Bibliografías temáticas / Syndrome sein

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Literatura académica sobre el tema "Syndrome sein"

Autor: Grafiati
Publicado: 30 de noviembre de 2024
Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Syndrome sein"

1

Imbert, B., and JL Debru. "Syndrome néphrotique et cancer du sein." La Revue de Médecine Interne 15 (January 1994): 97s. http://dx.doi.org/10.1016/s0248-8663(05)82645-1.

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Llambrich, Claire, Marie-Christine Falcou, Yann de Rycke, Paul Cottu, Sylvie Carrié, and Malika Medjbari. "Cancer du sein et syndrome mains-pieds." Soins 57, no. 766 (2012): 25–28. http://dx.doi.org/10.1016/j.soin.2012.04.015.

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Aziza, Claude. "Antiquités parallèles (8)Le syndrome du sein droit." Anabases, no. 27 (April 1, 2018): 161–65. http://dx.doi.org/10.4000/anabases.7127.

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Guedin, P., J. Chasle, C. Blanc-Fournier, and J. Lacroix. "Cancer du sein et chondrosarcome osseux : un nouveau syndrome ?" Journal de Radiologie 87, no. 11 (2006): 1700–1704. http://dx.doi.org/10.1016/s0221-0363(06)74150-6.

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Pelissier, A., J. Dumesnil, R. Levy, C. Charron, and R. Rouzier. "Syndrome du choc toxique staphylococcique après chirurgie du sein." Journal de Gynécologie Obstétrique et Biologie de la Reproduction 43, no. 7 (2014): 526–29. http://dx.doi.org/10.1016/j.jgyn.2014.02.003.

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Sulkowski, Udo, and Rudolf Mennigen. "Das Low anterior Resection Syndrome (LARS)." Zentralblatt für Chirurgie - Zeitschrift für Allgemeine, Viszeral-, Thorax- und Gefäßchirurgie 144, no. 04 (2019): 419–25. http://dx.doi.org/10.1055/a-0754-2482.

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Zusammenfassung Hintergrund Mit einem 5-Jahres-Überleben von mittlerweile 80% rückt die postoperative Lebensqualität nach onkologischer Rektumresektion zunehmend in den Fokus des Interesses. Das Low anterior Resection Syndrome (LARS) fasst die postoperative Morbidität infolge des operativen Eingriffes zusammen. Material und Methode Es wurde eine selektive Literaturrecherche durchgeführt, um das Bild des LARS näher zu definieren und Verständnis für seine Pathophysiologie, Diagnose, Therapie und Prophylaxe zu entwickeln. Ergebnisse LARS wird in bis zu 80% nach allen stomavermeidenden operativen
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Premont, Coralie. "Kinésithérapie et syndrome du sein fantôme chez les femmes mastectomisées." Kinésithérapie, la Revue 25, no. 279 (2025): 137. https://doi.org/10.1016/j.kine.2025.01.101.

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Gschossmann, J. M. "Irritable Bowel Syndrome - eine Standortbestimmung." Praxis 97, no. 9 (2008): 489–94. http://dx.doi.org/10.1024/1661-8157.97.9.489.

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Das Reizdarmsyndrom (Irritable Bowel Syndrome IBS) stellt durch seine hohe Prävalenz und seinen chronischen Krankheitsverlauf ein bedeutendes Krankheitsbild für den niedergelassenen Arzt dar. Gekennzeichnet ist das IBS vor allem durch chronisch rezidivierende Abdominalschmerzen und Stuhlgangsunregelmässigkeiten, ohne dass in der Routinediagnostik eine dafür erklärende Pathologie gefunden werden kann. Die Ursachen für die Entstehung eines IBS scheinen multifaktoriell und sowohl intrinsischer als auch extrinsischer Natur zu sein. Im Zentrum der pathophysiologischen Alterationen stehen Veränderun
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Cohen-Haguenauer, Odile. "Prédisposition héréditaire au cancer du sein (1)." médecine/sciences 35, no. 2 (2019): 138–51. http://dx.doi.org/10.1051/medsci/2019003.

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L’oncogénétique a pour objectif principal de caractériser une sous-population à haut risque de développement de cancers à un âge précoce afin de préconiser les recommandations pour un parcours optimisé de suivi et de soins. La consultation d’oncogénétique contribue à évaluer un risque individuel à partir d’une histoire familiale. Par une approche familiale de génétique formelle, il s’agit de repérer les familles avec une forte agrégation de cancers, éventuellement évocatrice d’un syndrome de prédisposition héréditaire. Cette démarche peut conduire à la proposition d’un test génétique constitut
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Djaroud, Z., K. Terki, F. Benlebna, B. Boumédiene Zellat, and F. El Abed. "Lymphœdème et syndrome du bras douloureux après néo du sein opéré." Douleurs : Evaluation - Diagnostic - Traitement 13 (November 2012): A78—A79. http://dx.doi.org/10.1016/j.douler.2012.08.215.

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Tesis sobre el tema "Syndrome sein"

1

Limpas, Yvon. "Le POEMS syndrome : entité particulière au sein des dyscrasies plasmocytaires." Bordeaux 2, 1989. http://www.theses.fr/1989BOR25325.

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DI, MARCO JEAN-NOEL. "Le syndrome de kearns-sayre : situation actuelle au sein des mitochondriopathies." Aix-Marseille 2, 1990. http://www.theses.fr/1990AIX20005.

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Bonnaud-Antignac, Angélique. "Etude des réactions psychologiques face au Syndrome Douloureux Post-Mastectomie : une approche intégrative." Toulouse 2, 2000. http://www.theses.fr/2000TOU20054.

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Cette etude longitudinale, menee au centre regional de lutte contre le cancer de la gironde, a etudie les reactions cognitives et emotionnelles a la douleur postoperatoire de quatre-vingtdeux femmes traitees chirurgicalement pour un cancer du sein (tumorectomie ou mastectomie). Les resultats ont montre que la moitie des patientes presentaient un syndrome douloureux post-mastectomie a six mois postoperatoires et que les reactions cognitives et affectives a la douleur postoperatoire chronique etaient influencees par l'anxiete-trait et l'investissement corporel, deux caracteristiques psychologiqu
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Dury, Alain. "Étude de la compartimentalisation de sous-populations de la Fragile X Mental Retardation Protein au sein de la cellule." Doctoral thesis, Université Laval, 2017. http://hdl.handle.net/20.500.11794/27704.

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Le syndrome du X fragile, première cause de retard mental héréditaire, est une maladie monogénique liée au chromosome X. Le syndrome affecte environ un homme sur 4000 et une femme sur 6000 dans la population générale. Il est causé par l'inactivation du gène Fragile Mental Retardation 1 (FMR1) entraînant l'absence de la Fragile X Mental Retardation Protein (FMRP). Celle-ci est une protéine de liaison à l'ARN ayant pour rôle présumé de coordonner le devenir et la traduction d'un grand nombre d'ARN messagers (ARNm). L'absence de FMRP provoquerait une dérégulation subtile du transport des ARNm, co
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Leman, Raphaël. "Développement d'outils biostatisques et bioinformatiques de prédiction et d'analyse des défauts de l'épissage : application aux gènes de prédisposition aux cancers du sein et de l'ovaire." Thesis, Normandie, 2019. http://www.theses.fr/2019NORMC418/document.

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L’analyse des défauts d’épissage est particulièrement complexe. Outre la diversité des transcrits présents à l’état physiologique, les variations nucléotidiques peuvent induire des modifications hétéroclites de l’épissage. Ces variations, appelées variants splicéogéniques, et leur impact au niveau de l’épissage, sont à même de modifier plus ou moins sévèrement le phénotype de l’individu.Au cours de ce travail de thèse, nous nous sommes intéressés à trois grands aspects de l’étude des défauts de l’épissage : (i) la prédiction de ces défauts d’épissage, (ii) l’analyse des données de RNA-seq et (
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Le, Gall Anne. "Variabilite antigenique et genomique du virus du syndrome dysgenesique et respiratoire porcin. Relations phylogenetiques au sein des arterivirus." Rennes, Agrocampus Ouest, 1997. http://www.theses.fr/1997NSARB093.

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Le virus du syndrome dysgenesique respiratoire porcin (sdrp) est un virus a arn positif simple brin, appartenant a la famille des arteriviridae. La variabilite antigenique de ce virus a ete etudiee par la comparaison des profils epitopiques de 18 isolats viraux a l'aide d'un panel d'anticorps monoclonaux, obtenus au laboratoire ou genereusement offerts par des equipes etrangeres. Les hybridomes ont ete obtenus en testant differents protocoles de purification de virus, et en utilisant des modalites d'immunisation classiques ou visant a orienter la reponse immunitaire des souris. La variabilite
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DESHAYES, STEPHANE. "Le syndrome de de morsier kallmann ou dysplasie olfacto-genitale : revue de la litterature a propos de deux observations au sein de la meme fratrie." Rennes 1, 1992. http://www.theses.fr/1992REN1M012.

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Couillault, Coline. "Hétérogénéité et mécanismes d’initiation de la réponse humorale dans les tumeurs du sein et de l’ovaire." Thesis, Lyon, 2019. http://www.theses.fr/2019LYSE1051/document.

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Les lymphocytes B (LB) et les plasmocytes (PC) émergent comme des cellules importantes dans la surveillance immunitaire des tumeurs, même si leur rôle pro- ou anti-tumoral reste activement débattu. Nous avons émis l’hypothèse que cette dualité fonctionnelle de la réponse B pourrait être dictée par l'identité des sous-populations de LB infiltrant la tumeur et/ou par la nature des anticorps (Ac) qu’ils produisent. Dans ce contexte, nous avons montré que les tumeurs du sein et de l’ovaire sont souvent infiltrées par des LB mémoires et des PC exprimant/produisant principalement des IgG ou des IgA.
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Martin-Blondel, Guillaume. "Migration et pathogénicité des lymphocytes T CD8 au sein du système nerveux central." Toulouse 3, 2014. http://www.theses.fr/2014TOU30255.

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Le système nerveux central (SNC) bénéficie localement d'un statut immunologique privilégié contrôlant activement les réponses immunitaires potentiellement délétères. Une réponse immunitaire peut toutefois s'y développer au cours de maladies infectieuses ou inflammatoires. Le syndrome inflammatoire de restauration immunitaire (SIRI) est une situation particulière dans laquelle les dommages tissulaires peuvent être dus à l'agent infectieux lui-même, à la réponse immunitaire qu'il a engendrée, ou aux deux. Notre premier objectif était de préciser le rôle des lymphocytes T CD8 (LTCD8), acteurs cru
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Fagherazzi, Guy. "Facteurs alimentaires, composantes du syndrome métabolique et risques de cancer du sein et de diabète de type II dans la cohorte E3N." Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00718783.

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Le cancer du sein et le diabète de type II sont deux pathologies chroniques majeures chez la femme, qui sont suspectées de partager de nombreux facteurs de risque. Mais leurs étiologies demeurent encore partiellement inconnues,notamment en ce qui concerne certains facteurs alimentaires, ou encore certaines composantes du syndrome métabolique. Les données de la cohorte française E3Nont ainsi été utilisées pour évaluer les associations entre la consommation d'alcool, decafé, de viande, les apports en vitamine D et les risques de cancer du sein et dediabète de type II. De plus, s'il est avéré que
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Libros sobre el tema "Syndrome sein"

1

Brown, Phil. Toxic exposures: Contested illnesses and the environmental health movement. Columbia University Press, 2007.

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Irene, Diekmann, Schoeps Julius H. 1942-, and Moses Mendelssohn-Zentrum für Europäisch-Jüdische Studien., eds. Das Wilkomirski-Syndrom: Eingebildete Erinnerungen, oder, Von der Sehnsucht, Opfer zu sein. Pendo, 2002.

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Brandl, Katrin. Hans-guck-in-die-Luft und Zappelphilipp in Musikschule und allgemein bildender Schule: Medizinische Grundlagen, heilpädagogische und soziale Aspekte des Aufmerksamkeitsdefizit/Hyperaktivititäts-Syndroms und seine Beeinflussbarkeit durch Musikerziehung. Musikverlag Muth, 2004.

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Brown, Phil. Toxic Exposures. Columbia University Press, 2007.

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Dionisi-Vici, Carlo, Diego Martinelli, Enrico Bertini, and Claude Bachmann. HHH Syndrome. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0020.

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Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is an autosomal recessive disorder of the urea cycle characterized by impaired transport of ornithine across the inner mitochondrial membrane. As seen in other urea cycle defects, in the acute phase the disease is characterized by intermittent episodes of hyperammonemia accompanied by vomiting, lethargy, and coma, with or without signs of acute liver failure. The disease course is characterized by a pyramidal tract dysfunction associated with myoclonic seizures and cerebellar symptoms. Most patients reaching adulthood manifest v
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Heidet, Laurence, Bertrand Knebelmann, and Marie Claire Gubler. Alport syndrome. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0322_update_001.

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This chapter describes the clinical features of Alport syndrome. The characteristic features of this familial condition are haematuria with progressive nephropathy and sensorineural hearing loss. Most cases are X-linked so this is typically seen in boys and young men, but female heterozygous (‘carriers’) of X-linked Alport syndrome are also at significant risk of renal disease in their lifetime. The average age of end-stage renal failure is in the third or fourth decade. Those with autosomal recessive disease (approximately 15%) show a similar phenotype. Hearing loss characteristically develop
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Pitt, Matthew. Nerve damage and entrapment syndromes. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0005.

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In this chapter, the pathological classification of nerve damage using the Sunderland classification is described. The neurophysiological findings that allow distinction between neurapraxia, axonotmesis, and neurotmesis are highlighted. Nerve entrapment syndromes involving the upper and lower limb are discussed according to the nerve involved, with particular emphasis on those commonly seen in children. In the upper limb, median, ulnar, and radial nerve entrapments are described with particular emphasis on the carpal tunnel syndrome in mucopolysaccharidosis. Also mentioned here are the thoraci
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Rajakrishna, Premil, Stewart Cameron, and Neil Turner. Nephrotic syndrome. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0052.

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Nephrotic syndrome is the constellation of manifestations seen in patients with such severe proteinuria that serum albumin falls below normal levels. Its severity and the risk of complications are graded by the severity of the protein loss. The risks of some complications begin to rise at levels of proteinuria below those conventionally associated with nephrotic syndrome. The main manifestation, oedema, is characterized by avid sodium retention and managed by sodium restriction and diuretics. A pronounced thrombotic tendency is particularly apparent within the first 6 months of diagnosis and i
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Niaudet, Patrick, and Alain Meyrier. Idiopathic nephrotic syndrome. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0054_update_001.

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Idiopathic nephrotic syndrome is defined by the combination of massive proteinuria, hypoalbuminaemia, hyperlipidaemia, and oedema, and of non-specific histological abnormalities of the glomeruli. Light microscopy may disclose minimal change disease, diffuse mesangial proliferation, or focal segmental glomerular sclerosis (FSGS). The two main causes of idiopathic nephrotic syndrome are characterized histologically. On electron microscopy the glomerular capillaries show a fusion of visceral epithelial cell (podocyte) foot processes and with the exception of some variants no significant deposits
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Yurdakul, Sebahattin, Emire Seyahi, and Hasan Yazici. Behçet’s syndrome. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0135.

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Behçet's syndrome is a systemic inflammatory panvasculitis (affecting all sizes of vessels) of unknown aetiology. It is in vogue to include it among the systemic autoinflammatory conditions. Behçet's syndrome is more frequent along the ancient 'Silk Route' across Asia than it is in Western countries. The usual onset is the second or third decade, equally affecting either gender. However, young patients and male patients have more severe disease. Almost all patients have recurrent oral ulceration. Scar-forming genital ulcers, a variety of skin lesions including acneiform, erythema nodosum-like
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Capítulos de libros sobre el tema "Syndrome sein"

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Wallhult, Elisabeth, Michelle Kenyon, and Barry Quinn. "Early and Acute Complications and the Principles of HSCT Nursing Care." In The European Blood and Marrow Transplantation Textbook for Nurses. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-23394-4_10.

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AbstractHaematopoietic stem cell transplantation (HSCT) generally includes preparative or conditioning regimens containing combinations of chemotherapy and/or radiotherapy and sometimes immunotherapy. These regimens, as well as other treatments before and after HSCT such as immunosuppressive drugs to prevent graft-versus-host disease (GvHD) (see Chap. 11), may affect the patient’s organs and tissues and cause both early and long-term complications. In the evolving field of stem cell therapies, some complications that traditionally have been regarded as early complications are now, due to chang
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2

Niklas, F. "Das BWS-Syndrom und seine physiotherapeutische Behandlung." In Brustwirbelsäulenerkrankungen, Engpaßsyndrome, Chemonukleolyse, Evozierte Potentiale. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70562-5_24.

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Shapiro, Daniel I., Huijun Li, and Larry J. Seidman. "Attenuated Psychosis Syndromes Seen Through the Cultural Prism: Relevance, Terminology, and Book Structure." In Handbook of Attenuated Psychosis Syndrome Across Cultures. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-17336-4_1.

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Chavoin, J. P., L. Foucras, A. Chichery, B. Chaput, A. André, and J. L. Grolleau. "Sein et syndrome de Poland." In Chirurgie Plastique et Reconstructive du Sein. Elsevier, 2012. http://dx.doi.org/10.1016/b978-2-294-71374-3.00009-x.

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Abou-Khalil, Bassel. "Select Epilepsy Syndromes Seen in Adulthood." In Atlas of EEG, Seizure Semiology, and Management, edited by Karl E. Misulis, Hasan H. Sonmezturk, Kevin C. Ess, and Bassel Abou-Khalil. Oxford University Press, 2022. http://dx.doi.org/10.1093/med/9780197543023.003.0011.

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Select epilepsy syndromes can begin in childhood but are also seen in adulthood. Among these are the family of absence epilepsies, generalized tonic-clonic seizures, Lennox-Gastaut syndrome, and a host of focal epilepsy syndromes. This chapter discusses the clinical features of many of these epilepsy syndromes.
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Clark, Robin D., and Cynthia J. Curry. "Overgrowth." In Genetic Consultations in the Newborn, edited by Robin D. Clark and Cynthia J. Curry. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780199990993.003.0003.

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This chapter reviews information on disorders that cause large birth weight, macrosomia, and/or segmental overgrowth. The most common of these conditions is seen in infants of diabetic mothers. Abnormal dosage of growth regulating genes make chromosomal microarray abnormalities a relatively common cause of overgrowth. Particularly notable is the distinctive Pallister Killian syndrome (12p tetrasomy). Other common overgrowth syndromes include Beckwith-Wiedemann syndrome, Sotos, Malan, and Weaver syndromes. The RASopathy syndromes including Noonan syndrome* and Costello syndrome are also often l
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"Seip syndrome." In Dermatology Therapy. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_2458.

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Gagliardi, Francesco. "A Cognitive Machine-Learning System to Discover Syndromes in Erythemato-Squamous Diseases." In Advances in Healthcare Information Systems and Administration. IGI Global, 2014. http://dx.doi.org/10.4018/978-1-4666-4619-3.ch005.

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A syndrome is a set of typical clinical features that appear together often enough to suggest they may represent a single, as yet unknown, disease. The discovery of syndromes and relative taxonomy formation is the critical early phase of the process of scientific discovery in the medical domain. The author proposes a machine learning system to discover syndromes (seen as prototypes of clinical cases) that is based on the Eleanor Rosch’s prototype theory on how the human mind categorizes and infers prototypes from observations. A comparison on a case study in erythemato-squamous diseases of the
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Rousset-Jablonski, C. "Contraception et prédispositions génétiques au risque de cancer du sein et/ou de l'ovaire (hors syndrome de Lynch)." In La contraception en pratique. Elsevier, 2024. http://dx.doi.org/10.1016/b978-2-294-78270-1.00033-8.

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Desai, Geetha, Santosh K. Chaturvedi, and Dinesh Bhugra. "Cultural Spectrum of Chronic Pain and Somatization Syndromes." In Overlapping Pain and Psychiatric Syndromes, edited by Geetha Desai, Santosh K. Chaturvedi, and Dinesh Bhugra. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190248253.003.0027.

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Chronic pain and somatization are common reasons for consultation in health settings, including psychiatric services, in India. These are often manifestations of underlying psychiatric illnesses such as depression, anxiety, and other stress-related disorders. Assessment of chronic pain and somatization is essential because it may be a means for the patient to communicate psychological distress, arising out of stress and conflicts within the environment. Sociocultural factors have an important role in the manifestations, help-seeking, and management of these chronic pain and somatizing syndrome
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Actas de conferencias sobre el tema "Syndrome sein"

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Polychronidou, Eleftheria, Ilias Kalamaras, Kostantinos Votis, and Dimitrios Tzovaras. "Towards visualizing primary Sjögren's Syndrome data from heterogeneous cohorts." In SETN '18: 10th Hellenic Conference on Artificial Intelligence. ACM, 2018. http://dx.doi.org/10.1145/3200947.3201040.

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Cracco, Luiz Augusto Fanhani, Marian Hanae Oda, Gustavo Koíti Kondo, et al. "ANTI-GLOMERULAR BASEMENT MEMBRANE DISEASE (GOODPASTURE SYNDROME) COMMONLY REMEMBERED BUT RARELY SEEN." In XL Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2023. http://dx.doi.org/10.47660/cbr.2023.1974.

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Admire, K. J., S. S. Aleem, A. N. Mahendra, S. Pourshahid, T. Uchel, and M. R. Cossio. "Air Space Jam: Vanishing Lung Syndrome Seen in a Competitive Basketball Player." In American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a2048.

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Kokikian, Collette, Ann Ly, and Lama Al-Khoury. "A rare case of Carotid Dissection seen in Vascular Eagle Syndrome (P3-5.024)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000203428.

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Li, Jianhua, Yueyang Teng, Shouliang Qi, et al. "Pancreatic malformations as seen in congenital syndromes — Developmental perspective with an alternative view." In 2016 IEEE International Conference on Information and Automation (ICIA). IEEE, 2016. http://dx.doi.org/10.1109/icinfa.2016.7831910.

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Aragon, Jose Gerald, Mohammed A. Rattu, Alex Gechlik, Nicholas Coan, James A. Espinosa, and Alan Lucerna. "Brief Review: The Refeeding Syndrome." In 28th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2024. https://doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.88_2024.

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Here we briefly review the definition, epidemiology, pathophysiology, clinical risk scenarios, prevention and treatment of the refeeding syndrome. Refeeding syndrome is a condition which arises when a severely malnourished individual has been restarted with increased nutrition in a relatively short period of time. The refeeding process can lead to shifts in a number of fluids and electrolytes. The hallmark feature is hypophosphatemia. The true incidence of refeeding syndrome is unknown. This is said to be partly due to the lack of a universally accepted definition. Populations that are likely
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Diaz, C., C. Geli, C. Diaz-Torne, et al. "FRI0230 Clinical presentation of 475 patients with primary sjÖgren’s syndrome who where seen by the rheumatologists." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.323.

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Gurian, Jordana Gaudie, Maria Ondina Machado Diniz, Amanda Nascimento Bispo, Aline Boaventura Ferreira, Fernando Elias Borges, and Ane Cristina Dunck. "Case report: stiff Person syndrome." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.346.

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Introduction: The rigid person syndrome is rare, characterized by blockade of the GAD enzyme, responsible for inhibiting muscle contraction. Although it is not mandatory for the diagnosis, most patients are positive for Anti-GAD. Objectives: To report a case of rigid person syndrome seen at Hospital Geral de Goiânia. Methods: Information was obtained through clinical follow-up in a neurology ward and outpatient clinic. Results: Patient, female, 32 years old, complaining of paresthesia ascending to upper limbs, worsening over a period of six months with paresis with gait impairment, increased t
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Monteiro, Ana Karoline da Costa, Paulo Filho Soares Marcelino, Marcello Holanda de Andrade, Rairis Barbosa Nascimento, Marx Lincoln Lima de Barros Araújo, and Samuel Pinheiro da Silva. "Fahr’s Syndrome: A Case Report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.110.

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Context: Fahr’s syndrome is a clinical entity of primary or secondary causes characterized by neurological and/or psychiatric symptoms associated with abnormal calcifications in basal ganglia, cerebellum and cerebral cortex. Case report: G.M.A, female, 49 years-old, presented athetosis in the distal extremity of the right upper limb (RUL) in December 2020, without seeking for medical help. Known to be diabetic, hypertensive and with diastolic heart failure (HF), in February 2021 she presented decompensated HF associated with worsening of involuntary movements in the RUL. During investigation,
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Gupta, Swati, Saritha Shamsunder, Roli Purwar, et al. "Growing teratoma syndrome: A case report." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685323.

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Introduction: Growing teratoma syndrome (GTS) or chemotherapeutic retro conversion is an extremely rare phenomenon seen in about 1.9-7.6% of patients being treated for non-seminomatous testicular germ cell tumor. It is even more rarely reported in females with only sporadic cases reported so far. It was described by logothetis et al and is described as conversion of immature teratoma to mature one after chemotherapy and presents as growing and metastasizing mass. Case Report: We report a case of 10 year old girl who underwent conservative surgery for an adnexal mass reported as immature terato
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Informes sobre el tema "Syndrome sein"

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Teja, Dr K. Pavana, Dr B. Indira, and Dr Blessy Manohar. YOUNGS SYNDROME - A RARE INHERITED SYNDROME IN YOUNG MALE ADULTS. World Wide Journals, 2023. http://dx.doi.org/10.36106/ijar/5408129.

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Youngs syndrome also known as azoospermia sinopulmonary infections,sinusitis -infertility syndrome and Barry - Perkins -Young syndrome is a rare, inherited syndrome commonly seen in middle aged men with chronic reccurent rhinosinusitis, bronchiectasis, infertility due to azoospermia. Diagnosis of youngs syndrome is based on the occurrence of early onset progression in adult life with the presence of clubbing, sinusitis, and cystic bronchiectasis1.Azoospermia is seen due to hypomotility and decreased sperm count.
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Whitaker, Stephen. Rocky intertidal community monitoring at Channel Islands National Park: 2018–19 annual report. National Park Service, 2023. http://dx.doi.org/10.36967/2299674.

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Channel Islands National Park includes the five northern islands off the coast of southern California (San Miguel, Santa Rosa, Santa Cruz, Anacapa, and Santa Barbara Islands) and the surrounding waters out one nautical mile. There are approximately 176 miles of coastline around the islands, about 80% of which is composed of rock. The diversity and undisturbed nature of the tidepools of this rocky coastline were recognized as special features of the islands in the enabling legislation. To conserve these communities unimpaired for future generations, the National Park Service has been monitoring
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