Literature DB >> 16234993

Paget's disease of bone or osteopetrosis?

Alexander Rozin1, Rachel Bar-Shalom, Sofia Ish-Shalom.   

Abstract

We report a previously undescribed case of diffuse, scan-negative, and low active form of bone disease carrying clinical, x-ray, and biochemistry signs of Paget's disease of bone, which is analyzed in comparison with different forms of osteopetrosis.

Entities:  

Mesh：

Year:  2005        PMID： 16234993     DOI： 10.1007/s10067-005-0035-y

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN： 0770-3198            Impact factor:   2.980


  18 in total

1.  Scintigraphy in a patient with complicated osteopetrosis.

Authors:  B K Adams
Journal:  Clin Nucl Med       Date:  1989-05       Impact factor: 7.794

Review 2.  Paget disease of bone: current status and a look back to 1943 and earlier.

Authors:  D Resnick
Journal:  AJR Am J Roentgenol       Date:  1988-02       Impact factor: 3.959

3.  Monostotic Paget's disease of the mandible presenting with progressive resorption of the teeth.

Authors:  N H Smith
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1978-08

4.  Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.

Authors:  E Cleiren; O Bénichou; E Van Hul; J Gram; J Bollerslev; F R Singer; K Beaverson; A Aledo; M P Whyte; T Yoneyama; M C deVernejoul; W Van Hul
Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

5.  Extensive personal experience: Paget's disease of bone.

Authors:  E S Siris
Journal:  J Clin Endocrinol Metab       Date:  1995-02       Impact factor: 5.958

6.  Osteopetrosis appearance on bone scan.

Authors:  M Dumont; J Lamoureux; F Lamoureux; S Danais; J P Soucy; R Taillefer
Journal:  Clin Nucl Med       Date:  1983-09       Impact factor: 7.794

7.  Skeletal distribution and biochemical parameters of Paget's disease.

Authors:  P J Meunier; C Salson; L Mathieu; M C Chapuy; P Delmas; C Alexandre; S Charhon
Journal:  Clin Orthop Relat Res       Date:  1987-04       Impact factor: 4.176

8.  Osteoclast-derived serum tartrate-resistant acid phosphatase 5b in Albers-Schonberg disease (type II autosomal dominant osteopetrosis).

Authors:  Sari L Alatalo; Kaisa K Ivaska; Steven G Waguespack; Michael J Econs; H Kalervo Väänänen; Jussi M Halleen
Journal:  Clin Chem       Date:  2004-03-11       Impact factor: 8.327

9.  Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis.

Authors:  Annalisa Frattini; Alessandra Pangrazio; Lucia Susani; Cristina Sobacchi; Massimiliano Mirolo; Mario Abinun; Marino Andolina; Adrienne Flanagan; Edwin M Horwitz; Ercan Mihci; Luigi D Notarangelo; Ugo Ramenghi; Anna Teti; Johan Van Hove; Dragana Vujic; Terri Young; Alberto Albertini; Paul J Orchard; Paolo Vezzoni; Anna Villa
Journal:  J Bone Miner Res       Date:  2003-10       Impact factor: 6.741

10.  Type II benign osteopetrosis (Albers-Schönberg disease) caused by a novel mutation in CLCN7 presenting with unusual clinical manifestations.

Authors:  C Letizia; A Taranta; S Migliaccio; C Caliumi; D Diacinti; E Delfini; E D'Erasmo; M Iacobini; M Roggini; O M E Albagha; S H Ralston; A Teti
Journal:  Calcif Tissue Int       Date:  2003-11-26       Impact factor: 4.333
View more
  1 in total

1.  Inheritance patterns, challenges, and outcomes of fracture management in osteopetrosis patients. CASE series and review of pertinent literature.

Authors:  Obada Hasan; Aly Zaheer Pathan; Hammad Naqi; Talal Aqueel; Pervaiz Hashmi; Riaz Hussain Lakdawala
Journal:  Ann Med Surg (Lond)       Date:  2018-11-08
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.