Výsledky vyhledávání - "J Ferrer-Calvete"

Autor: R.A. Pereda Pérez, J. Pastor Guillén, P. Ferrer González, J. Ferrer Calvete

Publikováno v: Anales de Pediatría, Vol 58, Iss 1, Pp 55-58 (2003)

Se presenta un niño de 13 años diagnosticado de fibrosis quística que desarrolló una infección grave del pulmón derecho con formación de abscesos y bronquiectasias localizadas. La evolución de su enfermedad se complicó con un síndrome nefr�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65bad905f2eb21f0e05d914689488fa6
https://doi.org/10.1016/s1695-4033(03)77992-2

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Utilidad de la colangiorresonancia magnética en el estudio de la enfermedad hepatobiliar en pacientes adultos con fibrosis quística

Autor: V. Martínez-Sanjuán, J Ferrer-Calvete, Julio Ponce, Joaquín Berenguer, M. Lloret, F. Pérez-Aguilar, G. Montoliú

Publikováno v: Gastroenterología y Hepatología. 24:122-126

IntroducciON Dado que las alteraciones de los conductos biliares en la fibrosis quistica remedan a las de la colangitis esclerosante primaria (CEP), la colangiorresonancia magnetica (CRM) podria ser de utilidad diagnostica, sobre todo teniendo en cue

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b59dfba386d9c803688971f7dab24b4e
https://doi.org/10.1016/s0210-5705(01)70137-9

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Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AAright-arrowG shows a severe phenotype

Autor: Mehmet Okyay Kilinc, Aslıhan Tolun, G. Glover, Teresa Casals, Fazilet Karakoc, Elif Dagli, Vasiliki Ninidu Ninis, J Pena, Xavier Estivill, J. Ferrer-Calvete, J L Seculi, Mübeccel Demirkol, Esen Demir, Ferda Ozkinay, I Kremenski, C Calvo, Gülden Huner, Alexey Savov, C Bousono

Publikováno v: Journal of Medical Genetics. 37:307-309

Editor—Cystic fibrosis (CF) is the most common lethal childhood disorder in white populations and occurs at a frequency of about 1/2500 with regional variations. Over 1000 mutations in the CF transmembrane conductance regulator ( CFTR ) gene accoun

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b023b654073e635de3ff3c83b99e9b8
https://doi.org/10.1136/jmg.37.4.307

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[Pneumonectomy in cystic fibrosis]

Autor: P, Ferrer González, A, Pereda Pérez, J, Pastor Guillén, J, Ferrer Calvete

Publikováno v: Anales de pediatria (Barcelona, Spain : 2003). 58(1)

We present the case of a 13-year-old boy with cystic fibrosis (CF) who developed severe right-sided lung infection with formation of abscess and localized bronchiectasis. The boy's lung disease was complicated by nephrotic syndrome and secondary amyl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a1178fab5db63a937a5720083b612219
https://pubmed.ncbi.nlm.nih.gov/12628120

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[Usefulness of magnetic cholangioresonance in the study of hepatobiliary disease in patients adults with cystic fibrosis]

Autor: F, Pérez-Aguilar, V, Martínez-Sanjuán, G, Montoliú, M, Lloret, J, Ferrer-Calvete, J, Ponce, J, Berenguer

Publikováno v: Gastroenterologia y hepatologia. 24(3)

Because alterations in the bile ducts found in cystic fibrosis mimic those found in primary sclerosing cholangitis, magnetic resonance cholangiography (MRC) could be a useful diagnosis technique, especially because it is non-invasive.We prospectively

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::90329aae41d2a86178a5357f91233266
https://pubmed.ncbi.nlm.nih.gov/11261222

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[Digestive alterations in cystic fibrosis. Retrospective study of a series of 46 adult patients]

Autor: F, Pérez-Aguilar, J, Ferrer-Calvete, D, Nicolás, J, Berenguer, J, Ponce

Publikováno v: Gastroenterologia y hepatologia. 22(2)

The clinical histories of 46 adult patients (24 men and 22 women, mean age 20.6 +/- 5.1 years) diagnosed of cystic fibrosis were reviewed evaluating the digestive alterations. The age at diagnosis of cystic fibrosis was 5.63 +/- 5.3 years (range: new

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::123b8501c1020f47e97706fe221c7cc3
https://pubmed.ncbi.nlm.nih.gov/10193090

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[Anderson's disease (steatorrhea due to the retention of chylomicrons): diagnostic criteria]

Autor: M, Oltra Benavent, M, Chirivella Casanova, A, Pereda Pérez, C, Ribes Konickx, J, Ferrer Calvete

Publikováno v: Anales espanoles de pediatria. 47(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b78747ea419e49ef598c0c923c10dca7
https://pubmed.ncbi.nlm.nih.gov/9382356

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[An alpha 1-antitrypsin aerosol in the treatment of cystic fibrosis]

Autor: J, Ferrer Calvete, J, Aznar Lucea, P, Morales Marín, A, Pereda Pérez, R, Llopis Carles, C, Ribes Koninckx, P, Ferrer González, V, Marco Martínez

Publikováno v: Anales espanoles de pediatria. 44(2)

Alpha-1-antitrypsin (a-1AT) is a natural inhibitor of the elastase that is released physiologically by neutrophils in the lung. As a result of the increased neutrophil degranulation secondary to chronic epithelial inflammation in cystic fibrosis pati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ac2c370d65e31802ea33e9d8bb9fb651
https://pubmed.ncbi.nlm.nih.gov/8830566

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