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G Toogeh

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Articles 8
Citations 94
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Recent Articles
1.
Ross C, Rangarajan S, Karimi M, Toogeh G, Apte S, Lissitchkov T, et al.
J Thromb Haemost . 2017 Dec; 16(2):253-261. PMID: 29220876
Summary: Background Human fibrinogen concentrate (HFC) corrects fibrinogen deficiency in congenital a-/hypofibrinogenemia. Objectives To assess pharmacokinetics (PK), effects on thromboelastometry maximum clot firmness (MCF), and safety of a new double...
2.
Mortazavi S, Haghpanah B, Ebrahiminasab M, Baghdadi T, Toogeh G
Haemophilia . 2016 Aug; 22(6):919-924. PMID: 27561958
Introduction: Haemophilic arthropathy (HA) is a debilitating complication of haemophilia which leads to TKA in severe cases. Aim: We conducted a prospective study of the outcome of TKA in our...
3.
Mortazavi S, Najafi A, Toogeh G
Haemophilia . 2016 Jun; 22(5):e451-3. PMID: 27353311
No abstract available.
4.
Mortazavi S, Haghpanah B, Ebrahiminasab M, Baghdadi T, Hantooshzadeh R, Toogeh G
Haemophilia . 2015 Nov; 22(2):303-307. PMID: 26536858
Introduction: Haemophilic arthropathy of the knee is usually a bilateral affliction. The patients usually refer for treatment in young ages and do not have major comorbidities, being fit for bilateral...
5.
Ferdowsi S, Atarodi K, Amirizadeh N, Toogeh G, Azarkeivan A, Shirkoohi R, et al.
Int J Lab Hematol . 2015 May; 37(5):661-7. PMID: 26011312
Introduction: The JAK2V617F mutation has emerged in recent years as a diagnostic as well as a treatment target in patients with polycythemia vera (PV) and essential thrombocythemia (ET). The disease...
6.
Fallah P, Amirizadeh N, Poopak B, Toogeh G, Arefian E, Kohram F, et al.
Int J Lab Hematol . 2015 Apr; 37(4):560-8. PMID: 25833191
Introduction: Chronic myeloid leukemia (CML) is caused by reciprocal translocation in hematopoietic stem cells (HSCs). This translocation forms the BCR-ABL1 oncogene, which alters several signaling pathways that control malignancy. CML...
7.
Toogeh G, Sharifian R, Lak M, Safaee R, Artoni A, Peyvandi F
Am J Hematol . 2004 Sep; 77(2):198-9. PMID: 15389911
Glanzmann thrombasthenia (GT) is a rare autosomal recessive disease characterized by prolonged bleeding time with normal platelet count and morphology. It is caused by the quantitative or qualitative deficiency of...
8.
Ghaemmaghami F, Behtash N, Yarandi F, Moosavi A, Modares M, Toogeh G, et al.
J Obstet Gynaecol . 2003 Jul; 23(4):422-5. PMID: 12881087
This study was designed to assess the role of first-line chemotherapy with 5-fluorouracil (5-FU) and platinum in the treatment of advanced or recurrent cervical cancer. Ten patients with advanced or...