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.
145 related articles for article (PubMed ID: 9134190)
1. The spectrum of arthrogryposis in 33 chinese children. Wong V Brain Dev; 1997 Apr; 19(3):187-96. PubMed ID: 9134190 [TBL] [Abstract][Full Text] [Related]
2. Congenital muscular dystrophy associated with lethal arthrogryposis multiplex congenita. Moerman P; Fryns JP; Van Dijck H; Lauweryns JM Virchows Arch A Pathol Anat Histopathol; 1985; 408(1):43-8. PubMed ID: 3933170 [TBL] [Abstract][Full Text] [Related]
3. Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: three new cases and review of the literature. Sombekke BH; Molenaar WM; van Essen AJ; Schoots CJ Pediatr Pathol; 1994; 14(2):277-85. PubMed ID: 8008690 [TBL] [Abstract][Full Text] [Related]
4. Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects. Hall JG J Pediatr Orthop B; 1997 Jul; 6(3):159-66. PubMed ID: 9260643 [TBL] [Abstract][Full Text] [Related]
5. Characterization of a group unrelated patients with arthrogryposis multiplex congenita. Valdés-Flores M; Casas-Avila L; Hernández-Zamora E; Kofman S; Hidalgo-Bravo A J Pediatr (Rio J); 2016; 92(1):58-64. PubMed ID: 26453511 [TBL] [Abstract][Full Text] [Related]
6. Tabulation of findings in the muscular dystrophies and in myotonia dystrophica. Danowski TS; Wissinger HA; Hohmann TC; Gerneth JA; Folkers K; Vester JW; Fisher ER Arch Phys Med Rehabil; 1971 May; 52(5):193-200. PubMed ID: 4931852 [No Abstract] [Full Text] [Related]
8. Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome? Seidahmed MZ; Sunada Y; Ozo CO; Hamid F; Campbell KP; Salih MA Neuropediatrics; 1996 Dec; 27(6):305-10. PubMed ID: 9050048 [TBL] [Abstract][Full Text] [Related]
9. Electromyographic characteristics of congenital and early onset motor unit diseases. Fowler WM; Taylor RG; Munsat TL Arch Phys Med Rehabil; 1971 Aug; 52(8):343-61. PubMed ID: 5284447 [No Abstract] [Full Text] [Related]
11. Arthrogryposis multiplex congenita, Pena-Shokeir phenotype, with gastroschisis and agenesis of the leg. Agapitos M; Georgiou-Theodoropoulou M; Koutselinis A; Papacharalambus N Pediatr Pathol; 1988; 8(4):409-13. PubMed ID: 2974953 [TBL] [Abstract][Full Text] [Related]
12. The Schwartz-Jampel syndrome. al Gazali LI Clin Dysmorphol; 1993 Jan; 2(1):47-54. PubMed ID: 8298738 [TBL] [Abstract][Full Text] [Related]
13. Orthopaedic aspects of the Schwartz syndrome. Horan F; Beighton P J Bone Joint Surg Am; 1975 Jun; 57(4):542-4. PubMed ID: 1141267 [No Abstract] [Full Text] [Related]
14. The distal arthrogryposes: delineation of new entities--review and nosologic discussion. Hall JG; Reed SD; Greene G Am J Med Genet; 1982 Feb; 11(2):185-239. PubMed ID: 7039311 [TBL] [Abstract][Full Text] [Related]
15. Arthrogryposis multiplex congenita: a report of two cases. Brooks JG; Coster DJ Aust N Z J Ophthalmol; 1994 May; 22(2):127-32. PubMed ID: 7917267 [TBL] [Abstract][Full Text] [Related]
16. Arthrogryposis. Hall JG Am Fam Physician; 1989 Jan; 39(1):113-9. PubMed ID: 2643273 [TBL] [Abstract][Full Text] [Related]
17. Extending the spectrum of distal arthrogryposis. Gripp KW; Scott CI; Brockett BC; Nicholson L; Mackenzie WG Am J Med Genet; 1996 Nov; 65(4):286-90. PubMed ID: 8923937 [TBL] [Abstract][Full Text] [Related]