnostics (Basel, Switzerland)|January 10, 2026
Yttrium-90 Selective Internal Radiation Therapy for Neuroendocrine Liver Metastases: An Institutional Case Series, Updated Systematic Review, and Meta-AnalysisXinlin Zheng, Fang Wen, Huan Xi, et al.
Journal of Neurology|October 31, 2014
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutationRita Barone, M Carrozzi, R Parini, et al.
The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.
Biochimica Et Biophysica Acta|March 3, 2011
Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin patternM Mohamed, M Guillard, S B Wortmann, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
British Journal of Cancer|June 13, 2015
Microsatellite instable vs stable colon carcinomas: analysis of tumour heterogeneity, inflammation and angiogenesisL De Smedt, J Lemahieu, S Palmans, et al.
Human Mutation|September 12, 2000
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)E Schollen, L Dorland, T J de Koning, et al.
British Journal of Cancer|March 15, 2012
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer familiesD J Osher, K De Leeneer, G Michils, et al.
Diagnostics (Basel, Switzerland)|January 10, 2026
Yttrium-90 Selective Internal Radiation Therapy for Neuroendocrine Liver Metastases: An Institutional Case Series, Updated Systematic Review, and Meta-AnalysisXinlin Zheng, Fang Wen, Huan Xi, et al.
Journal of Neurology|October 31, 2014
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutationRita Barone, M Carrozzi, R Parini, et al.
The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.
Biochimica Et Biophysica Acta|March 3, 2011
Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin patternM Mohamed, M Guillard, S B Wortmann, et al.
Pageof 16