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British Journal of Cancer
|
June 13, 2015
Microsatellite instable vs stable colon carcinomas: analysis of tumour heterogeneity, inflammation and angiogenesis
L 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 families
D 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-Analysis
Xinlin 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 mutation
Rita 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 If
B 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 synthesis
S Grünewald, T Imbach, K Huijben, et al.
Nature Genetics
|
February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
V 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 factor
A 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 pattern
M Mohamed, M Guillard, S B Wortmann, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 157) with videos related to
Sort By:
Page
of 16
British Journal of Cancer
|
June 13, 2015
Microsatellite instable vs stable colon carcinomas: analysis of tumour heterogeneity, inflammation and angiogenesis
L 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 families
D 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-Analysis
Xinlin 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 mutation
Rita 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 If
B 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 synthesis
S Grünewald, T Imbach, K Huijben, et al.
Nature Genetics
|
February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
V 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 factor
A 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 pattern
M Mohamed, M Guillard, S B Wortmann, et al.
Page
of 16