WordNet

divide or split up; "The cells segmented"
one of the parts into which something naturally divides; "a segment of an orange"
divide into segments; "segment an orange"; "segment a compound word" (同)section
divided or organized into speech segments or isolable speech sounds
loss of the myelin covering of some nerve fibers resulting in their impaired function

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1. 小児におけるギラン・バレー症候群の概要 overview of guillain barre syndrome in children
2. 神経伝導検査の概要 overview of nerve conduction studies
3. 免疫誘導性神経障害 immune mediated neuropathies
4. 浸透圧性脱髄症候群と低ナトリウム血症の過度に急速な補正 osmotic demyelination syndrome and overly rapid correction of hyponatremia
5. 慢性炎症性脱髄性多発神経炎：病因、臨床的特徴、および診断 chronic inflammatory demyelinating polyneuropathy etiology clinical features and diagnosis

Therapy of Vestibular Paroxysmia, Superior Oblique Myokymia, and Ocular Neuromyotonia.

Strupp M1,2, Dieterich M3,4,5, Brandt T3,6, Feil K3,4.
Current treatment options in neurology.Curr Treat Options Neurol.2016 Jul;18(7):34. doi: 10.1007/s11940-016-0417-2.
OPINION STATEMENT: Neurovascular compression syndromes are characterized by recurrent attacks of neurological symptoms and clinical signs depending on the cranial nerve affected. It is assumed that pulsatile compression of the nerve is caused mainly by an artery. The result is segmental demyelinatio
PMID 27306762

Immunotherapy-responsive Allodynia due to Distal Acquired Demyelinating Symmetric (DADS) Neuropathy.

Liewluck T1,2, Engelstad JK2, Mauermann ML2.
Muscle & nerve.Muscle Nerve.2016 Jun 2. doi: 10.1002/mus.25206. [Epub ahead of print]
INTRODUCTION: Distal acquired demyelinating symmetric (DADS) neuropathy is a distal variant of chronic inflammatory demyelinating polyradiculoneuropathy. It is characterized by chronic distal symmetric sensory or sensorimotor deficits. Sensory ataxia is a common clinical presentation. Nerve conducti
PMID 27251375

Laukka JJ1, Kamholz J2, Bessert D3.
Neuroscience letters.Neurosci Lett.2016 May 17. pii: S0304-3940(16)30340-8. doi: 10.1016/j.neulet.2016.05.028. [Epub ahead of print]
Pelizaeus-Merzbacher disease (PMD) is an X-linked inherited hypomyelinating disorder caused by mutations in the gene encoding proteolipid protein (PLP), the major structural protein in central nervous system (CNS) myelin. Prior to our study, whether hypomyelination in PMD was caused by demyelination
PMID 27222925