Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Farzaneh Jadali"'
Autor:
Seyyed Ahmad Tabatabaei, Abdollah Karimi, Sedigheh Rafiee Tabatabaei, Badiozzaman Radpay, Farzaneh Jadali, Farideh Shiva, Mana Hadipour Jahromy
Publikováno v:
Journal of Research in Medical Sciences, Vol 15, Iss 2, Pp 120-124 (2010)
Pulmonary alveolar proteinosis, (PAP) is a rare disease of unknown etiology, characterized by accumulation of intraalveolar proteinaceous material which is rich in lipid and positive on periodic acid-Schiff stain. Two clinically different pediatric t
Externí odkaz:
https://doaj.org/article/bbd6a1172b8f46ceae3587343739fde6
Autor:
Reza Dalirani, Saied Habibian, Farzaneh Jadali, Masoumeh Mohkam, Abdollah Karimi, Mostafa Sharifian
Publikováno v:
Medical Journal of The Islamic Republic of Iran, Vol 23, Iss 1, Pp 36-41 (2009)
Background:Hydronephrosis is the most common congenital condition that is detected by prenatal ultrasonography.Moreover,the widespread use of prenatal ultrasonography results in an increased recognition of fetal hydronephrosis.Prenatal hydronephrosis
Externí odkaz:
https://doaj.org/article/9aa1fa1078f44bafa801b6b31962ced6
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
Kawasaki disease (KD) is a systemic vasculitis of unknown etiology and a leading cause of acquired heart disease. It is assumed that there is an activation of the immune system by an infectious trigger in a genetically susceptible host. Neuroblastoma
Externí odkaz:
https://doaj.org/article/a5becce07d39477cb6e3c12b29c29f19
Autor:
Zeinab Saei, Mahnaz Agaeipoor, Roohollah Gholampour, Sasan Ghaffari, Farzaneh Jadali, Esmaeil Shahabi Satlsar, Mohammad Mosleh, Mahdieh Mehrpouri
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 80:87-92
Although AML-M3 (APL) and HLA-DR negative non-APL are characterized by negative HLA-DR antigen, they are different entities with similar morphology in some cases. The aim of this study is the precise, differential diagnosis of APL from HLA-DR negativ
Autor:
Zeinab, Falakian, Tina, Shahani, Razieh, Rezaie, Saeideh, Mazloomzadeh, Feridoon, Sirati, Ahmad, Jalilvand, Farzaneh, Jahangiri, Parisa, Bahmani, Farzaneh, Jadali, Shahrokh, Atarian, Reza, Eghdam-Zamir, Alireza, Biglari
Publikováno v:
Archives of Iranian medicine. 21(11)
Reduction in the level of tissue decorin is a hallmark of many types of cancer including breast carcinoma. However, reduced decorin expression has also been reported in several types of benign tumors to the extent that it has been proposed as a tissu
Autor:
Saadat Adabian, Mohsen Zahraei, Fatemeh Fallah, Abdol-Reza Esteghamati, Farzaneh Jadali, Abdollah Karimi, Masoumeh Navidinia
Publikováno v:
Archives of Pediatric Infectious Diseases. 1:23-26
Background: Rotaviruses a major group of viruses that cause severe gastroenteritis in young children worldwide. Many different viruses can cause gastroenteritis, including Noroviruses, Adenoviruses, Sapoviruses, and Astroviruses. Serum antibody studi
Autor:
Raheleh Sadat Sajadi Nia, Saadat Adabian, Farzaneh Jadali, Fatemeh Bitajian, Saeid Maham, Latif Gachkar, Sara Rahmati Roodsari
Publikováno v:
Archives of Pediatric Infectious Diseases. 1:57-60
Background: Noroviruses are one of the major viral pathogens responsible for gastroenteritis. Outbreaks of diarrhea due to Norovirus have been reported frequently. This study is performed to determine the prevalence of Norovirus in fecal specimens of
Publikováno v:
BioMed Research International, Vol 2013 (2013)
BioMed Research International
BioMed Research International
Objectives. The B-cell-specific moloney leukemia virus insertion site 1 (the Bmi-1) gene is an important member in the family of polycomb group (PcG) genes that plays an oncogenic role in several types of cancer, but it’s expression as a prognostic
Autor:
Zahra Pourpak, Mohammad Taghi Arzanian, Samin Alavi, Atoosa Gharib, Mona Hedayat, Bibi Shahin Shamsian, Ali Amin Asnafi, Farzaneh Jadali, Nima Rezaei
Publikováno v:
Pediatric Hematology and Oncology. 29:215-219
Hemophagocytic lymphohistiocytosis (HLH) is a rare condition characterized by fever, hepatosplenomegaly, and cytopenia, and widespread accumulation of lymphocytes and histiocytes, sometimes with hemophagocytosis, primarily involving the spleen, lymph
Autor:
Farzaneh Jadali, J Ghoroobi, Ghamartaj Khanbabaee, Alireza Khatami, Kourosh Sheibani, Nima Rezaei, Seyed Ahmad Tabatabaei, F Rahimpoor
Publikováno v:
Bratislavske lekarske listy. 114(10)
Background: Congenital cystic adenomatoid malformations (CCAMs) are considered rare develop- mental anomalies of the lower respiratory tract. These are hamartomatous abnormalities of the lung with adeno- matoid proliferation of cysts resembling bronc