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Journal of Medical Genetics
|
May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome
J van Reeuwijk, M Janssen, C van den Elzen, et al.
Alimentary Pharmacology & Therapeutics
|
September 16, 2017
Risk factors for thiopurine-induced myelosuppression and infections in inflammatory bowel disease patients with a normal TPMT genotype
M M T J Broekman, M J H Coenen, G J Wanten, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 11, 2024
Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing
R Baardman, H H Lemmink, V K Yenamandra, et al.
Zeitschrift Fur Gastroenterologie
|
March 17, 2015
[Improvement of cost allocation in gastroenterology by introduction of a novel service catalogue covering the complete spectrum of endoscopic procedures]
M Rathmayer, H Scheffer, M Braun, et al.
Alimentary Pharmacology & Therapeutics
|
December 13, 2016
Early prediction of thiopurine-induced hepatotoxicity in inflammatory bowel disease
D R Wong, M J H Coenen, L J J Derijks, et al.
The Pharmacogenomics Journal
|
January 4, 2017
The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine
M M T J Broekman, D R Wong, G J A Wanten, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M Snoeck, B G M van Engelen, B Küsters, et al.
Gastroenterology
|
December 29, 2023
Standard of Care Versus Octreotide in Angiodysplasia-Related Bleeding (the OCEAN Study): A Multicenter Randomized Controlled Trial
Lia C M J Goltstein, Karina V Grooteman, Lucas H P Bernts, et al.
American Journal of Human Genetics
|
December 20, 2011
Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement
Alejandro Estrada-Cuzcano, Kornelia Neveling, Susanne Kohl, et al.
Endoscopy International Open
|
October 13, 2023
Adherence to guideline recommendations for Barrett's esophagus (BE) surveillance endoscopies: Effects of dedicated BE endoscopy lists
I N Beaufort, A N Milne, Y A Alderlieste, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 154) with videos related to
Sort By:
Page
of 16
Journal of Medical Genetics
|
May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome
J van Reeuwijk, M Janssen, C van den Elzen, et al.
Alimentary Pharmacology & Therapeutics
|
September 16, 2017
Risk factors for thiopurine-induced myelosuppression and infections in inflammatory bowel disease patients with a normal TPMT genotype
M M T J Broekman, M J H Coenen, G J Wanten, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 11, 2024
Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing
R Baardman, H H Lemmink, V K Yenamandra, et al.
Zeitschrift Fur Gastroenterologie
|
March 17, 2015
[Improvement of cost allocation in gastroenterology by introduction of a novel service catalogue covering the complete spectrum of endoscopic procedures]
M Rathmayer, H Scheffer, M Braun, et al.
Alimentary Pharmacology & Therapeutics
|
December 13, 2016
Early prediction of thiopurine-induced hepatotoxicity in inflammatory bowel disease
D R Wong, M J H Coenen, L J J Derijks, et al.
The Pharmacogenomics Journal
|
January 4, 2017
The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine
M M T J Broekman, D R Wong, G J A Wanten, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M Snoeck, B G M van Engelen, B Küsters, et al.
Gastroenterology
|
December 29, 2023
Standard of Care Versus Octreotide in Angiodysplasia-Related Bleeding (the OCEAN Study): A Multicenter Randomized Controlled Trial
Lia C M J Goltstein, Karina V Grooteman, Lucas H P Bernts, et al.
American Journal of Human Genetics
|
December 20, 2011
Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement
Alejandro Estrada-Cuzcano, Kornelia Neveling, Susanne Kohl, et al.
Endoscopy International Open
|
October 13, 2023
Adherence to guideline recommendations for Barrett's esophagus (BE) surveillance endoscopies: Effects of dedicated BE endoscopy lists
I N Beaufort, A N Milne, Y A Alderlieste, et al.
Page
of 16