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5. [Description of a case of Camurati-Engelmann syndrome in a newborn infant]. Carbone R; Ponticelli A; Bernardo NS; Galasso GF Pediatria (Napoli); 1983; 91(2-3):261-4. PubMed ID: 6664733 [No Abstract] [Full Text] [Related]
6. [On Camurati-Engelmann disease: considerations on a case with hypacusis]. Cravario A; Pelocchino AM; Voena G Minerva Med; 1968 Apr; 59(34):2006-16. PubMed ID: 5653972 [No Abstract] [Full Text] [Related]
7. [Camurati-Engelmann disease]. FAZAKAS J; VASCULESCU T; GHERMAN E; MICLUTIA M; VOINA J Z Orthop Ihre Grenzgeb; 1959; 91(1):42-50. PubMed ID: 13648656 [No Abstract] [Full Text] [Related]
8. [The vascular origin of Camurati-Engelmann disease (familial symmetrical sclerotic polyosteopathy)]. BEDOGNI C Chir Organi Mov; 1962 Aug; 51():156-66. PubMed ID: 13970211 [No Abstract] [Full Text] [Related]
9. [Hereditary symetrical hyperostotic polyosteopathy (Camurati-Engelmann disease). Clinical and anatomopathological study]. BATTAGLIA L; VENTURI R Chir Organi Mov; 1960; 49():179-96. PubMed ID: 13687783 [No Abstract] [Full Text] [Related]
10. [Contribution on Camurati-Engelmann disease]. WETZEL H Dtsch Med Wochenschr; 1963 Jan; 88():188-90. PubMed ID: 14000156 [No Abstract] [Full Text] [Related]
11. [A new observation in a case of osteopathia hyperostotica Engelmann-Camurati]. WEINBRABER H Fortschr Geb Rontgenstr; 1954 Dec; 81(6):800-4. PubMed ID: 14365957 [No Abstract] [Full Text] [Related]
12. [HEREDITARY SYMMETRICAL CONDENSING POLYOSTEOPATHY. "CAMURATI-ENGELMANN DISEASE". FIRST CASE REPORTED IN THE HOSPITAL INFANTIL DE MEXICO]. FLORES A; SIERRAROJAS L Bol Med Hosp Infant Mex; 1965; 22():75-87. PubMed ID: 14262484 [No Abstract] [Full Text] [Related]
16. [Clinical and histological observations on generalized hyperostosis without pachyderma (Camurati-Engelmann)]. NEUMANN G Z Orthop Ihre Grenzgeb; 1962 Jul; 96():201-15. PubMed ID: 14479218 [No Abstract] [Full Text] [Related]
17. [On a case of Camurati-Engelmann disease in childhood]. Konstantinov D Radiol Diagn (Berl); 1968; 9(3):351-5. PubMed ID: 5688207 [No Abstract] [Full Text] [Related]
20. A mutation in TGF beta1 gene encoding the latency-associated peptide in a Chinese patient with Camurati-Engelmann disease. Liang YH; Li W; Li LY; Ye YY; Lu GX Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Oct; 23(5):502-4. PubMed ID: 17029195 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]