関: idiopathic intestinal pseudo-obstruction、intestinal pseudo-obstruction、intestinal pseudoobstruction、paralytic ileus

WordNet

relating to or affecting the viscera; "visceral bleeding"; "a splanchnic nerve" (同)splanchnic
internal organs collectively (especially those in the abdominal cavity); "`viscera is the plural form of `viscus" (同)entrails, innards
any pathology of the muscles that is not attributable to nerve dysfunction

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1. ミトコンドリアミオパシー：臨床的特徴および診断 mitochondrial myopathies clinical features and diagnosis
2. 慢性偽性腸閉塞 chronic intestinal pseudo obstruction
3. 先天性ミオパシー congenital myopathies
4. 代謝性ミオパチーへのアプローチ approach to the metabolic myopathies
5. 全身性疾患のミオパシー myopathies of systemic disease

Severe gastrointestinal dysmotility developed after treatment with gonadotropin-releasing hormone analogs.

Cordeddu L1, Bergvall M, Sand E, Roth B, Papadaki E, Li L, D Amato M, Ohlsson B.
Scandinavian journal of gastroenterology.Scand J Gastroenterol.2015 Mar;50(3):291-9. doi: 10.3109/00365521.2014.958098. Epub 2015 Jan 16.
Abstract Background. Sporadic cases of abdominal pain and dysmotility has been described after treatment with gonadotropin-releasing hormone (GnRH) analogs. The aim of the present study was to scrutinize for patients with severe gastrointestinal complaints after treatment with GnRH analogs, to descr
PMID 25592315

Quickly progressive amyotrophy of the thigh: An unusual cause of rapid chondrolysis of the knee.

Ferrari M1, Louati K1, Miquel A2, Behin A3, Benveniste O4, Sellam J5.
Joint, bone, spine : revue du rhumatisme.Joint Bone Spine.2015 Feb 10. pii: S1297-319X(15)00004-4. doi: 10.1016/j.jbspin.2014.12.013. [Epub ahead of print]
While rapidly destructive OA is more recognized in hip, we report the case of a 50-year-old woman who presented a rapid chondrolysis in the patellofemoral joint in a context of rapid loss of muscular strength. She had arthralgia, myalgia and proximal muscular deficit of the limbs. Creatine phospho k
PMID 25680228

Spontaneous abdominal esophageal perforation in a patient with mitochondrial neurogastrointestinal encephalomyopathy.

Kalkan IH, Köksal AŞ, Evcimen S, Sapmaz F, Öztaş E, Önder FO, Güliter S.
Acta clinica Belgica.Acta Clin Belg.2015 Feb;70(1):44-5. doi: 10.1179/2295333714Y.0000000053.
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive multisystem disorder caused by thymidine phosphorylase deficiency. Severe denutrition is almost constant during the course of the disease which leads to severe malnutrition and requires long-term parenteral nutri
PMID 25649531

崔吉道
ビタミン 84(12), 604-609, 2010-12-25
… SCD is an autosomal recessive disorder characterized by progressive cardiomyopathy, skeletal myopathy, hypoglycemia and hyperammonaemia. … Several pharmacokinetic studies using a SCD model mouse, jvs (juvenile visceral steatosis), have revealed that OCTN2 governs carntine disposition in vivo. …
NAID 110008006993