WordNet

relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
pain in the head caused by dilation of cerebral arteries or muscle contractions or a reaction to drugs (同)head ache, cephalalgia
a severe recurring vascular headache; occurs more frequently in women than men (同)megrim, sick_headache, hemicrania

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1. 片麻痺性片頭痛 hemiplegic migraine
2. 小児における片頭痛の分類 classification of migraine in children
3. 成人における片頭痛の病態生理、臨床症状、および診断 pathophysiology clinical manifestations and diagnosis of migraine in adults
4. 頭痛、片頭痛、および脳卒中 headache migraine and stroke
5. 脳幹の前兆を伴う片頭痛（脳底型片頭痛） migraine with brainstem aura basilar type migraine

Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study.

De Marchis ML1, Barbanti P, Palmirotta R, Egeo G, Aurilia C, Fofi L, Piroso S, Ialongo C, Della-Morte D, D'Andrea G, Ferroni P, Guadagni F.
The journal of headache and pain.J Headache Pain.2015 Dec;16:520. doi: 10.1186/s10194-015-0520-x. Epub 2015 Apr 30.
BACKGROUND: The study of COMT gene polymorphisms in migraine could be of particular interest since impaired catecholaminergic neurotransmission, namely chronic dopaminergic and noradrenergic hypofunction, is a peculiar migraine trait. In this study, for the first time, we focused on the role of COMT
PMID 25929431

Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations.

Schuh E1, Lohse P1, Ertl-Wagner B1, Witt M1, Krumbholz M1, Frankenberger M1, Gerdes LA1, Hohlfeld R1, Kümpfel T1.
Neurology® neuroimmunology & neuroinflammation.Neurol Neuroimmunol Neuroinflamm.2015 May 14;2(4):e109. doi: 10.1212/NXI.0000000000000109. eCollection 2015.
OBJECTIVE: To evaluate the frequency of the cryoporin/NLRP3 low-penetrance mutations V198M and Q703K in patients who reported at least 2 symptoms compatible with cryopyrin-associated periodic syndromes (CAPS) and to characterize the phenotype in mutation-positive patients.METHODS: The frequency of t
PMID 26020059

Association of age at onset of migraine with family history of migraine in children attending a pediatric headache clinic: A retrospective cohort study.

Eidlitz-Markus T1, Haimi-Cohen Y2, Zeharia A2.
Cephalalgia : an international journal of headache.Cephalalgia.2015 Jul;35(8):722-7. doi: 10.1177/0333102414554114. Epub 2014 Oct 10.
AIM: Migraine is known to run in families and has long been considered a strongly heritable disorder. This study sought to evaluate the relationship between age at onset of pediatric migraine and family history of migraine.METHODS: Review of the medical files of the headache clinic of a tertiary ped
PMID 25304765

辻貞俊
臨床神経学 54(12), 1003-1005, 2014
片頭痛とてんかんは一過性発作性脳疾患であるため，関連が議論されている．国際頭痛分類第3版では，てんかん発作と関連する頭痛として，片頭痛てんかん，てんかん性片側頭痛，てんかん発作後頭痛があり，関連性は複雑でかつ双方向性であるとしている．ミグラレプシーの多くは後頭葉てんかんの症状といわれている．国際抗てんかん連盟のてんかん分類には頭痛関連てんかんはない．複雑部分発作後に拍動性頭痛発作を呈する症例は，臨 …
NAID 130004921205

古和久典,中島健二
臨床神経学 52(11), 1006-1008, 2012
… Functional imaging studies of migraine patients have shown dramatic changes in blood flow and brain activity whose characteristics are similar to those of CSD, implicated in migraine visual aura. … Although the trigeminal nerve innervates the meninges and participates in the genesis of migraine headaches, triggering mechanisms remain controversial and poorly understood. …
NAID 130004505039

岩中行己男,岡田和将,赤松直樹,魚住武則,足立芳樹,辻貞俊
臨床神経学 49(5), 267-270, 2009
症例は34歳の男性である．小児期より体幹のバランス不良が緩徐に進行し,18歳頃よりろれつ不良が出現した.33歳時より右上下肢の異常感覚と脱力,運動性失語，健忘症状，嘔気をともなう左側頭部の激しい拍動性頭痛発作をくりかえした．発作間欠期の神経学的所見では軽度の失調性構音障害と体幹失調のみをみとめ,頭部MRIでは小脳上虫部から前葉に中等度萎縮をみとめた．頭痛発作間欠期の脳波では左前頭側頭部に間欠性δ波 …
NAID 130004504549

家族性偏頭痛 : 15 件
家族性片頭痛 : 19 件

リンク元	「家族性片頭痛」
関連記事	「familial」