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Literature DB >> 192120

Congenital hyperphosphatasia (juvenile Paget's disease). Eleven years follow-up of three sisters.

M Eroglu, N N Taneli.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 1977 PMID： 192120

Source DB: PubMed Journal: Ann Radiol (Paris) ISSN： 0003-4185

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3 in total

1. Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK.

Authors: Michael P Whyte; Cristina Tau; William H McAlister; Xiafang Zhang; Deborah V Novack; Virginia Preliasco; Eduardo Santini-Araujo; Steven Mumm
Journal: Bone Date: 2014-07-23 Impact factor: 4.398

Review 2. Craniotubular bone disorders.

Authors: R J Gorlin
Journal: Pediatr Radiol Date: 1994

Review 3. Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene.

Authors: Giacomina Brunetti; Flaviana Marzano; Silvia Colucci; Annamaria Ventura; Luciano Cavallo; Maria Grano; Maria Felicia Faienza
Journal: Endocrine Date: 2012-05-26 Impact factor: 3.633

3 in total