✦ LIBER ✦

Bunina bodies in neurons of the medullary reticular formation in amyotrophic lateral sclerosis

✍ Scribed by Imaharu Nakano; Takeshi Iwatsubo; Yoshio Hashizume; Toshio Mizutani

Publisher: Springer-Verlag
Year: 1993
Tongue: English
Weight: 1003 KB
Volume: 85
Category: Article
ISSN: 0001-6322
DOI: 10.1007/bf00230484

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Bunina bodies in neurons of the medullar

Bunina bodies in neurons of the medullary reticular formation in a case of amyotrophic lateral sclerosis

✍ I. Nakano; Y. Hashizume; T. Tomonaga 📂 Article 📅 1990 🏛 Springer-Verlag 🌐 English ⚖ 741 KB

In an autopsied case of amyotrophic lateral sclerosis (ALS) with dementia (a 65-year-old man with a 4-year course) showing numerous Bunina bodies in the lower motor neurons including those of cranial motor nuclei, eosinophilic inclusions were also observed in several neurons of the reticular formati

Selective appearance of Bunina bodies in

Selective appearance of Bunina bodies in amyotrophic lateral sclerosis

✍ M. Tomonaga 📂 Article 📅 1980 🏛 Springer 🌐 English ⚖ 918 KB

Bunina inclusion bodies were distribution abundantly in the nerve cell cytoplasm of case of amyothrophic lateral sclerosis (ALS). They appeared mainly in the motor nuclei of the brainstem and spinal cord on a routine examination. Although the oculomotor nucleus is known to be spared in ALS, Bunina b

Abnormalities of cortical inhibitory neu

Abnormalities of cortical inhibitory neurons in amyotrophic lateral sclerosis

✍ Mohammed Enterzari-Taher; Andrew Eisen; Heather Stewart; Masashi Nakajima 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 118 KB 👁 2 views

We have used peristimulus time histograms to study how paired, transcranial magnetic stimulation alters the firing of single motor units and the magnitude of unitary excitatory postsynaptic potentials (EPSPs) recorded from the extensor digitorum communis muscle. With stimulus intensity at threshold

Studies of the coding region of the neur

Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosis

✍ T. Meyer; U. Lenk; G. Küther; A. Weindl; A. Speer; Dr A. C. Ludolph 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 314 KB 👁 2 views

Functional significance of upper and low

Functional significance of upper and lower motor neuron impairment in amyotrophic lateral sclerosis

✍ Jane A. Kent-Braun; Christie H. Walker; Michael W. Weiner; Robert G. Miller 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 2 views

The objective of this study was to examine the contribution of lower motor neuron (LMN) and upper motor neuron (UMN) dysfunction to weakness and impaired motor control in 27 patients with amyotrophic lateral sclerosis (ALS). Isometric strength was measured by dorsiflexor maximum voluntary contractio

Progressive motor neuron impairment in a

Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

✍ Mimoun Azzouz; Nathalie Leclerc; Mark Gurney; Jean-Marie Warter; Philippe Poindr 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 2 views

Mutations of Cu,Zn superoxide dismutase cause an autosomal dominant form of familial amyotrophic lateral sclerosis. An animal model of the disease has been produced by expressing mutant human SOD1 in transgenic mice (G93A). In order to quantify the dysfunction of the motor unit in transgenic mice, e