Zobrazeno 1 - 10
of 1 290
pro vyhledávání: '"F, Hammer"'
Autor:
Y., Yang, F., Hammer, H., Li, S., Pawlowski M., L., Wang J., C., Babusiaux, A., Mamon G., P., Bonifacio, Y., Jiao, H., Wang
Gaia EDR3 has provided proper motions of Milky Way (MW) dwarf galaxies with an unprecedented accuracy, which allows us to investigate their orbital properties. We found that the total energy and angular momentum of MW dwarf galaxies are much larger t
Externí odkaz:
http://arxiv.org/abs/2306.17208
Publikováno v:
Biology Open, Vol 13, Iss 4 (2024)
Externí odkaz:
https://doaj.org/article/a78aba6b825b42bd8451cc4c181641ca
Publikováno v:
Journal of Sensors and Sensor Systems, Vol 9, Pp 143-155 (2020)
This paper presents the extension of an empirical study in which a universally applicable fault diagnosis method is used to analyse vibration data of bearings measured with accelerometers. The motivation for extending the previously published results
Externí odkaz:
https://doaj.org/article/fdaeef3d4bb641b387c1bab9c6b27dc4
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0238121 (2020)
Variants implicated in childhood epilepsy have been identified in all four voltage-gated sodium channels that initiate action potentials in the central nervous system. Previous research has focused on the functional effects of particular variants wit
Externí odkaz:
https://doaj.org/article/d446e92b8d5540128825178e307e1f2c
Publikováno v:
Parasites & Vectors, Vol 10, Iss 1, Pp 1-9 (2017)
Abstract Background Bovine theileriosis, caused by the haemoprotozoan Theileria orientalis, is an emerging disease in East Asia and Australasia. Previous studies have demonstrated transplacental transmission of various Theileria spp. but molecular co
Externí odkaz:
https://doaj.org/article/6de1b745f18044c39820f92b238e6d5b
Publikováno v:
Cleveland Clinic Journal of Medicine. 89:513-522
Autor:
Michael F. Hammer, Yanling Pan, Medhane Cumbay, Manuela Pendziwiat, Zaid Afawi, Hadassah Goldberg‐Stern, Laurel Johnstone, Ingo Helbig, Theodore R. Cummins
Publikováno v:
Epilepsia. 63:1970-1980
Family members carrying the same SCN1A variant often exhibit differences in the clinical severity of epilepsy. This variable expressivity suggests that other factors aside from the primary sodium channel variant influence the clinical manifestation.
Autor:
Elisabeth, Fabian, Thomas, Roskaric, Johann, Pfeifer, Heimo, Wenzl, Heinz F, Hammer, Carolin, Lackner, Georg, Rosanelli, Guenter J, Krejs
Publikováno v:
Wiener klinische Wochenschrift.
Autor:
Dinesh Talwar, Michael F. Hammer
Publikováno v:
Pediatric Neurology. 122:76-83
Understanding the precise genetic -basis of disease is one of the critical developments in medicine in the twenty-first century. Genetic testing has revolutionized the diagnosis and treatment of neurological diseases in children. Whole-genome and who
Publikováno v:
Pediatric Neurology Briefs, Vol 31, Iss 3 (2017)
Investigators from the University of British Columbia, Great Ormond Street Hospital for Children, and the National Hospital reported their findings on neurotransmitter deficiencies in two patients with mutations in voltage-gated sodium genes (SCN2A a
Externí odkaz:
https://doaj.org/article/276594c99bb34c1994bd9bb2549ae2e6