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2. The familial factor in exostosis multiplex cartilaginea. Bercu G; Străjescu N; Străjescu E; Sima F; Teodorescu M Helv Med Acta; 1969 Mar; 34(6):510-6. PubMed ID: 5305166 [No Abstract] [Full Text] [Related]
3. [Multiple familial exostoses. Apropos of 16 cases]. Guerrero Espejo A; Alonso Alonso JJ; Martińez López de Letona J; Frieyro Segui E; Bouza Santiago E; Masa Vázquez C; Pérez Maestu R; Buzón Rueda L; Alamo Antúnez A Rev Clin Esp; 1978 Feb; 148(4):385-9. PubMed ID: 306650 [No Abstract] [Full Text] [Related]
4. Radiographic findings in hereditary multiple exostoses and a new theory of the pathogenesis of exostoses. Pazzaglia UE; Pedrotti L; Beluffi G; Monafò V; Savasta S Pediatr Radiol; 1990; 20(8):594-7. PubMed ID: 2251004 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. The widened spectrum of multiple cartilaginous exostosis (MCE). Giedion A; Kesztler R; Muggiasca F Pediatr Radiol; 1975 Mar; 3(2):93-100. PubMed ID: 1085923 [TBL] [Abstract][Full Text] [Related]
10. [Review of exostosing disease apropos of the study of a family with 14 carriers of multiple exostoses]. Mota López A; García-Roméu García C; Sanjose Pacheco F; García Carlos E; Pedauye González JM; Caturla Such J Rev Clin Esp; 1977 Mar; 144(5):350-60. PubMed ID: 300890 [No Abstract] [Full Text] [Related]
11. Spastic disorder in patients with hereditary multiple exostoses, but without spinal cord compression: a new syndrome? Hamann G; Zankl M; Schimrigk K; Kloss R J Med Genet; 1992 Jul; 29(7):494-6. PubMed ID: 1640431 [TBL] [Abstract][Full Text] [Related]
12. [Familial multiple exostoses. Presentation of a case]. Rogai R; Renai P; Benedetti PA Minerva Pediatr; 1979 Mar; 31(6):435-42. PubMed ID: 314043 [No Abstract] [Full Text] [Related]
13. Multiple hereditary osteochondromatosis. Two cases with ankle and knee deformities. Glockenberg A; Sobel E; Levitz SJ J Am Podiatr Med Assoc; 1997 Feb; 87(2):70-3. PubMed ID: 9046752 [TBL] [Abstract][Full Text] [Related]
14. Incomplete penetrance and expressivity skewing in hereditary multiple exostoses. Legeai-Mallet L; Munnich A; Maroteaux P; Le Merrer M Clin Genet; 1997 Jul; 52(1):12-6. PubMed ID: 9272707 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Multiple cartilaginous exostoses in two generations of dogs. Chester DK J Am Vet Med Assoc; 1971 Oct; 159(7):895-7. PubMed ID: 5315272 [No Abstract] [Full Text] [Related]
18. Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostoses. Dominguez R; Young LW; Steele MW; Girdany BR Pediatr Radiol; 1984; 14(5):356-9. PubMed ID: 6332296 [TBL] [Abstract][Full Text] [Related]
19. Cartilaginous exostosis arising from the ventral surface of the scapula. A case report. Nercessian O; Denton JR Clin Orthop Relat Res; 1988 Nov; (236):145-7. PubMed ID: 3263242 [TBL] [Abstract][Full Text] [Related]
20. The Jansen type of metaphyseal chondrodysplasia: confirmation of dominant inheritance and review of radiographic manifestations in the newborn and adult. Charrow J; Poznanski AK Am J Med Genet; 1984 Jun; 18(2):321-7. PubMed ID: 6331768 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]