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Dissertations / Theses on the topic 'Disease manifestation'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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1

Herrett, Emily. "Myocardial infarction as the first manifestation of atherosclerotic disease." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590613.

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Shankar, Suma Prabhu. "Modifier genes in the phenotypic manifestation of primary disease-causing mutations." Diss., University of Iowa, 2005. http://ir.uiowa.edu/etd/108.

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3

Bohm, Marlies. "The comparative assessment of capillary and venous Babesia rossi parasitaemias on thin blood smears and their association with disease manifestation." Diss., University of Pretoria, 2006. http://hdl.handle.net/2263/24316.

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This observational study of 100 dogs naturally infected with Babesia rossi determined whether severity of parasitaemia was associated with outcome of infection and documented the relative distribution of parasitised red blood cells (pRBC) in capillary and venous circulation. The association between increased parasitaemias and outcome with a clinically compromised circulation was also investigated. Outcome was defined as either hospitalisation with death, or hospitalisation with eventual recovery or treatment as an outpatient. Dogs were enrolled if large babesias were found on stained thin capi

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4

Kyriacou, Helen M. "Var gene transcription and clinical disease manifestation in African P. falciparum malaria field isolates." Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/2583.

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The Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) variant surface antigens, encoded by the var gene family, play a crucial role in malaria pathogenesis through mediating immunomodulation and host cell adhesion. Var genes can be sub-grouped according to genetic or functional features. This thesis examined var gene transcription of conserved groups of var genes in the context of clinical malaria disease manifestation in African field isolates. Analysis of var gene transcription in 26 P. falciparum field isolates from Malian children revealed that field isolates from children with

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5

Claussen, Marie. "CMV-Infektion mit gastrointestinaler Manifestation: Vergleich der diagnostischen Möglichkeiten von endoskopischer, pathologischer und virologischer Untersuchung." Doctoral thesis, Universitätsbibliothek Leipzig, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-96771.

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Cytomegalievirus (CMV) ist bei immunsupprimierten Patienten nach Organ- oder Stammzelltransplantation sowie bei Patienten mit chronisch entzündlichen Darmerkrankungen und nicht immunsupprimierten kritisch kranken Patienten ein ernstzunehmender Risikofaktor für eine manifeste CMV-Infektion. Diese ist durch eine hohe Morbidität und Letalität gekennzeichnet. Daher ist eine zeitnahe und zuverlässige Diagnosestellung für die Einleitung einer adäquaten Therapie und damit für das klinische Ergebnis der Patienten von entscheidender Bedeutung. Ziel dieser retrospektiven Arbeit war es, die diagnostische

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6

Barber, Judith (Judith Anne) Carleton University Dissertation Sociology and Anthropology. "The Incorporation of visualizations into the western model of health and disease; a manifestation of cultural change." Ottawa, 1996.

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7

Jew, Kara Lynn. "Development of a Prolyl Endopeptidase Expression System In Lactobacillus reuteri to Reduce the Clinical Manifestation of Celiac Disease." DigitalCommons@CalPoly, 2019. https://digitalcommons.calpoly.edu/theses/2065.

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Celiac Disease (CD) is an autoimmune disorder that emerges due to the ingestion of gluten, a protein found in a variety of common grains such as wheat, rye, and barley. Approximately 1 in 100 individuals in the US suffer from CD, making it the most commonly diagnosed gastrointestinal disorder (Ciclitira et. al., 2005). These proline-rich gluten peptides are resistant to proteolysis and accumulate in the duodenum of the small intestine. Once in the duodenum, these peptides illicit an autoimmune response resulting in villous atrophy. Current treatment for CD requires a rigorous adherence to a gl

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8

Böhm, Marlies. "The comparative assessment of capillary and venous Babesia rossi parasitaemias on thin blood smears and their association with disease manifestation." Electronic thesis, 2006. http://upetd.up.ac.za/thesis/available/etd-05042007-154527/.

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9

Knauf, Sascha [Verfasser]. "Clinical manifestation and aetiology of a genital associated disease in Olive baboons (Papio hamadryas anubis) at Lake Manyara National Park, Tanzania / Sascha Knauf." Gießen : Universitätsbibliothek, 2011. http://d-nb.info/1061195716/34.

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10

Donis, Karina Carvalho. "História natural da ataxia espinocerebelar tipo 3/Doença de Machado-Joseph com início na infância." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2015. http://hdl.handle.net/10183/116803.

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Introdução: A Ataxia Espinocerebelar tipo 3 (SCA3), também chamada de Doença de Machado - Joseph (DMJ) é uma doença neurodegenerativa autossômica dominante causada pela expansão de uma sequência repetitiva CAG no gene ATXN3 localizado no cromossomo 14q32.1. Alelos normais contêm 12 a 43 repetições CAG; alelos causadores da doença contêm 51 ou mais repetições CAG (CAGexp). Existe uma forte correlação entre o tamanho da expansão e a gravidade da doença, e a antecipação é um fenômeno comum. Com idade de início média entre os 32 e os 40 anos, a SCA3/DMJ se apresenta com ataxia, disartria, disfagia

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11

Hempel, Maria. "Nicht-invasive Evaluation der hepatischen Manifestation bei Patienten mit Morbus Wilson mittels Transienter Elastographie, Acoustic Radiation Force Impulse (ARFI)-Elastographie und verschiedener laborbasierter Fibrose-Indices." Doctoral thesis, Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-160102.

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Die vorliegende medizinische Dissertation beschäftigt sich mit der Evaluation nicht-invasiver Diagnostikverfahren zur Detektion einer Leberfibrose bei Patienten mit Morbus Wilson. Untersucht wurden die Transiente Elastographie (TE), die Acoustic Radiation Force Impulse (ARFI)-Elastographie sowie verschiedene laborbasierte Fibrose-Indices bezüglich der Anwendbarkeit und ihres diagnostischen Nutzens. Der Morbus Wilson ist eine seltene hereditäre Kupferspeicherkrankheit, die über Kupferakkumulation im Leberparenchym zur Ausbildung einer Zirrhose führen kann. Die Kenntnis des Leberfibrosegrades is

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12

Chipangura, Sheila. "An investigation into the manifestation of stigma and discrimination and its consequences on HIV/AIDS prevention and treatment efforts amongst people living with HIV/AIDS." Thesis, Stellenbosch : Stellenbosch University, 2013. http://hdl.handle.net/10019.1/79945.

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Thesis (MPhil)--Stellenbosch University, 2013.<br>ENGLISH ABSTRACT: The AIDS epidemic has brought out both the best and the worst in people. The disease brings out the best when individuals group together in solidarity to combat the consequences of HIV/AIDS and to support and care for PLWHA. HIV/AIDS also brings out the worst when individuals are stigmatized and ostracized by their loved ones, their family and their communities and discriminated against individually as well as institutionally. This research has reviewed available scientific literature on HIV/AIDS stigma and discrimination. Th

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13

Bates, Matthew. "Cardiac manifestations of mitochondrial disease." Thesis, University of Newcastle upon Tyne, 2014. http://hdl.handle.net/10443/2525.

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Due to critical dependence of the heart on oxidative metabolism, cardiac involvement in mitochondrial disease is common and may occur as the principal clinical manifestation or part of multisystem disease. The basic features of cardiac mitochondrial disease expression remain uncertain and no effective treatment exists. Previous research has suggested that cardiac involvement in mitochondrial disease is an important cause of morbidity and early mortality in paediatric populations. In this thesis, a retrospective study confirms the frequent occurrence of cardiac involvement in adults, and demons

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14

Jeevaratnam, P. "Early manifestations of Anderson Fabry disease." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1396784/.

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This thesis examines some early renal and neurological manifestations in Anderson Fabry disease (AFD). First, estimating glomerular filtration rate in AFD using serum creatinine (Cr) based equations was assessed in 106 AFD patients. The Modification in diet in renal disease (MDRD) and the Chronic kidney disease epidemiology collaboration (CKD-EPI) equations had the least bias and were the best methods of estimating glomerular filtration rates in AFD patients with chronic kidney disease (CKD) stage 1 to 3. The monitoring of renal involvement in AFD use methods which assess glomerular function p

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15

Tsang, Chiu-shun Peter. "Oral biology of human immunodeficiency virus-infected individuals in Hong Kong /." [Hong Kong : Faculty of Dentistry, University of Hong Kong], 1997. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19900661.

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16

Tsang, Chiu-shun Peter, and 曾昭舜. "Oral biology of human immunodeficiency virus-infected individuals in Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1997. http://hub.hku.hk/bib/B31237770.

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17

Al-shair, Khaled. "Systemic Manifestations of Chronic Obstructive Pulmonary Disease." Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509061.

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18

Yiu, Kai-hang, and 姚啟恆. "Cardiovascular manifestations in systemic inflammatory diseases." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B48541011.

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Systemic inflammatory diseases, including those of rheumatology and dermatology, are associated with increased cardiovascular events. Evidence demonstrates that the chronic systemic inflammation associated with these diseases plays a pivotal role in all stages of atherosclerotic plaque formation, from initiation of the fatty streak to plaque rupture and consequent acute coronary syndrome. Although a number of studies have evaluated the cardiovascular manifestations in systemic inflammatory disease, this thesis offers additional observations, including the vascular atherosclerotic pattern, the

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19

Alhaddad, Maath. "Cardiopulmonary manifestations in chronic obstructive pulmonary disease (COPD)." Thesis, University of Nottingham, 2015. http://eprints.nottingham.ac.uk/30008/.

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Rationale Chronic obstructive pulmonary disease (COPD) is a progressive lung condition with extrapulmonary manifestations- cardiovascular diseases (CVD), impaired physical function, activity and increased frailty. Integrating measures of function into community assessments is hindered by the space and time required. The association of function, activity and CVD has not been extensively investigated in COPD. Objectives Explore the potential utility of Time Up and Go (TUG) as a measure of physical function in COPD Assess association of non-invasive measures of haemodynamics to physical function

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20

Davies, E. H. "Developing markers of neurological manifestations in Neuronopathic Gaucher Disease." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1310245/.

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Gaucher disease is a rare inherited lysosomal disorder caused by deficiency of the enzyme glucocerebrosidase. Classically, three forms of the disease are recognised: type I or nonneuronopathic, type 2 or acute neuronopathic, and type 3 or subacute or chronic neuronopathic. Neuronopathic Gaucher disease (NGD) is defined as a confirmed diagnosis of Gaucher disease in the presence of neurological symptoms and signs, for which there is no other cause. Horizontal gaze palsy is the clinical hallmark of NGD. Other neurological manifestations include seizures, cerebellar ataxia and pyramidal tract inv

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21

Presnell, Scott. "Whatever the individual says it is : a phenomenological analysis of chronic pain in people with Human Immunodeficiency Virus-associated distal symmetrical polyneuropathy /." [St. Lucia, Qld.], 2004. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe18066.pdf.

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22

Zagten, Maria Sophia Gerarda van. "Cerebral small-vessel disease vascular risk factor profiles, clinical manifestations, and disease progression in stroke /." Maastricht : Maastricht : Universiteit Maastricht ; University Library, Maastricht University [Host], 1997. http://arno.unimaas.nl/show.cgi?fid=6019.

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23

Kilpi, Anu. "Characterization of mononuclear cells of inflammatory infiltrates in oral tissues a histochemical and immunohistochemical study of labial salivary glands in Sjögren syndrome and oral lesions in systemic lupus erythematosus and in lichen planus /." Helsinki : Yliopistopaino, 1987. http://catalog.hathitrust.org/api/volumes/oclc/17456505.html.

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24

Biancalana, Helenice. "Manifestações bucais em crianças com doença falciforme." [s.n.], 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/312073.

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Orientador: Silvia Regina Brandalise<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas<br>Made available in DSpace on 2018-08-07T00:03:46Z (GMT). No. of bitstreams: 1 Biancalana_Helenice_M.pdf: 2127698 bytes, checksum: c684b76f616b7c6c6ee06e1debd4e145 (MD5) Previous issue date: 2006<br>Resumo: INTRODUÇÃO: Doença Falciforme é uma anemia hemolítica genético-hereditária, causada por uma mutação do gene da hemoglobina, que altera sua estabilidade e característica físico-química, resultando numa hemácia que, sob determinadas condições, tem seu formato al

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25

Tsai, Chi-Chun Wirongrong Chierakul. "Rheumatological manifestations in melioidosis patients /." Abstract, 2006. http://mulinet3.li.mahidol.ac.th/thesis/2549/cd387/4838796.pdf.

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26

Lee, Alice. "An exploratory study of the behavioural manifestations in a group of patients with binswanger's disease." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1985. http://hub.hku.hk/bib/B29648233.

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27

Pitcher, Alex. "Cardiovascular manifestations of Marfan syndrome : insights from advanced cardiovascular magnetic resonance." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:e47f70d4-a777-4c1d-8bb4-3758231ef38a.

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Marfan syndrome (MFS) is the commonest inherited disorder of connective tissue and is associated with a high risk of potentially life-threatening complications, including aortic aneurysm, dissection and rupture, and, perhaps, ventricular disease. This work describes the prospective application of advanced cardiovascular magnetic resonance techniques to the aorta and heart of consecutive, unselected subjects with MFS, and to appropriately matched control populations. Comprehensive 3D visualisation of blood flow in the entire thoracic aorta of subjects with MFS was achieved using a time-resolved

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28

Whalan, Comus John. "Mechanisms of post-operative sepsis and renal impairment in obstructive jaundice /." Title page, abstract, contents and introduction only, 1998. http://web4.library.adelaide.edu.au/theses/09MD/09mdw552.pdf.

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29

Ranganathan, Megha. "The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu152409456533713.

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30

Sanchez, Phyllis Nancy. "Psychiatric diagnosis vs medical diagnosis: Are mental health professionals aware?" Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184826.

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For years research has demonstrated a varying incidence of medical disorders manifesting with psychiatric symptoms. A relatively conservative estimate of such so called "medical masquerades" is around 10%. It is important to ascertain whether health care professionals are aware of possible medical masquerades perhaps most especially in a mental health center outpatient setting where non-medically trained clinicians are the first line therapists for treatment in the majority of cases. This study set about to find out how aware three types of health care clinicians (psychiatrists, nonpsychiatric

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31

Behardien, Nashreen. "Oral mucosal and facial manifestations of HIV/AIDS in children (Cape Peninsula, South Africa)." Thesis, University of the Western Cape, 2006. http://etd.uwc.ac.za/index.php?module=etd&amp.

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Currently, HIV/AIDS is one of the greatest threats to child survival in South Africa. It is estimated that approximately 6000 newborn babies become infected with the HIV virus monthly i.e. approximately 200 babies per day. During a 24 month period (October 1999 &ndash<br>October 2001), a descriptive prevalence study of the oro-facial manifestations affecting HIV-positive children was conducted in the Cape Peninsula, South Africa. The study population consisted of 268 vertically infected HIV-positive children. The study was motivated by the lack of data regarding oral mucosal lesions in childre

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32

Aung, Thu Wichai Supanaranond. "Gastrointestinal manifestations of septic patients with scrub typhus in Maharat Nakhon Ratchasima hospital /." Abstract, 2003. http://mulinet3.li.mahidol.ac.th/thesis/2546/4538024.pdf.

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33

Marshall, Jonathan Charles Walter. "The interdisciplinary relationship between alcohol consumption and liver disease on the prevalence and disease manifestations of Helicobacter pylori : a clinical, histological and in vitro study." Thesis, University College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.402117.

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34

Viglino, Damien. "Douleur et stéatopathie hépatiques, des manifestations systémiques sous estimées de la BPCO." Thesis, Université Grenoble Alpes (ComUE), 2018. http://www.theses.fr/2018GREAS023.

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La bronchopneumopathie chronique obstructive (BPCO) est une des maladies chroniques les plus fréquentes et constitue une des premières causes de mortalité dans le monde avec un impact sociétal majeur et des couts de santé considérables. La BPCO est aujourd’hui considérée comme une maladie multi-systémique dont le pronostic est lié en grande partie à ses comorbidités et à la survenue d’exacerbations. Les exacerbations qui vont ponctuer l’évolution de la BPCO précipitent le déclin de la fonction respiratoire et favorisent la décompensation des comorbidités et la survenue d’événements cardiovascu

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35

Gånemo, Agneta. "Hereditary ichthyosis : Causes, Skin Manifestations, Treatments and Quality of Life." Doctoral thesis, Uppsala University, Dermatology and Venereology, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1780.

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<p>Hereditary ichthyosis is a collective name for many dry and scaly skin disorders ranging in frequency from common to very rare. The main groups are autosomal recessive lamellar ichthyosis, autosomal dominant epidermolytic hyperkeratosis and ichthyosis vulgaris, and x-linked recessive ichthyosis. Anhidrosis, ectropion and keratodermia are common symptoms, especially in lamellar ichthyosis, which is often caused by mutations in the transglutaminase 1 (TGM1) gene. The aim of this work was to study patients with different types of ichthyosis regarding (i) the patho-aetiology (TGM1 and electron

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36

Tala, Hazel Marie Bituin Linan. "The oral health status and dental awareness of young Hong Kong Chinese with insulin dependent diabetes mellitus (IDDM)." Click to view the E-thesis via HKUTO, 2000. http://sunzi.lib.hku.hk/hkuto/record/B31954145.

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37

La, Cock Charles J. R. "Mitochondrial DNA heteroplasmy in radiation induced myelodysplasia and leukaemia." Thesis, Cape Technikon, 1996. http://hdl.handle.net/20.500.11838/2251.

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Thesis (MTech (Medical Technology))--Cape Technikon, 1996.<br>Haematological defects observed in clonal deletions of mtDNA and the inhibition of mitochondrial function by benzene and chloramphenicol, suggest a role for mtDNA in the pathogenesis of radiation - induced preleukaemia (MDS). The fact that leukaemia cells contain abnormal mitochondria and abnormally structured mtDNA, makes it reasonable to assume mtDNA mutations could be central to the pathogenesis of both MDS and leukaemia. It was decided to examine MDS patients for the presence of mtDNA length mutations (dimers and cocanta

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38

Haggard, Claire Louise. "Making sense of the lived and told experience of the 'ill' body : a phenomenological exploration into the storied and embodied nature of somatic or medically unexplained symtoms." Thesis, Rhodes University, 2013. http://hdl.handle.net/10962/d1008364.

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Despite a wealth of literature on the aetiology of somatic distress or somatization, somatic theory has failed to expand beyond a dualistic epistemology of causation. Within the primary health context where medically unexplained symptoms are characteristically articulated as literal, symbolic gestures of internal psychological processes, individuals' subjective accounts of somatic distress are reduced to objective phenomena and thus articulated on the grounds of absence. Within this context, the body as a lived, meaningful, perceiving subjectivity is silenced in favour of the corpse, thus rend

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39

Dunder, Kristina. "Clinical Manifestations of Coronary Heart Disease and the Metabolic Syndrome : A Population-based Study in Middle-aged Men in Uppsala." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4280.

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40

Saunders, Lucy C. (Lucy Chloe). "Psychological and endocrine indicators of stress : health and management implications." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53563.

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Thesis (MSc)--University of Stellenbosch, 2003.<br>ENGLISH ABSTRACT: Introduction: This is a multidisciplinary investigation of stress in working males. The physiological aspect of the stress response is focused primarily on the hypothalamic-pituitary-adrenal axis; the health outcomes focus on cardiovascular risk and the psychological aspect focuses on both personality and state. Aims: To assess psychological and physiological measures of stress and determine if they are associated. To assess the effect of massage as a relaxation intervention on these measures. Abstract: Section 1 Thi

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Yamakawa, Noriyuki. "A Clinical, Pathological and Genetic Characterization of Methotrexate-Associated Lymphoproliferative Disorders." Kyoto University, 2014. http://hdl.handle.net/2433/188632.

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Sato, Takeshi. "Anti-U1RNP antibodies in cerebrospinal fluid are associated with central neuropsychiatric manifestations in systemic lupus erythematosus and mixed connective tissue disease." Kyoto University, 2011. http://hdl.handle.net/2433/142082.

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Mathiba, Olorato P. "An Oral Health Survey among HIV-infected children younger than twelve years of age presenting at the Paediatric Infectious Diseases Clinic at Tygerberg Hospital." The University of the Western Cape, 2017. http://hdl.handle.net/11394/5531.

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Magister Scientiae Dentium - MSc(Dent)<br>HIV/AIDS remains a global health problem. Orofacial manifestations of HIV/AIDS have been found to be among the first signs of immune suppression and have been used in the clini-cal staging of the disease. Infants and children are prone to opportunistic infections because of the immature immune system. Orofacial manifestations of HIV can therefore be used to predict prog-nosis and progression of infection. The introduction of highly active anti-retroviral therapy (HAART) has since seen a decline in the development of opportunistic infections and HIV-rel

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La, Cock Charles JR. "Mitochondrial DNA heteroplasmy in radiation induced myelodysplasia and leukaemia." Thesis, Cape Technikon, 1996. http://hdl.handle.net/20.500.11838/1493.

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Thesis (MTech(Medical Technology))--Cape Technikon, Cape Town, 1996<br>Haematol.ogical defects observed in cl.onal deletions of mtDNA and the inhibition of mitochondrial function by benzene and chloramphenicol., suggest a role for mtDNA in the pathogenesis of radiation - induced preleukaemia (MDS). The fact that leukaemia cell.s contain abnormal mitochondria and abnormally structured mtDNA, makes it reasonable to assume mtDNA mutations could be central to the pathogenesis of both MDS and l.eukaemia. It was decided to examine MDS patients for the presence of mtDNA length mutatio

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45

Nejem, R'afat Mahmoud. "Enantioselective sensors and biosensors for clinical analysis." Pretoria ; [s.n.], 2004. http://upetd.up.ac.za/thesis/available/etd-01242005-114455.

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46

Baltyde, Kizzy-Clara. "Implication de la voie adénosine/adénosine récepteur A2B dans les mécanismes physiopathologiques de deux manifestations drépanocytaires : l'hémolyse et le priapisme." Thesis, Antilles, 2016. http://www.theses.fr/2016ANTI0039/document.

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La drépanocytose résulte d’une mutation du gène β-globine entrainant la synthèse d’une hémoglobine anormale, l’HBS, qui polymérise en condition désoxygénée. Le globule rouge deviendra plus rigide et plus fragile, donnant lieu a deux conséquences majeures : l’hémolyse accrue et l’occlusion vasculaire.Récemment, un nouvel acteur moléculaire, l’adénosine, a été identifie. Ce nucléoside présente des effets bénéfiques sur les atteintes pulmonaires en inhibant l’activation des cellules « tueur naturel t inductibles », mais aussi délétères en favorisant la polymérisation de l’HBS et la survenue du pr

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47

Hamilton-Shield, J. P. "Sub-clinical manifestations of microvascular disease in childhood onset insulin dependent diabetes mellitus (IDDM) : a follow up study on the 'Avon Childhood Diabetes Cohort'." Thesis, University of Bristol, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387992.

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48

GalvÃo, LÃvia Monteiro. "Beta globin s gene haplotypes study, vascular endothelial growth factor-a (VEGF-A), fetal hemoglobin and clinical manifestations in patients with sickle cell disease." Universidade Federal do CearÃ, 2016. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17633.

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CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior<br>A anemia falciforme (AF) Ã uma doenÃa hereditÃria decorrente de uma mutaÃÃo pontual no gene da globina βS gerando uma hemoglobina anormal denominada de hemoglobina S (HbS) , que quando desoxigenada sofre polimerizaÃÃo favorecendo o fenÃmeno de vaso-oclusÃo, dano endotelial vascular e a expressÃo de fatores angiogÃnicos. Fatores genÃticos como os haplÃtipos da beta globina S sÃo responsÃveis pelas diferenÃas clÃnicas entre os pacientes. O objetivo deste trabalho foi verificar a associaÃÃo dos haplÃtipos da globina βs com o

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Oliveira, Gisele Ramos de. "ManifestaÃÃes neurolÃgicas em pacientes com doenÃa de Crohn e retocolite ulcerativa." Universidade Federal do CearÃ, 2008. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=1566.

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CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior<br>VÃrios distÃrbios neurolÃgicos foram observados em pacientes com doenÃa inflamatÃria intestinal (DII), porÃm sua prevalÃncia exata Ã desconhecida. Estudamos prospectivamente a incidÃncia e a prevalÃncia das manifestaÃÃes neurolÃgicas em uma coorte de 82 pacientes com DII (protocolo 1) e a presenÃa e gravidade de tremor em pacientes com DII e voluntÃrios sadios (Protocolo 2). Os pacientes do protocolo 1 foram avaliados no ambulatÃrio de DII do Hospital Walter CantÃdio por um perÃodo de pelo menos 1 ano, realizando avaliaÃÃes neurol

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Tang, Linyun [Verfasser]. "Chemogenetic investigation of amyotrophic lateral sclerosis (ALS): controlling signaling in astrocytes and in motoneurons to affect disease manifestations in an ALS mouse model / Linyun Tang." Ulm : Universität Ulm, 2020. http://d-nb.info/1205001743/34.

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