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Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
May 1, 1980
Estimates of radiation absorbed doses from radioxenons in lung imaging
H L Atkins, J S Robertson, B Y Croft, et al.
Applied and Environmental Microbiology
|
January 5, 2002
Spatial and resource factors influencing high microbial diversity in soil
Jizhong Zhou, Beicheng Xia, David S Treves, et al.
Surgical Neurology
|
January 22, 2008
Single-dose vs multiple-dose antibiotic prophylaxis in instrumented lumbar fusion--a prospective study
Leslie C Hellbusch, Michele Helzer-Julin, Stephen E Doran, et al.
Human Molecular Genetics
|
December 14, 2001
Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis
N Tilgen, F Zorzato, B Halliger-Keller, et al.
Alcohol, Clinical & Experimental Research
|
November 26, 2024
Visium spatial transcriptomics and proteomics identifies novel hepatic cell populations and transcriptomic signatures of alcohol-associated hepatitis
Tyler C Gripshover, Rui S Treves, Eric C Rouchka, et al.
The Journal of Clinical Investigation
|
November 1, 1980
Lung growth and airway function after lobectomy in infancy for congenital lobar emphysema
J T McBride, M E Wohl, D J Strieder, et al.
Neuromuscular Disorders : NMD
|
December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire study
E van Ruitenbeek, J A E Custers, C Verhaak, et al.
Biochemistry and Biophysics Reports
|
April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody disease
J P Molenaar, M M Snoeck, S Treves, et al.
Annals of Neurology
|
September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nuclei
J M Wilmshurst, S Lillis, H Zhou, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M Snoeck, B G M van Engelen, B Küsters, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 192) with videos related to
Sort By:
Page
of 20
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
May 1, 1980
Estimates of radiation absorbed doses from radioxenons in lung imaging
H L Atkins, J S Robertson, B Y Croft, et al.
Applied and Environmental Microbiology
|
January 5, 2002
Spatial and resource factors influencing high microbial diversity in soil
Jizhong Zhou, Beicheng Xia, David S Treves, et al.
Surgical Neurology
|
January 22, 2008
Single-dose vs multiple-dose antibiotic prophylaxis in instrumented lumbar fusion--a prospective study
Leslie C Hellbusch, Michele Helzer-Julin, Stephen E Doran, et al.
Human Molecular Genetics
|
December 14, 2001
Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis
N Tilgen, F Zorzato, B Halliger-Keller, et al.
Alcohol, Clinical & Experimental Research
|
November 26, 2024
Visium spatial transcriptomics and proteomics identifies novel hepatic cell populations and transcriptomic signatures of alcohol-associated hepatitis
Tyler C Gripshover, Rui S Treves, Eric C Rouchka, et al.
The Journal of Clinical Investigation
|
November 1, 1980
Lung growth and airway function after lobectomy in infancy for congenital lobar emphysema
J T McBride, M E Wohl, D J Strieder, et al.
Neuromuscular Disorders : NMD
|
December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire study
E van Ruitenbeek, J A E Custers, C Verhaak, et al.
Biochemistry and Biophysics Reports
|
April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody disease
J P Molenaar, M M Snoeck, S Treves, et al.
Annals of Neurology
|
September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nuclei
J M Wilmshurst, S Lillis, H Zhou, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M Snoeck, B G M van Engelen, B Küsters, et al.
Page
of 20