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Journal Abstract Search
242 related items for PubMed ID: 6822598
1. Osteogenesis imperfecta with dominant inheritance and normal sclerae. Paterson CR, McAllion S, Miller R. J Bone Joint Surg Br; 1983 Jan; 65(1):35-9. PubMed ID: 6822598 [Abstract] [Full Text] [Related]
2. CLINICAL FEATURES AND PATTERN OF FRACTURES AT THE TIME OF DIAGNOSIS OF OSTEOGENESIS IMPERFECTA IN CHILDREN. Brizola E, Zambrano MB, Pinheiro BS, Vanz AP, Félix TM. Rev Paul Pediatr; 2017 Jan; 35(2):171-177. PubMed ID: 28977334 [Abstract] [Full Text] [Related]
4. Osteogenesis imperfecta. Review of the literature with presentation of 29 cases. Shoenfeld Y. Am J Dis Child; 1975 Jun; 129(6):679-87. PubMed ID: 1098447 [Abstract] [Full Text] [Related]
5. Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta? Beighton P. J Med Genet; 1981 Apr; 18(2):124-8. PubMed ID: 7241530 [Abstract] [Full Text] [Related]
6. A new look at osteogenesis imperfecta. A clinical, radiological and biochemical study of forty-two patients. Bauze RJ, Smith R, Francis MJ. J Bone Joint Surg Br; 1975 Feb; 57(1):2-12. PubMed ID: 1117018 [Abstract] [Full Text] [Related]
7. Natural history of blue sclerae in osteogenesis imperfecta. Sillence D, Butler B, Latham M, Barlow K. Am J Med Genet; 1993 Jan 15; 45(2):183-6. PubMed ID: 8456800 [Abstract] [Full Text] [Related]
9. Four patients with Sillence type I osteogenesis imperfecta and mild bone fragility, complicated by left ventricular cardiac valvular disease and cardiac tissue fragility caused by type I collagen mutations. Vandersteen AM, Lund AM, Ferguson DJ, Sawle P, Pollitt RC, Holder SE, Wakeling E, Moat N, Pope FM. Am J Med Genet A; 2014 Feb 15; 164A(2):386-91. PubMed ID: 24311407 [Abstract] [Full Text] [Related]
13. [A contribution to the recording and study of the disease pattern of osteogenesis imperfecta tarda (author's transl)]. Matzen KA, Werner KC. Z Orthop Ihre Grenzgeb; 1979 Feb 15; 117(1):21-30. PubMed ID: 425623 [Abstract] [Full Text] [Related]