WordNet

the presence of abnormally high levels of calcium in the urine; usually the result of excessive bone resorption in hyperparathyroidism or osteoporosis (同)hypercalcinuria

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/05/14 20:49:01」(JST)

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1. 成人におけるカルシウム結石の危険因子 risk factors for calcium stones in adults
2. 成人における再発性カルシウム結石の予防 prevention of recurrent calcium stones in adults
3. 小児における腎結石症の疫学および危険因子 epidemiology of and risk factors for nephrolithiasis in children
4. 腎石灰沈着症 nephrocalcinosis
5. 小児における顕微鏡的血尿の評価 evaluation of microscopic hematuria in children

GENETICS IN ENDOCRINOLOGY: Gain and Loss of Function Mutations of the Calcium Sensing Receptor and Associated Proteins: Current Treatment Concepts.

Mayr BM1, Schnabel D2, Dörr HG3, Schöfl C4.
European journal of endocrinology / European Federation of Endocrine Societies.Eur J Endocrinol.2015 Dec 8. pii: EJE-15-1028. [Epub ahead of print]
The calcium-sensing receptor (CASR) is the main calcium sensor in the maintenance of calcium metabolism. Mutations of the CASR, the G protein alpha 11 (GNA11) and the adaptor-related protein complex 2 sigma 1 subunit (AP2S1) genes can shift the set point for calcium sensing causing hyper- or hypocal
PMID 26646938

Calcium and bone homeostasis in heterozygous carriers of CYP24A1 mutations: A cross-sectional study.

Cools M1, Goemaere S2, Baetens D3, Raes A4, Desloovere A5, Kaufman JM6, De Schepper J7, Jans I8, Vanderschueren D9, Billen J10, De Baere E11, Fiers T12, Bouillon R13.
Bone.Bone.2015 Dec;81:89-96. doi: 10.1016/j.bone.2015.06.018. Epub 2015 Jun 25.
BACKGROUND: Bi-allelic CYP24A1 mutations can cause idiopathic infantile hypercalcemia (IIH), adult-onset nephrocalcinosis, and possibly bone metabolism disturbances. It is currently unclear if heterozygous carriers experience clinical problems or biochemical abnormalities. Our objective is to gain i
PMID 26117226

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics.

Claverie-Martin F1.
Clinical kidney journal.Clin Kidney J.2015 Dec;8(6):656-664. Epub 2015 Sep 1.
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC) is an autosomal-recessive renal tubular disorder characterized by excessive urinary losses of magnesium and calcium, bilateral nephrocalcinosis and progressive chronic renal failure. Presentation with FHHNC symptoms generally
PMID 26613020

Upregulation of calbindin D28k in the late distal tubules in the potassium-loaded adrenalectomized mouse kidney

KOBAYASHI Mizuka,YASUOKA Yukiko,SATO Yuichi,ZHOU Ming,ABE Hiroshi,KAWAHARA Katsumasa,OKAMOTO Hirotsugu
Clinical and experimental nephrology 15(3), 355-362, 2011-06-01
NAID 10029005679