Relevant bibliographies by topics / Macroglosia

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Macroglosia'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Macroglosia"

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Benavente-Fernández, A., H. Husein-El Ahmed, and A. Romero-Ortiz. "Macroglosia." Revista Clínica Española 215, no. 7 (2015): 415. http://dx.doi.org/10.1016/j.rce.2015.02.014.

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Rivas-Nieto, Andrea C., and Germán Málaga. "Macroglosia." Revista Medica Herediana 23, no. 4 (2012): 263. http://dx.doi.org/10.20453/rmh.v23i4.850.

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Martínez, Laura Pilar. "Macroglosia: Etiología multifactorial, manejo múltiple." Colombia Medica 37, no. 1 (2006): 67–73. http://dx.doi.org/10.25100/cm.v37i1.414.

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Calvo Hernadez, Luz Marina, Eduardo Riol López, Luis Peña Ferrera, and Rosa Apolinario Hidalgo. "Macroglosia secundaria a enfermedad de Madelung." Medicina Clínica 147, no. 10 (2016): e59. http://dx.doi.org/10.1016/j.medcli.2016.03.045.

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Albarrán-Planelles, Cristina, David Jiménez-Gallo, Mario Linares-Barrios, and Jose María Báez-Perea. "Macroglosia como manifestación de amiloidosis primaria." Piel 29, no. 3 (2014): 196–97. http://dx.doi.org/10.1016/j.piel.2013.06.014.

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Diéguez, Antoni Monner. "Macroglosia y el síndrome de Down." Revista Médica Internacional sobre el Síndrome de Down 12, no. 2 (2008): 17. http://dx.doi.org/10.1016/s1138-2074(08)70019-8.

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ROSADO COELLO, LINDEMBERTH, PRISCILLA NAVARRETE ROSADO, and FERNANDO MONCAYO ASNALEMA. "TRAUMA LINGUAL COMO COMPLICACIÓN DE MACROGLOSIA DE COVID-19: CASO CLÍNICO." REVISTA FACULTAD DE CIENCIAS MÉDICAS 4, no. 2 (2023): 17–21. http://dx.doi.org/10.53591/10.53591revfcm.v4i2.2582.

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La macroglosia en la hipertrofia del órgano (lengua) generalmente sin deformación, aunque en algunas ocasiones puede presentar cierta alteración en su forma. Los diferentes patólogos están de acuerdo en que no todos los elementos que forman la lengua se hipertrofian sino se realiza a expensas de dos tejidos: el linfático y el muscular con esclerosis del tejido conjuntivo. La aparición de la covid-19 nos ha llevado a encontrar síntomas no comunes en cierto tipo de pacientes, como el que mostraremos a continuación, paciente en el que se puede describir la macroglosia no tanto como un síntoma sin
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Gómez-Piña, Juan José, Dulce Mariana Quiroz, Amairani Sierra-Hernández, Sergio Alberto Mendoza-Álvarez, and Olga Lidia Vera-Lastra. "[Giant tongue leading to dysphagia in light chain amyloidosis patient]." Revista Médica el Instituto Mexicano del Seguro Social 61, no. 6 (2023): 863–67. https://doi.org/10.5281/zenodo.10064470.

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<strong>Abstract</strong><strong>Introduction:</strong> Macroglossia as a clinical manifestation of systemic amyloidosis is a rare condition, occurring in less than 9% of all types of amyloidosis. The aim of this report is to present the diagnostic approach of a patient with macroglossia, providing a systematic approach and considering relevant diagnostic possibilities during their evaluation.<strong>Clinical case:</strong> We present the case of a 60-year-old man who presented with a progressively enlarging giant tongue for six months, causing dysphagia and reduced oral opening. A tongue biop
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Molinos Castro, S., P. M. Pesqueira Fontán, J. A. Díaz Peromingo, and A. Lirola Delgado. "Shoulder pad y macroglosia: dos signos de amiloidosis." Revista Clínica Española 209, no. 10 (2009): 521–22. http://dx.doi.org/10.1016/s0014-2565(09)72641-4.

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Acosta-Aragón, María A., Álvaro Narváez-Gómez, and Oscar Ramirez-Wurttemberg. "Tratamiento de mucopolisacaridosis tipo I con trasplante de células madre de sangre de cordón umbilical de donante no emparentado: informe del primer caso exitoso en Colombia." Medicina y Laboratorio 21, no. 9-10 (2015): 445–54. http://dx.doi.org/10.36384/01232576.140.

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Se presenta el primer caso exitoso en Colombia de trasplante de células madre de sangre de cordón umbilical no relacionadas, en un niño de 30 meses de edad con diagnóstico de mucopolisacaridosis tipo I. El paciente fue recibido a los seis meses de edad por presentar signos y síntomas típicos de la enfermedad, por lo que se realizó confirmación diagnóstica por bioquímica y se determinó la mutación genética. Se inició terapia de reemplazo enzimático con laronidasa a los 13 meses de edad y se llevó a cabo un trasplante de sangre de cordón umbilical de un donante no emparentado a los 30 meses, alc
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Dissertations / Theses on the topic "Macroglosia"

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GIULIETTI, FEDERICO. "Predictors of moderate and severe obstructive sleep apnea and association of nocturnal oximetry parameters with cardiovascular organ damage." Doctoral thesis, Università Politecnica delle Marche, 2022. https://hdl.handle.net/11566/295289.

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Introduzione: L’apnea ostruttiva nel sonno (OSA) colpisce quasi un miliardo di persone nel mondo, con prevalenza crescente. La maggior parte del rischio di morbilità e mortalità associato all'OSA è legato ad aumentato rischio di sviluppo e/o progressione di malattie cardiovascolari (CV). Il marker più usato per definire sia gravità di malattia che rischio di danno d'organo è l'indice-apnea-ipopnea (AHI). La ricerca di predittori di OSA è in continuo sviluppo. Lo scopo di questo studio è stato valutare i predittori di malattia di grado moderato e grave in un ampio campione non selezionato di pa
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Coutinho, Maria da Cunha. "Macroglossia como manifestação de amiloidose : caso clínico." Master's thesis, 2014. http://hdl.handle.net/10451/24369.

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Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Lisboa, 2014<br>Amyloidosis is any of a group of conditions caused by extracellular deposition of insoluble protein fibres polymer [1] . The amyloid has a regular β-structure, that makes it insoluble and gives it the ability to show a characteristic green birefringence to microscopy with polarized light, when stained with Congo red.[1] Amyloid diseases are defined by biochemical nature of the amyloid protein. There are at least 18 types of proteins that can form amyloid deposits. These protein
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Caron, Paré Eugénie. "Manifestations orales du syndrome de Beckwith-Wiedemann." Thèse, 2017. http://hdl.handle.net/1866/20376.

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Book chapters on the topic "Macroglosia"

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Alshafei, Abdulrahman, and Thambipillai Sri Paran. "Macroglossia." In Pediatric Surgery. Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/978-3-662-43588-5_43.

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Alshafei, Abdulrahman, and Thambipillai Sri Paran. "Macroglossia." In Pediatric Surgery. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-642-38482-0_43-1.

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Teiga, Pedro Saraiva, Kishore Sandu, and Lluís Nisa. "Macroglossia." In Neonatal Surgery. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-93534-8_7.

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Inai, Kei, Alexander K. C. Leung, Jouni Uitto, et al. "Exomphalos-Macroglossia-Gigantism Syndrome." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_7213.

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Kruijt Spanjer, E. C., and R. J. J. van Es. "Chirurgische behandeling van macroglossie." In Het tandheelkundig jaar 2016. Bohn Stafleu van Loghum, 2015. http://dx.doi.org/10.1007/978-90-368-0889-7_17.

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Napolitano, Marcello, Alice Munari, Anna Ravelli, and Anna Venegoni. "Congenital Subcutaneous Mixed Venous-Lymphatic Orofacial Malformation Associated with Macroglossia: Prenatal Diagnosis with Ultrasound and Fetal MRI." In Prenatal Diagnosis of Orofacial Malformations. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-32516-3_14.

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"Macroglossia." In Diagnostic Imaging: Obstetrics. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39256-3.50088-1.

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"Macroglossia." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_9725.

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Youngson, George. "Macroglossia." In Newborn Surgery 3E. CRC Press, 2011. http://dx.doi.org/10.1201/b13478-29.

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"Macroglossia." In Newborn Surgery 3E. CRC Press, 2011. http://dx.doi.org/10.1201/b13478-32.

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Conference papers on the topic "Macroglosia"

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Wilkinson, J., C. E. Drolen, P. Y. Beah, I. Barjaktarevic, and S. S. Oh. "Hirudotherapy in the Management of Post-Intubation Macroglossia." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a2984.

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Tieppo, Eduardo Macedo de Souza, Miriam Eva Koch, and Alzira Alves de Siqueira Carvalho. "A deletion in CFL-2 gene associated with Severe Nemaline Myopathy with peculiar features." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.362.

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Context: Nemaline myopathy (NM) is the most common congenital myopathy characterized by muscle weakness and presence of nemaline bodies (rods) in muscle biopsy. Phenotype ranges from neonatal death to normal lifespan. 13 genes have been reported. We describe a new variant in cofilin 2 gene (CFL2;OMIM*601443). Case report: A 5-year-old boy born severely hypotonic and unable to breathe, in need of mechanic ventilation. Healthy non-consanguineous parents. Physical examination: severe hypotonia with only extraocular motricity preserved and multiple contractures. Dysmorphic features were observed a
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Watts, A., B. Duong, C. Pham, M. Baig, and M. F. Zaidan. "Acute Disseminated Encephalomyelitis and Macroglossia in COVID-19-Infected Patient: A Case Report." 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.a1647.

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Bosselmann, Stephan, Angela Lihs, and Gunther Mielke. "Prenatal presentation of pseudo-macroglossia caused by a tongue fibroma as the only sign of neurofibromatosis type 1." In 46. Dreiländertreffen der DEGUM in Zusammenarbeit mit ÖGUM & SGUM. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1772340.

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PONOMARI, Dorina. "The specifics of phonetic-phonematic disorders in children with Down syndrome." In Ştiință și educație: noi abordări și perspective", conferinţă ştiinţifică internaţională. Ion Creangă Pedagogical State University, 2024. https://doi.org/10.46727/c.v1.21-22-03-2024.p327-333.

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Language presents an important faculty that makes possible the insertion of the child into the environment. One of the important components of the language is the phonetic-phonematic one, pronunciation skills evolve with age and allow the child to interact with those around them, to expand the vocabulary, to train the correct model of expression, so the language develops. In the case of genetic conditions, namely Down Syndrome, the phonetic-phonemic side is deeply affected, which slows down the evolution of language and communication. The underdevelopment of the phonetic-phonemic side in child
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Rocha, Maria Eduarda Araújo Machado da, Andrey Luis de Oliveira Gonçalves Dias, and Nilson Ramirez de Jesus. "Síndrome em espelho associada a síndrome de Beckwith-Wiedemann fetal: um relato de caso." In 45º Congresso da SGORJ XXIV Trocando Ideias. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/jbg-0368-1416-20211311209.

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Introdução: A síndrome em espelho (SE) é uma condição materna rara, definida pela tríade hidropsia fetal, hidropsia placentária e edema materno generalizado. Neste relato, descrevemos um caso de SE associada à síndrome de Beckwith-Wiedemann (SBW), uma anomalia congênita rara. Foi atribuída a expressão “síndrome em espelho” pelo fato de o edema materno refletir o edema fetal. Pode ocorrer em qualquer período da gravidez, mas é mais comum no final do segundo e no início do terceiro trimestre. Está associada a elevada morbimortalidade materna e perinatal. Sua etiopatogenia é variada, e a maioria
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