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Juvenile form, typeⅢ [Kugelberg-Welander] 어깨종아리형Scapuloperoneal form G12.2즐겨찾기 운동신경세포병Motor neuron disease G12.20즐겨찾기 가족성 근위축측삭경화증Familial amyotrophic lateral sclerosis 가족성 운동신경세포병Familial motor...

of GGTs are heterogeneous with clinical diagnoses ranging from frontotemporal dementia, Pick’s disease, PSP, CBS, motor neuron disease (MND) and primary lateral sclerosis [52]. A subgroup of GGT was previously referred as atypical PSP...

R. G., and Moore, D. H. (2017). Gamma aminobutyric acid (GABA) modulators for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database. Syst. Rev. 1:Cd006049. doi: 10.1002/14651858.CD006049.pub2 PubMed Abstract | CrossRef...

and Pennybacker [104] were the first to record individual twitches from the fasciculations of motor units in patients with motor neuron disease, using an indirect pneumatic transducer. Buchthal and Schmalbruch [105] used a mechanical...

for Kennedy’s disease Spinal bulbar muscular atrophy (SBMA), commonly known as Kennedy's disease (KD), is an X-linked motor neuron disease affecting males. Aims This project will use next-generation DNA designer drugs called antisense...

NSE: Neuron-Specific Enolase, TRPV1: Transient Receptor Potential Cation Channel Subfamily V Member 1, RT97: Neurofilament Monoclonal Antibody. 3.3. Type and Localization of Nerve Receptors In order to carry out effective work, the...

Glued, encoded by the DCTN1 gene, has been identified as the cause of the late-onset and slowly progressive motor neuron disease HMN7B (Puls et al., 2003). Thus, mutations in DCTN1 can be considered as a very rare cause of ALS (Chia et...

인하여 야기되는 행동장애를 보이는 질환을 포함하는데, 여기 기술하고 있는 픽병, 전두엽변성, 그리고 운동신경원병(motor neuron disease) 등을 포함하고 있습니다. 이들 가운데 가장 흔한 것은 전두엽과 측두엽에 신경세포의 소실을 보이며, 미세공포...

and neuropathy,5 including pure motor variants, which have been reported to have EMG changes consistent with motor neuron disease.6 There was no evidence of ataxia or peripheral neuropathy, however, in the present case. Celiac disease...