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1Academic Journal
المؤلفون: Andolfo, I., Martone, S., Rosato, B.E., Marra, R., Gambale, A., Forni, G.L., Pinto, V., Göransson, M., Papadopoulou, V., Gavillet, M., Elalfy, M., Panarelli, A., Tomaiuolo, G., Iolascon, A., Russo, R.
المصدر: Genes, vol. 12, no. 7, pp. 958
مصطلحات موضوعية: PIEZO1, SPTA1, multi-locus inheritance, red blood cell defects, targeted next-generation sequencing
وصف الملف: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/34201899; info:eu-repo/semantics/altIdentifier/eissn/2073-4425; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_130682967E5B0; https://serval.unil.ch/notice/serval:BIB_130682967E5B; https://serval.unil.ch/resource/serval:BIB_130682967E5B.P001/REF.pdf
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2Academic Journal
المؤلفون: Pinto, V.M., Graziadei, G., Voi, V., Quota, A., Rigano, P., Spadola, V., Fidone, C., Gianesin, B., Franceschi, L. De, Forni, G.L.
المصدر: HemaSphere ; volume 3, issue S1, page 322-323 ; ISSN 2572-9241
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3Academic Journal
المؤلفون: Udeze, C., Dovizio, M., Veronesi, C., Degli Esposti, L., Li, N., Dang, T.X.M.P., Forni, G.L.
المصدر: Value in Health ; volume 26, issue 6, page S133 ; ISSN 1098-3015
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4Academic Journal
المؤلفون: Udeze, C., Dovizio, M., Veronesi, C., Degli Esposti, L., Li, N., Dang, T.X.M.P., Forni, G.L.
المصدر: Value in Health ; volume 26, issue 6, page S69-S70 ; ISSN 1098-3015
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5Academic Journal
المؤلفون: Iolascon, A., Bianchi, P., Andolfo, I., Russo, R., Barcellini, W., Fermo, E., Toldi, G., Ghirardello, S., Rees, D., Wijk, R. van, Kattamis, A., Gallagher, P.G., Roy, N., Taher, A., Mohty, R., Kulozik, A., Franceschi, L. de, Gambale, A., Montalembert, M. de, Forni, G.L., Harteveld, C.L., Prchal, J., SWG Red Cell & Iron EHA & EuroBloo
المصدر: American Journal of Hematology
وصف الملف: application/pdf
Relation: lumc-id: 122190055; https://hdl.handle.net/1887/3249335
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6Academic Journal
المؤلفون: Iolascon, A., Andolfo, I., Russo, R., Barcellini, W., Fermo, E., Toldi, G., Ghirardello, S., Rees, D., Wijk, R. van, Kattamis, A., Gallagher, P.G., Roy, N., Taher, A., Mohty, R., Kulozik, A., Franceschi, L. de, Gambale, A., Montalembert, M. de, Forni, G.L., Harteveld, C.L., Prchal, J., Bianchi, P., SWG Red Cell Iron EHA EuroBloodNet
المصدر: HemaSphere
وصف الملف: application/pdf
Relation: https://journals.lww.com/hemasphere/Fulltext/2021/12000/Summary_of_Joint_European_Hematology_Association.5.aspx; lumc-id: 122190216; https://hdl.handle.net/1887/3249336
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7Academic Journal
المؤلفون: Derchi G, Balocco M, Bina P, Caruso V, D'Ascola DG, Littera R, ORIGA, RAFFAELLA, Cappellini MD, Forni G.L.
المساهمون: Derchi, G, Balocco, M, Bina, P, Caruso, V, D'Ascola, Dg, Littera, R, Origa, Raffaella, Cappellini, Md, Forni, G. L.
Relation: info:eu-repo/semantics/altIdentifier/pmid/24497563; info:eu-repo/semantics/altIdentifier/wos/WOS:000336253900002; volume:99; issue:2; firstpage:17; lastpage:18; numberofpages:2; journal:HAEMATOLOGICA; http://hdl.handle.net/11584/90762; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84896713401
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8Academic Journal
المؤلفون: Galanello R., Neufeld E.J., Viprakasit V., Aydinok Y., Piga A., Harmatz P., Forni G.L., Shah F.T., Grace R.F., Porter J.B., Wood J.C., Peppe J., Jones A., Rienhoff Jr. H.Y.
Relation: Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Blood; https://hdl.handle.net/11454/18816; https://doi.org/10.1182/blood-2011-10-386268; 119; 14; 3263; 3268
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9Academic Journal
المؤلفون: Derchi, G., Formisano, F., Lamagna, M., Galanello, R., Bina, P., Cappellini, M.D., Piga, A., Quarta, G., Forni, G.L.
مصطلحات موضوعية: Abstracts
وصف الملف: text/html
Relation: http://eurjhfsupp.oxfordjournals.org/cgi/content/short/7/Suppl_1/24; http://dx.doi.org/10.1016/S1567-4215(08)60066-1
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12Electronic Resource
المؤلفون: Tomaiuolo G., Unal S., Forni G.L., Iolascon A., Russo R., Andolfo I., Manna F., Gambale A., Marra R., Rosato B.E., Caforio P., Pinto V., Pignataro P., Radhakrishnan K.
مصطلحات الفهرس: enzyme defect, epilepsy, female, gene mutation, genetic association, genetic susceptibility, genotype, hereditary spherocytosis, homozygosity, human, iron overload, major clinical study, male, molecular diagnosis, next generation sequencing, ohtahara syndrome, pathogenicity, phenotype, practice guideline, software, stomatocytosis, workflow, caspase activated deoxyribonuclease, endogenous compound, conference abstract, congenital dyserythropoietic anemia type 2, Blackfan Diamond anemia, diagnosis, diagnostic value, adult, cohort analysis, Conference Abstract
URL:
https://repository.monashhealth.org/monashhealthjspui/handle/1/37793
Click here for full text options
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13Electronic Resource
المؤلفون: Forni G.L., Caforio P., Pinto V., Pignataro P., Radhakrishnan K., Unal S., Tomaiuolo G., Iolascon A., Russo R., Andolfo I., Manna F., Gambale A., Marra R., Rosato B.E.
مصطلحات الفهرس: hereditary anemia/di [Diagnosis], Blackfan Diamond anemia/di [Diagnosis], Blackfan Diamond anemia/et [Etiology], brain disease, child, clinical feature, cohort analysis, congenital dyserythropoietic anemia/cn [Congenital Disorder], congenital dyserythropoietic anemia/di [Diagnosis], controlled study, diagnostic procedure, diagnostic value, disease association, disease severity, epilepsy, family, female, gene, gene mutation, genetic analysis, genetic disorder/cn [Congenital Disorder], genetic disorder/di [Diagnosis], genetic disorder/et [Etiology], genotype, hemolytic anemia/cn [Congenital Disorder], hemolytic anemia/di [Diagnosis], hemolytic anemia/et [Etiology], hereditary spherocytosis/cn [Congenital Disorder], hereditary spherocytosis/di [Diagnosis], hereditary spherocytosis/et [Etiology], high throughput sequencing, homozygote, human, infant, inheritance, iron overload/co [Complication], major clinical study, male, patient care, phenotype, preschool child, priority journal, school child, stomatocytosis/cn [Congenital Disorder], stomatocytosis/di [Diagnosis], stomatocytosis/et [Etiology], genomic DNA/ec [Endogenous Compound], CAD gene, hereditary anemia/cn [Congenital Disorder], hereditary anemia/et [Etiology], infantile epileptic encephalopathy, piezo1 gene, PKLR gene, SEC23B gene, adolescent, anemia/cn [Congenital Disorder], anemia/di [Diagnosis], anemia/et [Etiology], article, Blackfan Diamond anemia/cn [Congenital Disorder], Article
URL:
https://repository.monashhealth.org/monashhealthjspui/handle/1/37000
American Journal of Hematology
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14Academic Journal
المؤلفون: Pinto, V, Balocco, M, Derchi, G, Forni, G.l., AMBAGLIO, ILARIA, MALCOVATI, LUCA
المساهمون: Pinto, V, Balocco, M, Ambaglio, Ilaria, Derchi, G, Malcovati, Luca, Forni, G. l.
مصطلحات موضوعية: Myelodysplastic syndrome, Iron overload, Iron chelation therapy
وصف الملف: ELETTRONICO
Relation: info:eu-repo/semantics/altIdentifier/pmid/26576280; info:eu-repo/semantics/altIdentifier/wos/WOS:000364329300012; volume:3; issue:11; firstpage:952; lastpage:954; numberofpages:3; journal:CLINICAL CASE REPORTS; http://hdl.handle.net/11571/1152962
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15Academic Journal
المؤلفون: MATTIOLI, FRANCESCA, Puntoni M, MARINI, VALERIA, FUCILE, CARMEN, Milano G, ROBBIANO, LUIGI, Perrotta S, Pinto V, MARTELLI, ANTONIETTA MARIA, Forni G.L.
المساهمون: Mattioli, Francesca, Puntoni, M, Marini, Valeria, Fucile, Carmen, Milano, G, Robbiano, Luigi, Perrotta, S, Pinto, V, Martelli, ANTONIETTA MARIA, Forni, G. L.
مصطلحات موضوعية: deferasirox, bioavailability, thalassemia, iron chelation therapy, therapeutic drug monitoring
وصف الملف: STAMPA
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000351628000005; volume:94; firstpage:310; lastpage:317; numberofpages:8; journal:EUROPEAN JOURNAL OF HAEMATOLOGY; http://hdl.handle.net/11567/761992; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84925426274
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16Academic Journal
المؤلفون: Balleari, E., Salvetti, C., Del Corso, L., Filiberti, R., Bacigalupo, A., Bellodi, A., Beltrami, G., Bergamaschi, M., Berisso, G., Calzamiglia, T., Carella, A.M., Cavalleri, M., Da Col, A., Favorini, S., Forni, G.L., Goretti, R., Miglino, M., Mitscheuning, L., Molinari, E., Racchi, O., Scudeletti, M., Tassara, R., Gobbi, M., Lemoli, R., Clavio, M.
المساهمون: Fondazione Italiana Sindromi Mielodisplastiche (FISM)
المصدر: Leukemia Research ; volume 39, issue 8, page 846-852 ; ISSN 0145-2126
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17Academic Journal
المؤلفون: Del Corso, L., Salvetti, C., Filiberti, R., Clavio, M., Lemoli, R., Carella, A.M., Forni, G.L., Scudeletti, M., Tassara, R., Berisso, G., Calzamiglia, T., Arboscello, E., Bellodi, A., Beltrami, G., Bergamaschi, M., Cavalleri, M., Dominietto, A., Favorini, S., Ghiso, A., Goretti, R., Miglino, M., Mitscheunig, L., Racchi, O., Molinari, E., Vignolo, L., Gobbi, M., Balleari, E.
المصدر: Leukemia Research ; volume 39, page S100-S101 ; ISSN 0145-2126
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18Academic Journal
المؤلفون: Cossu G, Abbruzzese G, Matta G, Murgia D, Melis M, Ricchi V, Galanello R, Barella S, ORIGA, RAFFAELLA, Balocco M, Pelosin E, Marchese R, Ruffinengo U, Forni G.L.
المساهمون: Cossu, G, Abbruzzese, G, Matta, G, Murgia, D, Melis, M, Ricchi, V, Galanello, R, Barella, S, Origa, Raffaella, Balocco, M, Pelosin, E, Marchese, R, Ruffinengo, U, Forni, G. L.
Relation: info:eu-repo/semantics/altIdentifier/pmid/24661465; info:eu-repo/semantics/altIdentifier/wos/WOS:000336877900018; volume:20; issue:6; firstpage:651; lastpage:654; numberofpages:4; journal:PARKINSONISM & RELATED DISORDERS; http://hdl.handle.net/11584/90183; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84900024340
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19Academic Journal
المؤلفون: Forni, G.L., Giusti⁎, A., Pinto, V., Perrotta, S., Borgna Pignatti, C., D'Ascola, D.G., Nobili, B., Pitrolo, L., Quarta, G., Rigano, P., Zanaboni, L., Barone, A., Palummeri, E.
المصدر: Bone ; volume 50, page S153 ; ISSN 8756-3282
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20Academic Journal
المؤلفون: Cossu, G., Murgia, D., Melis, M., Matta, G., Galanello, R., Barella, S., Balocco, M., Paribello, A., Marcia, E., Marchese, R., Ruffinengo, U., Bonuccelli, U., Forni, G.L., Abbruzzese, G.
المصدر: Basal Ganglia ; volume 2, issue 4, page 264-265 ; ISSN 2210-5336