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M Verheij

Showing results (431-440 of 456) with videos related to

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Scientific Reports|June 25, 2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone MonochromacyElena Buena-Atienza, Klaus Rüther, Britta Baumann, et al.
BMJ (Clinical Research Ed.)|February 22, 2023
Effect of a multifaceted antibiotic stewardship intervention to improve antibiotic prescribing for suspected urinary tract infections in frail older adults (ImpresU): pragmatic cluster randomised controlled trial in four European countriesEsther A R Hartman, Alma C van de Pol, Silje Rebekka Heltveit-Olsen, et al.
Science Advances|June 5, 2021
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defectsMireia Coll-Tané, Naihua N Gong, Samuel J Belfer, et al.
The British Journal of Surgery|April 14, 2018
Association between hospital volume and quality of gastric cancer surgery in the CRITICS trialY H M Claassen, J W van Sandick, H H Hartgrink, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 6, 2018
Surgical morbidity and mortality after neoadjuvant chemotherapy in the CRITICS gastric cancer trialY H M Claassen, H H Hartgrink, J L Dikken, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 21, 2016
The added value of C-reactive protein measurement in diagnosing pneumonia in primary care: a meta-analysis of individual patient dataMargaretha C Minnaard, Joris A H de Groot, Rogier M Hopstaken, et al.
Investigative Ophthalmology & Visual Science|October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformationsBarbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Human Molecular Genetics|December 10, 2015
ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis SyndromeDanny Halim, Robert M W Hofstra, Luca Signorile, et al.
American Journal of Human Genetics|April 4, 2015
Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liabilityQian Jiang, Stacey Arnold, Tiffany Heanue, et al.
American Journal of Human Genetics|July 6, 2010
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liabilityEileen Sproat Emison, Merce Garcia-Barcelo, Elizabeth A Grice, et al.
Pageof 46

Showing results (431-440 of 456) with videos related to

Sort By:
Pageof 46
Scientific Reports|June 25, 2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone MonochromacyElena Buena-Atienza, Klaus Rüther, Britta Baumann, et al.
BMJ (Clinical Research Ed.)|February 22, 2023
Effect of a multifaceted antibiotic stewardship intervention to improve antibiotic prescribing for suspected urinary tract infections in frail older adults (ImpresU): pragmatic cluster randomised controlled trial in four European countriesEsther A R Hartman, Alma C van de Pol, Silje Rebekka Heltveit-Olsen, et al.
Science Advances|June 5, 2021
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defectsMireia Coll-Tané, Naihua N Gong, Samuel J Belfer, et al.
The British Journal of Surgery|April 14, 2018
Association between hospital volume and quality of gastric cancer surgery in the CRITICS trialY H M Claassen, J W van Sandick, H H Hartgrink, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 6, 2018
Surgical morbidity and mortality after neoadjuvant chemotherapy in the CRITICS gastric cancer trialY H M Claassen, H H Hartgrink, J L Dikken, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 21, 2016
The added value of C-reactive protein measurement in diagnosing pneumonia in primary care: a meta-analysis of individual patient dataMargaretha C Minnaard, Joris A H de Groot, Rogier M Hopstaken, et al.
Investigative Ophthalmology & Visual Science|October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformationsBarbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Human Molecular Genetics|December 10, 2015
ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis SyndromeDanny Halim, Robert M W Hofstra, Luca Signorile, et al.
American Journal of Human Genetics|April 4, 2015
Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liabilityQian Jiang, Stacey Arnold, Tiffany Heanue, et al.
American Journal of Human Genetics|July 6, 2010
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liabilityEileen Sproat Emison, Merce Garcia-Barcelo, Elizabeth A Grice, et al.
Pageof 46