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Disability and Rehabilitation
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September 2, 2021
The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy
Andras Fogarasi, Elisa Fazzi, Ana R P Smorenburg, et al.
American Journal of Medical Genetics. Part A
|
October 8, 2020
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum
Yanick J Crow, Heather Marshall, Gillian I Rice, et al.
Nature Genetics
|
January 24, 2012
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
Beverley H Anderson, Paul R Kasher, Josephine Mayer, et al.
Nature Genetics
|
August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 5, 2018
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care
Ivan Ivanovski, Olivera Djuric, Stefano Giuseppe Caraffi, et al.
Physical Review Letters
|
August 29, 2014
Search for supersymmetry with like-sign lepton-tau events at CDF
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
April 8, 2014
First search for exotic Z Boson decays into photons and neutral pions in hadron collisions
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
December 27, 2014
Measurements of direct CP-violating asymmetries in charmless decays of bottom baryons
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
June 28, 2014
Evidence for s-channel single-top-quark production in events with one charged lepton and two jets at CDF
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
August 29, 2014
Search for resonant top-antitop production in the lepton plus jets decay mode using the full CDF data set
T Aaltonen, S Amerio, D Amidei, et al.
Page
of 52
Search research articles
Search
Showing results (271-280 of 519) with videos related to
Sort By:
Page
of 52
Disability and Rehabilitation
|
September 2, 2021
The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy
Andras Fogarasi, Elisa Fazzi, Ana R P Smorenburg, et al.
American Journal of Medical Genetics. Part A
|
October 8, 2020
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum
Yanick J Crow, Heather Marshall, Gillian I Rice, et al.
Nature Genetics
|
January 24, 2012
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
Beverley H Anderson, Paul R Kasher, Josephine Mayer, et al.
Nature Genetics
|
August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 5, 2018
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care
Ivan Ivanovski, Olivera Djuric, Stefano Giuseppe Caraffi, et al.
Physical Review Letters
|
August 29, 2014
Search for supersymmetry with like-sign lepton-tau events at CDF
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
April 8, 2014
First search for exotic Z Boson decays into photons and neutral pions in hadron collisions
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
December 27, 2014
Measurements of direct CP-violating asymmetries in charmless decays of bottom baryons
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
June 28, 2014
Evidence for s-channel single-top-quark production in events with one charged lepton and two jets at CDF
T Aaltonen, S Amerio, D Amidei, et al.
Physical Review Letters
|
August 29, 2014
Search for resonant top-antitop production in the lepton plus jets decay mode using the full CDF data set
T Aaltonen, S Amerio, D Amidei, et al.
Page
of 52