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American Journal of Medical Genetics. Part A
|
July 4, 2020
A homozygous variant in growth and differentiation factor 2 (GDF2) may cause lymphatic dysplasia with hydrothorax and nonimmune hydrops fetalis
Sietse M Aukema, Gerdien A Ten Brinke, Wim Timens, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
December 16, 2006
A prospective multi-centre study of the value of FDG-PET as part of a structured diagnostic protocol in patients with fever of unknown origin
Chantal P Bleeker-Rovers, Fidel J Vos, Aart H Mudde, et al.
Healthcare (Basel, Switzerland)
|
September 27, 2025
Early Palliative Care in Patients with Glioblastoma: Co-Design of an Integrated Care Pathway
Esmée K J van der Poort, Monique C M Baas-Thijssen, Marleen Oomes, et al.
Molecular Cancer Therapeutics
|
May 22, 2012
MLN0905, a small-molecule plk1 inhibitor, induces antitumor responses in human models of diffuse large B-cell lymphoma
Judy Quiju Shi, Kerri Lasky, Vaishali Shinde, et al.
Journal of Clinical Monitoring and Computing
|
July 20, 2024
Comparing the haemodynamic effects of high- and low-dose opioid anaesthesia: a secondary analysis of a randomised controlled trial
O M Marges, J P Nieboer, I N de Keijzer, et al.
European Journal of Human Genetics : EJHG
|
September 19, 2019
Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy
Diantha Terlouw, Manon Suerink, Sunny S Singh, et al.
Hereditary Cancer in Clinical Practice
|
August 14, 2010
A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
Els van Riel, Margreet Gem Ausems, Frans Bl Hogervorst, et al.
European Heart Journal. Case Reports
|
October 27, 2021
Case series, chemotherapy-induced cardiomyopathy: mind the family history!
Setareh Moghadasi, Rienke Fijn, Saskia L M A Beeres, et al.
American Journal of Medical Genetics. Part A
|
January 24, 2009
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstruction
Marja W Wessels, Ingrid M B H van de Laar, Jolien Roos-Hesselink, et al.
Annals of Vascular Surgery
|
November 13, 2019
Adverse Cardiac Events and Mortality in Patients with Critical Limb Ischemia
Joost J P Roijers, Bastiaan Y S Rakké, Niels C J Hopmans, et al.
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of 57
Search research articles
Search
Showing results (501-510 of 566) with videos related to
Sort By:
Page
of 57
American Journal of Medical Genetics. Part A
|
July 4, 2020
A homozygous variant in growth and differentiation factor 2 (GDF2) may cause lymphatic dysplasia with hydrothorax and nonimmune hydrops fetalis
Sietse M Aukema, Gerdien A Ten Brinke, Wim Timens, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
December 16, 2006
A prospective multi-centre study of the value of FDG-PET as part of a structured diagnostic protocol in patients with fever of unknown origin
Chantal P Bleeker-Rovers, Fidel J Vos, Aart H Mudde, et al.
Healthcare (Basel, Switzerland)
|
September 27, 2025
Early Palliative Care in Patients with Glioblastoma: Co-Design of an Integrated Care Pathway
Esmée K J van der Poort, Monique C M Baas-Thijssen, Marleen Oomes, et al.
Molecular Cancer Therapeutics
|
May 22, 2012
MLN0905, a small-molecule plk1 inhibitor, induces antitumor responses in human models of diffuse large B-cell lymphoma
Judy Quiju Shi, Kerri Lasky, Vaishali Shinde, et al.
Journal of Clinical Monitoring and Computing
|
July 20, 2024
Comparing the haemodynamic effects of high- and low-dose opioid anaesthesia: a secondary analysis of a randomised controlled trial
O M Marges, J P Nieboer, I N de Keijzer, et al.
European Journal of Human Genetics : EJHG
|
September 19, 2019
Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy
Diantha Terlouw, Manon Suerink, Sunny S Singh, et al.
Hereditary Cancer in Clinical Practice
|
August 14, 2010
A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
Els van Riel, Margreet Gem Ausems, Frans Bl Hogervorst, et al.
European Heart Journal. Case Reports
|
October 27, 2021
Case series, chemotherapy-induced cardiomyopathy: mind the family history!
Setareh Moghadasi, Rienke Fijn, Saskia L M A Beeres, et al.
American Journal of Medical Genetics. Part A
|
January 24, 2009
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstruction
Marja W Wessels, Ingrid M B H van de Laar, Jolien Roos-Hesselink, et al.
Annals of Vascular Surgery
|
November 13, 2019
Adverse Cardiac Events and Mortality in Patients with Critical Limb Ischemia
Joost J P Roijers, Bastiaan Y S Rakké, Niels C J Hopmans, et al.
Page
of 57