183 related articles for article (PubMed ID: 643415)
1. Arthrogryposis multiplex congenita as part of an inherited symptom complex: two case reports and a review of the literature.
Beckerman RC; Buchino JJ
Pediatrics; 1978 Mar; 61(3):417-22. PubMed ID: 643415
[TBL] [Abstract][Full Text] [Related]
2. Arthrogryposis multiplex congenita and the Turner phenotype.
Krieger I; Espiritu CE
Am J Dis Child; 1972 Feb; 123(2):141-4. PubMed ID: 5025860
[No Abstract] [Full Text] [Related]
3. Arthrogryposis multiplex congenita. Review with comment.
Hageman G; Willemse J
Neuropediatrics; 1983 Feb; 14(1):6-11. PubMed ID: 6339980
[TBL] [Abstract][Full Text] [Related]
4. Non-lethal arthrogryposis multiplex congenita presenting with cystic hygroma at 13 weeks gestational age.
Scott H; Hunter A; Bédard B
Prenat Diagn; 1999 Oct; 19(10):966-71. PubMed ID: 10521824
[TBL] [Abstract][Full Text] [Related]
5. Multiple Pterygium Syndrome (Escobar Syndrome): A Rare Form of Prenatal Myasthenia Presenting With Arthrogryposis Multiplex Congenita.
Manjunathan S; Singh K; Saini L
Neurology; 2024 Jul; 103(2):e209602. PubMed ID: 38870465
[No Abstract] [Full Text] [Related]
6. [The pterygium syndrome; status Bonnevie-Ullrich, dystrophia brevicollis congenita, Turner's syndrome and congenital arthromyodysplasia].
ROSSI E; CAFLISCH A
Helv Paediatr Acta; 1951 Apr; 6(2):119-48. PubMed ID: 14831862
[No Abstract] [Full Text] [Related]
7. Successful pregnancy outcome by caesarean section in a woman with arthrogryposis multiple congenita (AMC).
Singhal SR; Paul A; Nanda S; Singhal SK
Afr J Reprod Health; 2010 Sep; 14(3):233-4. PubMed ID: 21495617
[TBL] [Abstract][Full Text] [Related]
8. Arthrogryposis multiplex congenita: dental and maxillofacial phenotype - A scoping review.
Taqi D; Nematollahi S; Lemin S; Rauch F; Hamdy R; Dahan-Oliel N
Bone; 2024 Feb; 179():116955. PubMed ID: 37951521
[TBL] [Abstract][Full Text] [Related]
9. A family with autosomal dominant distal arthrogryposis multiplex congenita and brown syndrome.
Lobefalo LT; Mancini AT; Petitti MT; Verrotti AE; Della Loggia GE; Di Muzio AE; Chiarelli FE; Gallenga PE
Ophthalmic Genet; 1999 Dec; 20(4):233-41. PubMed ID: 10617921
[TBL] [Abstract][Full Text] [Related]
10. Disease coding systems for arthrogryposis multiplex congenita.
Bedard T; Lowry RB
Am J Med Genet C Semin Med Genet; 2019 Sep; 181(3):304-309. PubMed ID: 31232506
[TBL] [Abstract][Full Text] [Related]
11. Arthrogryposis multiplex congenita (AMC), a hereditary disease in swine, maps to chromosome 5 by linkage analysis.
Genini S; Malek M; Spilar S; Nguyen TT; Ménétrey F; Gebert S; Hagger C; Neuenschwander S; Kadarmideen HN; Stranzinger G; Vögeli P
Mamm Genome; 2004 Nov; 15(11):935-41. PubMed ID: 15672597
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A mild phenotype of LGI4-Related arthrogryposis multiplex congenita with intrafamilial variability.
Mishra S; Rai A; Srivastava P; Phadke SR
Eur J Med Genet; 2020 Mar; 63(3):103756. PubMed ID: 31513940
[TBL] [Abstract][Full Text] [Related]
14. Genetics of arthrogryposis: linkage analysis approach.
Narkis G; Landau D; Manor E; Ofir R; Birk OS
Clin Orthop Relat Res; 2007 Mar; 456():30-5. PubMed ID: 17195815
[TBL] [Abstract][Full Text] [Related]
15. Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care.
Dieterich K; Kimber E; Hall JG
Am J Med Genet C Semin Med Genet; 2019 Sep; 181(3):345-353. PubMed ID: 31410997
[TBL] [Abstract][Full Text] [Related]
16. A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.
Shohat M; Lotan R; Magal N; Shohat T; Fischel-Ghodsian N; Rotter JI; Jaber L
Am J Hum Genet; 1997 Nov; 61(5):1139-43. PubMed ID: 9345093
[TBL] [Abstract][Full Text] [Related]
17. Anaesthesia in arthrogryposis multiplex congenita: case report.
Oberoi GS; Kaul HL; Gill IS; Batra RK
Can J Anaesth; 1987 May; 34(3 ( Pt 1)):288-90. PubMed ID: 3581399
[TBL] [Abstract][Full Text] [Related]
18. [Problems with reference to genetic counseling in arthrogryposis multiplex congenits].
Gericke GS; Retief AE; Van Niekerk WA
S Afr Med J; 1975 Mar; 49(14):573-6. PubMed ID: 1145379
[TBL] [Abstract][Full Text] [Related]
19. A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita.
Latypova X; Creadore SG; Dahan-Oliel N; Gustafson AG; Wei-Hung Hwang S; Bedard T; Shazand K; van Bosse HJP; Giampietro PF; Dieterich K
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356068
[TBL] [Abstract][Full Text] [Related]
20. The range of publications on arthrogryposis multiplex congenita from 1995 to 2022-A scoping review.
Hermansen MV; Wekre LL; Lidal IB
Am J Med Genet A; 2023 Jul; 191(7):1693-1703. PubMed ID: 37009761
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
