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Dissertations / Theses on the topic 'Arnold Chiari type I malformation'

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Published: 5 June 2025

Last updated: 2 August 2025

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1

Richards, Rachel. "Morphometric-Based Classification For Chiari Malformation Type I." University of Akron / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=akron1438941369.

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2

NOVELLO, GUY. "L'echographie trans-fontanellaire chez les enfants porteurs d'une myelomeningocele." Limoges, 1988. http://www.theses.fr/1988LIMO0151.

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3

Shaffer, Nicholas. "A Study of Impedance to Cerebrospinal Fluid Flow in Type I Chiari Malformation." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1301674180.

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4

Nwotchouang, Blaise Simplice Talla. "SKULL-BASED MORPHOMETRICS AND BRAIN TISSUE DEFORMATION CHARACTERIZATION OF CHIARI MALFORMATION TYPE I." University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1595877233083287.

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5

Shaffer, Nicholas. "Magnetic Resonance Image-Based Hydrodynamic Analysis of Cerebrospinal Fluid Motion in Type I Chiari Malformation." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1417545898.

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6

VIDAL, Claudio Henrique Fernandes. "Tratamento cirurgico da malformação de Chiari do tipo I:importância da abertura do forame de Magendie e ressecção das tonsilas." Universidade Federal de Pernambuco, 2014. https://repositorio.ufpe.br/handle/123456789/17973.

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Submitted by Natalia de Souza Gonçalves (natalia.goncalves@ufpe.br) on 2016-10-10T12:57:26Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) CLAUDIO VIDAL - COLACAO.pdf: 6023190 bytes, checksum: d165c8659f0d2b209cb4a7a228a33bd7 (MD5)<br>Made available in DSpace on 2016-10-10T12:57:26Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) CLAUDIO VIDAL - COLACAO.pdf: 6023190 bytes, checksum: d165c8659f0d2b209cb4a7a228a33bd7 (MD5) Previous issue date: 2014-06-13<br>A alta prevalência de malformação da

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7

Rodrigues, Andre Broggin Dutra. "Marcadores prognósticos em recém-nascidos portadores de mielomeningocele." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-20062016-144207/.

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Introdução: Pacientes com mielomeningocele apresentam elevada mortalidade e desenvolvem déficits neurológicos que ocorrem, primariamente, pelo desenvolvimento anormal da medula e de raízes nervosas e, secundariamente, por complicações adquiridas no período pós-natal. O desafio no cuidado desses pacientes é o reconhecimento precoce dos recém-nascidos de risco para evolução desfavorável a fim de estabelecer estratégias terapêuticas individualizadas. Objetivo: Este estudo tem como objetivo identificar marcadores prognósticos de curto prazo para recém-nascidos com mielomeningocele. As característi

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8

Eppelheimer, Maggie S. "Identification of Chiari Malformation Type I Brain Morphology and Biomechanics: A Multi-Faceted Approach to Determine Diagnostic and Treatment Criteria." University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1595680107882868.

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9

OLIVEIRA, FILHO Marcos Antonio Inacio de. "Cefaleia de esforço em pacientes com má-formação de Chiari tipo I: características anatômicas da fossa posterior e junção crânio-cervical." Universidade Federal de Pernambuco, 2016. https://repositorio.ufpe.br/handle/123456789/18642.

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Submitted by Fabio Sobreira Campos da Costa (fabio.sobreira@ufpe.br) on 2017-04-26T15:31:25Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) TESE COMPLETA - MARCOS ANTONIO INACIO DE OLIVEIRA FILHO.pdf: 2169493 bytes, checksum: e337756cb83d4d2819ca9c84d87d318c (MD5)<br>Made available in DSpace on 2017-04-26T15:31:25Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) TESE COMPLETA - MARCOS ANTONIO INACIO DE OLIVEIRA FILHO.pdf: 2169493 bytes, checksum: e337756cb83d4d2819ca9c84d87d318c (MD5) Previo

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10

Urbizu, Serrano Aintzane. "Bases genètiques en la malformació de Chiari tipus i." Doctoral thesis, Universitat de Barcelona, 2013. http://hdl.handle.net/10803/145244.

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La malformació de Chiari de tipus I (MCI) s'ha definit tradicionalment com una alteració congènita caracteritzada pel descens de les amígdales cerebel.loses a travès del forat magne en 3 o més mm. Es creu que és conseqüència d'una fosa cranial posterior (FCP) hipoplàstica, amb un os occipital anormalment curt, que resulta d'un mesoderma paraxial insuficient. La simptomatologia descrita pels pacients és molt variada: mals de cap occipitals, cervicàlgies, marejos, vertígens, pèrdua de sensibilitat i de força a les extremitats, alteracions de la son i problemes en la deglució entre d'altres, atri

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11

Moncho, Rodríguez Dulce María. "Estudio neurofisiológico mediante potenciales evocados auditivos de tronco cerebral y somatosensoriales en pacientes con malformación de Chiari tipo 1." Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/399570.

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La malformación de Chiari de tipo 1 (MC-1) es una anomalía congénita de la charnela craneo-cervical, descrita por primera vez por Chiari como un desplazamiento de las amígdalas del cerebelo hacia el canal raquídeo. El diagnóstico neurorradiológico clásico de esta entidad exige un descenso amigdalar de más de 3-5 mm por debajo del foramen magnum (FM). La teoría etiopatogénica más aceptada sugiere que estos pacientes presentan una reducción patológica del volumen de la fosa posterior (FP). El descenso de las amígdalas cerebelosas dificulta el paso de líquido cefalorraquídeo a través de la unión

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12

Mestres, i. Soler Olga. "Repercusiones de la malformación de Chiari 1 en la calidad de vida del paciente." Doctoral thesis, Universitat de Barcelona, 2015. http://hdl.handle.net/10803/318809.

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La malformación de Chiari tipo 1 (MC-1) es una patología congénita de baja prevalencia codificada dentro del grupo de enfermedades raras. Se define por la presencia de una herniación de las amígdalas del cerebelo por debajo del foramen magnum. Las manifestaciones clínicas de la MC-1 son muy variables, aunque las más frecuentes son las cefaleas occipitonucales, que aumentan con el esfuerzo y las maniobras de Valsalva, parestesias, debilidad en las extremidades, vértigos, cansancio y alteraciones respiratorias durante el sueño, entre otras. Su evolución viene determinada en gran parte por las pa

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13

Brock, Roger Schmidt. "Ultrassonografia intraoperatória para avaliação da necessidade de duroplastia no tratamento cirúrgico de doentes com malformação de Chiari tipo I." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-28072017-093016/.

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Objetivos: Malformação de Chiari do tipo I (MC-I) é a principal doença malformativa congênita da junção craniovertebral, manifestando-se com ampla variedade de sinais e sintomas neurológicos. A melhor técnica cirúrgica a ser empregada no tratamento dos pacientes com malformação de Chiari do tipo I é ainda controversa. A descompressão das estruturas da fossa craniana posterior com plástica de ampliação dural é considerada procedimento padrão. Embora efetiva e de baixa morbidade, a craniectomia occipital isolada, sem abertura e ampliação dural, implica maior taxa de recidiva dos sintomas. Método

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14

Salman, Michael S. "Saccades and saccadic adaptation in children with spina bifida and Arnold-Chiari type II malformation." 2004. http://link.library.utoronto.ca/eir/EIRdetail.cfm?Resources__ID=80315&T=F.

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15

Jesus, Ana Rita Patrocínio de. "Spring mediated cranial vault expansion in infants : an alternative treatment for symptomatic multisutural craniosynostosis associated Chiari malformation type I." Master's thesis, 2015. http://hdl.handle.net/10451/24907.

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Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Lisboa, 2015<br>Chiari malformation type 1 is a frequent finding in patients with craniosynostosis. The performance of suboccipital decompression as a standard treatment has been progressively questioned. Two symptomatic patients presenting multiple suture craniosynostosis associated Chiari malformation type 1 underwent cranial vault expansion using spring-mediated distraction at an early age (at 2 and 6 weeks). A complete resolution of Chiari symptoms was observed postoperatively and the postope

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16

Markunas, Christina Ann. "Genetic Dissection of Chiari Type I Malformation." Diss., 2013. http://hdl.handle.net/10161/7128.

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<p>Chiari Type I Malformation (CMI) is a developmental disorder characterized by displacement of the cerebellar tonsils below the base of the skull, resulting in significant neurologic morbidity. While there are multiple proposed mechanisms for tonsillar herniation, "classical" CMI is thought to occur due to a compromised posterior cranial fossa (PF). As CMI patients display a high degree of clinical variability, it is hypothesized that this heterogeneous disorder has a complex etiology influenced by multiple genetic and environmental factors. Despite the fact that multiple lines of eviden

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17

Stahl, Kerstin. "Auswirkung zentraler Apnoen auf die zerebrale Oxygenierung bei Kindern mit Chiari-II-Malformation, gemessen mit der Nahinfrarot-Spektroskopie." Doctoral thesis, 2011. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-66004.

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Das Ziel dieser Studie lag darin, die Auswirkung zentraler schlafbezogener Atemstörungen (zSBA) auf die zerebrale Oxygenierung bei Kindern mit Meningomyelozele (MMC) und Chiari-II-Malformation zu untersuchen. Im Schlaflabor der Universitäts-Kinderklinik Würzburg wurden Kinder mit MMC und Chiari-II-Malformation, bei denen zuvor eine zentrale Atemstörung diagnostiziert worden war, polysomnographisch untersucht. Zusätzlich zur standardisierten Polysomnographie (PSG) wurde die zerebrale Sauerstoffsättigung mittels Nahinfrarotspektroskopie (NIRS) abgeleitet. Die Nahinfrarotspektroskopie ermöglicht

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18

Lemay, Philippe. "Malformation Chiari-Like : l’investigation d’une maladie complexe par l’utilisation d’un modèle canin." Thèse, 2012. http://hdl.handle.net/1866/8575.

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La malformation de Chiari type 1 (MCI) est une anomalie congénitale de la jonction cranio-cérébrale fréquente avec une incidence de 1:1280. MCI est caractérisée par la descente des amygdales cérébelleuses à travers le foramen magnum et est souvent associée à la syringomyélie. Les causes de cette maladie semblent être multifactorielles incluant des facteurs génétiques. La MCI est similaire à une malformation fréquente chez la race des Griffon Bruxellois (GB) connue sous le nom de Malformation Chiari-like (MCL). Le modèle canin offre l’avantage d’une forte homogénéité génétique réduisant ainsi l

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