与继发性低钙血症相关的低镁血症的影像学表现。 - Suppr

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超能文献

Imaging findings in -Related hypomagnesemia with secondary hypocalcemia.

作者信息

Malik Prateek, Bidkar Sayli Umakant, Yoganathan Sangeetha, Mathai Sarah, Danda Sumita, Koshy Beena

机构信息

Department of Radiodiagnosis, Department of Child Health, Christian Medical College, Vellore, Tamil Nadu, India.

Department of Neurological Sciences, Department of Child Health, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):247-248. doi: 10.4103/aian.AIAN_243_20. Epub 2021 Apr 28.

DOI:10.4103/aian.AIAN_243_20

PMID:34220071

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8232497/

Abstract

摘要

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本文引用的文献

Case of hypomagnesemia with secondary hypocalcemia with a novel mutation.伴有新型突变的继发性低钙血症性低镁血症病例

Neurol India. 2018 Nov-Dec;66(6):1795-1800. doi: 10.4103/0028-3886.246240.

Differential Diagnosis of Cerebellar Atrophy in Childhood: An Update.儿童小脑萎缩的鉴别诊断：最新进展

Neuropediatrics. 2015 Dec;46(6):359-70. doi: 10.1055/s-0035-1564620. Epub 2015 Oct 7.

Severe hypomagnesaemia causing reversible cerebellopathy.严重低镁血症导致可逆性小脑病变。

Cerebellum. 2014 Oct;13(5):659-62. doi: 10.1007/s12311-014-0567-2.

Cerebellar syndrome in chronic cyclic magnesium depletion.

Cerebellum. 2013 Aug;12(4):587-8. doi: 10.1007/s12311-012-0431-1.

J Am Soc Nephrol. 2005 Oct;16(10):3061-9. doi: 10.1681/ASN.2004110989. Epub 2005 Aug 17.

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.TRPM6基因突变导致家族性低镁血症伴继发性低钙血症。

Nat Genet. 2002 Jun;31(2):171-4. doi: 10.1038/ng901. Epub 2002 May 28.

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