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Brain : a Journal of Neurology
|
October 6, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects
Lama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac, et al.
Neuropediatrics
|
June 1, 2017
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease
Gillian I Rice, Naoki Kitabayashi, Magalie Barth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, et al.
Human Mutation
|
March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Bobby G Ng, Paulina Sosicka, Satish Agadi, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 9, 2025
Efficacy of adjuvant therapy in patients with stage IIIA cutaneous melanoma
P Grover, S N Lo, I Li, et al.
Physical Review Letters
|
June 4, 2008
Upper limit on the diffuse flux of ultrahigh energy tau neutrinos from the Pierre Auger Observatory
J Abraham, P Abreu, M Aglietta, et al.
Physical Review Letters
|
September 26, 2012
Measurement of the proton-air cross section at √s=57 TeV with the Pierre Auger Observatory
P Abreu, M Aglietta, E J Ahn, et al.
Physical Review Letters
|
September 4, 2008
Observation of the suppression of the flux of cosmic rays above 4 x 10 (19) eV
J Abraham, P Abreu, M Aglietta, et al.
Physical Review Letters
|
April 7, 2010
Measurement of the depth of maximum of extensive air showers above 10{18} eV
J Abraham, P Abreu, M Aglietta, et al.
Page
of 27
Search research articles
Search
Showing results (261-270 of 269) with videos related to
Sort By:
Page
of 27
You have reached the last page of results.
This site can display upto 269 results.
Brain : a Journal of Neurology
|
October 6, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects
Lama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac, et al.
Neuropediatrics
|
June 1, 2017
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease
Gillian I Rice, Naoki Kitabayashi, Magalie Barth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, et al.
Human Mutation
|
March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Bobby G Ng, Paulina Sosicka, Satish Agadi, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 9, 2025
Efficacy of adjuvant therapy in patients with stage IIIA cutaneous melanoma
P Grover, S N Lo, I Li, et al.
Physical Review Letters
|
June 4, 2008
Upper limit on the diffuse flux of ultrahigh energy tau neutrinos from the Pierre Auger Observatory
J Abraham, P Abreu, M Aglietta, et al.
Physical Review Letters
|
September 26, 2012
Measurement of the proton-air cross section at √s=57 TeV with the Pierre Auger Observatory
P Abreu, M Aglietta, E J Ahn, et al.
Physical Review Letters
|
September 4, 2008
Observation of the suppression of the flux of cosmic rays above 4 x 10 (19) eV
J Abraham, P Abreu, M Aglietta, et al.
Physical Review Letters
|
April 7, 2010
Measurement of the depth of maximum of extensive air showers above 10{18} eV
J Abraham, P Abreu, M Aglietta, et al.
Page
of 27