Relevant bibliographies by topics / Mucovisidosis

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Mucovisidosis'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Mucovisidosis"

1

"Dépistage néonatal de la mucovisidose." Revue Française des Laboratoires 2000, no. 326 (2000): 14. http://dx.doi.org/10.1016/s0338-9898(00)80048-7.

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2

Balasubramanian, Thiagarajan. "Nasal polyposis in children." Otolaryngology online, June 19, 2017. https://doi.org/10.5281/zenodo.811157.

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Abstract:
This article discusses various causative factors of nasal polyposis in children. It is a review of literature on this subject, supplemented by the author's personal experience. Even though nasal polyposis is rather uncommon in children, when present they should be throughly investigated to rule out other sinister lesions. Imaging has a vital role to play in diagnosis of these patients. Antrochonal polyp is currently the commonest nasal polyp seen in children. This record was migrated from the OpenDepot repository service in June, 2017 before shutting down.
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3

Daniels, T., K. van Calsteren, and L. Dupont. "Maternele en obstetrische uitkomsten in vrouwen met mucovisidose: een retrospectieve case series van patiënten uit UZ Leuven." Tijdschrift voor Geneeskunde, September 27, 2024. http://dx.doi.org/10.47671/tvg.80.24.036.

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Maternal and obstetric outcomes in women with cystic fibrosis: a retrospective case series of patients in UZ Leuven Introduction: Cystic fibrosis (CF) is a genetic disease, caused by a mutation in the CFTR gene. This mutation may lead to pulmonary and endocrine complications. With CF therapies improving, the life expectancy of CF patients has increased and so has the number of pregnancies. Methodology: The case series describes the maternal and obstetric outcomes for 8 patients who had their pregnancy follow-up and delivery at the University Hospital of Leuven between January 2015 and December
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Dissertations / Theses on the topic "Mucovisidosis"

1

Annereau, Jean-Philippe. "Une approche structurale et fonctionnelle du domaine NBF1 de la protéine CFTR : implications pour la mucovisidose." Palaiseau, Ecole polytechnique, 1998. http://www.theses.fr/1998EPXX0015.

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Dans 70% des cas, la mucoviscidose est due à une délétion de la phenylalanine 508 dans la protéine cftr (cystic fibrosis transmembrane conductance regulator), canal membranaire de la famille des transporteurs abc (atp binding cassette). Cette délétion, située dans un domaine cytoplasmique : nbf1 (nucleotide binding fold 1), altère l'intégrité structurale de la protéine cftr. De nombreuses études in vitro ont permis de prédire que le rôle de cftr est de réguler les mouvements d'ions chlorures à travers la membrane apicale des cellules épithéliales. Cependant, la mucoviscidose ne peut s'explique
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2

Jouneau, Stéphane. "Etude de l'implication de l' "extracellular matrix metalloproteinase inducer" (EMMPRIN) dans l'inflammation pulmonaire et systémique de la mucovisidose et la bronchopneumopathie chronique obstructive." Rennes 1, 2007. http://www.theses.fr/2007REN1B107.

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L'inflammation et le remodelage bronchique, impliquant les métalloprotéinases matricielles (MMPs), tiennent une place majeure dans la physiopathologie de la mucovisidose et de la BPCO. Nous avons étudié la précense et l'implication de l'EMMPRIN, inducteur de MMPs, dans ces pathologies. Nous avons montré la présence d'EMMPRIN dans les expectorations et les plasmas des patients atteints de mucovisidose. Les taux d'EMMPRIN plasmatiques des patients stables sont corrolés à la sévérité de la maladie. En immunohistochimie, l'EMMPRIN est très fortement exprimé au niveau des macrophages alvéolaires et
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