نتایج جستجو برای: مدل sma

تعداد نتایج: 138859  

Journal: :Journal of neurophysiology 2002
Atsushi Nambu Katsuyuki Kaneda Hironobu Tokuno Masahiko Takada

To analyze the organization of corticostriatal motor inputs, we examined the neuronal responses in the putamen (Put) to stimulation in the primary motor cortex (MI) and the supplementary motor area (SMA). Stimulating electrodes were chronically implanted in the distal and proximal parts of the forelimb representation of the MI and in the forelimb representation of the SMA in Japanese monkeys (M...

Journal: :Pediatrics 2004
Brian H Y Chung Virginia C N Wong Patrick Ip

OBJECTIVE Spinal muscular atrophy (SMA) is common. The prevalence of SMA in southern Chinese is 1 in 53,000. The clinical course is variable. The traditional classification of SMA includes age of onset, age of death, achievement of motor milestones, and ambulatory status as criteria. There was a lack of inclusion of the best lifetime functional status of any child with SMA. With the advances in...

Journal: :Human molecular genetics 2008
Vicki L McGovern Tatiana O Gavrilina Christine E Beattie Arthur H M Burghes

Spinal muscular atrophy (SMA) is caused by reduced levels of survival motor neuron (SMN) protein. Previously, cultured SMA motor neurons showed reduced growth cone size and axonal length. Furthermore, reduction of SMN in zebrafish resulted in truncation followed by branching of motor neuron axons. In this study, motor neurons labeled with green fluorescent protein (GFP) were examined in SMA mic...

2014
Francesco Vergani Luis Lacerda Juan Martino Johannes Attems Christopher Morris Patrick Mitchell Michel Thiebaut de Schotten Flavio Dell’Acqua

To cite: Vergani F, Lacerda L, Martino J, et al. J Neurol Neurosurg Psychiatry 2014;85: 1377–1385. ABSTRACT Introduction The supplementary motor area (SMA) is frequently involved by brain tumours (particularly WHO grade II gliomas). Surgery in this area can be followed by the ‘SMA syndrome’, characterised by contralateral akinesia and mutism. Knowledge of the connections of the SMA can provide ...

2017
Cathy Lally Cynthia Jones Wildon Farwell Sandra P. Reyna Suzanne F. Cook W. Dana Flanders

BACKGROUND Spinal muscular atrophy (SMA) is a progressive, devastating disease and a leading inherited cause of infant mortality. The limited population-based literature is confined to small regional studies. Estimates of prevalence are needed to characterize the burden of SMA and to understand trends in prevalence by disease type as new treatments become available. The reported estimates of SM...

Journal: :Brain : a journal of neurology 1999
A Ikeda S Yazawa T Kunieda S Ohara K Terada N Mikuni T Nagamine W Taki J Kimura H Shibasaki

To clarify the functional role of human pre-supplementary motor area (pre-SMA) in 'cognitive' motor control as compared with other non-primary motor cortices (SMA-proper and lateral premotor areas) and prefrontal area, we recorded epicortical field potentials by using subdural electrodes in five epileptic patients during presurgical evaluation, whose pre-SMA, SMA-proper, prefrontal and lateral ...

Journal: :Diagnostic and interventional radiology 2013
Umberto G Rossi Paolo Rigamonti M'Hamed Dahmane Maurizio Cariati

The outcome of endovascular treatment in acute superior mesenteric artery (SMA) thromboembolic occlusion is variable at best. We describe three patients who underwent urgent endovascular manual aspiration thrombectomy of the SMA, illustrating the good, the bad, and the ugly. The good: a 63-year-old male patient was admitted to our hospital for acute abdominal pain. Contrast-enhanced multidetect...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1999
K Sakai O Hikosaka S Miyauchi Y Sasaki N Fujimaki B Pütz

In preceding studies (Hikosaka et al., 1996; Sakai et al., 1998) we have shown that the presupplementary motor area (pre-SMA), an anterior part of the medial premotor cortex, is active during visuo-motor sequence learning. However, the paradigm required the subjects first to acquire correct visuo-motor association and then to acquire correct sequence, and it was still unknown which of the two p...

Journal: :Human molecular genetics 2015
Hansjörg Rindt Zhihua Feng Chiara Mazzasette Jacqueline J Glascock David Valdivia Noah Pyles Thomas O Crawford Kathryn J Swoboda Teresa N Patitucci Allison D Ebert Charlotte J Sumner Chien-Ping Ko Christian L Lorson

Systemically low levels of survival motor neuron-1 (SMN1) protein cause spinal muscular atrophy (SMA). α-Motor neurons of the spinal cord are considered particularly vulnerable in this genetic disorder and their dysfunction and loss cause progressive muscle weakness, paralysis and eventually premature death of afflicted individuals. Historically, SMA was therefore considered a motor neuron-auto...

1998
Srikant Krishna Lisa L. Maduzia Richard W. Padgett

In C. elegans, the TGFβ-like type II receptor daf-4 is required for two distinct signaling pathways. In association with the type I receptor daf-1, it functions in the dauer pathway. In addition, it is also required for body size determination and male tail patterning, roles which do not require daf-1. In an effort to determine how two different signals are transmitted through daf-4, we looked ...

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