<?xml version="1.0"?>
<Articles JournalTitle="International Journal of Hematology-Oncology and Stem Cell Research">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of Leptin Levels in Major beta-Thalassemic Patients</title>
    <FirstPage>1</FirstPage>
    <LastPage>4</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Hamid</FirstName>
        <LastName>Choobineh</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Sciences, Faculty of Para- Medicine, Tehran University of Medical Sciences</affiliation>
      </Author>
      <Author>
        <FirstName>SJ</FirstName>
        <LastName>Dehghani</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Sciences, Faculty of Para- Medicine, Tehran University of Medical Sciences</affiliation>
      </Author>
      <Author>
        <FirstName>Shaban</FirstName>
        <LastName>Alizadeh</LastName>
        <affiliation locale="en_US">Department of Hematology and Blood Banking, Faculty of Para- Medicine, Tehran University of Medical Sciences</affiliation>
      </Author>
      <Author>
        <FirstName>V</FirstName>
        <LastName>Ghobadi Dana</LastName>
        <affiliation locale="en_US">Department of Pediatrics, Faculty of Medicine, Tehran University of Medical Sciences</affiliation>
      </Author>
      <Author>
        <FirstName>N</FirstName>
        <LastName>Saiepour</LastName>
        <affiliation locale="en_US">Department of Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences</affiliation>
      </Author>
      <Author>
        <FirstName>R</FirstName>
        <LastName>Meshkani</LastName>
        <affiliation locale="en_US">Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences</affiliation>
      </Author>
      <Author>
        <FirstName>N</FirstName>
        <LastName>Einollahi</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Sciences, Faculty of Para- Medicine, Tehran University of Medical Sciences</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: Leptin is an adipocyte-derived hormone. Exogenous leptin allows the recovery of the reproductive function. In humans, leptin correlates positively with the body mass index (BMI). The aim of this study was to investigate the association of leptin with the toxic effects of iron overload.
Methods: 219 Major Beta thalassemic patients (119 men, 100 women) and 137 non thalassemic individuals (86 men, 51 women) were investigated on the basis of a case control study. Data was gathered from six hospitals related to Tehran University during a seven month petiod (July 2006&#x2013; January 2007). Blood samples of all major beta thalassemic patients who were admitted to these hospitals for recurrent blood transfusion were collected. Non thalassemic individuals were selected from outpatients who without significant medical problems, had come to these hospitals and had extra blood sample. The similarities of the two groups in age, gender and BMI also were considered.
Results: The serum leptin level median was 5.00 (interquartile range: 6.50) for major beta thalassemic patients and 6.10 (interquartile range: 7.00) for healthy individuals. Serum leptin level was significantly lower in thalassemic patients (P value &lt;0.001). Major beta thalassemic men had significantly lower leptin level (median, interquartile range: 2.90, 3.60) than major beta thalassemic women (median, interquartile range: 6.45, 16.02; P value &lt;0.001).
Conclusions: This study confirmed that the adipocytes of major beta thalassemic patients are unable to maintain adequate leptin production. These results suggest that adipose tissue dysfunction can be considered one of the endocrinopathies affecting major beta thalassemic patients.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/223</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/223/216</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Human Dental Pulp Stem Cells: The Culture Optimization for Increased Growth</title>
    <FirstPage>5</FirstPage>
    <LastPage>13</LastPage>
    <AuthorList>
      <Author>
        <FirstName>MR</FirstName>
        <LastName>Baghaban Eslaminejad</LastName>
        <affiliation locale="en_US">Department of Stem Cell and Developmental Biology, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>H</FirstName>
        <LastName>Nazarian</LastName>
        <affiliation locale="en_US">Department of Stem Cell and Developmental Biology, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>M</FirstName>
        <LastName>Shariati</LastName>
        <affiliation locale="en_US">Department of Periodontics, Dental Scool of Shahid Beheshti University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>S</FirstName>
        <LastName>Vahabi</LastName>
        <affiliation locale="en_US">Department of Periodontics, Dental Scool of Shahid Beheshti University, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: Dental pulp-derived mesenchymal stem cells (MSCs) have emerged as a promising tool for use in regenerative medicine. The in vitro growth kinetic and culture requirement of the cells derived from human dental pulp, which is the subject of this present study, is poorly described.
Materials and Methods: Stem cells were derived from human third molar and then characterized. The in vitro growth kinetics of the cells was examined by colonogenic assay and a determination of the population doubling number (PDN). Finally, the culture conditions were optimized for pulp stem cell maximum proliferation.
Results: Propagated dental pulp cells tended to differentiate into odontoblast, osteoblast, adipose and cartilage cells. Typically surface antigens were expressed as mesenchymal stem cells. The cells tended to be very proliferative with a PDN value of about 11. The colonogenic efficiency was about 60% and an average colony size was about 10.75&#xB1;1.58 mm2. The best culture condition for enhanced proliferation was achieved when the cells were seeded at 100 cells/cm2 in a the presence of 20% FBS in a medium (P&lt;0.05).
Conclusion: Taken together, the optimal culture conditions for human dental pulp-derived MSCs were determined. This information is helpful with respect to cell in vitro propagation which is greatly needed prior to their transplantation.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/224</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/224/217</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">fms Like Tyrosine kinase3- Internal Tandem Duplication (FLT3-ITD) in Acute Myeloid Leukemia, Mutation Frequency and its Relation with Complete Remission, 2007- 2008</title>
    <FirstPage>14</FirstPage>
    <LastPage>20</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Amir Hossein</FirstName>
        <LastName>Emami</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ramin</FirstName>
        <LastName>Shekarriz</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>A</FirstName>
        <LastName>Meysamie</LastName>
        <affiliation locale="en_US">Community Medicine Department, Faculty of Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ramazanali</FirstName>
        <LastName>Sharifian</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>R</FirstName>
        <LastName>Safaei</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ghlamreza</FirstName>
        <LastName>Toogheh</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Manouchehr</FirstName>
        <LastName>Keihani</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>R</FirstName>
        <LastName>Shekarriz</LastName>
        <affiliation locale="en_US">Community Medicine Department, Faculty of Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: About half of acute myeloid leukemia (AML) adult patients have no cytogenetic abnormalities as a main determinant of complete remission after treatment, so other markers are needed such as FLT3-ITD (Fms-like Tyrosine kinase3-internal tandem duplication) mutations in patients with normal karyotype. The objective of this study was assessing the frequency of FLT3-ITD mutations and its relation with complete remission in different FAB (French- American- British) and cytogenetic subgroups of AML patients who had been hospitalized at Tehran Imam Khomeini Hospital, hematology ward.
Methods: The current study, was a cross sectional descriptive study which was performed during the years 2007-2008. Population frame were consecutive patients whose diseases were confirmed and who had been hospitalizedin Tehran Imam Khomeini Hospital, hematology ward. Contemporary, flowcytometry, cytogenetic and chromosomal studies were performed for the cytogenetic subgroup assessment and to investigate the presence of FLT3-ITD mutation. Finally, complete remission achievement after induction chemotherapy were assessed. The obtained data was entered onto the information forms and analyzed by statistical tests.
Results: Out of 40 patients who participated in this study, 18 (45%) were female and 22 (55%) were male. The median age of the patients with mutation was 33 years of age, and the ones without mutation were 39.5. M1, M2and M4 FAB subgroups, with respectively 60, 37.5 and 35.7%, had the most occurrence of mutation. There was no significant relationship between mutation and the FAB subgroups (P=0.45). Favorable, intermediate and adverse cytogenetic risk groups had respectively 10, 37 and 66.7% mutations and 69.2% of the patients were in the normal karyotype group. Seventeen (42.5%) of the 40 patients achieved complete remission. 17.6% of them had mutations. There was no relationship between mutation and complete remission (P=0.085).
Conclusion: There was no relationship between thepresence ofFLT3-ITD mutation and complete remission achievement following chemotherapy.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/225</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/225/218</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Primary Gasterointestinal Lymphoma, Clinicopathologic Study of 49 Small Intestinal Lymphoma Casess and the Treatment Option of Choice</title>
    <FirstPage>21</FirstPage>
    <LastPage>23</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Taleb</FirstName>
        <LastName>Azarm</LastName>
        <affiliation locale="en_US">Hematology- Oncology Department, Esfahan University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>H</FirstName>
        <LastName>Mohajer</LastName>
        <affiliation locale="en_US">Internal Medicin Department, Esfahan University of Medical Siences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>H</FirstName>
        <LastName>Daghaghzadeh</LastName>
        <affiliation locale="en_US">Gastrointrology Department, Esfahan University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Kamran</FirstName>
        <LastName>Alimoghaddam</LastName>
        <affiliation locale="en_US">Hematology- Oncology and Stem Cell Research Center, Tehran University of Medical Sciences,Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Jahani</LastName>
        <affiliation locale="en_US">Hematology- Oncology and Stem Cell Research Center, Tehran University of Medical Sciences,Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ardeshir</FirstName>
        <LastName>Ghavamzadeh</LastName>
        <affiliation locale="en_US">Hematology- Oncology and Stem Cell Research Center, Tehran University of Medical Sciences,Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: A study was made conserning 142 patients who were suffering from gastrointestinal lymphoma, were seen at the department of Hematology and Oncology, Esfahan Medical School, during the period 1982-2002.
Method: All patients had laparotomy, and biopsy of the site lesion. Histopathological subtypes were done in the International Working Formulation. Stage groupings were done applying the Crowther and Blackledge staging system. The post-laparotomy was made depending on the patient's general condition, the completeness of surgery and histological subtype.
Results: There were 52 cases of gastrointestinal lymphoma in the stomach, 49 in the small intestine, 12 in the ileocecal region, 22 in the rectosigmoid and in seven of the cases, multiple sites in the gastrointestinal tract were involved.
Conclusion: The overall survival rate was 47.8% at 5 years. Early stage disease and high-grade lymphoma have a better prognosis if treated adequately. Patients who had complete surgical removal of primary tumour (befor any metastasis) had a longer survival.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/226</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/226/520</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">A New Method for Diagnosis and Predicting Blood Disorder and Cancer Using Artificial Intelligence (Artificial Neural Networks)</title>
    <FirstPage>25</FirstPage>
    <LastPage>33</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mehrdad</FirstName>
        <LastName>Payandeh</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Faculty of Medical Science, Kermanshah University of Medical Science,Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mehrnoush</FirstName>
        <LastName>Aeinfar</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Faculty of Medical Science, Kermanshah University of Medical Science, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Vahid</FirstName>
        <LastName>Aeinfar</LastName>
        <affiliation locale="en_US">Electronic Department, Faculty of Technology, Razi University, Kermanshah, Iran&#xD;
Computational Intelligence Research Center, Razi University, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>Hayati</LastName>
        <affiliation locale="en_US">Electronic Department, Faculty of Technology, Razi University, Kermanshah, Iran&#xD;
Computational Intelligence Research Center, Razi University, Kermanshah, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">This paper represents a novel use of artificial neural networks in medical science. The proposed technique involves training a Multi Layer Perceptron (MLP) (a kind of artificial neural network) with a BP learning algorithm to recognize a pattern for the diagnosing and prediction of five blood disorders, through the results of blood tests from H1 machine. The blood test parameters and diagnosis of physician about the diseases of 450 patients from Taleghani Hospital in Kermanshah, Iran, are used in a supervised training method to update network parameters. This method was implemented to diagnose these disorder and cancer: Megaloblastic Anaemia, Thalassemia, Idiopathic thrombocytopenic pupura (ITP), Chronic myelogenous leukemia and Lymphoproliferative.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/227</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/227/220</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Metastatic Colo-Rectal Cancer, 2005-2008: Treatment results</title>
    <FirstPage>34</FirstPage>
    <LastPage>37</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mozaffar</FirstName>
        <LastName>Aznab</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Kermanshah University of Medical Science (KUMS)</affiliation>
      </Author>
      <Author>
        <FirstName>A</FirstName>
        <LastName>Tabarroki</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Kermanshah University of Medical Science (KUMS)</affiliation>
      </Author>
      <Author>
        <FirstName>Gh</FirstName>
        <LastName>Mohsseni</LastName>
        <affiliation locale="en_US">Hematology-Oncology Department, Kermanshah University of Medical Science (KUMS)</affiliation>
      </Author>
      <Author>
        <FirstName>F</FirstName>
        <LastName>Farshian</LastName>
        <affiliation locale="en_US">Faculty of Medical Sciences, Kermanshah University of Medical Science (KUMS)</affiliation>
      </Author>
      <Author>
        <FirstName>K</FirstName>
        <LastName>Kavyani</LastName>
        <affiliation locale="en_US">Statistic Department, Kermanshah University of Medical Science (KUMS)</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: Colo-rectal cancer has 10% prevalence, among all of the cancer proportionally and also it is the third common cancer in the both sexes. Two recently introduced active drugs in the treatment of advanced colorectal cancer (ACC) are irinotecan and oxaliplatin. The combinations of oxaliplatin (OXA) or irinotecan (IRI) with 5FU-LV have been accepted as standard treatment for metastatic colorectal cancer.
Patients and Methods: fifty four patients with colo-rectal cancer who came to the Oncology Clinic of Kermanshah University were assessed over a period of 4 years (2005-2008). All cases in stage III were treated by FOLFOX, unlike the patients in Stage IV treated with FOLFOX during 8 cycles fallowed by FOLFIRI in the same cycles (Sequential method).
Results: the age average was less (49.1 years versus 55 years) than in other studies (6). A parallel analyzation of solid data, overall survival (OS), progression free survival (PFS) were 18 and 17.3 months, respectively.
Conclusion: FOLFOX and FOLFIRI were administrated in 8 cycles each concomitantly (Sequential form) which provided considerable response with manageable complications. The result of the treatment in the study was correlated with other trials utilizing more modern procedures of medication like &#x2018;Target therapies&#x2019; (OS; 18.4m for CT versus 19-20m for target therapies).</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/228</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/228/221</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Gastric Cancer in South East of Iran</title>
    <FirstPage>38</FirstPage>
    <LastPage>42</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mohammadali</FirstName>
        <LastName>Mashhadi</LastName>
        <affiliation locale="en_US">Hematology- Oncology Department, Zahedan University of Medical Sciences, Zahedan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>K</FirstName>
        <LastName>Nazem</LastName>
        <affiliation locale="en_US">Gastroentrology Department, Zahedan University of Medical Scienceshaveisi Zadeh</LastName>
        <affiliation locale="en_US">Medical Genetics Department, Faculty of Medicine, Shahid Beheshti University of Medical Sciences and Heaith Services, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Myeloproliferative neoplasms (MPNs) such as polycythemia vera, essential thrombocythemia, primary myelofibrosis and chronic myeloid leukemia have too similar and accurate way to differentiate their is study of genetic disorders in these patients. Philadelphia chromosome is a sure way to definitively diagnose CML. Recently, JAK2V617F mutation introduced as a diagnostic marker for other Myeloproliferative neoplasms. Many studies show that the absence of the JAK2 mutation in chronic phase Philadelphia positive CML. In contrast with these reports, more recently, several cases with the coexistence of Philadelphia positive chromosome and JAK2V617F mutation in blood and bone marrow samples were reported. Here, we report a patient that have the Philadelphia chromosome disorder and JAK2V617F mutation in same time.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/278</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/278/271</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>5</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2011</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Central Serous Chorioretinopathy in a Patient with B-cell Non-Hodgkin Lymphoma</title>
    <FirstPage>38</FirstPage>
    <LastPage>40</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Nasim</FirstName>
        <LastName>Valizadeh</LastName>
        <affiliation locale="en_US">Hematology- Oncology Department, Imam Khomeini Hospital, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Negar</FirstName>
        <LastName>Haghighi</LastName>
        <affiliation locale="en_US">Internal Medicine Department, Imam Khomeini Hospital, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Negar</FirstName>
        <LastName>Aghamohammadi</LastName>
        <affiliation locale="en_US">Internal Medicine Department, Imam Khomeini Hospital, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Mohammadzadeh</LastName>
        <affiliation locale="en_US">Vitreo- retinal Subspecialty ward, Ophthalmology Department, Shafa Hospital, Urmia University of Medical, Sciences, Urmia, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Central serous chorioretinopathy (CSCR) is an ocular disease which fluid is collected under retina and leads to retinal detachment and blurred vision. Risk factors for development of central serous chorioretinopathy are included: alcohol use, uncontrolled hypertension, pregnancy, type A personalityand different ways of corticosteroid use. We want to present central serous chorioretinopathy in a case of B-cell type Non-Hodgkin lymphoma (NHL)after taking 6th course of CHOP regimen which was presented with left- sided blurred vision.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/279</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/279/272</pdf_url>
  </Article>
</Articles>
titter on Hela cells. Then, the CD34+ cells of cord blood can be pre-stimulated in a serum- free media supplemented with SCF, Flt3,TPO,IL6 in the presence and absence of 50 ng/ml MIP-1&#x3B1;. Transduction efficiency was assessed by a semi-quantitative PCR for the neomycin gene.
Results: A PCR analysis of the neomycin gene in CD34+ cells revealed an improved transduction of cord blood cells in the presence of MIP-1&#x3B1; 65%, in comparison to its absence: 40.7%.
Conclusion: the addition of MIP-1&#x3B1; to the cytokine cocktail improves the transduction efficiency of cord blood hematopoietic progenitor cells. Further studies are required to clarify its effect on the functional properties of CD34+ cells.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/212</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/212/205</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>3</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">A Randomized Comparison of Granisetron Plus Dexamethason with Granisetron alone for the Control of Acute Chemotherapy-Induced Emesis and Nausea</title>
    <FirstPage>27</FirstPage>
    <LastPage>30</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Shahrbanou</FirstName>
        <LastName>Keyhanian</LastName>
        <affiliation locale="en_US">Oncology- Hematology Department, School of Medicine, Islamic Azad University, Tonekabon, Mazandaran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>O</FirstName>
        <LastName>Taziki</LastName>
        <affiliation locale="en_US">Nephrology Department, Medical University of Mazandaran</affiliation>
      </Author>
      <Author>
        <FirstName>MM</FirstName>
        <LastName>Saravi</LastName>
        <affiliation locale="en_US">Radiology Department, Imam Sajjad Hospital, Ramsar, Mazandaran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Z</FirstName>
        <LastName>Fotokian</LastName>
        <affiliation locale="en_US">School of Nursing and Midwifery, Ramsar, Babol Medical Sciences university, Mazandaran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Yea