يعرض 1 - 10 نتائج من 122 نتيجة بحث عن '"Cirilli, N."', وقت الاستعلام: 0.97s تنقيح النتائج
  1. 1
    دورية أكاديمية
    P007 A novel cystic fibrosis-causing mutation identified in a newborn of African origin

    المؤلفون: Cirilli, N., Varriale, L., Baffico, A.M., Caporelli, N., Fabrizzi, B.

    المصدر: Journal of Cystic Fibrosis ; volume 20, page S40-S41 ; ISSN 1569-1993

    مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/s1569-1993Test(21)01034-1
    https://api.elsevier.com/content/article/PII:S1569199321010341?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1569199321010341?httpAccept=text/plainTest

    View record in BASE

    أضف إلى المفضلة
  2. 2
    دورية أكاديمية
    P020 CFTR mutation panel in detecting cystic fibrosis screen positive inconclusive diagnosis patients (CFSPIDs) in the Marche Region, Italy

    المؤلفون: Cirilli, N., Ciatti, R., Fortuna, F., Tarsi, E., Varriale, L., Vagnini, A., Banfi, M., Caporelli, N., Fabriazzi, B.

    المصدر: Journal of Cystic Fibrosis ; volume 20, page S44 ; ISSN 1569-1993

    مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/s1569-1993Test(21)01047-x
    https://api.elsevier.com/content/article/PII:S156919932101047X?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S156919932101047X?httpAccept=text/plainTest

    View record in BASE

    أضف إلى المفضلة
  3. 3
    دورية أكاديمية
    Two novel and correlated CF-causing insertions in the (TG)mTn tract of the CFTR gene

    المؤلفون: Pierandrei S., Blacona G., Fabrizzi B., Cimino G., Cirilli N., Caporelli N., Angeloni A., Cipolli M., Lucarelli M.

    المساهمون: Pierandrei, S., Blacona, G., Fabrizzi, B., Cimino, G., Cirilli, N., Caporelli, N., Angeloni, A., Cipolli, M., Lucarelli, M.

    مصطلحات موضوعية: Cystic Fibrosi, CFTR gene, novel pathogenic variant, (TG)mTn tract, anomalous splicing, functional characterization, clinical characterization

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31593572; info:eu-repo/semantics/altIdentifier/wos/WOS:000532431700003; volume:14; issue:10; firstpage:e0222838; numberofpages:14; journal:PLOS ONE; http://hdl.handle.net/11573/1344888Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85073079506

    الإتاحة: https://doi.org/10.1371/journal.pone.0222838Test
    http://hdl.handle.net/11573/1344888Test

    View record in BASE

    أضف إلى المفضلة
  4. 4
    دورية أكاديمية
    Cystic Fibrosis Defective Response to Infection Involves Autophagy and Lipid Metabolism

    المؤلفون: Mingione A., Ottaviano E., Barcella M., Merelli I., Rosso L., Armeni T., Cirilli N., Ghidoni R., Borghi E., Signorelli P.

    المساهمون: A. Mingione, E. Ottaviano, M. Barcella, I. Merelli, L. Rosso, T. Armeni, N. Cirilli, R. Ghidoni, E. Borghi, P. Signorelli

    مصطلحات موضوعية: Aspergillus fumigatu, autophagy, cystic fibrosi, myriocin, sphingolipids, Settore MED/21 - Chirurgia Toracica, Settore MED/07 - Microbiologia e Microbiologia Clinica, Settore MED/14 - Nefrologia, Settore BIO/10 - Biochimica

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32781626; info:eu-repo/semantics/altIdentifier/wos/WOS:000568174900001; volume:9; issue:8; numberofpages:22; journal:CELLS; http://hdl.handle.net/2434/758838Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089360279

    الإتاحة: https://doi.org/10.3390/cells9081845Test
    http://hdl.handle.net/2434/758838Test

    View record in BASE

    أضف إلى المفضلة
  5. 5
    دورية أكاديمية
    P005 Lessons from 5T;TG12

    المؤلفون: Cirilli, N., Munaretto, R., Perticaroli, F., Bruni, A., Baiocco, N., Fabrizzi, B.

    المصدر: Journal of Cystic Fibrosis ; volume 19, page S56 ; ISSN 1569-1993

    مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/s1569-1993Test(20)30342-8
    https://api.elsevier.com/content/article/PII:S1569199320303428?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1569199320303428?httpAccept=text/plainTest

    View record in BASE

    أضف إلى المفضلة
  6. 6
    دورية أكاديمية
    P029 Validation of new sweat test control materials

    المؤلفون: Cirilli, N., Maggi, T., Fabrizzi, B., Baiocco, N., Sbaragli, G., Bianchi, L.

    المصدر: Journal of Cystic Fibrosis ; volume 19, page S63 ; ISSN 1569-1993

    مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/s1569-1993Test(20)30366-0
    https://api.elsevier.com/content/article/PII:S1569199320303660?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1569199320303660?httpAccept=text/plainTest

    View record in BASE

    أضف إلى المفضلة
  7. 7
    دورية أكاديمية
    Clinical expression of cystic fibrosis in a large cohort of Italian siblings

    المؤلفون: Terlizzi V., Lucarelli M., Salvatore D., Angioni A., Bisogno A., Braggion C., Buzzetti R., Carnovale V., Casciaro R., Castaldo G., Cirilli N., Collura M., Colombo C., Di Lullo A. M., Elce A., Lucidi V., Madarena E., Padoan R., Quattrucci S., Raia V., Seia M., Termini L., Zarrilli F.

    المساهمون: Terlizzi, V., Lucarelli, M., Salvatore, D., Angioni, A., Bisogno, A., Braggion, C., Buzzetti, R., Carnovale, V., Casciaro, R., Castaldo, G., Cirilli, N., Collura, M., Colombo, C., Di Lullo, A. M., Elce, A., Lucidi, V., Madarena, E., Padoan, R., Quattrucci, S., Raia, V., Seia, M., Termini, L., Zarrilli, F.

    مصطلحات موضوعية: CFTR, FEV1, genotype, modifier gene, phenotype, pseudomonas aeruginosa, carrier state, cystic fibrosi, cystic fibrosis transmembrane conductance regulator, diabetes mellitu, exocrine pancreatic insufficiency, liver disease, meconium ileu, nasal polyp, siblings

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30577776; info:eu-repo/semantics/altIdentifier/wos/WOS:000454239000001; volume:18; issue:1; firstpage:1; lastpage:8; numberofpages:8; journal:BMC PULMONARY MEDICINE; http://hdl.handle.net/11573/1281958Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85058920504

    الإتاحة: https://doi.org/10.1186/s12890-018-0766-6Test
    http://hdl.handle.net/11573/1281958Test

    View record in BASE

    أضف إلى المفضلة
  8. 8
    دورية أكاديمية
    Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis

    المؤلفون: Sofia VM, Surace C, Terlizzi V, Da Sacco L, Alghisi F, Angiolillo A, Braggion C, Cirilli N, Colombo C, Di Lullo A, Padoan R, Quattrucci S, Raia V, Tuccio G, Zarrilli F, Tomaiuolo AC, Novelli A, Lucidi V, Lucarelli M, Castaldo G, Angioni A

    المساهمون: Sofia, Vm, Surace, C, Terlizzi, V, Da Sacco, L, Alghisi, F, Angiolillo, A, Braggion, C, Cirilli, N, Colombo, C, Di Lullo, A, Padoan, R, Quattrucci, S, Raia, V, Tuccio, G, Zarrilli, F, Tomaiuolo, Ac, Novelli, A, Lucidi, V, Lucarelli, M, Castaldo, G, Angioni, A

    مصطلحات موضوعية: CFTR gene, Cystic fibrosi, Pancreatic pathway, Recurrent/chronic pancreatiti, Trans-heterozogosity, Trypsin

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000440071700001; volume:24; issue:38; firstpage:1; lastpage:10; numberofpages:10; journal:MOLECULAR MEDICINE; https://hdl.handle.net/11588/720212Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85054962143

    الإتاحة: https://doi.org/10.1186/s10020-018-0041-6Test
    https://hdl.handle.net/11588/720212Test

    View record in BASE

    أضف إلى المفضلة
  9. 9
    دورية أكاديمية
    P413 How to use telemonitoring for the detection of respiratory exacerbations in cystic fibrosis: effectiveness and adherence

    المؤلفون: Luciani, L., Peruzzi, A., Giovagnoli, L., Cirilli, N., Caporelli, N., Fabrizzi, B.

    المصدر: Journal of Cystic Fibrosis ; volume 22, page S190 ; ISSN 1569-1993

    مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/s1569-1993Test(23)00783-x
    https://api.elsevier.com/content/article/PII:S156919932300783X?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S156919932300783X?httpAccept=text/plainTest

    View record in BASE

    أضف إلى المفضلة
  10. 10
    دورية أكاديمية
    P040 Sweat chloride values in cystic fibrosis patients after one year on elexacaftor/tezacaftor/ivacaftor

    المؤلفون: Cirilli, N., D’Antuono, A., Masseria, F., Caporelli, N., Fabrizzi, B.

    المصدر: Journal of Cystic Fibrosis ; volume 22, page S75 ; ISSN 1569-1993

    مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/s1569-1993Test(23)00415-0
    https://api.elsevier.com/content/article/PII:S1569199323004150?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1569199323004150?httpAccept=text/plainTest

    View record in BASE

    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS — أرسل هذا البحث بالبريد الإلكتروني — حفظ البحث