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Ophthalmology. Retina
|
May 4, 2019
Straylight as an Indicator for Cataract Extraction in Patients with Retinal Dystrophy
Maartje C J van Bree, Laurence Pierrache, Bart L M Zijlmans, et al.
BMC Nephrology
|
December 21, 2018
Association of plasma somatostatin with disease severity and progression in patients with autosomal dominant polycystic kidney disease
A Lianne Messchendorp, Edwin M Spithoven, Niek F Casteleijn, et al.
The Biochemical Journal
|
December 1, 1989
Isolation and partial characterization of heparan sulphate proteoglycan from the human glomerular basement membrane
L P van den Heuvel, J van den Born, T J van de Velden, et al.
Journal of Hypertension
|
December 22, 2018
High-salt intake affects sublingual microcirculation and is linked to body weight change in healthy volunteers: a randomized cross-over trial
Nienke M G Rorije, Emma Rademaker, Esmee M Schrooten, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
October 28, 2025
Spontaneous coronary artery dissection: dissecting an underdiagnosed problem
Deborah N Kalkman, Arja S Vink, Marcel A M Beijk, et al.
Hypertension (Dallas, Tex. : 1979)
|
March 12, 2008
Association between thrombotic microangiopathy and reduced ADAMTS13 activity in malignant hypertension
Bert-Jan H van den Born, Niels V van der Hoeven, Evelyn Groot, et al.
Journal of Medical Genetics
|
August 19, 2018
Homozygous variants in <i>KIAA1549</i>, encoding a ciliary protein, are associated with autosomal recessive retinitis pigmentosa
Suzanne E de Bruijn, Sanne K Verbakel, Erik de Vrieze, et al.
Pharmaceutics
|
January 25, 2025
Development of an Adaptable Qualification Test Set for Personnel Involved in Visual Inspection Procedures of Parenteral Drug Products Manufactured Under Good Manufacturing Practice Conditions in Hospital Pharmacy Compounding Facilities
Tessa van den Born-Bondt, Harmen P S Huizinga, Koen R Kappert, et al.
Investigative Ophthalmology & Visual Science
|
March 23, 2011
Autosomal recessive Stickler syndrome in two families is caused by mutations in the COL9A1 gene
Konstantinos Nikopoulos, Isabelle Schrauwen, Marleen Simon, et al.
Medical & Biological Engineering & Computing
|
January 22, 2023
Automated analysis of finger blood pressure recordings provides insight in determinants of baroreflex sensitivity and heart rate variability-the HELIUS study
D Collard, B E Westerhof, J M Karemaker, et al.
Page
of 72
Search research articles
Search
Showing results (301-310 of 717) with videos related to
Sort By:
Page
of 72
Ophthalmology. Retina
|
May 4, 2019
Straylight as an Indicator for Cataract Extraction in Patients with Retinal Dystrophy
Maartje C J van Bree, Laurence Pierrache, Bart L M Zijlmans, et al.
BMC Nephrology
|
December 21, 2018
Association of plasma somatostatin with disease severity and progression in patients with autosomal dominant polycystic kidney disease
A Lianne Messchendorp, Edwin M Spithoven, Niek F Casteleijn, et al.
The Biochemical Journal
|
December 1, 1989
Isolation and partial characterization of heparan sulphate proteoglycan from the human glomerular basement membrane
L P van den Heuvel, J van den Born, T J van de Velden, et al.
Journal of Hypertension
|
December 22, 2018
High-salt intake affects sublingual microcirculation and is linked to body weight change in healthy volunteers: a randomized cross-over trial
Nienke M G Rorije, Emma Rademaker, Esmee M Schrooten, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
October 28, 2025
Spontaneous coronary artery dissection: dissecting an underdiagnosed problem
Deborah N Kalkman, Arja S Vink, Marcel A M Beijk, et al.
Hypertension (Dallas, Tex. : 1979)
|
March 12, 2008
Association between thrombotic microangiopathy and reduced ADAMTS13 activity in malignant hypertension
Bert-Jan H van den Born, Niels V van der Hoeven, Evelyn Groot, et al.
Journal of Medical Genetics
|
August 19, 2018
Homozygous variants in <i>KIAA1549</i>, encoding a ciliary protein, are associated with autosomal recessive retinitis pigmentosa
Suzanne E de Bruijn, Sanne K Verbakel, Erik de Vrieze, et al.
Pharmaceutics
|
January 25, 2025
Development of an Adaptable Qualification Test Set for Personnel Involved in Visual Inspection Procedures of Parenteral Drug Products Manufactured Under Good Manufacturing Practice Conditions in Hospital Pharmacy Compounding Facilities
Tessa van den Born-Bondt, Harmen P S Huizinga, Koen R Kappert, et al.
Investigative Ophthalmology & Visual Science
|
March 23, 2011
Autosomal recessive Stickler syndrome in two families is caused by mutations in the COL9A1 gene
Konstantinos Nikopoulos, Isabelle Schrauwen, Marleen Simon, et al.
Medical & Biological Engineering & Computing
|
January 22, 2023
Automated analysis of finger blood pressure recordings provides insight in determinants of baroreflex sensitivity and heart rate variability-the HELIUS study
D Collard, B E Westerhof, J M Karemaker, et al.
Page
of 72