These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. [Congenital multiple arthrogryposis. Description of a case of myogenic origin]. Marzetti G; Ermini M; Ferrante E Minerva Pediatr; 1968 Nov; 20(45):2348-54. PubMed ID: 5742970 [No Abstract] [Full Text] [Related]
10. Syndrome of osteopetrosis and muscular degeneration associated with cerebro-oculo-facio-skeletal changes. Lerman-Sagie T; Levi Y; Kidron D; Grünebaum M; Nitzan M Am J Med Genet; 1987 Sep; 28(1):137-42. PubMed ID: 3674107 [TBL] [Abstract][Full Text] [Related]
11. [Myogenic muscular atrophy, neurogenic muscular atrophy and congenital generalized arthrogryposis. The distinctiveness of each of these genetic diseases and the significance of their relative definitions based on the system in which the disease is most noticeable]. Salvioli G Clin Pediatr (Bologna); 1968 Oct; 50(10):605-24. PubMed ID: 5743023 [No Abstract] [Full Text] [Related]
12. ["An autopsy case of severe congenital muscular dystrophy with arthrogryposis multiplex"]. Itagaki Y; Yoshioka M; Sakamoto Y; Nishitani H; Haebara H Rinsho Shinkeigaku; 1982 Oct; 22(10):896-900. PubMed ID: 7182092 [No Abstract] [Full Text] [Related]
13. [Congenital muscular dystrophy]. Mumenthaler M Z Kinderheilkd; 1969; 106(2):131-62. PubMed ID: 5802055 [No Abstract] [Full Text] [Related]
14. [Granular body myopathy (so-called reducing body myopathy)]. Hübner G; Pongratz D Pathologe; 1982 Mar; 3(2):111-3. PubMed ID: 7088899 [No Abstract] [Full Text] [Related]
15. [Nonprogressive congenital myopathy (central core disease)]. Jean R; Bonnet H; Pages A; Dumas R; Rey JM Pediatrie; 1970; 25(7):796. PubMed ID: 5482535 [No Abstract] [Full Text] [Related]
17. [A contribution to the pathogenesis of arthrogryposis multiplex congenita]. Kozik M; Wróblewski T Reumatologia; 1968; 6(4):315-9. PubMed ID: 5714612 [No Abstract] [Full Text] [Related]