Rein AJ[au] - Search Results

Year	Number of Results
1976	1
1982	3
1983	1
1984	5
1985	4
1986	2
1987	3
1988	5
1989	2
1990	2
1992	3
1993	1
1994	2
1995	6
1996	4
1997	3
1998	3
1999	4
2000	5
2001	4
2002	2
2003	3
2004	2
2005	3
2006	5
2007	4
2008	1
2009	3
2010	1
2012	2
2013	3
2014	2
2015	2
2016	1
2017	1
2018	1
2020	1
2022	0

1

The natriuretic peptides as biomarkers for adults with congenital heart disease.

Nir A, Luchner A, Rein AJ. Nir A, et al. Among authors: rein aj. Biomark Med. 2012 Dec;6(6):827-37. doi: 10.2217/bmm.12.73. Biomark Med. 2012. PMID: 23227849 Review.

2

Immune-Mediated Fetal Complete Atrioventricular Block: Can Dexamethasone Therapy Revert the Process?

Perles Z, Ishay Y, Nir A, Gavri S, Golender J, Ta-Shma A, Abu-Zahira I, Natsheh J, Elchalal U, Mevorach D, Rein AJ. Perles Z, et al. Among authors: rein aj. Isr Med Assoc J. 2020 Nov;11(22):711-716. Isr Med Assoc J. 2020. PMID: 33249793 Free article. Review.

3

Cardiovascular abnormalities associated with the Stuve-Wiedemann syndrome.

Raas-Rothschild A, Ergaz-Schaltiel Z, Bar-Ziv J, Rein AJ. Raas-Rothschild A, et al. Among authors: rein aj. Am J Med Genet A. 2003 Aug 30;121A(2):156-8. doi: 10.1002/ajmg.a.20066. Am J Med Genet A. 2003. PMID: 12910496 Review.

4

Prevention of complete heart block in children of mothers with anti-SSA/Ro and anti-SSB/La autoantibodies: detection and treatment of first-degree atrioventricular block.

Mevorach D, Elchalal U, Rein AJ. Mevorach D, et al. Among authors: rein aj. Curr Opin Rheumatol. 2009 Sep;21(5):478-82. doi: 10.1097/BOR.0b013e32832ed817. Curr Opin Rheumatol. 2009. PMID: 19584727 Review.

5

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

Ta-Shma A, Hjeij R, Perles Z, Dougherty GW, Abu Zahira I, Letteboer SJF, Antony D, Darwish A, Mans DA, Spittler S, Edelbusch C, Cindrić S, Nöthe-Menchen T, Olbrich H, Stuhlmann F, Aprea I, Pennekamp P, Loges NT, Breuer O, Shaag A, Rein AJJT, Gulec EY, Gezdirici A, Abitbul R, Elias N, Amirav I, Schmidts M, Roepman R, Elpeleg O, Omran H. Ta-Shma A, et al. Among authors: rein ajjt. PLoS Genet. 2018 Aug 27;14(8):e1007602. doi: 10.1371/journal.pgen.1007602. eCollection 2018 Aug. PLoS Genet. 2018. PMID: 30148830 Free PMC article.

6

Congenital valvular defects associated with deleterious mutations in the PLD1 gene.

Ta-Shma A, Zhang K, Salimova E, Zernecke A, Sieiro-Mosti D, Stegner D, Furtado M, Shaag A, Perles Z, Nieswandt B, Rein AJ, Rosenthal N, Neiman AM, Elpeleg O. Ta-Shma A, et al. Among authors: rein aj. J Med Genet. 2017 Apr;54(4):278-286. doi: 10.1136/jmedgenet-2016-104259. Epub 2016 Oct 31. J Med Genet. 2017. PMID: 27799408

7

Absent ductus venosus in the fetus: review of the literature and first report of direct umbilical venous drainage to the coronary sinus.

Perles Z, Nir A, Nadjari M, Ergaz Z, Raas-Rothschild A, Rein AJ. Perles Z, et al. Among authors: rein aj. Fetal Diagn Ther. 2003 Jul-Aug;18(4):247-51. doi: 10.1159/000070804. Fetal Diagn Ther. 2003. PMID: 12835584 Review.

8

The coronary sinus in the fetus.

Rein AJ, Nir A, Nadjari M. Rein AJ, et al. Ultrasound Obstet Gynecol. 2000 Jun;15(6):468-72. doi: 10.1046/j.1469-0705.2000.00142.x. Ultrasound Obstet Gynecol. 2000. PMID: 11005113 Free article.

9

A human laterality disorder associated with recessive CCDC11 mutation.

Perles Z, Cinnamon Y, Ta-Shma A, Shaag A, Einbinder T, Rein AJ, Elpeleg O. Perles Z, et al. Among authors: rein aj. J Med Genet. 2012 Jun;49(6):386-90. doi: 10.1136/jmedgenet-2011-100457. Epub 2012 May 10. J Med Genet. 2012. PMID: 22577226

10

A human laterality disorder caused by a homozygous deleterious mutation in MMP21.

Perles Z, Moon S, Ta-Shma A, Yaacov B, Francescatto L, Edvardson S, Rein AJ, Elpeleg O, Katsanis N. Perles Z, et al. Among authors: rein aj. J Med Genet. 2015 Dec;52(12):840-7. doi: 10.1136/jmedgenet-2015-103336. Epub 2015 Oct 1. J Med Genet. 2015. PMID: 26429889 Free PMC article.

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