Zobrazeno 1 - 10
of 139
pro vyhledávání: '"C Scotton"'
Publikováno v:
Ocean Science, Vol 12, Iss 2, Pp 403-415 (2016)
The self-organizing map (SOM) technique is considered and extended to assess the extremes of a multivariate sea wave climate at a site. The main purpose is to obtain a more complete representation of the sea states, including the most severe states t
Externí odkaz:
https://doaj.org/article/c8bc39e5e1cd4311a82628f88bf9d732
Autor:
J Mandizha, M Gibbons, S Lines, G Brown, A Jorge Da Ponte, A Duckworth, R Shuttleworth, M Steward, C Scotton, M Cosby, A Berry, A Russell
Publikováno v:
01.04 - M-Health/e-health.
Autor:
R Shuttleworth, M Althobiani, A Duckworth, J Conway, J Dainton, S Lines, J Mandizha, A Jorge Da Ponte, C Scotton, M Gibbons, A Russell
Publikováno v:
12.01 - Idiopathic interstitial pneumonias.
Autor:
J Mandizha, A Duckworth, H Almond, G Brown, S Lines, A Jorge Da Ponte, R Shuttleworth, J Lanario, M Steward, R Sayers, C Scotton, M Gibbons, A Russell
Publikováno v:
01.01 - Clinical problems - no related to asthma or COPD.
Akademický článek
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Autor:
Alessandra Ferlini, Francesca Gualandi, Mert Karakaya, Rocco Liguori, Stefano Squarzoni, Fernanda Fortunato, V. Simioni, Marcella Neri, Elisabetta Sette, Domenico De Grandis, Alex Incensi, Vincent Timmerman, Markus Storbeck, Rita Selvatici, Valeria Tugnoli, C. Scotton, Brunhilde Wirth, Stefania Bigoni, Vincenzo Donadio
Publikováno v:
Neuromuscular disorders
We describe a novel ATP7A gene mutation associated with distal motor neuropathy, mild connective tissue abnormalities and autonomic disturbances. Next-generation sequencing analysis of a lower-motor neuron diseases gene panel was performed in two sib
Autor:
Qinghai Liu, Shuhan He, Leonid Groysman, David Shaked, Jonathan Russin, Thomas C Scotton, Steven Cen, William J Mack
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e84802 (2013)
The C5 complement protein is a potent inflammatory mediator that has been implicated in the pathogenesis of both stroke and neurodegenerative disease. Microvascular failure is proposed as a potential mechanism of injury. Along these lines, this inves
Externí odkaz:
https://doaj.org/article/8a05aea2c9354d7098e14c81c7a60589
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
Autor:
Anikó Gál, David Weaver, Daniele Ghezzi, Massimo Zeviani, Alice Donati, Marika Pane, Alessandra Ferlini, Annarita Armaroli, Eugenio Mercuri, Rita Selvatici, Marcella Neri, Rachele Rossi, Rahul Phadke, Francesco Muntoni, Alessia Nasca, Imelda Hughes, György Hajnóczky, Antonella Cecconi, Olafur Thor Magnusson, Anna Sarkozy, C. Scotton, Irina Zaharieva
Publikováno v:
Human Mutation
We report here the first families carrying recessive variants in the MSTO1 gene: compound heterozygous mutations were identified in two sisters and in an unrelated singleton case, who presented a multisystem complex phenotype mainly characterized by