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Relevant bibliographies by topics / Leiomyomatose

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Dissertations / Theses
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Academic literature on the topic 'Leiomyomatose'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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Journal articles on the topic "Leiomyomatose"

1

Schumacher, A., G. Saile, H. Brühwiler, and K. Lüscher. "Intravenöse Leiomyomatose." Geburtshilfe und Frauenheilkunde 55, no. 10 (1995): 602–4. http://dx.doi.org/10.1055/s-2007-1023533.

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Kommoss, F., T. Ebel, J. Drusenheimer, et al. "Die intravenöse Leiomyomatose." Der Pathologe 40, no. 1 (2019): 80–84. http://dx.doi.org/10.1007/s00292-019-0566-7.

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Padberg, B. C., A. Emmermann, C. Zornig, M. Germer, and S. Schröder. "Leiomyomatose des Rektums." Der Pathologe 28, no. 2 (2007): 161–65. http://dx.doi.org/10.1007/s00292-007-0898-6.

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Braun, S. A., S. Hanneken, J. Reifenberger, D. Helbig, and J. Frank. "Hereditäre kutane Leiomyomatose." Der Hautarzt 63, no. 4 (2012): 276–78. http://dx.doi.org/10.1007/s00105-012-2357-4.

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Acid, S., S. Marciano-Chagnaud, P. Kbaier, et al. "AGF14 Leiomyomatose peritoneale disseminee." Journal de Radiologie 87, no. 10 (2006): 1440. http://dx.doi.org/10.1016/s0221-0363(06)87509-8.

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Bergmann, M., B. Seelbach-Göbel, and H. Müller-Hermelink. "Intravenöse Leiomyomatose des Uterus." Geburtshilfe und Frauenheilkunde 51, no. 11 (1991): 942–44. http://dx.doi.org/10.1055/s-2008-1026241.

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Scharlau, L.-L. L.-L., J. Scharlau, Cl Mathuis, and C.-N. C.-N. Schremmer. "Diffuse peritoneale Leiomyomatose - Eine klinische Fallstudie - Diffuse Peritoneal Leiomyomatosis: A Case Report -." Geburtshilfe und Frauenheilkunde 60, no. 4 (2000): 225–28. http://dx.doi.org/10.1055/s-2000-10014.

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Versini, M., PY Jeandel, A. Rahili, et al. "Leiomyomatose surrénalienne : une localisation exceptionnelle." La Revue de Médecine Interne 32 (June 2011): S179—S180. http://dx.doi.org/10.1016/j.revmed.2011.03.305.

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Kruczynski, D., E. Merz, Th Beck, et al. "Minimal invasive Therapie bei peritonealer Leiomyomatose." Geburtshilfe und Frauenheilkunde 54, no. 03 (1994): 181–83. http://dx.doi.org/10.1055/s-2007-1023578.

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Werthemann, A., B. Unger, H. Lobeck, and H. Wenisch. "Die verzögerte Ösophagusresektion bei diffuser Leiomyomatose." Zentralblatt für Chirurgie 136, no. 03 (2010): 282–83. http://dx.doi.org/10.1055/s-0030-1247322.

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Dissertations / Theses on the topic "Leiomyomatose"

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SALOBIR, BERNADETTE. "La leiomyomatose peritoneale disseminee associee a une endometriose : a propos d'un cas." Lille 2, 1990. http://www.theses.fr/1990LIL2M028.

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ESTANOVE, JEAN-GREGOIRE. "Syndrome d'alport et leiomyomatose viscerale : deux observations dans une meme famille." Lyon 1, 1988. http://www.theses.fr/1988LYO1M028.

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BECETTE, VERONIQUE. "La lymphangioleiomyomatose pulmonaire diffuse : a propos d'un cas, revue de la litterature." Lille 2, 1989. http://www.theses.fr/1989LIL2M323.

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CANAL, GUY. "Leiomyomatose intraveineuse d'origine uterine avec extension cardiaque : a propos de 1 cas." Reims, 1989. http://www.theses.fr/1989REIMM116.

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MIGNOT, THEVENET FLORENCE. "La lymphangioleiomyomatose pulmonaire : transplantation pulmonaire et traitement hormonal ; a propos d'un cas ; revue de la litterature." Lyon 1, 1994. http://www.theses.fr/1994LYO1M222.

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Kiuru, Maija. "Molecular basis of hereditary leiomyomatosis and renal cell cancer (HLRCC)." Helsinki : University of Helsinki, 2002. http://ethesis.helsinki.fi/julkaisut/laa/kliin/vk/kiuru/.

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Alam, Naaz Afrina. "Clinical and genetic features of multiple cutaneous and uterine leiomyomatosis syndrome." Thesis, Queen Mary, University of London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.414008.

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Pollard, Patrick John. "Genetic and functional analysis of tumourigenesis in hereditary leiomyomatosis and renal cell cancer and hereditary paragangliomatosis syndromes." Thesis, University College London (University of London), 2006. http://discovery.ucl.ac.uk/1446046/.

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Hereditary leiomyomatosis and renal cell cancer (HLRCC) and hereditary paragangliomatosis (HPGL) are familial cancer syndromes, caused by germline mutations in genes encoding the Tricarboxylic Acid Cycle (TCAC) enzymes fumarate hydratase (FH) and succinate dehydrogenase (SDH) respectively. Both FH and SDH function as tumour-suppressor genes and the conditions are inherited as autosomal dominant traits. Germline FH mutations predispose individuals to develop benign smooth muscle tumours of the skin and uterus (leiomyomas) and renal carcinoma, whilst individuals with mutations in SDHB, -C, and -

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Pinlou, Elizabeth. "Tumeurs cardiaques du nouveau-né : difficultés diagnostiques echocardiographiques et anatomo-pathologiques à propos d'un cas de tumeur leiomyomateuse." Bordeaux 2, 1993. http://www.theses.fr/1993BOR2M112.

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Zhang, Xu. "Basal lamina genes affected in leiomyomatosis and congenital muscular dystrophy : structure and mutation analyses of the collagen COL4A6 and laminin LAMA2 genes." Stockholm, 1997. http://diss.kib.ki.se/1997/91-628-2780-4.

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Books on the topic "Leiomyomatose"

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Sybert, Virginia P. Tumors/Hamartomas. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0010.

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Basal Cell Nevus Syndrome – Bathing Trunk Nevus – Cowden Disease – Cylindromatosis – Dysplastic Nevus Syndrome – Epidermal Nevus – Gardner Syndrome – Hereditary Keratoacanthomas – Infantile Myofibromatosis – Multiple Endocrine Neoplasia Types 1, 2A, and 2B/3 – Multiple Leiomyomatosis – Pilomatricoma – Proteus Syndrome – Sebaceous Nevus Syndrome – Tumoral Calcinosis

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Sybert, Virginia P. Tumors/Hamartomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0010.

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Chapter 10 covers Basal Cell Nevus Syndrome, Cowden Syndrome, Cylindromatosis, Dysplastic Nevus Syndrome, Epidermal Nevus, Gardner Syndrome, Giant congenital nevocytic nevus, Hereditary Keratoacanthomas, Hereditary Leiomyomatosis and renal cell cancer, Infantile Myofibromatosis, Multiple Endocrine Neoplasia Types 1, 2A, and 2B/3, Pilomatricoma, Proteus Syndrome, Sebaceous Nevus Syndrome, and Tumoral Calcinosis. Each condition is discussed in detail, including dermatologic features, associated anomalies, histopathology, basic defect, treatment, mode of inheritance, prenatal diagnosis, and diffe

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Jafri, Mariam, and Eamonn R. Maher. Genetics and molecular biology of renal cancer. Edited by James W. F. Catto. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0084.

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Renal cell carcinoma (RCC) is the exemplar of how the understanding of the molecular pathogenesis of rare inherited disorders can inform an understanding of the key pathways involved in the pathogenesis of sporadic cancer. In this chapter we describe the clinical and pathological features of the inherited kidney cancer syndromes: von Hippel Lindau disease (VHL); Birt-Hogg-Dube syndrome; hereditary leiomyomatosis and renal cancer syndrome; succinate dehydrogenase disorders; hereditary papillary renal cancer; and translocation-associated kidney cancer. Though individually rare, recognition of in

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Heidet, Laurence, Bertrand Knebelmann, and Marie Claire Gubler. Alport syndrome. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0323.

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The diagnosis of Alport syndrome is suspected from the clinical features and confirmed by identifying the almost pathognomonic ultrastructural changes to the basement membrane in a family member with early disease (so that glomeruli are not too sclerosed), or in modern times by identifying a causative mutation in one or more of the three implicated COL4 genes. Genetic testing is becoming simpler and cheaper, but is still out of the reach of many. Eighty-five per cent of cases are caused by COL4A5 mutations and 10–15% by autosomal recessive disease. A significant proportion of morbidity in X-li

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Book chapters on the topic "Leiomyomatose"

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Nucci, Marisa R. "Disseminated Peritoneal Leiomyomatosis (Leiomyomatosis Peritonealis Disseminata)." In Encyclopedia of Pathology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-28845-1_5415-1.

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Mocellin, Simone. "Disseminated Peritoneal Leiomyomatosis." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_76.

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Scharnagl, Hubert, Winfried März, Markus Böhm, et al. "Alport Syndrome – Diffuse Leiomyomatosis Complex." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8690.

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Rübe, Claudia E., Bernadine R. Donahue, Jay S. Cooper, et al. "Hereditary Leiomyomatosis Renal Cell Carcinoma." In Encyclopedia of Radiation Oncology. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-85516-3_165.

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Fang, Ligang, Jing Ping Sun, and Yining Wang. "Intravenous Leiomyomatosis with Cardiac Metastases." In Comparative Cardiac Imaging. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119453192.ch40.

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Hauschild, A., C. Petres-Dunsche, C. Maier, and E. Christophers. "Schmerzkontrolle bei Leiomyomatosis cutis et uteri." In Fortschritte der operativen und onkologischen Dermatologie. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-79336-3_33.

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Zimmermann, Arthur. "Leiomyomatous Tumors of the Hepatobiliary Tract." In Tumors and Tumor-Like Lesions of the Hepatobiliary Tract. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26587-2_63-1.

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Zimmermann, Arthur. "Leiomyomatous Tumors of the Hepatobiliary Tract." In Tumors and Tumor-Like Lesions of the Hepatobiliary Tract. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26956-6_63.

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Leung, Alexander K. C., William Lane M. Robson, Carsten Büning, et al. "Leiomyomatosis and Renal Cell Cancer, Hereditary." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_3203.

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Metze, Dieter, Vanessa F. Cury, Ricardo S. Gomez, et al. "Hereditary Leiomyomatosis and Renal Cell Cancer." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_9218.

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Conference papers on the topic "Leiomyomatose"

1

Brautzsch, A., M. Brychcy, and J. Schnabel. "Disseminierte peritoneale Leiomyomatose – Ein Fallbericht." In Kongressabstracts zur 13. Jahrestagung der Mitteldeutschen Gesellschaft für Frauenheilkunde und Geburtshilfe e.V. (MGFG). Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1692099.

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Stilidi, I., J. Paianidi, K. Zgordania, V. Bochian, and A. Shevchuk. "303 Intravenous leiomyomatosis." In IGCS 2020 Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2020. http://dx.doi.org/10.1136/ijgc-2020-igcs.260.

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Thota, A., A. Geevarghese, and G. Acash. "A Case of Not so "Benign" Metastasizing Leiomyomatosis." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a6292.

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Serraj, M., A. Assal, O. Baroud, M. Benhessou, M. Ennachit, and M. El Karroumi. "EP1088 Pelvic leiomyomatosis (about a case and literature review)." In ESGO Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/ijgc-2019-esgo.1130.

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Bjerk, Sonja, Petr Bachan, and Ken M. Kunisaki. "Persistent Micronodular Pulmonary Infiltrates Caused By Benign Metastasizing Pulmonary Leiomyomatosis." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a6470.

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Uyanık, E., G. Özten, OC Zaim, M. Gültekin, and MC Salman. "EP761 Incidentally detected intravenous leiomyomatosis limited to uterus: a case report." In ESGO Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/ijgc-2019-esgo.812.

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Vocke, Cathy D., Christopher J. Ricketts, Lindsay A. Middelton, Youfeng Yang, and W. Marston Linehan. "Abstract 3179: Germline deletion of FH in hereditary leiomyomatosis and renal cell carcinoma (HLRCC)." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-3179.

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Vats, Pankaj, Yuping Zhang, Sarvana Mohan Dhanashekaran, et al. "Abstract 730: Genomic characterization of hereditary leiomyomatosis and renal cell carcinoma (HLRCC), a rare and aggressive kidney cancer." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-730.

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Vats, Pankaj, Yuping Zhang, Sarvana Mohan Dhanashekaran, et al. "Abstract 730: Genomic characterization of hereditary leiomyomatosis and renal cell carcinoma (HLRCC), a rare and aggressive kidney cancer." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-730.

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Koski, Taru A., Pia Vahteristo, Laura Näätsaari, et al. "Abstract 1844: No evidence for genetic factor increasing renal cell cancer risk in Hereditary Leiomyomatosis and Renal Cell Cancer syndrome." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-1844.

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