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        <title>International Archives of Medicine - Most accessed articles</title>
        <link>http://www.intarchmed.com</link>
        <description>The most accessed research articles published by International Archives of Medicine</description>
        <dc:date>2012-01-26T00:00:00Z</dc:date>
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        <title>Feasibility of combination allogeneic stem cell therapy for spinal cord injury: a case report</title>
        <description>Cellular therapy for spinal cord injury (SCI) is overviewed focusing on bone marrow mononuclear cells, olfactory ensheathing cells, and mesenchymal stem cells. A case is made for the possibility of combining cell types, as well as for allogeneic use. We report the case of 29 year old male who suffered a crush fracture of the L1 vertebral body, lacking lower sensorimotor function, being a score A on the ASIA scale. Stem cell therapy comprised of intrathecal administration of allogeneic umbilical cord blood ex-vivo expanded CD34 and umbilical cord matrix MSC was performed 5 months, 8 months, and 14 months after injury. Cell administration was well tolerated with no adverse effects observed. Neuropathic pain subsided from intermittent 10/10 to once a week 3/10 VAS. Recovery of muscle, bowel and sexual function was noted, along with a decrease in ASIA score to &quot;D&quot;. This case supports further investigation into allogeneic-based stem cell therapies for SCI.</description>
        <link>http://www.intarchmed.com/content/3/1/30</link>
                <dc:creator>Thomas Ichim</dc:creator>
                <dc:creator>Fabio Solano</dc:creator>
                <dc:creator>Fabian Lara</dc:creator>
                <dc:creator>Eugenia Paris</dc:creator>
                <dc:creator>Federico Ugalde</dc:creator>
                <dc:creator>Jorge Paz Rodriguez</dc:creator>
                <dc:creator>Boris Minev</dc:creator>
                <dc:creator>Vladimir Bogin</dc:creator>
                <dc:creator>Famela Ramos</dc:creator>
                <dc:creator>Erik Woods</dc:creator>
                <dc:creator>Michael Murphy</dc:creator>
                <dc:creator>Amit Patel</dc:creator>
                <dc:creator>Robert Harman</dc:creator>
                <dc:creator>Neil Riordan</dc:creator>
                <dc:source>International Archives of Medicine 2010, null:30</dc:source>
        <dc:date>2010-11-11T00:00:00Z</dc:date>
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        <item rdf:about="http://www.intarchmed.com/content/1/1/23">
        <title>Muscle disorders and dentition-related aspects in temporomandibular disorders: controversies in the most commonly used treatment modalities</title>
        <description>This review explores the aetiology of temporomandibular disorders and discusses the controversies in variable treatment modalities.Pathologies of the temporomandibular joint (TMJ) and its&apos; associated muscles of mastication are jointly termed temporomandibular disorders (TMDs).TMDs present with a variety of symptoms which include pain in the joint and its surrounding area, jaw clicking, limited jaw opening and headaches. It is mainly reported by middle aged females who tend to recognize the symptoms more readily than males and therefore more commonly seek professional help.Several aetiological factors have been acknowledged including local trauma, bruxism, malocclusion, stress and psychiatric illnesses. The Research Diagnostic Criteria of the Temporomandibular Disorders (RDC/TMD) is advanced to other criteria as it takes into consideration the socio-psychological status of the patient.Several treatment modalities have been recommended including homecare practices, splint therapy, occlusal adjustment, analgesics and the use of psychotropic medication; as well as surgery, supplementary therapy and cognitive behavioural therapy. Although splint therapy and occlusal adjustment have been extensively used, there is no evidence to suggest that they can be curative; a number of evidence-based trials have concluded that these appliances should not be suggested as part of the routine care.Surgery, except in very rare cases, is discouraged since it is the most invasive alternative; recent studies have shown healthier outcome with cognitive behavioural therapy.</description>
        <link>http://www.intarchmed.com/content/1/1/23</link>
                <dc:creator>Waseem Jerjes</dc:creator>
                <dc:creator>Tahwinder Upile</dc:creator>
                <dc:creator>Syedda Abbas</dc:creator>
                <dc:creator>Panagiotis Kafas</dc:creator>
                <dc:creator>Michael Vourvachis</dc:creator>
                <dc:creator>Jubli Rob</dc:creator>
                <dc:creator>Eileen Mc Carthy</dc:creator>
                <dc:creator>Nikolaos Angouridakis</dc:creator>
                <dc:creator>Colin Hopper</dc:creator>
                <dc:source>International Archives of Medicine 2008, null:23</dc:source>
        <dc:date>2008-10-30T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-1-23</dc:identifier>
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        <prism:startingPage>23</prism:startingPage>
        <prism:publicationDate>2008-10-30T00:00:00Z</prism:publicationDate>
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        <title>Combination stem cell therapy for heart failure</title>
        <description>Patients with congestive heart failure (CHF) that are not eligible for transplantation have limited therapeutic options. Stem cell therapy such as autologous bone marrow, mobilized peripheral blood, or purified cells thereof has been used clinically since 2001. To date over 1000 patients have received cellular therapy as part of randomized trials, with the general consensus being that a moderate but statistically significant benefit occurs. Therefore, one of the important next steps in the field is optimization. In this paper we discuss three ways to approach this issue: a) increasing stem cell migration to the heart; b) augmenting stem cell activity; and c) combining existing stem cell therapies to recapitulate a &quot;therapeutic niche&quot;. We conclude by describing a case report of a heart failure patient treated with a combination stem cell protocol in an attempt to augment beneficial aspects of cord blood CD34 cells and mesenchymal-like stem cells.</description>
        <link>http://www.intarchmed.com/content/3/1/5</link>
                <dc:creator>Thomas Ichim</dc:creator>
                <dc:creator>Fabio Solano</dc:creator>
                <dc:creator>Fabian Lara</dc:creator>
                <dc:creator>Jorge Paz Rodriguez</dc:creator>
                <dc:creator>Octav Cristea</dc:creator>
                <dc:creator>Boris Minev</dc:creator>
                <dc:creator>Famela Ramos</dc:creator>
                <dc:creator>Erik Woods</dc:creator>
                <dc:creator>Michael Murphy</dc:creator>
                <dc:creator>Doru Alexandrescu</dc:creator>
                <dc:creator>Amit Patel</dc:creator>
                <dc:creator>Neil Riordan</dc:creator>
                <dc:source>International Archives of Medicine 2010, null:5</dc:source>
        <dc:date>2010-04-14T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-3-5</dc:identifier>
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        <item rdf:about="http://www.intarchmed.com/content/3/1/24">
        <title>Dopaminergic reward system: a short integrative review</title>
        <description>Memory is an essential element to adaptive behavior since it allows consolidation of past experience guiding the subject to consider them in future experiences. Among the endogenous molecules that participate in the consolidation of memory, including the drug-seeking reward, considered as a form of learning, is dopamine. This neurotransmitter modulates the activity of specific brain nucleus such as nuclei accumbens, putamen, ventral tegmental area (VTA), among others and synchronizes the activity of these nuclei to establish the neurobiological mechanism to set the hedonic element of learning. We review the experimental evidence that highlights the activity of different brain nuclei modulating the mechanisms whereby dopamine biases memory towards events that are of motivational significance.</description>
        <link>http://www.intarchmed.com/content/3/1/24</link>
                <dc:creator>Oscar Arias-Carrion</dc:creator>
                <dc:creator>Maria Stamelou</dc:creator>
                <dc:creator>Eric Murillo-Rodriguez</dc:creator>
                <dc:creator>Manuel Menendez-Gonzalez</dc:creator>
                <dc:creator>Ernst Poppel</dc:creator>
                <dc:source>International Archives of Medicine 2010, null:24</dc:source>
        <dc:date>2010-10-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-3-24</dc:identifier>
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        <prism:startingPage>24</prism:startingPage>
        <prism:publicationDate>2010-10-06T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.intarchmed.com/content/4/1/35">
        <title>The optimal sequence of radiotherapy and chemotherapy in adjuvant treatment of breast cancer </title>
        <description>Background:
The optimal time sequences for chemotherapy and radiation therapy after breast surgery for patients with breast cancer remains unknown. Most of published studies were done for early breast cancer patients. However, in Egypt advanced stages were the common presentation. This retrospective analysis aimed to assess the optimum sequence for our population.
Methods:
267 eligible patients planned to receive adjuvant chemotherapy [FAC] and radiotherapy. Majority of patients (87.6%) underwent modified radical mastectomy while, 12.4% had conservative surgery.We divided the patients into 3 groups according to the sequence of chemotherapy and radiotherapy. Sixty-seven patients (25.1%) received postoperative radiotherapy before chemotherapy [group A]. One hundred and fifty patients (56.2%) were treated in a sandwich scheme (group B), which means that 3 chemotherapy cycles were given prior to radiotherapy followed by 3 further chemotherapy cycles. A group of 50 patients (18.7%) was treated sequentially (group C), which means that radiotherapy was supplied after finishing the last chemotherapy cycle. Patients&apos; characteristics are balanced between different groups.
Results:
Disease free survival was estimated at 2.5 years, and it was 83.5%, 82.3% and 80% for patient receiving radiation before chemotherapy [group A], sandwich [group B] and after finishing chemotherapy [group C] respectively (p &gt; 0.5). Grade 2 pneumonitis, which necessitates treatment with steroid, was detected in 3.4% of our patients, while grade 2 radiation dermatitis was 17.6%. There are no clinical significant differences between different groups regarded pulmonary or skin toxicities.
Conclusion:
Regarding disease free survival and treatment toxicities, in our study, we did not find any significant difference between the different radiotherapy and chemotherapy sequences.</description>
        <link>http://www.intarchmed.com/content/4/1/35</link>
                <dc:creator>Hamza Abbas</dc:creator>
                <dc:creator>Ashraf Elyamany</dc:creator>
                <dc:creator>Mohamed Salem</dc:creator>
                <dc:creator>Ahmed Salem</dc:creator>
                <dc:creator>Salah Binzaid</dc:creator>
                <dc:creator>Basem Gamal</dc:creator>
                <dc:source>International Archives of Medicine 2011, null:35</dc:source>
        <dc:date>2011-10-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-4-35</dc:identifier>
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                <prism:publicationName>International Archives of Medicine</prism:publicationName>
        <prism:issn>1755-7682</prism:issn>
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        <prism:startingPage>35</prism:startingPage>
        <prism:publicationDate>2011-10-16T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.intarchmed.com/content/5/1/2">
        <title>Neutrophil lymphocyte ratio as a measure of systemic inflammation in prevalent chronic diseases in Asian population.</title>
        <description>Background:
Preliminary evidence has suggested the role of inflammation in development and prognosis of cardiovascular diseases and cancers. Most of the prognostic studies failed to account for the effects of co-morbid conditions as these might have raised the systemic inflammation. We used neutrophil lymphocyte ratio (NLR) as a measure of systemic inflammation and investigated its association with prevalent chronic conditions.
Methods:
Present study is a cross sectional study conducted on population of Karachi, Pakistan. A detailed questionnaire about the demographic details of all subjects was filled and an informed consent obtained for blood sampling. Multinomial regression analyses were carried out to investigate the relationship between NLR and prevalent chronic conditions.
Results:
1070 apparently healthy individuals participated in the study. Proportion of individuals with hypertension was higher in middle and highest tertile of NLR as compared to the lowest tertile (18.2% &amp; 16.1% compared to 11.8%). Individuals with hypertension were 43% (RRR = 1.43, 95% CI 0.94-2.20) and 66% (RRR = 1.69, 95% CI 1.09-2.54) more likely to be in the middle and highest tertile of NLR respectively compared to the baseline group. Similarly, individuals with diabetes mellitus were 53% (RRR = 1.53, 95% CI 0.93-2.51) and 65% (RRR = 1.65, 95% CI 1.01-2.71) more likely to be in the middle or highest tertile of NLR as compared to the baseline NLR group.
Conclusions:
Systemic inflammation measured by NLR has a significant association with prevalent chronic conditions. Future research is needed to investigate this relationship with longitudinal data to establish the temporal association between these variables.</description>
        <link>http://www.intarchmed.com/content/5/1/2</link>
                <dc:creator>Fauzia Imtiaz</dc:creator>
                <dc:creator>Kashif Shafique</dc:creator>
                <dc:creator>Saira Mirza</dc:creator>
                <dc:creator>Zeenat Ayoob</dc:creator>
                <dc:creator>Priya Vart</dc:creator>
                <dc:creator>Saddiyah Rao</dc:creator>
                <dc:source>International Archives of Medicine 2012, null:2</dc:source>
        <dc:date>2012-01-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-5-2</dc:identifier>
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                <prism:publicationName>International Archives of Medicine</prism:publicationName>
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        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2012-01-26T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.intarchmed.com/content/3/1/36">
        <title>LDLR-Gene therapy for familial hypercholesterolaemia: problems, progress, and perspectives</title>
        <description>Coronary artery diseases (CAD) inflict a heavy economical and social burden on most populations and contribute significantly to their morbidity and mortality rates. Low-density lipoprotein receptor (LDLR) associated familial hypercholesterolemia (FH) is the most frequent Mendelian disorder and is a major risk factor for the development of CAD. To date there is no cure for FH. The primary goal of clinical management is to control hypercholesterolaemia in order to decrease the risk of atherosclerosis and to prevent CAD. Permanent phenotypic correction with single administration of a gene therapeutic vector is a goal still needing to be achieved. The first ex vivo clinical trial of gene therapy in FH was conducted nearly 18 years ago. Patients who had inherited LDLR gene mutations were subjected to an aggressive surgical intervention involving partial hepatectomy to obtain the patient&apos;s own hepatocytes for ex vivo gene transfer with a replication deficient LDLR-retroviral vector. After successful re-infusion of transduced cells through a catheter placed in the inferior mesenteric vein at the time of liver resection, only low-level expression of the transferred LDLR gene was observed in the five patients enrolled in the trial. In contrast, full reversal of hypercholesterolaemia was later demonstrated in in vivo preclinical studies using LDLR-adenovirus mediated gene transfer. However, the high efficiency of cell division independent gene transfer by adenovirus vectors is limited by their short-term persistence due to episomal maintenance and the cytotoxicity of these highly immunogenic viruses. Novel long-term persisting vectors derived from adeno-associated viruses and lentiviruses, are now available and investigations are underway to determine their safety and efficiency in preparation for clinical application for a variety of diseases. Several novel non-viral based therapies have also been developed recently to lower LDL-C serum levels in FH patients. This article reviews the progress made in the 18 years since the first clinical trial for gene therapy of FH, with emphasis on the development, design, performance and limitations of viral based gene transfer vectors used in studies to ameliorate the effects of LDLR deficiency.</description>
        <link>http://www.intarchmed.com/content/3/1/36</link>
                <dc:creator>Faisal Al-Allaf</dc:creator>
                <dc:creator>Charles Coutelle</dc:creator>
                <dc:creator>Simon Waddington</dc:creator>
                <dc:creator>Anna David</dc:creator>
                <dc:creator>Richard Harbottle</dc:creator>
                <dc:creator>Michael Themis</dc:creator>
                <dc:source>International Archives of Medicine 2010, null:36</dc:source>
        <dc:date>2010-12-13T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-3-36</dc:identifier>
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        <prism:startingPage>36</prism:startingPage>
        <prism:publicationDate>2010-12-13T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.intarchmed.com/content/4/1/17">
        <title>Sclerosing Mesenteritis:  Diverse clinical presentations and dissimilar treatment options.  A case series and review of the literature. 
</title>
        <description>Sclerosing mesenteritis (SM) is a rare pathological condition affecting the mesentery. It is a benign, non-specific inflammation of the adipose tissue of the mesentery of the small intestine and colon. It is characterized by a variable amount of chronic fibrosis. Its etiology is unknown, the pathogenesis is obscure, while the pathological characteristics of the disease are unspecific. The initial clinical presentation varies from typically asymptomatic to that of an acute abdomen. The diagnosis is suggested by computed tomography but is usually confirmed by surgical biopsies. Treatment is largely empirical; it is decided upon on the basis of the clinical condition of the patient, and usually a few specific drugs are used. Surgical resection is sometimes attempted for definitive therapy, although the surgical approach is often limited. We will present five cases of SM as well as a review of the available literature in order to state and compare a variety of clinical presentations, diverse possible etiologies and dissimilar treatment options.</description>
        <link>http://www.intarchmed.com/content/4/1/17</link>
                <dc:creator>Konstantinos Vlachos</dc:creator>
                <dc:creator>Fotis Archontovasilis</dc:creator>
                <dc:creator>Evangelos Falidas</dc:creator>
                <dc:creator>Stavros Mathioulakis</dc:creator>
                <dc:creator>Stefanos Konstandoudakis</dc:creator>
                <dc:creator>Constantinos Villias</dc:creator>
                <dc:source>International Archives of Medicine 2011, null:17</dc:source>
        <dc:date>2011-06-02T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-4-17</dc:identifier>
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        <prism:startingPage>17</prism:startingPage>
        <prism:publicationDate>2011-06-02T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.intarchmed.com/content/4/1/39">
        <title>Africa&apos;s health: could the private sector accelerate the progress towards health MDGs?</title>
        <description>Background:
Out of 1.484 billion disability-adjusted life years lost globally in 2008, 369.1 million (25%) were lost in the WHO African Region. Despite the heavy disease burden, the majority of countries in the Region are not on track to achieve Millennium Development Goals (MDG) 4 (reducing child mortality), 5 (improving maternal health), and 6 (combating HIV/AIDS, malaria and other diseases). This article provides an overview of the state of public health, summarizes 2010-2015 WHO priorities, and explores the role that private sector could play to accelerate efforts towards health MDGs in the African Region.DiscussionOf the 752 total resolutions adopted by the WHO Regional Committee for Africa (RC) between years 1951 and 2010, 45 mention the role of the private sector. We argue that despite the rather limited role implied in RC resolutions, the private sector has a pivotal role in supporting the achievement of health MDGs, and articulating efforts with 2010-2015 priorities for WHO in the African Region: provision of normative and policy guidance as well as strengthening partnerships and harmonization; supporting the strengthening of health systems based on the Primary Health Care approach; putting the health of mothers and children first; accelerating actions on HIV/AIDS, malaria and tuberculosis; intensifying the prevention and control of communicable and noncommunicable diseases; and accelerating response to the determinants of health.
Conclusion:
The very high maternal and children mortality, very high burden of communicable and non-communicable diseases, health systems challenges, and inter-sectoral issues related to key determinants of health are too heavy for the public sector to address alone. Therefore, there is clear need for the private sector, given its breadth, scope and size, to play a more significant role in supporting governments, communities and partners to develop and implement national health policies and strategic plans; strengthen health systems capacities; and implement roadmaps for accelerating the attainment of health MDGs relating to maternal and child health, reducing disease burden, and promoting social determinants of health.In order for governments to further explore the potential benefits of the private sector towards improved performance of health systems, there is need for accurate evidence on the private sector capacity in areas of prevention, promotion, treatment and rehabilitation; dialogue and negotiation; clear definition of roles and responsibilities; and regulatory frameworks.</description>
        <link>http://www.intarchmed.com/content/4/1/39</link>
                <dc:creator>Luis Sambo</dc:creator>
                <dc:creator>Joses Kirigia</dc:creator>
                <dc:source>International Archives of Medicine 2011, null:39</dc:source>
        <dc:date>2011-11-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1755-7682-4-39</dc:identifier>
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        <prism:startingPage>39</prism:startingPage>
        <prism:publicationDate>2011-11-25T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.intarchmed.com/content/3/1/11">
        <title>Interleukin 8 (IL-8) - a universal biomarker? </title>
        <description>Many clinical conditions including various types of cancers are complex and generally require invasive, laborious, expensive and time-consuming investigations for their diagnosis, treatment and follow-up. There is therefore a general need for exploring non-invasive markers in clinical medicine. Interleukin 8 (IL-8) is currently being applied in various subspecialties of medicine either for the purpose of rapid diagnosis or as a predictor of prognosis. Nevertheless, there is need for large-scale studies to substantiate accuracy and outcome. This article will summarize current evidence suggesting that Interleukin 8 (IL-8) may serve as a useful biomarker.</description>
        <link>http://www.intarchmed.com/content/3/1/11</link>
                <dc:creator>Aamir Shahzad</dc:creator>
                <dc:creator>Martin Knapp</dc:creator>
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