المؤلفون: Suppressa P., Maiorano E., Gaetani E., Matti E., Lenato G. M., Serio I., Masala M. S., Passali G. C., Aguglia M., Crocione C., Lopalco P. L., Caneschi F., Musella V., De Silvestri A., Gambini G., Spinozzi G., Sabba C., Pagella F.

المساهمون: Suppressa, P., Maiorano, E., Gaetani, E., Matti, E., Lenato, G. M., Serio, I., Masala, M. S., Passali, G. C., Aguglia, M., Crocione, C., Lopalco, P. L., Caneschi, F., Musella, V., De Silvestri, A., Gambini, G., Spinozzi, G., Sabba, C., Pagella, F.

مصطلحات موضوعية: Arteriovenous malformation, COVID-19, Hereditary hemorrhagic telangiectasia, Rare disease, SARS-CoV-2 infection

Relation: info:eu-repo/semantics/altIdentifier/pmid/37140873; info:eu-repo/semantics/altIdentifier/wos/WOS:000981363100003; volume:18; firstpage:1109; lastpage:1118; numberofpages:10; journal:INTERNAL AND EMERGENCY MEDICINE; https://hdl.handle.net/11586/432020

الاتاحة: https://hdl.handle.net/11586/432020
https://doi.org/10.1007/s11739-023-03287-8
https://link.springer.com/article/10.1007/s11739-023-03287-8

المؤلفون: Dupuis-Girod, S, Shovlin, CL, Kjeldsen, AD, Mager, H-J, Sabba, C, Droege, F, Fargeton, A-E, Fialla, AD, Gandolfi, S, Hermann, R, Lenato, GM, Manfredi, G, Post, MC, Rennie, C, Suppressa, P, Sure, U, Buscarini, E, Crocione, C, Blom, R, Botella, LM, Brocca, F, Coxall, C, Druckman, KT, Erasme, D, Federici, P, Grabowski, C, Lundgren, M, Søderman, T, Woods, D

المصدر: 8 ; 1

مصطلحات موضوعية: 0604 Genetics, 1103 Clinical Sciences, Genetics & Heredity

Relation: European Journal of Medical Genetics; http://hdl.handle.net/10044/1/99201

الاتاحة: http://hdl.handle.net/10044/1/99201
https://doi.org/10.1016/j.ejmg.2022.104575

المؤلفون: Dupuis-Girod S., Shovlin C. L., Kjeldsen A. D., Mager H. -J., Sabba C., Droege F., Fargeton A. -E., Fialla A. D., Gandolfi S., Hermann R., Lenato G. M., Manfredi G., Post M. C., Rennie C., Suppressa P., Sure U., Crocione C., Blom R., Botella L. M., Brocca F., Coxall C., Druckman K. T., Erasme D., Federici P., Grabowski C., Lundgren M., Soderman T., Woods D., Buscarini E.

المساهمون: Dupuis-Girod, S., Shovlin, C. L., Kjeldsen, A. D., Mager, H. -J., Sabba, C., Droege, F., Fargeton, A. -E., Fialla, A. D., Gandolfi, S., Hermann, R., Lenato, G. M., Manfredi, G., Post, M. C., Rennie, C., Suppressa, P., Sure, U., Crocione, C., Blom, R., Botella, L. M., Brocca, F., Coxall, C., Druckman, K. T., Erasme, D., Federici, P., Grabowski, C., Lundgren, M., Soderman, T., Woods, D., Buscarini, E.

مصطلحات موضوعية: Anaemia, Bevacizumab, Digestive bleeding, Hereditary haemorrhagic telangiectasia, Iron deficiency, Nosebleeds

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000888569400004; volume:65; issue:10; firstpage:104575; journal:EUROPEAN JOURNAL OF MEDICAL GENETICS; https://hdl.handle.net/11586/447092; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85135948315

الاتاحة: https://hdl.handle.net/11586/447092
https://doi.org/10.1016/j.ejmg.2022.104575

المؤلفون: Suppressa P., Pagella F., Lenato G. M., Gaetani E., Serio I., Masala M. S., Spinozzi G., Lizzio R., Matti E., De Silvestri A., Passali G. C., Aguglia M., Crocione C., Sabba C.

المساهمون: Suppressa, P., Pagella, F., Lenato, G. M., Gaetani, E., Serio, I., Masala, M. S., Spinozzi, G., Lizzio, R., Matti, E., De Silvestri, A., Passali, G. C., Aguglia, M., Crocione, C., Sabba, C.

مصطلحات موضوعية: COVID-19, Hereditary hemorrhagic telangiectasia, PANDEMICS 2020, Rare disease, SARS-CoV-2 infection, Communicable Disease Control, Cross-Sectional Studie, Human, Italy, Retrospective Studie, SARS-CoV-2, Telangiectasia, Hereditary Hemorrhagic

Relation: info:eu-repo/semantics/altIdentifier/pmid/34496900; info:eu-repo/semantics/altIdentifier/wos/WOS:000693846100003; volume:16; issue:1; firstpage:378; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/11586/392811; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85114514796

الاتاحة: http://hdl.handle.net/11586/392811
https://doi.org/10.1186/s13023-021-02000-2

المؤلفون: Buscarini E., Botella L. M., Geisthoff U., Kjeldsen A. D., Mager H. J., Pagella F., Suppressa P., Zarrabeitia R., Dupuis-Girod S., Shovlin C. L., Federici P., Crocione C.

المساهمون: Buscarini, E., Botella, L. M., Geisthoff, U., Kjeldsen, A. D., Mager, H. J., Pagella, F., Suppressa, P., Zarrabeitia, R., Dupuis-Girod, S., Shovlin, C. L., Federici, P., Crocione, C.

مصطلحات موضوعية: Adverse event, Arteriovenous malformation, Bevacizumab, Bleeding, Cardiac failure, Epistaxi, Hereditary hemorrhagic telangiectasia, Nosebleed, Thalidomide, Adolescent, Adult, Female, Hemorrhage, Human, Male, Retrospective Studie, Surveys and Questionnaire, Telangiectasia, Hereditary Hemorrhagic, Young Adult

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/30717761; info:eu-repo/semantics/altIdentifier/wos/WOS:000457787300001; volume:14; issue:1; firstpage:28; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/11571/1361014; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85061058896

الاتاحة: http://hdl.handle.net/11571/1361014
https://doi.org/10.1186/s13023-018-0982-4