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H Willemsen

Showing results (121-130 of 180) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|April 27, 2013
Targeted phosphotyrosine profiling of glycoprotein VI signaling implicates oligophrenin-1 in platelet filopodia formationOnno B Bleijerveld, Thijs C van Holten, Christian Preisinger, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletionsMarjolein H Willemsen, Nicole de Leeuw, Catherine Mercer, et al.
Cancer Medicine|December 9, 2022
The predictive and prognostic value of weight loss and body composition prior to and during immune checkpoint inhibition in recurrent or metastatic head and neck cancer patientsAnna C H Willemsen, Nina De Moor, Jeroen Van Dessel, et al.
Frontiers in Endocrinology|September 13, 2023
Key features of puberty onset and progression can help distinguish self-limited delayed puberty from congenital hypogonadotrophic hypogonadismYuri Aung, Vasilis Kokotsis, Kyla Ng Yin, et al.
Clinical Nutrition (Edinburgh, Scotland)|December 17, 2019
Prediction model for tube feeding dependency during chemoradiotherapy for at least four weeks in head and neck cancer patients: A tool for prophylactic gastrostomy decision makingAnna C H Willemsen, Annemieke Kok, Sander M J van Kuijk, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Adaptive and maladaptive functioning in Kleefstra syndrome compared to other rare genetic disorders with intellectual disabilitiesKarlijn Vermeulen, Anneke de Boer, Joost G E Janzing, et al.
Clinical Genetics|January 6, 2011
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletionsM H Willemsen, G Beunders, M Callaghan, et al.
Clinical Endocrinology|June 15, 2007
Long-term effects of growth hormone (GH) treatment on body composition and bone mineral density in short children born small-for-gestational-age: six-year follow-up of a randomized controlled GH trialRuben H Willemsen, Nicolette J T Arends, Willie M Bakker-van Waarde, et al.
Neuro-Oncology Advances|April 27, 2022
Temporal muscle thickness as an independent prognostic imaging marker in newly diagnosed glioblastoma patients: A validation studyMartinus P G Broen, Rueben Beckers, Anna C H Willemsen, et al.
Journal of Medical Genetics|February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defectsMarjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Pageof 18

Showing results (121-130 of 180) with videos related to

Sort By:
Pageof 18
Arteriosclerosis, Thrombosis, and Vascular Biology|April 27, 2013
Targeted phosphotyrosine profiling of glycoprotein VI signaling implicates oligophrenin-1 in platelet filopodia formationOnno B Bleijerveld, Thijs C van Holten, Christian Preisinger, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletionsMarjolein H Willemsen, Nicole de Leeuw, Catherine Mercer, et al.
Cancer Medicine|December 9, 2022
The predictive and prognostic value of weight loss and body composition prior to and during immune checkpoint inhibition in recurrent or metastatic head and neck cancer patientsAnna C H Willemsen, Nina De Moor, Jeroen Van Dessel, et al.
Frontiers in Endocrinology|September 13, 2023
Key features of puberty onset and progression can help distinguish self-limited delayed puberty from congenital hypogonadotrophic hypogonadismYuri Aung, Vasilis Kokotsis, Kyla Ng Yin, et al.
Clinical Nutrition (Edinburgh, Scotland)|December 17, 2019
Prediction model for tube feeding dependency during chemoradiotherapy for at least four weeks in head and neck cancer patients: A tool for prophylactic gastrostomy decision makingAnna C H Willemsen, Annemieke Kok, Sander M J van Kuijk, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Adaptive and maladaptive functioning in Kleefstra syndrome compared to other rare genetic disorders with intellectual disabilitiesKarlijn Vermeulen, Anneke de Boer, Joost G E Janzing, et al.
Clinical Genetics|January 6, 2011
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletionsM H Willemsen, G Beunders, M Callaghan, et al.
Clinical Endocrinology|June 15, 2007
Long-term effects of growth hormone (GH) treatment on body composition and bone mineral density in short children born small-for-gestational-age: six-year follow-up of a randomized controlled GH trialRuben H Willemsen, Nicolette J T Arends, Willie M Bakker-van Waarde, et al.
Neuro-Oncology Advances|April 27, 2022
Temporal muscle thickness as an independent prognostic imaging marker in newly diagnosed glioblastoma patients: A validation studyMartinus P G Broen, Rueben Beckers, Anna C H Willemsen, et al.
Journal of Medical Genetics|February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defectsMarjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Pageof 18