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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 5. 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

6. Familial idiopathic hypertrophic osteoarthropathy and cranial suture defects in children.

Authors: A J Reginato; V Schiapachasse; R Guerrero
Journal: Skeletal Radiol Date: 1982 Impact factor: 2.199

7. 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

8. Camurati-engelmann disease association with hypogonadism and primary hypothyroidism.

Authors: Soo Fin Low; Norzailin Abu Bakar; Chai Soon Ngiu
Journal: Iran Red Crescent Med J Date: 2014-08-01 Impact factor: 0.611

8 in total