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44. [Kniest syndrome. Contribution of a new case]. Casanova Bellido M; Martín M; Moreno AM; Hernández A; Rico S An Esp Pediatr; 1986 Oct; 25(4):297-9. PubMed ID: 3492163 [No Abstract] [Full Text] [Related]
45. [Multiple exostoses disease (observations in 21 reported cases)]. Di Giovanni C; Rosa MA; Pallotta F Arch Putti Chir Organi Mov; 1989; 37(2):335-43. PubMed ID: 2696447 [TBL] [Abstract][Full Text] [Related]
46. Hemothorax: unusual complication of hereditary multiple exostosis. Camera A; Potter RT; Siegel M N Y State J Med; 1981 Feb; 81(2):243-4. PubMed ID: 6970353 [No Abstract] [Full Text] [Related]
47. The radiographic patterns in dyschondrostosis. Hoeffel JC; Brauer B; Jimenez J; Hoeffel F Aust Paediatr J; 1972 Aug; 8(4):191-4. PubMed ID: 4539409 [No Abstract] [Full Text] [Related]
48. [Exostosing disease. One case report. Review of the literature]. Safary A; Limbosch JM; Baillon JM Acta Orthop Belg; 1978; 44(4):485-95. PubMed ID: 310626 [No Abstract] [Full Text] [Related]
50. Stüve-Wiedemann syndrome and related bent bone dysplasias. Akawi NA; Ali BR; Al-Gazali L Clin Genet; 2012 Jul; 82(1):12-21. PubMed ID: 22300393 [TBL] [Abstract][Full Text] [Related]
51. The development of the upper end of the femur in multiple hereditary exostosis. Weiner DS; Hoyt WA Clin Orthop Relat Res; 1978; (137):187-90. PubMed ID: 311266 [TBL] [Abstract][Full Text] [Related]
52. [Multiple cartilaginous exostoses with polyposis of stomach and colon: a new, hereditary combination different from Gardner's syndrome (author's transl)]. Fuchs GA Dtsch Med Wochenschr; 1975 Nov; 100(45):2316-9. PubMed ID: 1081041 [TBL] [Abstract][Full Text] [Related]
53. One-bone forearm as a salvage procedure for recalcitrant forearm deformity in hereditary multiple exostoses. Rodgers WB; Hall JE J Pediatr Orthop; 1993; 13(5):587-91. PubMed ID: 8376557 [TBL] [Abstract][Full Text] [Related]
54. [Radiographic evaluation of skeletal changes in metaphyseal and vertebro-metaphyseal osteochondrodysplasias]. Winkielman J Pol Przegl Radiol; 1983; 47(2):109-13. PubMed ID: 6364055 [No Abstract] [Full Text] [Related]
55. [Certain mechanisms of genetic transmission in the field of osteochondro-embryopathies (Case reports)]. Ravetto F; Crua G Minerva Pediatr; 1967 Nov; 19(46):2035-41. PubMed ID: 5304440 [No Abstract] [Full Text] [Related]
56. Hereditary multiple exostoses. Report of a case with spinal cord compression. Vinstein AL; Franken EA Am J Roentgenol Radium Ther Nucl Med; 1971 Jun; 112(2):405-7. PubMed ID: 5314313 [No Abstract] [Full Text] [Related]
57. Hereditary multiple exostoses. Report of a family. Crandall BF; Field LL; Sparkes RS; Spence MA Clin Orthop Relat Res; 1984 Nov; (190):217-9. PubMed ID: 6333306 [TBL] [Abstract][Full Text] [Related]
58. Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses-mental retardation syndrome (Langer-Giedion syndrome). Miyamoto K; Sakaguchi Y; Hosoe H; Mori A; Yamazaki S; Hattori S; Shimizu K Spinal Cord; 2005 Mar; 43(3):190-4. PubMed ID: 15583707 [TBL] [Abstract][Full Text] [Related]
60. Hereditary deforming dyschondroplasia. Two case report followed through four generations of each family. Pandey S Int Surg; 1970 Oct; 54(4):264-7. PubMed ID: 5311860 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]