Academic literature on the topic 'Urbach-Wiethe disease'

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Journal articles on the topic "Urbach-Wiethe disease"

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Rallis, Efstathios, Dimitrios G. Balatsouras, Pavlos Papadakis, Nicolas C. Economou, Antonis Kaberos, and Stavros Korres. "Urbach–Wiethe disease." International Journal of Pediatric Otorhinolaryngology Extra 1, no. 1 (2006): 1–4. http://dx.doi.org/10.1016/j.pedex.2005.10.001.

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Tiwary, Anup Kumar. "Urbach-Wiethe Disease." Indian Pediatrics 55, no. 10 (2018): 923. http://dx.doi.org/10.1007/s13312-018-1413-2.

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Koganti, Deepthi. "Urbach-Wiethe Disease: A Rare Cause of Hoarseness of Voice." International Journal of Phonosurgery & Laryngology 3, no. 2 (2013): 61–64. http://dx.doi.org/10.5005/jp-journals-10023-1065.

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ABSTRACT Urbach-Wiethe disease is a rare, autosomal recessive disorder, characterized by infiltration of periodic acid-Schiff positive hyaline material into the skin, oral cavity, larynx and internal organs. The clinical manifestations include hoarseness of voice, beaded papules along the eyelid margins, skin scarring and an inability to protrude the enlarged and thickened tongue. Laryngeal involvement is typical and causes hoarseness of voice. In this paper, we present a case of a middle-aged female with clinical features suggestive of Urbach-Wiethe disease. This entity is of interest to the
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Kucuk, Ulku, IsinG Erdogan, Umit Bayol, Nazife Hacioglu, Ibrahim Cukurova, and Cengiz Bicakci. "Urbach-Wiethe disease (lipoid proteinosis)." Indian Journal of Pathology and Microbiology 55, no. 3 (2012): 375. http://dx.doi.org/10.4103/0377-4929.101749.

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KELLY, J. E., M. T. SIMPSON, D. JONATHAN, and T. E. HOLLWAY. "LIPOID PROTEINOSIS: URBACH-WIETHE DISEASE." British Journal of Anaesthesia 63, no. 5 (1989): 609–11. http://dx.doi.org/10.1093/bja/63.5.609.

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Cinaz, P., T. Güvenir, and G. Gönlügen. "Lipoid proteinosis: Urbach-Wiethe disease." Acta Paediatrica 82, no. 11 (1993): 892–93. http://dx.doi.org/10.1111/j.1651-2227.1993.tb12590.x.

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Cinaz, P., T. Güvenir, and G. Gönlügen. "Lipoid proteinosis: Urbach-Wiethe disease." Acta Paediatrica 82, no. 10 (1993): 892–93. http://dx.doi.org/10.1111/j.1651-2227.1993.tb17638.x.

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Costagliola, C., M. Verolino, P. Landolfo, N. R. Winkler, L. Mastropasqua, and V. Landolfo. "Lipoid Proteinosis (Urbach-Wiethe Disease)." Ophthalmologica 213, no. 6 (1999): 392–96. http://dx.doi.org/10.1159/000027461.

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Staut, Claudio C. V., and Thomas P. Naidich. "Urbach-Wiethe Disease(Lipoid Proteinosis)." Pediatric Neurosurgery 28, no. 4 (1998): 212–14. http://dx.doi.org/10.1159/000028653.

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Kurtuluş, B., O. Dog?an Onur, V. Olgac, A. Balik, and B. Batur. "OC12 Lipoid proteinosis (Urbach-Wiethe disease)." Oral Diseases 12, s1 (2006): 12. http://dx.doi.org/10.1111/j.1601-0825.2006.01308_12.x.

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Dissertations / Theses on the topic "Urbach-Wiethe disease"

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Fourie, Jorique. "Social and economic decision-making in Urbach-Wiethe Disease." Master's thesis, Faculty of Health Sciences, 2020. http://hdl.handle.net/11427/32253.

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Background: Rodent and primate research have identified the basolateral amygdala as indispensable for social decision-making. This finding has not yet been translated to humans, and has even been partially contradicted by previous findings in patients with amygdala lesions that show generous economic investments in strangers. This thesis therefore aimed to determine whether selective basolateral amygdala damage in humans, caused by Urbach-Wiethe Disease, impairs instrumental non-social economic decision-making. Methods: Using an adapted reinforcement-learning task, the performance of basolater
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Baasch, Roland. "FMRI guided DTI at the grey-white matter interface : with application to a connectivity analysis of the default mode network in Urbach-Wiethe disease." Master's thesis, University of Cape Town, 2011. http://hdl.handle.net/11427/12246.

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Includes abstract.<br>Includes bibliographical references.<br>The cerebral cortex is composed of a thin layer of Grey Matter (GM), functionally subdivided into discrete regions which are connected in a large scale network via White Matter (WM) tracts. With fMRI (Functional Magnetic Resonance Imaging) it is possible to identify cortical regions involved in specific tasks, and with DTI (Diffusion Tensor Imaging) the structural connections between these areas can be mapped. The aim of this thesis is to to identify and track only those WM tracts entering and leaving a GM Region Of Interest (ROI) d
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Book chapters on the topic "Urbach-Wiethe disease"

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Rappold, Gudrun, John-John B. Schnog, Victor E. A. Gerdes, et al. "Urbach-Wiethe Disease." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8789.

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"Urbach-Wiethe disease." In Dermatology Therapy. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_2793.

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"Eyelid Diseases." In Medical Atlas of Cornea and External Diseases in Middle Eastern Populations. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-7998-6937-5.ch001.

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This chapter reviews eyelid malpositions, benign and malignant tumors, infections, and inflammatory diseases of the eyelid. Eyelid lesions can originate in any layer or structure within the eyelid and eyelid adnexa. Benign tumors of the eyelid can often be diagnosed based on their characteristic appearance. A biopsy should be performed if an eyelid lesion is not easily diagnosed based on clinical appearance. Blepharitis and meibomitis are very common disorders. Despite their prevalence, these diseases are often overlooked and misdiagnosed. Meibomian gland dysfunction is a major cause of evapor
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Conference papers on the topic "Urbach-Wiethe disease"

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"EMOTIONAL DISTURBANCES IN URBACH-WIETHE DISEASE WITHOUT VISIBLE AMYGDALA DAMAGE." In International Psychological Applications Conference and Trends. inScience Press, 2023. http://dx.doi.org/10.36315/2023inpact013.

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Kimpo, J., S. Abu-Ghanem, and L. M. Chen. "New-onset Dyspnea and Stridor in a Patient With Urbach-wiethe Disease." In American Thoracic Society 2023 International Conference, May 19-24, 2023 - Washington, DC. American Thoracic Society, 2023. http://dx.doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1916.

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Declan, Brennan, Greene Chris, Togher Zara, Hutchinson Siobhan, Doherty Colin, and Campbell Matthew. "Urbach Wiethe Disease: uncovering the role of an ECM1 mutation in BBB dysfunction." In Association of British Neurologists: Annual Meeting Abstracts 2023. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/jnnp-2023-abn.44.

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