WordNet

an automatic instinctive unlearned reaction to a stimulus (同)reflex response, reflex action, instinctive reflex, innate reflex, inborn reflex, unconditioned_reflex, physiological reaction
abnormally inactive (同)underactive

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1. 成人における詳細な神経学的検査 the detailed neurologic examination in adults
2. 多発性神経障害の概要 overview of polyneuropathy
3. 全身疾患と関連した遺伝性ニューロパチー hereditary neuropathies associated with generalized disorders
4. 新生児の神経学的検査 neurological examination of the newborn
5. 脳性麻痺の診断および分類 diagnosis and classification of cerebral palsy

A morbid coexistence: thrombosed descending thoracic aorta aneurysm and aortic insufficiency with aortic diastolic reverse flow.

Yildiz S1, Boyaci N1, Yildiz A1.
Quantitative imaging in medicine and surgery.Quant Imaging Med Surg.2014 Oct;4(5):437-8. doi: 10.3978/j.issn.2223-4292.2014.10.01.
A 76-year-old woman presented with difficulty in speech and weakness on right arm and leg. Her medical history was remarkable only for uncontrolled hypertension for a long period. Dysarthria, right central facial paralysis, right hemiparesis and hypoactive deep tendon reflexes were noticed on neurol
PMID 25392831

A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles.

Fujii T1, Hayashi S1, Kawamura N1, Higuchi MA2, Tsugawa J2, Ohyagi Y1, Hayashi YK3, Nishino I4, Kira J5.
Journal of the neurological sciences.J Neurol Sci.2014 Aug 15;343(1-2):206-10. doi: 10.1016/j.jns.2014.05.056. Epub 2014 Jun 2.
We herein report a 32-year-old woman with adult-onset reducing body myopathy (RBM) who had a mutation in the four-and-a-half LIM domain 1 gene (FHL1) and showed a marked asymmetrical involvement of sternocleidomastoid and trapezius muscles. At 30 years of age she noticed bilateral foot drop, and ove
PMID 24928078

結城奈津子,吉岡亮,堀尾玲子,大道卓摩,安田怜,岡伸幸
臨床神経学 54(8), 671-674, 2014
症例は79歳の男性である．緩徐進行性の両手握力低下を主訴に当科を受診した．左側優位の上肢脱力，腱反射低下を呈し，表在感覚，深部感覚は正常であった．神経伝導検査で感覚運動神経の脱髄が示唆され，腓腹神経生検で髄鞘周期間線の開大，髄鞘のinfoldingがみとめられた．IgM-κ型M蛋白血症，抗myelin-associated glycoprotein（MAG）抗体がみとめられ，抗MAG抗体関連脱髄性 …
NAID 130004679013

荒井元美,楠進
臨床神経学 49(2/3), 123-126, 2009
57歳の女性例である．約3年前から手のこむら返りと手指，とくに左母指の脱力が徐々に進行した．脳神経は正常であった．小手筋に徒手筋力検査で4程度の脱力と軽度の萎縮，線維束性収縮がみとめられ，四肢の腱反射は消失していた．病的反射や感覚障害はみられなかった．IgMκ M蛋白血症があり，M蛋白は抗GM2抗体活性を示した．一方，GM1とGA1に結合するIgMλ抗体もみられた．運動神経の遠位潜時と伝導速度およ …
NAID 130004504540