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Viruses|October 27, 2017
Protoparvovirus Cell EntryCarlos Ros, Nooshin Bayat, Raphael Wolfisberg, et al.Journal of Medical Case Reports|February 8, 2012
Hemoglobin Q-Iran detected in family members from Northern Iran: a case reportMohammad Khorshidi, Payam Roshan, Nooshin Bayat, et al.The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology|September 28, 2011
Acute pancreatitis: an initial presentation of systemic lupus erythematosusMohammad Ebrahim Ghamarchehreh, Gholamhossein Alishiri, Nooshin Bayat, et al.JPMA. the Journal of the Pakistan Medical Association|July 5, 2012
Report of haemoglobin J-Toronto and alpha thalassemia in a family from North of IranMohammad Reza Mahdavi, Nooshin Bayat, Valeh Hadavi, et al.Hemoglobin|September 22, 2010
β-Thalassemia mutations in the Kurdish population of northeastern IraqSana D Jalal, Nasir A S Al-Allawi, Nooshin Bayat, et al.Expert Review of Hematology|November 3, 2015
Point mutations which should not be overlooked in Hb H diseaseSamaneh Farashi, Nooshin Bayat, Shadi Vakili, et al.Hemoglobin|May 16, 2014
Characterizing a cohort of α-thalassemia couples collected during screening for hemoglobinopathies: 14 years of an Iranian experienceNima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, et al.Hemoglobin|December 11, 2012
The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern IraqNasir A S Al-Allawi, Sana D Jalal, Najeeb S Rasheed, et al.Hemoglobin|June 13, 2012
The XmnI and BCL11A single nucleotide polymorphisms may help predict hydroxyurea response in Iranian β-thalassemia patientsMehdi Banan, Hadi Bayat, Azita Azarkeivan, et al.Hemoglobin|February 14, 2013
Novel mutations responsible for α-thalassemia in Iranian familiesNooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, et al.Pageof 2