Literature DB >> 19981348

Case for Diagnosis.

E A Cockayne.   

Abstract

Year:  1920        PMID： 19981348      PMCID： PMC2152594     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  13 in total

1.  An unusual bone dysplasia.

Authors:  S P GHOSAL
Journal:  Indian J Pediatr       Date:  1957-12       Impact factor: 1.967

2.  Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann disease.

Authors:  S Herrera; R Soriano; X Nogués; R Güerri-Fernandez; D Grinberg; N García-Giralt; N Martínez-Gil; S Castejón; A González-Lizarán; S Balcells; A Diez-Perez
Journal:  Osteoporos Int       Date:  2017-08-25       Impact factor: 4.507

3.  Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.

Authors:  S Simsek; K Janssens; M L Kwee; W Van Hul; J Veenstra; J C Netelenbos
Journal:  Osteoporos Int       Date:  2005-06-16       Impact factor: 4.507

4.  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

Review 5.  Craniotubular bone disorders.

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

6.  Engelmann's disease with optic atrophy.

Authors:  J P Soni; B D Gupta; M Soni; V Mund; Rajesh Aneja
Journal:  Indian J Pediatr       Date:  2002-09       Impact factor: 1.967

Review 7.  Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment.

Authors:  K Janssens; F Vanhoenacker; M Bonduelle; L Verbruggen; L Van Maldergem; S Ralston; N Guañabens; N Migone; S Wientroub; M T Divizia; C Bergmann; C Bennett; S Simsek; S Melançon; T Cundy; W Van Hul
Journal:  J Med Genet       Date:  2005-05-13       Impact factor: 6.318

Review 8.  Camurati-Engelmann Disease.

Authors:  Wim Van Hul; Eveline Boudin; Filip M Vanhoenacker; Geert Mortier
Journal:  Calcif Tissue Int       Date:  2019-02-05       Impact factor: 4.333

Review 9.  Significant Improvement After Surgery for a Symptomatic Osteoblastoma in a Patient with Camurati-Engelmann Disease: Case Report and Literature Review.

Authors:  Hirotaka Yonezawa; Katsuhiro Hayashi; Norio Yamamoto; Akihiko Takeuchi; Kaoru Tada; Shinji Miwa; Kentaro Igarashi; Hiroaki Kimura; Yu Aoki; Sei Morinaga; Yoshihiro Araki; Yohei Asano; Keisuke Sakurakichi; Hiroko Ikeda; Takayuki Nojima; Hiroyuki Tsuchiya
Journal:  Calcif Tissue Int       Date:  2021-02-08       Impact factor: 4.333

10.  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
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