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Journal Abstract Search
149 related items for PubMed ID: 20684007
21. Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations. Naveh Y, Kaftori JK, Alon U, Ben-David J, Berant M. Pediatrics; 1984 Sep; 74(3):399-405. PubMed ID: 6472973 [Abstract] [Full Text] [Related]
22. Scintigraphic findings in progressive diaphyseal dysplasia. Lundy MM, Billingsley JL, Redwine MD, Turnbull GL, Brown TJ. J Nucl Med; 1982 Apr; 23(4):324-5. PubMed ID: 6461731 [Abstract] [Full Text] [Related]
26. The Erlenmeyer flask bone deformity in the skeletal dysplasias. Faden MA, Krakow D, Ezgu F, Rimoin DL, Lachman RS. Am J Med Genet A; 2009 Jun; 149A(6):1334-45. PubMed ID: 19444897 [Abstract] [Full Text] [Related]
27. Progressive diaphyseal dysplasia (Engelmann's disease). Report of a sporadic case of the mild form. Fallon MD, Whyte MP, Murphy WA. J Bone Joint Surg Am; 1980 Apr; 62(3):465-72. PubMed ID: 7364820 [No Abstract] [Full Text] [Related]
28. Radiographic features of craniometadiaphyseal dysplasia, wormian bone type. Langer LO, Brill PW, Afshani E, Williams CA, Thomas IT, Frias JL. Skeletal Radiol; 1991 Apr; 20(1):37-41. PubMed ID: 2000503 [Abstract] [Full Text] [Related]
29. Diaphyseal dysplasia (englemann's syndrome). A case report demonstrating a deficiency in cortical haversian system formation. Wirth CR, Kay J, Bourke R. Clin Orthop Relat Res; 1982 Apr; (171):186-95. PubMed ID: 7140069 [No Abstract] [Full Text] [Related]
30. Camurati-Engelmann disease: a late and sporadic case with metaphyseal involvement. Brat HG, Hamoir X, Matthijs P, Lambin P, Van Campenhoudt M. Eur Radiol; 1999 Apr; 9(1):159-62. PubMed ID: 9933401 [Abstract] [Full Text] [Related]
31. Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. II. Multiple epiphyseal dysplasia; its relation to other disorders of epiphyseal development. JACKSON WP, HANELIN J, ALBRIGHT F. AMA Arch Intern Med; 1954 Dec; 94(6):886-901. PubMed ID: 13217487 [No Abstract] [Full Text] [Related]
32. The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis. Park SJ, Yoon CS, Park HW, Choi JR, Chung JS, Lee KA. J Korean Med Sci; 2009 Aug; 24(4):737-40. PubMed ID: 19654961 [Abstract] [Full Text] [Related]
33. [Camurati-Engelmann disease: description of a case in a child]. Calandi C, Pacciani G, Silenzi M, Mannori C, Aulisi A, Adami-Lami Conti C. Radiol Med; 1980 Oct; 66(10):711-2. PubMed ID: 7221031 [No Abstract] [Full Text] [Related]