Medullary nephrocalcinosis in an adult patient with idiopathic infantile hypercalcaemia and a novel CYP24A1 mutation

Author： Meusburger Edgar Mündlein Axel Zitt Emanuel Obermayer-Pietsch Barbara Kotzot Dieter Lhotta Karl

ISSN： 2048-8505

Source： Clinical Kidney Journal, Vol.6, Iss.2, 2013-04, pp. : 211-215

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Cellular congenital mesoblastic nephroma with contralateral medullary nephrocalcinosis

By Ozturk A Haliloglu M Akpinar E Tekgul S

British Journal of Radiology, Vol. 77, Iss. 917, 2004-05 ,pp. : 436-437

British Institute of Radiology

Access to resources Recommend Favorite

Expression of the vitamin D metabolizing enzyme CYP24A1 at the annulus of human spermatozoa may serve as a novel marker of semen quality

By Blomberg Jensen M. Jørgensen A. Nielsen J. E. Bjerrum P. J. Skalkam M. Petersen J. H. Egeberg D. L. Bangsbøll S. Andersen A. N. Skakkebæk N. E. Juul A. Rajpert-De Meyts E. Dissing S. Leffers H. Jørgensen N.

International Journal of Andrology, Vol. 35, Iss. 4, 2012-08 ,pp. : 499-510

Blackwell Publishing

Access to resources Recommend Favorite

Novel Mutation in the ABCA1 Gene Identified in a Chinese Patient with Dementia and Atherothrombotic Cerebral Infarction

Dementia and Geriatric Cognitive Disorders, Vol. 26, Iss. 3, 2008-10 ,pp. : 234-238

Karger

Access to resources Recommend Favorite

A Novel GFAP Mutation and Disseminated White Matter Lesions: Adult Alexander Disease?

European Neurology, Vol. 50, Iss. 2, 2003-09 ,pp. : 100-105

Karger

Access to resources Recommend Favorite

A patient with pseudohypoaldosteronism type II caused by a novel mutation in WNK4 gene

By Gong Hui

Endocrine Journal, Vol. 33, Iss. 3, 2008-06 ,pp. : 230-234

Humana Press, Inc

Access to resources Recommend Favorite