Salonen Riitta[au] - Search Results

Year	Number of Results
2002	6
2003	5
2004	7
2005	4
2006	3
2007	2
2008	3
2009	2
2010	1
2012	1
2014	1
2016	1
2024	0

1

Periderm prevents pathological epithelial adhesions during embryogenesis.

Richardson RJ, Hammond NL, Coulombe PA, Saloranta C, Nousiainen HO, Salonen R, Berry A, Hanley N, Headon D, Karikoski R, Dixon MJ. Richardson RJ, et al. Among authors: salonen r. J Clin Invest. 2014 Sep;124(9):3891-900. doi: 10.1172/JCI71946. Epub 2014 Aug 18. J Clin Invest. 2014. PMID: 25133425 Free PMC article.

2

Clinical utility gene card for: Meckel syndrome - update 2016.

Bergmann C, Frank V, Salonen R. Bergmann C, et al. Among authors: salonen r. Eur J Hum Genet. 2016 Aug;24(8). doi: 10.1038/ejhg.2016.33. Epub 2016 Apr 20. Eur J Hum Genet. 2016. PMID: 27094752 Free PMC article. No abstract available.

3

Mutant CHUK and severe fetal encasement malformation.

Lahtela J, Nousiainen HO, Stefanovic V, Tallila J, Viskari H, Karikoski R, Gentile M, Saloranta C, Varilo T, Salonen R, Kestilä M. Lahtela J, et al. Among authors: salonen r. N Engl J Med. 2010 Oct 21;363(17):1631-7. doi: 10.1056/NEJMoa0911698. N Engl J Med. 2010. PMID: 20961246 Free article.

4

A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm.

Luukkonen TM, Pöyhönen M, Palotie A, Ellonen P, Lagström S, Lee JH, Terwilliger JD, Salonen R, Varilo T. Luukkonen TM, et al. Among authors: salonen r. J Med Genet. 2012 Oct;49(10):621-9. doi: 10.1136/jmedgenet-2012-100977. J Med Genet. 2012. PMID: 23054244 Free PMC article.

5

Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis.

Paetau A, Honkala H, Salonen R, Ignatius J, Kestilä M, Herva R. Paetau A, et al. Among authors: salonen r. J Neuropathol Exp Neurol. 2008 Aug;67(8):750-62. doi: 10.1097/NEN.0b013e318180ec2e. J Neuropathol Exp Neurol. 2008. PMID: 18648327

6

Inflammation, abdominal obesity, and smoking as predictors of hypertension.

Niskanen L, Laaksonen DE, Nyyssönen K, Punnonen K, Valkonen VP, Fuentes R, Tuomainen TP, Salonen R, Salonen JT. Niskanen L, et al. Among authors: salonen r. Hypertension. 2004 Dec;44(6):859-65. doi: 10.1161/01.HYP.0000146691.51307.84. Epub 2004 Oct 18. Hypertension. 2004. PMID: 15492131

7

Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1.

Mee L, Honkala H, Kopra O, Vesa J, Finnilä S, Visapää I, Sang TK, Jackson GR, Salonen R, Kestilä M, Peltonen L. Mee L, et al. Among authors: salonen r. Hum Mol Genet. 2005 Jun 1;14(11):1475-88. doi: 10.1093/hmg/ddi157. Epub 2005 Apr 20. Hum Mol Genet. 2005. PMID: 15843405

8

Learning curve in ultrasonographic screening for selected fetal structural anomalies in early pregnancy.

Taipale P, Ammälä M, Salonen R, Hiilesmaa V. Taipale P, et al. Among authors: salonen r. Obstet Gynecol. 2003 Feb;101(2):273-8. doi: 10.1016/s0029-7844(02)02590-5. Obstet Gynecol. 2003. PMID: 12576250

9

Sex hormones, inflammation and the metabolic syndrome: a population-based study.

Laaksonen DE, Niskanen L, Punnonen K, Nyyssönen K, Tuomainen TP, Salonen R, Rauramaa R, Salonen JT. Laaksonen DE, et al. Among authors: salonen r. Eur J Endocrinol. 2003 Dec;149(6):601-8. doi: 10.1530/eje.0.1490601. Eur J Endocrinol. 2003. PMID: 14641004

10

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations.

Patrakka J, Martin P, Salonen R, Kestilä M, Ruotsalainen V, Männikkö M, Ryynänen M, Rapola J, Holmberg C, Tryggvason K, Jalanko H. Patrakka J, et al. Among authors: salonen r. Lancet. 2002 May 4;359(9317):1575-7. doi: 10.1016/S0140-6736(02)08504-5. Lancet. 2002. PMID: 12047969

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