[PDF] Top 20 El mapa conceptual como herramienta del aprendizaje significativo en Secundaria
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Refining eligibility criteria for amyotrophic lateral sclerosis clinical trials
... Escorial criteria are registered centrally at The Netherlands ALS ...a clinical trial in the same time period. In addition, clinical data were collected to determine an individual’s ... See full document
25
Amyotrophic lateral sclerosis
... diagnostic criteria [8] and the revised 2000 'Airlie House' criteria [9] to aid in diagnosing and classifying patients for research studies and drug ...House criteria are shown in Table 1, and based ... See full document
8
<p>Clinical and research applications of neuromuscular ultrasound in amyotrophic lateral sclerosis</p>
... giving 25% of patients greater diagnostic certainty, likely because MUS enables assessment of a larger area of muscle, including deeper muscle layers, compared to EMG. 7,9,16 It also has a potential role in guiding ... See full document
9
Respiratory measures in amyotrophic lateral sclerosis
... large clinical trials (EMPOWER and BENEFIT-ALS) and an ALS trial database (PRO-ACT) found that rate of decline in SVC strongly predicts the likelihood of death ... See full document
143
Electrophysiological and spinal imaging evidences for sensory dysfunction in amyotrophic lateral sclerosis
... Electrophysiological investigations were performed the same day as the MRI in each participant. Median and ulnar nerves were stimulated (1 ms rectangular electrical stimulation; DS7A, Digitimer Ltd, Hertfordshire, UK) at ... See full document
175
Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-U
... the clinical and pathologic findings of three cases of aFTLD-U and two cases of late- onset BIBD which have not been previously described in ...exhibit clinical and pathologic features that are distinct ... See full document
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Risk factors for amyotrophic lateral sclerosis
... between inflammatory conditions around the motor unit and ALS may shed light on the pathological development of ALS. Clinically, early symptoms of ALS can be difficult to differ- entiate from symptoms of other ... See full document
11
Interneuron dysfunction in amyotrophic lateral sclerosis
... the clinical presentation of both the genetic and non-genetic forms of the disease have led to the suggestion of a commonality in the final neurodegenerative pathway (Byrne et al ... See full document
287
Analysis of riluzole’s profile of use in a Central Hospital in Lisbon
... Despite the extended enrollment period, only 77 patients met the criteria to be included in the study, which indicates the paucity of this disease. Nonetheless, statistical data with regard to our population is in ... See full document
17
Analysis of microRNA from archived formalin-fixed paraffin-embedded specimens of amyotrophic lateral sclerosis
... that miRNAs may be good biomarkers for cancer diag- nosis and prognosis [5]. The role of miRNAs has also been studied in neurodegenerative conditions such as Alzheimer?s disease [6-22], Parkinson? s disease [19,23-27], ... See full document
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Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report
... the clinical course of the two concomitant neurological disorders evokes the previous reports of Dynes et ...simultaneous clinical progression of both ALS and ...although clinical and instrumental ... See full document
6
A patient with amyotrophic lateral sclerosis and atypical clinical and electrodiagnostic features: a case report
... Amyotrophic lateral sclerosis (ALS) is a progressive neu- rodegenerative disorder characterized by anterior horn cell and corticospinal degeneration, primarily involving motor neurons in the cerebral ... See full document
12
Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion
... of clinical, neuroimaging [37], and neuro pathological [45,46] parameters will probably improve the ability to predict the presence of a mutation in sporadic cases, but careful attention to patients in whom the ... See full document
75
Amyotrophic lateral sclerosis mimic syndromes
... Amyotrophic lateral sclerosis (ALS) is a progressive and almost always devastating neurodegenerative disorder. It is a kind of a heterogeneous group of disorders known as motor neuron diseases ... See full document
8
Genetics of amyotrophic lateral sclerosis: an update
... For clinical phenotype, C9ORF72 mutation mani- fests FTD and ALS as well as other features including memory loss, psychosis, akinetic-rigid and cerebellar signs ... See full document
14
How common are ALS plateaus and reversals?
... These results are major findings that could have important consequences for future clinical trial design and selection of outcome measures. Patients who do not progress during a clinical trial may cause ... See full document
36
Comparing methods to combine functional loss and mortality in clinical trials for amyotrophic lateral sclerosis
... Objective: Amyotrophic lateral sclerosis (ALS) clinical trials based on single end points only partially capture the full treatment effect when both function and mortality are affected, ... See full document
7
Cognitive and behavioral features of c9FTD/ALS
... hippocampal sclerosis or a retrieval- based deficit due to frontosubcortical ...hippocampal sclerosis is not present, an encoding deficit could relate to dysfunction associated with ubiquitin-, ubiquilin-, ... See full document
5
Language contributions to health related quality of life in Amyotrophic Lateral Sclerosis
... Language contributions to health related quality of life in Language contributions to health related quality of life in Amyotrophic Lateral Sclerosis.. Amyotrophic Lateral Sclerosis K[r] ... See full document
12
A blended psychosocial support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: protocol of a randomized controlled trial
... with Amyotrophic Lateral Sclerosis (ALS) or Progressive Muscular Atrophy (PMA) face stressful demands due to severe impairments and prospect of early death of the patients they care ... See full document
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