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Titlebook: Electrodiagnostic Medicine; A Practical Approach Nestor Galvez-Jimenez,Alexandra Soriano,John A. Mo Book 2021 Springer Nature Switzerland A

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Handbuch Kinder- und Jugendliteraturies. These studies not only help to identify the single peripheral nerve involved, but also the site of the lesion, the type of fibers involved (sensory and/or motor), the character of the lesion (axonal vs. demyelinating), and the age/chronicity of the lesion. There is also the potential to obtain
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Heinz-Hermann Krüger,Cathleen Grunertf peripheral nerves. Most commonly, patients present with sensory symptoms such as numbness or paresthesia starting in the toes/feet (i.e. following a length-dependent pattern). Common causes of polyneuropathy are diabetes mellitus, chronic alcoholism, nutritional deficiencies such as vitamin B12 an
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,Angststörungen in der Kindheit,eneration of the motor neuron. It can affect both the upper motor neurons (UMN) and/or the lower motor neurons (LMN), depending on the variant type. Amyotrophic Lateral Sclerosis (ALS) belongs to this group of diseases, causing dysfunction of the UMN and LMN. ALS is mostly considered sporadic, but a
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Armutsgebiete im kommunalen Sozialraum,s, especially myasthenia gravis (MG). It is particularly useful in cases where other test results are not sufficient for diagnosis. The goal of SFEMG is to measure impairment in NMJ transmission (manifested by increased jitter and/or blocking) which can be seen in 95–99% percent of patients with mya
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Manfred Kirchgeorg,Christiane Springerh the goal of interpreting the results in a clear way that can be understood by the referring physician, and that explains the diagnosis, correlated with the findings- including the nature/character (e.g. axon loss or demyelinating), localization/distribution, and severity of nerve, muscle or neurom
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