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<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle></ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Myelofibrosis due to Secondary Hyperparathyroidism in a Case of Celiac Disease</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract>Myelofibrosis is reported in patents with primary hyperparathyroidism. It is also was reported in patents with sec-
ondary hyperparathyroidism due to end-stage renal disease or Vitamin D dependent rickets .We present a case of
celiac disease and osteomalacia which leads to secondary hyperparathyroidism and myelofibrosis.</Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Congenital Leukemia: A Case Report</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Restless Legs Syndrome Prevalence in Major Thalasemia Tabriz Children Hospital</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Applying Totally Implantable Venous Access Devices (TIVAD) in Children: the First Iranian Experience</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Density of Platelet GPIIb-IIIa and Bleeding Severity in Iranian Patients with Glanzmann’s Thrombasthenia</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Pediatric Non Hodgkin’s Lymphomas</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Patterns of Gelatinase-B Expression in Leukemic Cell Lines</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Future</ArticleTitle>
	<FirstPage>0</FirstPage>
	<LastPage>0</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract></Abstract>


</Article>
<Article>
<Journal>
<PublisherName>Iranian Pediatric Hematology and Oncology Society</PublisherName>
<JournalTitle>Iranian Journal of Blood and Cancer</JournalTitle>
<Issn>2008-4595</Issn>
<Volume>2</Volume>
<Issue>3</Issue>
<PubDate PubStatus = "ppublish">
<Year>2010</Year>
<Month>5</Month>
<Day>1</Day>
</PubDate>
</Journal>


	<ArticleTitle>Intra articular Injection of Rifampin in Iranian Children with Haemophilic Arthropathy</ArticleTitle>
	<FirstPage>123</FirstPage>
	<LastPage>127</LastPage>
	<Language>EN</Language>
<AuthorList>
</AuthorList>
<Abstract>Background:Chronic synovitis is one of the most important complications in haemophilic patients. Rifampin is anantibiotic which its intra-articular injecion leads to destruction of the synovial membrane of haemophilic patientsmedically.Materials and Methods: Between September 2003 and November 2005, we administered intra-articular rifampinin ١۶ haemophilic joints of ٨ haemophilic patients.Results:Median age of our patients was 14.5 year-old. There were 11 knee joints and 5 elbow joints. Atier treatmentwe observed significant improvement in treated joints.Conclusion:This study reveals that intra-articular injection of rifampin may improve arthropathy in haemophilicpatients.</Abstract>


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