Popp R - Search Results

1

The MTHFD1 c.1958 G>A polymorphism and recurrent spontaneous abortions.

Crişan TO, Trifa A, Farcaş M, Militaru M, Netea M, Pop I, Popp R. Crişan TO, et al. Among authors: popp r. J Matern Fetal Neonatal Med. 2011 Jan;24(1):189-92. doi: 10.3109/14767051003702794. Epub 2010 Mar 24. J Matern Fetal Neonatal Med. 2011. PMID: 20334533 Free article.

2

Development of a reliable PCR-RFLP assay for investigation of the JAK2 rs10974944 SNP, which might predispose to the acquisition of somatic mutation JAK2(V617F).

Trifa AP, Cucuianu A, Popp RA. Trifa AP, et al. Acta Haematol. 2010;123(2):84-7. doi: 10.1159/000264954. Epub 2009 Dec 11. Acta Haematol. 2010. PMID: 20016140 No abstract available.

3

Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania.

Lazăr C, Popp R, Trifa A, Mocanu C, Mihut G, Al-Khzouz C, Tomescu E, Figan I, Grigorescu-Sido P. Lazăr C, et al. Among authors: popp r. Int J Pediatr Otorhinolaryngol. 2010 Apr;74(4):351-5. doi: 10.1016/j.ijporl.2009.12.015. Epub 2010 Jan 21. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20096468

4

The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms.

Trifa AP, Cucuianu A, Petrov L, Urian L, Militaru MS, Dima D, Pop IV, Popp RA. Trifa AP, et al. Ann Hematol. 2010 Oct;89(10):979-83. doi: 10.1007/s00277-010-0960-y. Epub 2010 Apr 27. Ann Hematol. 2010. PMID: 20422415

5

Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.

Militaru MS, Popp RA, Trifa AP. Militaru MS, et al. J Gastrointestin Liver Dis. 2010 Jun;19(2):191-3. J Gastrointestin Liver Dis. 2010. PMID: 20593054 Free article.

6

JAK2 46/1 haplotype seems not to be associated with lower limb deep venous thrombosis.

Trifa AP, Crişan S, Popp RA, Cucuianu A, Buzoianu AD. Trifa AP, et al. Blood Cells Mol Dis. 2010 Oct 15;45(3):199-200. doi: 10.1016/j.bcmd.2010.07.004. Epub 2010 Aug 5. Blood Cells Mol Dis. 2010. PMID: 20691622 Clinical Trial. No abstract available.

7

TLR1 polymorphisms in Europeans and spontaneous pregnancy loss.

Crişan TO, Farcaş MF, Trifa AP, Plantinga TS, Militaru MS, Pop IV, Netea MG, Popp RA. Crişan TO, et al. Gene. 2012 Feb 15;494(1):109-11. doi: 10.1016/j.gene.2011.12.008. Epub 2011 Dec 16. Gene. 2012. PMID: 22200569

8

Association of 276G>T adiponectin gene polymorphism to plasma adiponectin and albuminuria in type 2 diabetic patients.

Kacso IM, Trifa AP, Popp RA, Kacso G. Kacso IM, et al. Int Urol Nephrol. 2012 Dec;44(6):1771-7. doi: 10.1007/s11255-011-0118-4. Epub 2012 Jan 6. Int Urol Nephrol. 2012. PMID: 22222620

9

Absence of BRAF V600E mutation in a cohort of 402 patients with various chronic and acute myeloid neoplasms.

Trifa AP, Popp RA, Cucuianu A, Coadă CA, Urian LG, Militaru MS, Bănescu C, Dima D, Farcaş MF, Crişan TO, Petrov L, Gug C, Pop IV. Trifa AP, et al. Leuk Lymphoma. 2012 Dec;53(12):2496-7. doi: 10.3109/10428194.2012.668188. Epub 2012 Apr 18. Leuk Lymphoma. 2012. PMID: 22339435 No abstract available.

10

HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.

Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV. Trifa AP, et al. J Gastrointestin Liver Dis. 2012 Jun;21(2):177-80. J Gastrointestin Liver Dis. 2012. PMID: 22720307 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

579 results

Search Page

Filters