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Ugeskrift for Laeger
|
October 22, 1984
[Screening for serum alpha-fetoprotein for the detection of congenital malformations in the 16-18th weeks of pregnancy. Results of 24,023 pregnancy screenings]
B N Pedersen, P V Bagger, J Bang, et al.
The American Journal of Pathology
|
October 9, 1999
Megalin knockout mice as an animal model of low molecular weight proteinuria
J R Leheste, B Rolinski, H Vorum, et al.
The Journal of Biological Chemistry
|
September 13, 2000
Evidence for the role of megalin in renal uptake of transthyretin
M M Sousa, A G Norden, C Jacobsen, et al.
Medical Physics
|
June 17, 2017
Accuracy of deformable image registration on magnetic resonance images in digital and physical phantoms
Rachel B Ger, Jinzhong Yang, Yao Ding, et al.
Prehospital Emergency Care
|
October 16, 2019
Disparity in Receipt and Utilization of Telecommunicator CPR Instruction
Amanda Amen, Patrick Karabon, Cherie Bartram, et al.
The Western Journal of Emergency Medicine
|
November 18, 2020
CODE BLUE-19: Proposal to Mitigate COVID-19 Transmission in the Emergency Department for Out-of-hospital Cardiac Arrest
David Nguyen, Nima Sarani, Kenneth D Marshall, et al.
Cold Spring Harbor Molecular Case Studies
|
July 12, 2017
Compound heterozygous <i>SLC19A3</i> mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease
Whitney Whitford, Isobel Hawkins, Emma Glamuzina, et al.
Genes
|
February 27, 2026
Foundations of an Ovine Model of Fragile X Syndrome
Victoria Hawkins, Skye R Rudiger, Clive J McLaughlan, et al.
Brachytherapy
|
August 23, 2023
Feasibility of quantitative diffusion-weighted imaging during intra-procedural MRI-guided brachytherapy of locally advanced cervical and vaginal cancers
Megan C Jacobsen, Bastien Rigaud, Samantha J Simiele, et al.
JIMD Reports
|
November 22, 2017
Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q<sub>10</sub> Deficiency in a Female Sib-Pair
Jessie C Jacobsen, Whitney Whitford, Brendan Swan, et al.
Page
of 33
Search research articles
Search
Showing results (271-280 of 327) with videos related to
Sort By:
Page
of 33
Ugeskrift for Laeger
|
October 22, 1984
[Screening for serum alpha-fetoprotein for the detection of congenital malformations in the 16-18th weeks of pregnancy. Results of 24,023 pregnancy screenings]
B N Pedersen, P V Bagger, J Bang, et al.
The American Journal of Pathology
|
October 9, 1999
Megalin knockout mice as an animal model of low molecular weight proteinuria
J R Leheste, B Rolinski, H Vorum, et al.
The Journal of Biological Chemistry
|
September 13, 2000
Evidence for the role of megalin in renal uptake of transthyretin
M M Sousa, A G Norden, C Jacobsen, et al.
Medical Physics
|
June 17, 2017
Accuracy of deformable image registration on magnetic resonance images in digital and physical phantoms
Rachel B Ger, Jinzhong Yang, Yao Ding, et al.
Prehospital Emergency Care
|
October 16, 2019
Disparity in Receipt and Utilization of Telecommunicator CPR Instruction
Amanda Amen, Patrick Karabon, Cherie Bartram, et al.
The Western Journal of Emergency Medicine
|
November 18, 2020
CODE BLUE-19: Proposal to Mitigate COVID-19 Transmission in the Emergency Department for Out-of-hospital Cardiac Arrest
David Nguyen, Nima Sarani, Kenneth D Marshall, et al.
Cold Spring Harbor Molecular Case Studies
|
July 12, 2017
Compound heterozygous <i>SLC19A3</i> mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease
Whitney Whitford, Isobel Hawkins, Emma Glamuzina, et al.
Genes
|
February 27, 2026
Foundations of an Ovine Model of Fragile X Syndrome
Victoria Hawkins, Skye R Rudiger, Clive J McLaughlan, et al.
Brachytherapy
|
August 23, 2023
Feasibility of quantitative diffusion-weighted imaging during intra-procedural MRI-guided brachytherapy of locally advanced cervical and vaginal cancers
Megan C Jacobsen, Bastien Rigaud, Samantha J Simiele, et al.
JIMD Reports
|
November 22, 2017
Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q<sub>10</sub> Deficiency in a Female Sib-Pair
Jessie C Jacobsen, Whitney Whitford, Brendan Swan, et al.
Page
of 33