Literature DB >> 5503688

Corticosteroids in the treatment of Engelmann's disease: progressive diaphyseal dysplasia.

D T Allen, A M Saunders, W H Northway, G F Williams, I A Schafer.   

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Year:  1970        PMID： 5503688

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  9 in total

1.  Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3.

Authors:  M Ghadami; Y Makita; K Yoshida; G Nishimura; Y Fukushima; K Wakui; S Ikegawa; K Yamada; S Kondo; N Niikawa; H a Tomita
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

Review 2.  Sclerosing bone dysplasias--a target-site approach.

Authors:  A Greenspan
Journal:  Skeletal Radiol       Date:  1991       Impact factor: 2.199

3.  Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature.

Authors:  R S Sparkes; C B Graham
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

4.  Successful treatment with corticosteroid in a patient with progressive diaphyseal dysplasia.

Authors:  K Bourantas; S Tsiara; A A Drosos
Journal:  Clin Rheumatol       Date:  1995-07       Impact factor: 2.980

5.  Ghosal haemato-diaphyseal dysplasia: a new disorder.

Authors:  F Gümrük; A Besim; C Altay
Journal:  Eur J Pediatr       Date:  1993-03       Impact factor: 3.183

6.  Progressive diaphyseal dysplasia masquerading as shoulder capsulitis in an adult.

Authors:  D Schapira; D Militeanu; O Israel; I Misselevich; Y Scharf
Journal:  Clin Rheumatol       Date:  1995-09       Impact factor: 2.980

7.  Case report 202. Engelmann disease of bone (diaphyseal dysplasia) with bilateral shortened fibulae.

Authors:  A J Crisp; D P Brenton; D G Shaw
Journal:  Skeletal Radiol       Date:  1982       Impact factor: 2.199

8.  Engelmann's disease of bone--a systemic disorder?

Authors:  A J Crisp; D P Brenton
Journal:  Ann Rheum Dis       Date:  1982-04       Impact factor: 19.103

9.  Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.

Authors:  Michael P Whyte; William G Totty; Deborah V Novack; Xiafang Zhang; Deborah Wenkert; Steven Mumm
Journal:  J Bone Miner Res       Date:  2011-05       Impact factor: 6.741
  9 in total

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