139 related articles for article (PubMed ID: 24254849)
41. Clinical and pathological findings in cases of truncus arteriosus in infancy.
TAUSSIG HB
Am J Med; 1947 Jan; 2(1):26-34. PubMed ID: 20278447
[No Abstract] [Full Text] [Related]
42. Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.
Tenenbaum-Rakover Y; Weinberg-Shukron A; Renbaum P; Lobel O; Eideh H; Gulsuner S; Dahary D; Abu-Rayyan A; Kanaan M; Levy-Lahad E; Bercovich D; Zangen D
J Med Genet; 2015 Jun; 52(6):391-9. PubMed ID: 25873734
[TBL] [Abstract][Full Text] [Related]
43. Cardiac outflow tract: a review of some embryogenetic aspects of the conotruncal region of the heart.
Restivo A; Piacentini G; Placidi S; Saffirio C; Marino B
Anat Rec A Discov Mol Cell Evol Biol; 2006 Sep; 288(9):936-43. PubMed ID: 16892424
[TBL] [Abstract][Full Text] [Related]
44. Long-term follow-up of truncus arteriosus repaired in infancy: a twenty-year experience.
Rajasinghe HA; McElhinney DB; Reddy VM; Mora BN; Hanley FL
J Thorac Cardiovasc Surg; 1997 May; 113(5):869-78; discussion 878-9. PubMed ID: 9159620
[TBL] [Abstract][Full Text] [Related]
45. [Common truncus arteriosus].
GONZALEZ ALVAREZ J; MUNOZ CARDONA P; SANZ FERNANDEZ P
Rev Esp Cardiol; 1963 Apr; 16():336-55. PubMed ID: 13963358
[No Abstract] [Full Text] [Related]
46. 46,XY disorders of sex development and congenital diaphragmatic hernia: a case with dysmorphic facies, truncus arteriosus, bifid thymus, gut malrotation, rhizomelia, and adactyly.
Esplin ED; Chaib H; Haney M; Martin B; Homeyer M; Urban AE; Bernstein JA
Am J Med Genet A; 2015 Jun; 167(6):1360-4. PubMed ID: 25898814
[TBL] [Abstract][Full Text] [Related]
47. Perioperative and Anesthetic Considerations in Truncus Arteriosus.
Parikh R; Eisses M; Latham GJ; Joffe DC; Ross FJ
Semin Cardiothorac Vasc Anesth; 2018 Sep; 22(3):285-293. PubMed ID: 29808750
[TBL] [Abstract][Full Text] [Related]
48. [Truncus arteriosus. Comments of 4 cases].
BAUDINO C; BAUDINO CH; CLAVERO JN; SONEIRA G
Rev Med Cordoba; 1962; 50():109-28. PubMed ID: 13966894
[No Abstract] [Full Text] [Related]
49. Exome sequencing identifies a c.148-1G>C mutation of TBX5 in a Holt-Oram family with unusual genotype-phenotype correlations.
Guo Q; Shen J; Liu Y; Pu T; Sun K; Chen S
Cell Physiol Biochem; 2015; 37(3):1066-74. PubMed ID: 26401820
[TBL] [Abstract][Full Text] [Related]
50. Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patients.
van der Zwaag B; Verzijl HT; Wichers KH; Beltran-Valero de Bernabe D; Brunner HG; van Bokhoven H; Padberg GW
Pediatr Neurol; 2004 Aug; 31(2):114-8. PubMed ID: 15301830
[TBL] [Abstract][Full Text] [Related]
51. ENU induced mutations causing congenital cardiovascular anomalies.
Yu Q; Shen Y; Chatterjee B; Siegfried BH; Leatherbury L; Rosenthal J; Lucas JF; Wessels A; Spurney CF; Wu YJ; Kirby ML; Svenson K; Lo CW
Development; 2004 Dec; 131(24):6211-23. PubMed ID: 15548583
[TBL] [Abstract][Full Text] [Related]
52. Familial truncus arteriosus: a possible autosomal-recessive trait.
Abushaban L; Uthaman B; Kumar AR; Selvan J
Pediatr Cardiol; 2003; 24(1):64-6. PubMed ID: 12574981
[TBL] [Abstract][Full Text] [Related]
53. ["Pseudo-truncus arteriosus" in an adult].
BETOULIERES P; LATOUR H; PUECH P; VIALLA M
J Radiol Electrol Med Nucl; 1962 May; 43():318-22. PubMed ID: 13868632
[No Abstract] [Full Text] [Related]
54. Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects.
Bloch-Zupan A; Jamet X; Etard C; Laugel V; Muller J; Geoffroy V; Strauss JP; Pelletier V; Marion V; Poch O; Strahle U; Stoetzel C; Dollfus H
Am J Hum Genet; 2011 Dec; 89(6):773-81. PubMed ID: 22152679
[TBL] [Abstract][Full Text] [Related]
55. Prenatal sonographic appearance of truncus arteriosus on wide-band Doppler imaging.
Hidaka N; Anami A; Yoshitomi T; Tsukimori K; Wake N
J Clin Ultrasound; 2009 Jun; 37(5):295-7. PubMed ID: 19105238
[TBL] [Abstract][Full Text] [Related]
56. ASK1 mediates the teratogenicity of diabetes in the developing heart by inducing ER stress and inhibiting critical factors essential for cardiac development.
Wang F; Wu Y; Quon MJ; Li X; Yang P
Am J Physiol Endocrinol Metab; 2015 Sep; 309(5):E487-99. PubMed ID: 26173459
[TBL] [Abstract][Full Text] [Related]
57. PlexinD1 and semaphorin signaling are required in endothelial cells for cardiovascular development.
Gitler AD; Lu MM; Epstein JA
Dev Cell; 2004 Jul; 7(1):107-16. PubMed ID: 15239958
[TBL] [Abstract][Full Text] [Related]
58. Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome.
Haghighi A; Tiwari A; Piri N; Nürnberg G; Saleh-Gohari N; Haghighi A; Neidhardt J; Nürnberg P; Berger W
PLoS One; 2014; 9(11):e112747. PubMed ID: 25392994
[TBL] [Abstract][Full Text] [Related]
59. Persistent truncus arteriosus on dual source CT.
Sharma A; Priya S; Jagia P
Jpn J Radiol; 2016 Jul; 34(7):486-93. PubMed ID: 27262857
[TBL] [Abstract][Full Text] [Related]
60. Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.
Gerards M; Kamps R; van Oevelen J; Boesten I; Jongen E; de Koning B; Scholte HR; de Angst I; Schoonderwoerd K; Sefiani A; Ratbi I; Coppieters W; Karim L; de Coo R; van den Bosch B; Smeets H
Brain; 2013 Mar; 136(Pt 3):882-90. PubMed ID: 23423671
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]