<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet href="/rss.css" type="text/css"?>
<rdf:RDF xmlns="http://purl.org/rss/1.0/"
    xmlns:cc="http://web.resource.org/cc/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:extra="http://www.w3.org/1999/xhtml"
    xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#">
    <channel rdf:about="http://www.thyroidresearchjournal.com/feeds/latestarticles/journal?quantity=&amp;format=rss&amp;version=">
        <title>Thyroid Research - Latest Articles</title>
        <link>http://www.thyroidresearchjournal.com</link>
        <description>The latest research articles published by Thyroid Research</description>
        <dc:date>2013-05-16T00:00:00Z</dc:date>
        <items>
            <rdf:Seq>
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/8" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/7" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/6" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/5" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/4" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/3" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/2" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/6/1/1" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/5/1/26" />
                                <rdf:li rdf:resource="http://www.thyroidresearchjournal.com/content/5/1/25" />
                            </rdf:Seq>
        </items>
                 <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </channel>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/8">
        <title>TSH receptor antibodies have predictive value for breast cancer &#191; retrospective analysis</title>
        <description>Background:
Associations between breast cancer and thyroid disorders are reported in numerous studies. Relationships between thyroperoxidase antibodies (TPOAb), thyroglobulin antibodies (TgAb) and breast cancer have been previously demonstrated. However, no analysis has been performed concerning an association between thyrotropin (TSH) receptor antibodies (TSHRAb) and breast cancer. The aim of the study was to evaluate the prevalence of breast cancer or benign breast tumors in patients with Graves&#8217; disease and to analyze a possible relationship between Graves&#8217; disease and these two groups of breast diseases with emphasis to epidemiology and laboratory findings.Patients and methodsClinical and laboratory details of 2003 women hospitalized for endocrine disorders were retrospectively analyzed, using an unpaired Student&#8217;s t-test, logistic regression analysis, &#967;
						2 test of independence or the two-sided ratio comparison test.
Results:
The coexistence of Graves&#8217; disease and breast cancer was statistically significant. We observed TSHRAb and TgAb more frequently in patients with breast cancer. We found that TSHRAb is the only variable possessing predictive value for breast cancer.
Conclusions:
The strong relationship between Graves&#8217; disease and breast cancer is proposed. We suggest that TSHRAb could be described as a positive determinant of breast cancer. The present data call attention to the usefulness of screening for breast cancer in long-term follow-up of patients with autoimmune thyroid disorders, especially of those with Graves&#8217; disease. Similarly, screening for autoimmune thyroid disorders should be performed in patients with nodular breast disease. Additionally, the article draws ideas for further research in order to develop targeted treatment for more successful outcome in patients with breast cancer.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/8</link>
                <dc:creator>Pawe¿ Szychta</dc:creator>
                <dc:creator>Wojciech Szychta</dc:creator>
                <dc:creator>Adam Gesing</dc:creator>
                <dc:creator>Andrzej Lewi¿ski</dc:creator>
                <dc:creator>Ma¿gorzata Karbownik-Lewi¿ska</dc:creator>
                <dc:source>Thyroid Research 2013, null:8</dc:source>
        <dc:date>2013-05-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-8</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-8-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2013-05-16T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/7">
        <title>A solitary hyperfunctioning thyroid nodule harboring thyroid carcinoma: review of the literature</title>
        <description>Hyperfunctioning nodules of the thyroid are thought to only rarely harbor thyroid cancer, and thus are infrequently biopsied. Here, we present the case of a patient with a hyperfunctioning thyroid nodule harboring thyroid carcinoma and, using MEDLINE literature searches, set out to determine the prevalence of and characteristics of malignant &#8220;hot&#8221; nodules as a group. Historical, biochemical and radiologic characteristics of the case subjects and their nodules were compared to those in cases of benign hyperfunctioning nodules. A literature review of surgical patients with solitary hyperfunctioning thyroid nodules managed by thyroid resection revealed an estimated 3.1% prevalence of malignancy. A separate literature search uncovered 76 cases of reported malignant hot thyroid nodules, besides the present case. Of these, 78% were female and mean age at time of diagnosis was 47 years. Mean nodule size was 4.13 &#177; 1.68 cm. Laboratory assessment revealed T3 elevation in 76.5%, T4 elevation in 51.9%, and subclinical hyperthyroidism in 13% of patients. Histological diagnosis was papillary thyroid carcinoma (PTC) in 57.1%, follicular thyroid carcinoma (FTC) in 36.4%, and Hurthle cell carcinoma in 7.8% of patients. Thus, hot thyroid nodules harbor a low but non-trivial rate of malignancy. Compared to individuals with benign hyperfunctioning thyroid nodules, those with malignant hyperfunctioning nodules are younger and more predominantly female. Also, FTC and Hurthle cell carcinoma are found more frequently in hot nodules than in general. We were unable to find any specific characteristics that could be used to distinguish between malignant and benign hot nodules.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/7</link>
                <dc:creator>Sasan Mirfakhraee</dc:creator>
                <dc:creator>Dana Mathews</dc:creator>
                <dc:creator>Lan Peng</dc:creator>
                <dc:creator>Stacey Woodruff</dc:creator>
                <dc:creator>Jeffrey Zigman</dc:creator>
                <dc:source>Thyroid Research 2013, null:7</dc:source>
        <dc:date>2013-05-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-7</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-7-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2013-05-04T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/6">
        <title>Proposed algorithm for management of patients with thyroid nodules/focal lesions, based on ultrasound (US) and fine-needle aspiration biopsy (FNAB); our own experience</title>
        <description>Background:
The standard management in patients with thyroid nodules is to assess the risk of malignancy, based on cytological examination. On the other hand, there are thyroid patterns of ultrasound (US) image, associated with an increased risk of malignancy.The aim of our study was to create a diagnostic algorithm that would employ both data from US examination (expressed by a total score, according to our scoring system) and FNAB results, classified according to Bethesda system (The Bethesda System for Reporting Thyroid Cytopathology - TBSRTC categories).Material and methods100 thyroid cancer foci (94 papillary carcinomas, 4 medullary carcinomas, 2 undifferentiated carcinomas) and 100 benign focal lesions were selected during postoperative histopathological examination of thyroid glands excised during surgery from 111 patients. The corresponding US images of each lesion &#8211; performed in the course of preoperative diagnostics &#8211; were evaluated for the presence of seven (7) different features in US image, suggesting a malignant character of lesion, viz. vascularity, i.e., the increased central intranodular blood flows, microcalcifications, &#8220;taller-than-wide&#8221; orientation, solid composition, hypoechogenicity, irregular margin and either absence of peripheral halo or the presence of outer shell of uneven thickness, surrounding the lesion. The sensitivity, specificity, positive predictive values, negative predictive values and odds ratios for each US feature were calculated.
Results:
In US image of the analyzed cancer foci, we obtained the following values of odds ratio for each of the above mentioned features suggesting malignancy: &#8220;taller-than-wide&#8221; orientation - odds ratio - 301.0, microcalcifications - 24.67, increased intranodular vascularity - 20.44, hypoechogenicity - 18.61, irregular margins - 7.81, absence of halo - 5.88, and solid composition - 4.16.Taking into account our own experience and the present data, in juxtaposition with the opinions of other authors, we propose a division of US features into 3 groups of different prognostic importance, expressed by a total score calculated based on our scoring system. Accordingly, microcalcifications, &#8220;taller-than-wide&#8221; orientation, the increased intranodular vascularity, and hypoechogenicity constitute one group - each of the features in this group is awarded 1 point. In turn, the characteristics of minor prognostic importance, such as irregular margin, absence of halo, solid composition, and large size (a diameter longer than 3.0&#160;cm) - are associated with the granting 0.5 points each. The most important prognostic features &#8211; a rapid growth (enlargement) of nodules/focal lesions and a presence of pathologically altered lymph nodes are associated with the granting 3 points for each.Our scoring system can be applied in order to better assessment of thyroid US patterns in whole. In patients with a total score ranging from 0&#8201;&lt;&#8201;4 points there is US pattern of a low risk of malignancy, with&#8201;&#8805;&#8201;4&#8201;&lt;&#8201;7 points - intermediate risk, and in patients with a score&#8201;&#8805;&#8201;7 points &#8211; a high risk in question.
Conclusion:
Complementary use of our scoring system and FNAB TBSRTC categories can help to make optimal clinical decisions as regards the selection of treatment strategy.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/6</link>
                <dc:creator>Zbigniew Adamczewski</dc:creator>
                <dc:creator>Andrzej Lewi¿ski</dc:creator>
                <dc:source>Thyroid Research 2013, null:6</dc:source>
        <dc:date>2013-04-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-6</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-6-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2013-04-20T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/5">
        <title>Thyroid heterogeneity, as indicated by the CV of ultrasonographic intensities, correlates with anti-thyroid peroxidase antibodies in euthyroid Hashimoto&apos;s thyroiditis</title>
        <description>ObjectiveTo prospectively evaluate the heterogeneous appearance of the thyroid gland, reflecting inflammation and destruction in euthyroid Hashimoto&#8217;s thyroiditis (HT), we investigated the clinical utilities of the heterogeneity index (HI) [the coefficient of variance (CV) of the ultrasonographic (US) intensities], focusing on anti-thyroid peroxidase antibodies (TPO-Ab), which represent not only disease activity but also subsequent thyroid destruction of HT.
Methods:
Forty-four consecutive patients with euthyroid HT [60.5&#8201;&#177;&#8201;2.7&#8201;years old (mean &#177; SE)] and 30 age-matched normal controls were studied. HI was calculated as the CV (SD/mean) of US intensities of either four points per lobe of the thyroid gland along a horizontal line at the depth of the right common carotid artery. Evaluation included serum levels of free thyroxine (FT4), free triiodothyronine (FT3), thyroid stimulating hormone (TSH), anti-thyroid peroxidase antibodies (TPO-Ab), anti-thyroglobulin antibodies (Tg-Ab), thyroglobulin and thyroid volume.
Results:
While no differences were observed for TSH, FT4 and FT3, thyroglobulin and thyroid volume between the two groups, HI exhibited a tendency towards a significant difference (3.59&#8201;&#177;&#8201;0.20% in HT patients vs 3.23&#8201;&#177;&#8201;0.19% in normal group, p&#8201;=&#8201;0.089). In HT patients, there was a significant and positive correlation of HI with TPO-Ab (r&#8201;=&#8201;0.396, p&#8201;=&#8201;0.034), whereas such a correlation was absent in normal controls. In both groups, there were no significant correlations of HI with Tg-Ab, FT3, FT4 or TSH.
Conclusions:
This is the first report of the close relation between heterogeneity of US of the thyroid gland and TPO-Ab in euthyroid HT patients before the heterogeneity becomes distinguishable from normal thyroid glands. Furthermore, at this stage, subsequent thyroid destruction in HT might be already be predicted through the heterogeniety of the thyroid tissue.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/5</link>
                <dc:creator>Yosuke Wakita</dc:creator>
                <dc:creator>Toshiki Nagasaki</dc:creator>
                <dc:creator>Yuki Nagata</dc:creator>
                <dc:creator>Yasuo Imanishi</dc:creator>
                <dc:creator>Shinsuke Yamada</dc:creator>
                <dc:creator>Koichiro Yoda</dc:creator>
                <dc:creator>Masanori Emoto</dc:creator>
                <dc:creator>Eiji Ishimura</dc:creator>
                <dc:creator>Masaaki Inaba</dc:creator>
                <dc:source>Thyroid Research 2013, null:5</dc:source>
        <dc:date>2013-03-23T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-5</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-5-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2013-03-23T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/4">
        <title>Iodine-131 induced hepatotoxicity in previously healthy patients with Grave&#191;s disease</title>
        <description>ObjectiveTo describe the association of the rare and serious complication of liver toxicity in previously healthy Grave&#8217;s disease (GD) patients after the treatment with radioactive iodine 131I (RAI).Case presentationWe report the clinical, laboratory and pathologic findings of 2 cases of severe liver toxicity associated with the treatment with RAI in previously healthy patients with GD. Clinical examination and laboratory investigations excluded viral hepatitis, autoimmune hepatitis, granulomatous disease, primary biliary disease, extrahepatic biliary obstruction, and heart failure.Case 1: A previously healthy 52-years old man reportedly having a typical GD but following RAI treatment, concomitantly developed severe liver toxicity that required 1&#160;week of treatment in hospital.Case 2: A previously healthy 34-years old woman is reported as having a typical GD but developed jaundice following RAI treatment that required several weeks of in hospital treatment in the hepato-biliary department.In both cases, the liver dysfunction resolved after intensive treatment with hepato-protective agents. In this report the therapeutic considerations as well as the pathogenetic possibilities are reviewed.
Conclusion:
To the best of our knowledge, this is the first description of the association observed, which is rare but may be severe and should be considered in any case of thyrotoxicosis where a liver dysfunction develops after the treatment with radioactive iodine 131I.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/4</link>
                <dc:creator>Navina Jhummon</dc:creator>
                <dc:creator>Bhavna Tohooloo</dc:creator>
                <dc:creator>Shen Qu</dc:creator>
                <dc:source>Thyroid Research 2013, null:4</dc:source>
        <dc:date>2013-03-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-4</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-4-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2013-03-16T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/3">
        <title>Spectrum of lithium induced thyroid abnormalities: a current perspective</title>
        <description>Background:
Lithium is an integral drug used in the management of acute mania, unipolar and bipolar depression and prophylaxis of bipolar disorders. Thyroid abnormalities associated with treatment with lithium have been widely reported in medical literature to date. These include goitre, hypothyroidism, hyperthyroidism and autoimmune thyroiditis. This current review explores the varied thyroid abnormalities frequently encountered among patients on lithium therapy and their management, since lithium is still a fundamental and widely drug used in psychiatry and Internal Medicine.
Methods:
PubMed database and Google scholar were used to search for relevant English language articles relating to lithium therapy and thyroid abnormalities up to December 2012. The search terms used were lithium treatment, thyroid abnormalities, thyroid dysfunction, goitre, hypothyroidism, hyperthyroidism, thyrotoxicosis, autoimmune thyroiditis, lithium toxicity, treatment of affective disorders and depression and side effects of antipsychotic drugs. Reference lists of the identified articles were further used to identify other studies.
Results:
Lithium affects normal thyroid functioning through multiple mechanisms. At the cellular level, it decreases thyroid hormone synthesis and release. It also decreases peripheral deiodination of tetraiodothyronine (T4) or thyroxine by decreasing the activity of type I 5&#8217; de-iodinase enzyme. Hypothyroidism and goitre (clinically and/ultrasonographically detected) are the most prevalent thyroid abnormalities among patients on long term lithium therapy. Lithium induced hyperthyroidism is very infrequent. Lithium increases the propensity to thyroid autoimmunity in susceptible individuals due to its effect of augmenting the activity of B lymphocytes and reducing the ratio of circulating suppressor to cytotoxic T cells.
Conclusions:
Thyroid function tests (serum thyroid stimulating hormone, free thyroid hormones-T4 and triiodothyronine [T3] concentrations and thyroid auto-antibodies) and assessment of thyroid size clinically and by thyroid ultrasonography ought to be performed among patients initiating lithium therapy at baseline and later annually. More frequent assessment of thyroid function status and size during the course of therapy is recommended among middle aged females (&#8805;50 years), patients with a family history of thyroid disease and those positive for thyroid auto-antibodies (anti-thyroid peroxidase and TSH receptor antibodies).</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/3</link>
                <dc:creator>Davis Kibirige</dc:creator>
                <dc:creator>Kenneth Luzinda</dc:creator>
                <dc:creator>Richard Ssekitoleko</dc:creator>
                <dc:source>Thyroid Research 2013, null:3</dc:source>
        <dc:date>2013-02-07T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-3</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-3-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>3</prism:startingPage>
        <prism:publicationDate>2013-02-07T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/2">
        <title>Managing thyroid dysfunction in selected special situations</title>
        <description>Managing thyroid dysfunction is simple at first glance, the idea is to bring hormone levels in the euthyroid range, treat with antithyroid drugs, radio-iodine or surgery if toxic and replace with thyroxine or T3 if hypothyroid. Complexities arise when there are coexisting conditions that affect the thyroid or are affected by thyroid dysfunction and this review will deal with the special situations that need care when correcting thyroid hormone levels.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/2</link>
                <dc:creator>Durr Sabih</dc:creator>
                <dc:creator>Mohammad Inayatullah</dc:creator>
                <dc:source>Thyroid Research 2013, null:2</dc:source>
        <dc:date>2013-02-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-2</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-2-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2013-02-04T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/6/1/1">
        <title>Case report: rare case of infiltration of small lymphocytic B-cell lymphoma in the thyroid gland of female patient with B-cell chronic lymphocytic leukemia (CLL-B/SLL-B)</title>
        <description>The article presents a case of 57-year-old woman with the infiltration of rare small lymphocytic B cell lymphoma in the thyroid gland. Initially, the patient was followed-up due to chronic lymphocytic B-cell leukemia diagnosed on the basis of histopathological examination of cervical lymph node. Eight months later, general symptoms occurred along with lymphocytosis and exacerbation of lesions in lymph nodes, and therefore, chemotherapy was started according to COP regimen. After four chemotherapy cycles, further progression of the disease was observed during chemotherapy. Computed tomography (CT) performed at that time showed generalized lymphadenopathy and the presence of an irregular area in left thyroid lobe. On palpation, the thyroid was asymmetrical, with enlarged left lobe and palpable lymph node packages on the left side of the neck. The levels of thyroid hormones and anti-thyroid antibodies were normal. Ultrasound examination of the thyroid gland showed non-homogeneous hypoechogenic structure of the left lobe and complete focal remodeling. Cytological examination of left-lobe lesion obtained during fine needle aspiration biopsy showed multiple small lymphoid cells, suggestive of small lymphocytic lymphoma. To confirm this diagnosis, flow cytometry of the biopsy material sampled from the left lobe was performed showing B cellimmunophenotype: CD19+/CD20+/CD22 dim/FMC-7, CD23+/CD5+, sCD79b-+, CD38-, CD10-, kappa and lambda-/weak reaction. The results of flow cytometry of the thyroid bioptate and blood were nearly identical, confirming leukemic nature of the infiltration in left thyroid lobe. Cytogenetic findings included the presence of 17p deletion (TP53 gene). The patient received immunochemotherapy with alemtuzumab. The progression of the disease occurred in the sixth week of therapy. The treatment was discontinued after 8 weeks due to worsening of patient&#8217;s general status. The patient died 15 months after the diagnosis.</description>
        <link>http://www.thyroidresearchjournal.com/content/6/1/1</link>
                <dc:creator>El¿bieta Andrysiak-Mamos</dc:creator>
                <dc:creator>Rafa¿ Becht</dc:creator>
                <dc:creator>El¿bieta Sowi¿ska-Przepiera</dc:creator>
                <dc:creator>Jakub Pob¿ocki</dc:creator>
                <dc:creator>Justyna Syrenicz</dc:creator>
                <dc:creator>Barbara Zdziarska</dc:creator>
                <dc:creator>Katarzyna Karpi¿ska-Kaczmarczyk</dc:creator>
                <dc:creator>Anhelli Syrenicz</dc:creator>
                <dc:source>Thyroid Research 2013, null:1</dc:source>
        <dc:date>2013-01-02T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-6-1</dc:identifier>
                                <prism:require>/content/figures/1756-6614-6-1-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>1</prism:startingPage>
        <prism:publicationDate>2013-01-02T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/5/1/26">
        <title>Role of metallothioneins in benign and malignant thyroid lesions</title>
        <description>Recent findings in the past two decades have brought many insights into the biology of thyroid benign and malignant lesions, in particular the papillary and follicular thyroid cancers. Although, much progress have been made, thyroid cancers still pose diagnostic problems regarding differentiation of follicular lesions in relation to their aggressiveness and the treatment of advanced and undifferentiated thyroid cancers. Metallothioneins (MTs) were shown to induce cancer cells proliferation, mediate resistance to apoptosis, certain chemotherapeutics and radiotherapy. Therefore, MTs may be of utility in diagnosis and management of patients with benign and malignant lesions of the thyroid.</description>
        <link>http://www.thyroidresearchjournal.com/content/5/1/26</link>
                <dc:creator>Bartosz Pula</dc:creator>
                <dc:creator>Pawel Domoslawski</dc:creator>
                <dc:creator>Marzena Podhorska-Okolow</dc:creator>
                <dc:creator>Piotr Dziegiel</dc:creator>
                <dc:source>Thyroid Research 2012, null:26</dc:source>
        <dc:date>2012-12-28T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-5-26</dc:identifier>
                                <prism:require>/content/figures/1756-6614-5-26-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>26</prism:startingPage>
        <prism:publicationDate>2012-12-28T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.thyroidresearchjournal.com/content/5/1/25">
        <title>Oxidative damage to macromolecules in the thyroid - experimental evidence</title>
        <description>Whereas oxidative reactions occur in all tissues and organs, the thyroid gland constitutes such an organ, in which oxidative processes are indispensable for thyroid hormone synthesis. It is estimated that huge amount of reactive oxygen species, especially of hydrogen peroxide (H2O2), are produced in the thyroid under physiological conditions, justifying the statement that the thyroid gland is an organ of &#8220;oxidative nature&#8221;. Apart from H2O2, also other free radicals or reactive species, formed from iodine or tyrosine residues, participate in thyroid hormone synthesis. Under physiological conditions, there is a balance between generation and detoxification of free radicals. Effective protective mechanisms, comprising antioxidative molecules and the process of compartmentalization of potentially toxic molecules, must have been developed in the thyroid to maintain this balance. However, with additional oxidative abuse caused by exogenous or endogenous prooxidants (ionizing radiation being the most spectacular), increased damage to macromolecules occurs, potentially leading to different thyroid diseases, cancer included.</description>
        <link>http://www.thyroidresearchjournal.com/content/5/1/25</link>
                <dc:creator>Ma¿gorzata Karbownik-Lewi¿ska</dc:creator>
                <dc:creator>Agnieszka Kokoszko-Bilska</dc:creator>
                <dc:source>Thyroid Research 2012, null:25</dc:source>
        <dc:date>2012-12-27T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1756-6614-5-25</dc:identifier>
                                <prism:require>/content/figures/1756-6614-5-25-toc.gif</prism:require>
                <prism:publicationName>Thyroid Research</prism:publicationName>
        <prism:issn>1756-6614</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>25</prism:startingPage>
        <prism:publicationDate>2012-12-27T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <cc:License rdf:about="http://creativecommons.org/licenses/by/2.0/">
        <cc:permits rdf:resource="http://creativecommons.org/ns#Reproduction" />
        <cc:permits rdf:resource="http://creativecommons.org/ns#Distribution" />
        <cc:permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks" />
    </cc:License>
</rdf:RDF>
