Search details
1.
Enhancing evacuation plans with a situation awareness system based on end-user knowledge provision.
Sensors (Basel)
; 14(6): 11153-78, 2014 Jun 24.
Article
in English
| MEDLINE | ID: mdl-24961212
2.
On the support of scientific workflows over Pub/Sub brokers.
Sensors (Basel)
; 13(8): 10954-80, 2013 Aug 20.
Article
in English
| MEDLINE | ID: mdl-23966191
3.
Analysis of EEG patterns and genotypes in patients with Angelman syndrome.
Epilepsy Behav
; 23(3): 261-5, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-22341959
4.
Enabling flexible and continuous capability invocation in mobile prosumer environments.
Sensors (Basel)
; 12(7): 8930-54, 2012.
Article
in English
| MEDLINE | ID: mdl-23012526
5.
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease.
Cold Spring Harb Mol Case Stud
; 2(4): a001107, 2016 Jul.
Article
in English
| MEDLINE | ID: mdl-27551684
6.
Unusual clinical presentations in four cases of Leigh disease, cytochrome C oxidase deficiency, and SURF1 gene mutations.
J Child Neurol
; 20(8): 670-4, 2005 Aug.
Article
in English
| MEDLINE | ID: mdl-16225813
7.
Congenital livedo reticularis and recurrent strokes in two unrelated young children.
Clin Pediatr (Phila)
; 45(4): 367-72, 2006 May.
Article
in English
| MEDLINE | ID: mdl-16703162
8.
Vagus nerve stimulation for the management of seizures in children: an 8-year experience.
J Pediatr Surg
; 45(7): 1479-83, 2010 Jul.
Article
in English
| MEDLINE | ID: mdl-20638528
9.
Microcephaly and congenital grouped pigmentation of the retinal pigment epithelium associated with submicroscopic deletions of 13q33.3-q34 and 11p15.4.
Ophthalmic Genet
; 30(3): 136-41, 2009 Sep.
Article
in English
| MEDLINE | ID: mdl-19941418
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