Nooshin Bayat - Search Results

Year	Number of Results
2010	1
2011	2
2012	4
2013	2
2014	1
2015	2
2016	1
2017	1
2024	0

1

Ros C, Bayat N, Wolfisberg R, Almendral JM. Ros C, et al. Among authors: bayat n. Viruses. 2017 Oct 26;9(11):313. doi: 10.3390/v9110313. Viruses. 2017. PMID: 29072600 Free PMC article. Review.

2

Point mutations which should not be overlooked in Hb H disease.

Farashi S, Bayat N, Vakili S, Faramarzi Garous N, Ashki M, Imanian H, Najmabadi H, Azarkeivan A. Farashi S, et al. Among authors: bayat n. Expert Rev Hematol. 2016 Jan;9(1):107-13. doi: 10.1586/17474086.2016.1107470. Epub 2015 Nov 2. Expert Rev Hematol. 2016. PMID: 26523940

3

Genotype-phenotype correlation in Iranian patients with Hb H disease.

Ebrahimkhani S, Azarkeivan A, Bayat N, Houry-Parvin M, Jalil-Nejad S, Zand S, Golkar Z, Hadavi V, Imanian H, Oberkanins C, Najmabadi H. Ebrahimkhani S, et al. Among authors: bayat n. Hemoglobin. 2011;35(1):40-6. doi: 10.3109/03630269.2010.546314. Hemoglobin. 2011. PMID: 21250880

4

Acute pancreatitis: an initial presentation of systemic lupus erythematosus.

Ghamarchehreh ME, Alishiri G, Bayat N, Khajehpoor H, Nooranipour M. Ghamarchehreh ME, et al. Among authors: bayat n. Turk J Gastroenterol. 2011 Aug;22(4):433-6. doi: 10.4318/tjg.2011.0263. Turk J Gastroenterol. 2011. PMID: 21948578 Free article.

5

The XmnI and BCL11A single nucleotide polymorphisms may help predict hydroxyurea response in Iranian β-thalassemia patients.

Banan M, Bayat H, Azarkeivan A, Mohammadparast S, Kamali K, Farashi S, Bayat N, Khani MH, Neishabury M, Najmabadi H. Banan M, et al. Among authors: bayat n. Hemoglobin. 2012;36(4):371-80. doi: 10.3109/03630269.2012.691147. Epub 2012 Jun 11. Hemoglobin. 2012. PMID: 22686296

6

Report of haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran.

Mahdavi MR, Bayat N, Hadavi V, Karami H, Roshan P, Najmabadi H, Rohanizadeh H. Mahdavi MR, et al. Among authors: bayat n. J Pak Med Assoc. 2012 Apr;62(4):396-8. J Pak Med Assoc. 2012. PMID: 22755290

7

Hemoglobin Q-Iran detected in family members from Northern Iran: a case report.

Khorshidi M, Roshan P, Bayat N, Mahdavi MR, Najmabadi H. Khorshidi M, et al. Among authors: bayat n. J Med Case Rep. 2012 Feb 6;6:47. doi: 10.1186/1752-1947-6-47. J Med Case Rep. 2012. PMID: 22309992 Free PMC article.

8

Novel mutations responsible for α-thalassemia in Iranian families.

Bayat N, Farashi S, Hafezi-Nejad N, Faramarzi N, Ashki M, Vakili S, Imanian H, Khosravi M, Azar-Keivan A, Najmabadi H. Bayat N, et al. Hemoglobin. 2013;37(2):148-59. doi: 10.3109/03630269.2013.763821. Epub 2013 Feb 12. Hemoglobin. 2013. PMID: 23402770

9

The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern Iraq.

Al-Allawi NA, Jalal SD, Rasheed NS, Bayat N, Imanian H, Najmabadi H, Faraj A. Al-Allawi NA, et al. Among authors: bayat n. Hemoglobin. 2013;37(1):56-64. doi: 10.3109/03630269.2012.749490. Epub 2012 Dec 7. Hemoglobin. 2013. PMID: 23215864

10

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.

Farashi S, Bayat N, Faramarzi Garous N, Ashki M, Montajabi Niat M, Vakili S, Imanian H, Zeinali S, Najmabadi H, Azarkeivan A. Farashi S, et al. Among authors: bayat n. Hemoglobin. 2015;39(3):201-6. doi: 10.3109/03630269.2015.1027914. Epub 2015 Jun 18. Hemoglobin. 2015. PMID: 26084319

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