Progressive diaphyseal dysplasia and a low muscle carnitineBYE, A. M. E; HODSON, E; KEWLEY, G et al.Pediatric radiology. 1988, Vol 18, Num 4, issn 0301-0449, 340Article

Progressive diaphyseal dysplasia-Engelmann's diseaseMISHRA, G. K; MISHRA, M; VERNEKAR, J et al.Indian pediatrics. 1987, Vol 24, Num 11, pp 1052-1054, issn 0019-6061Article

Diaphyseal dysplasia associated with anemiaGHOSAL, S. P; MUKHERJEE, A. K; MUKHERJEE, D et al.The Journal of pediatrics. 1988, Vol 113, Num 1, pp 49-57, issn 0022-3476, 1Article

Progressive diaphyseal dysplasia (Camurati-Engelmann): radiographic follow-up and CT findingsKAFTORI, J. K; KLEINHAUS, U; NAVEH, Y et al.Radiology. 1987, Vol 164, Num 3, pp 777-782, issn 0033-8419Article

Facial-skeletal manifestations of Engelmann's diseaseDEMAS, P. N; SOTEREANOS, G. C.Oral surgery, oral medicine, oral pathology. 1989, Vol 68, Num 6, pp 686-690, issn 0030-4220Article

Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan familySIMSEK, S; JANSSENS, K; KWEE, M. L et al.Osteoporosis international. 2005, Vol 16, Num 9, pp 1167-1170, issn 0937-941X, 4 p.Article

Domain-specific mutations in TGFB1 result in Camurati-Engelmann diseaseKINOSHITA, Akira; SAITO, Takashi; FUKUSHIMA, Yoshimitsu et al.Nature genetics. 2000, Vol 26, Num 1, pp 19-20, issn 1061-4036Article

Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reportsWRIGHT, M; MILLER, N. R; MCFADZEAN, R. M et al.British journal of ophthalmology. 1998, Vol 82, Num 9, pp 1042-1048, issn 0007-1161Article

Engelmann's disease : A 45-year follow-upGREY, A. C; WALLACE, R; CRONE, M et al.Journal of bone and joint surgery. British volume. 1996, Vol 78, Num 3, pp 488-491, issn 0301-620XArticle

Camurati-Engelmann disease: Contribution of bone scintigraphy to genetic counselingCLYBOUW, C; DESMYTTERE, S; BONDUELLE, M et al.Genetic counseling. 1994, Vol 5, Num 2, pp 195-198, issn 1015-8146Conference Paper

Deflazacort treatment in progressive diaphyseal dysplasia (Camurati-Engelmann disease)BAS, F; DARENDELILER, F; PETORAK et al.Journal of paediatrics and child health. 1999, Vol 35, Num 4, pp 401-405, issn 1034-4810Article

Bone scintigraphy in a patient with progressive diaphyseal dysplasiaSHUKE, N; TAKASHIO, T; YAMAMOTO, W et al.Clinical nuclear medicine. 1997, Vol 22, Num 11, pp 791-792, issn 0363-9762Article

Ribbing disease (multiple diaphyseal sclerosis) : Imaging and differential diagnosisSEEGER, L. L; HEWEL, K. C; YAO, L et al.American journal of roentgenology (1976). 1996, Vol 167, Num 3, pp 689-694, issn 0361-803XConference Paper

Zufallsbefund einer progressiven diaphysären Dysplasie (Camurati-Engelmann-Syndrom) = Incidental finding of a progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)ALTEHOEFER, C; GRÜN, B; BARES, R et al.Nuclear-Medizin. 1993, Vol 32, Num 6, pp 325-327, issn 0029-5566Article

Monocytic origin of fibroblasts : spontaneous transformation of blood monocytes into neo-fibroblastic structures in osteomyelosclerosis and Engelmann's diseaseLABAT, M. L; BRINGUIER, A. F; SEEBOLD, C et al.Biomedicine & pharmacotherapy. 1991, Vol 45, Num 7, pp 289-299, issn 0753-3322Article

Camurati-Engelmann disease: imaging, clinical features and differential diagnosisBARTUSEVICIENE, Aldona; SAMUILIS, Arturas; SKUCAS, Jovitas et al.Skeletal radiology. 2009, Vol 38, Num 11, pp 1037-1043, issn 0364-2348, 7 p.Article

Progressive diaphyseal dysplasia (Camurati-Engelmann's diseae) improvement of clinical signs and of bone scintigraphy during pregnancyDE VITS, A; KEYMEULEN, B; BOSSUYT, A et al.Clinical nuclear medicine. 1994, Vol 19, Num 2, pp 104-107, issn 0363-9762Article

Correlation between bone imaging and the clinical picture in two unsuspected cases of progressive diaphyseal dysplasia (Engelmann's disease)D'ADDABBO, A; MACARINI, L; RUBINI, G et al.Clinical nuclear medicine. 1993, Vol 18, Num 4, pp 324-328, issn 0363-9762Article

Intrafamilial phenotypic variability in Engelmann disease (ED) : Are ED and Ribbing disease the same entity?MAKITA, Y; NISHIMURA, G; IKEGAWA, S et al.American journal of medical genetics. 2000, Vol 91, Num 2, pp 153-156, issn 0148-7299Article

Engelmann's disease with cardiomyopathyCHOUDHURY, Panna; BATRA, Vandana; BATRA, Bobby et al.Indian pediatrics. 2000, Vol 37, Num 12, pp 1373-1376, issn 0019-6061Article

Bone scan in Camurati-Engelmann diseaseVIDAL-SICART, S; PONS, F; GUANABENS, N et al.Clinical nuclear medicine. 1998, Vol 23, Num 4, pp 237-238, issn 0363-9762Article

Progressive diaphyseal dysplasia presenting as neuromuscular diseaseSTENZLER, S; GROGAN, D. P; FRENCHMAN, S. M et al.Journal of pediatric orthopedics. 1989, Vol 9, Num 4, pp 463-467, issn 0271-6798, 5 p.Article

Hearing impairment in Engelmann diseaseHIGASHI, K; MATSUKI, C.The American journal of otology (New York, NY). 1996, Vol 17, Num 1, pp 26-29, issn 0192-9763Article

MR of multiple cranial neuropathies in a patient with Camurati-Engelmann disease : case reportAPPLEGATE, L. J; APPLEGATE, G. R; KEMP, S. S et al.American journal of neuroradiology. 1991, Vol 12, Num 3, pp 557-559, issn 0195-6108, 3 p.Conference Paper

Early manifestation of ghosal-type hemato-diaphyseal dysplasiaALEBOUYEH, Mardawig; VOSSOUGH, Parvanch; TABARROK, Firouz et al.Pediatric hematology and oncology. 2003, Vol 20, Num 5, pp 409-415, issn 0888-0018, 7 p.Article