المؤلفون: Di Palma, M., Santopietro, M., Cardarelli, L., Palumbo, G., Di Pippo, T., De Benedictis, D., Monaco, N., Moleti, M. L., Testi, A. M., Giona, F.

مصطلحات موضوعية: pediatrico, piastrinopenia, itp

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3686::989448176e0e634e73ed2c2f1eee5186
http://hdl.handle.net/11573/1335588

المؤلفون: Mauro, M., Camoglio, F., Piccoli, P., De Bortoli, M., Balter, R., Pegoraro, A., Cesaro, Simone

مصطلحات موضوعية: piastrinopenia, splenectomia, trapianto di cellule staminali emopoietiche, piastrinopenia, splenectomia, trapianto di cellule staminali emopoietiche

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1943::bc3606a2e13449543a74b809519c16b9
http://hdl.handle.net/11562/945257

المؤلفون: Felisa C. Molinas, Carlo L. Balduini, Fernando Negro, Patrizia Noris, Daniela De Rocco, Ana C. Glembotsky, Yesica Romina Espasandin, Nora Paula Goette, Chiara Gnan, Anna Savoia, Rosana F. Marta, Alessandro Pecci, Paula G. Heller

المساهمون: Glembotsky, A. C., Marta, R. F., Pecci, A., DE ROCCO, Daniela, Gnan, Chiara, Espasandin, Y. R., Goette, N. P., Negro, F., Noris, P., Savoia, Anna, Balduini, C. L., Molinas, F. C., Heller, P. G.

المصدر: Europe PubMed Central
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET

مصطلحات موضوعية: Male, Pediatrics, Heredity, International Cooperation, DNA Mutational Analysis, Fluorescent Antibody Technique, Pedigree chart, Medicina Clínica, Disease, Health Services Accessibility, Thrombospondin 1, MNKRD26 mutation, purl.org/becyt/ford/3.2 [https], Medicine, Cooperative Behavior, Young adult, Child, Referral and Consultation, Hematologic Tests, Molecular Motor Proteins, Hematology, Middle Aged, Flow Cytometry, Prognosis, Pedigree, Leukemia, Phenotype, Italy, Child, Preschool, Predictive value of tests, Cohort, Female, purl.org/becyt/ford/3 [https], Algorithms, Adult, medicine.medical_specialty, CIENCIAS MÉDICAS Y DE LA SALUD, Adolescent, Platelet Function Tests, Platelet disorder, Argentina, Gray platelet syndrome, Young Adult, Predictive Value of Tests, Inherited thrombocytopenia, Humans, Genetic Predisposition to Disease, Hematología, Genetic Testing, Piastrinopenia ereditaria, ricerca di mutazioni, Developing Countries, Aged, Myosin Heavy Chains, Platelet Count, business.industry, medicine.disease, Thrombocytopenia, Immunology, Feasibility Studies, Platelet disorders, business, Biomarkers

وصف الملف: application/pdf; STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe7d7c381fd2bbaaf8d15e540792c9d9
https://doi.org/10.1111/j.1538-7836.2012.04805.x

المؤلفون: Rogier Kersseboom, Caterina Marconi, Paula G. Heller, James B. Bussel, Patrizia Noris, Marco Seri, Karen Y. Niederhoffer, Chiara Gnan, Ginevra Biino, Daniela De Rocco, William Cohen, Rémi Favier, Allison Imahiyerobo, Françoise Boehlen, Anna Savoia, Alessandro Pecci, Carlo L. Balduini, Pamela Magini, Elisa Civaschi, Shinji Kunishima, Gian Marco Podda, Nicola Vianelli, Dorsaf Ghalloussi, Anne Auvrignon, Marie-Christine Alessi, Amy E. Geddis, Jennifer C. Yu, Paola Giordano, Akihiro Iguchi

المساهمون: Noris P, Favier R, Alessi MC, Geddis AE, Kunishima S, Heller PG, Giordano P, Niederhoffer KY, Bussel JB, Podda GM, Vianelli N, Kersseboom R, Pecci A, Gnan C, Marconi C, Auvrignon A, Cohen W, Yu JC, Iguchi A, Miller Imahiyerobo A, Boehlen F, Ghalloussi D, De Rocco D, Magini P, Civaschi E, Biino G, Seri M, Savoia A, Balduini CL, P., Nori, R., Favier, M. C., Alessi, A. E., Geddi, S., Kunishima, P. G., Heller, P., Giordano, K. Y., Niederhoffer, J. B., Bussel, G. M., Podda, N., Vianelli, R., Kersseboom, A., Pecci, Gnan, Chiara, C., Marconi, A., Auvrignon, W., Cohen, J. C., Yu, A., Iguchi, A., Miller Imahiyerobo, F., Boehlen, D., Ghalloussi, DE ROCCO, Daniela, P., Magini, E., Civaschi, G., Biino, M., Seri, Savoia, Anna, C. L., Balduini

المصدر: Blood, Vol. 122, No 11 (2013) pp. 1987-1989
Blood (Online) 122 (2013): 1987–1989. doi:10.1182/blood-2013-04-499319
info:cnr-pdr/source/autori:Noris P, Favier R, Alessi MC, Geddis AE, Kunishima S, Heller PG, Giordano P, Niederhoffer KY, Bussel JB, Podda GM, Vianelli N, Kersseboom R, Pecci A, Gnan C, Marconi C, Auvrignon A, Cohen W, Yu JC, Iguchi A, Miller Imahiyerobo A, Boehlen F, Ghalloussi D, De Rocco D, Magini P, Civaschi E, Biino G, Seri M, Savoia A, Balduini CL/titolo:ANKRD26-related thrombocytopenia and myeloid malignancies/doi:10.1182%2Fblood-2013-04-499319/rivista:Blood (Online)/anno:2013/pagina_da:1987/pagina_a:1989/intervallo_pagine:1987–1989/volume:122

مصطلحات موضوعية: Piastrinopenia, Leucemia, Untranslated region, Myeloid, Immunology, myeloid malignancies, medicine.disease_cause, Biochemistry, Myelogenous, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, medicine, Humans, Genetic Predisposition to Disease, 5' Untranslated Regions/genetics, Myelodysplastic Syndromes/genetics, inherited thrombocytopenias, ddc:616, Family Health, Family health, Mutation, Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics, business.industry, Genetic Predisposition to Disease/genetics, Myelodysplastic syndromes, Nuclear Proteins, Cancer, Cell Biology, Hematology, medicine.disease, Thrombocytopenia, Nuclear Proteins/genetics, Leukemia, medicine.anatomical_structure, Leukemia, Myeloid, Myelodysplastic Syndromes, Acute Disease, Thrombocytopenia/genetics, Cancer research, Intercellular Signaling Peptides and Proteins, 5' Untranslated Regions, business, Leukemia, Myeloid/genetics

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e5e35a5e5449f31b7828def548ba10f
https://doi.org/10.1182/blood-2013-04-499319

المؤلفون: Annalisa Pastore, Carlos T. Moraes, Cristina Cerqua, Giovanna Russo, Leonardo Salviati, Paola Goffrini, Francesca Meloni, Elena Nicchia, Daniela De Rocco, Anna Savoia, Alessandro Pecci

المساهمون: DE ROCCO, Daniela, Cerqua, C, Goffrini, P, Russo, G, Pastore, A, Meloni, F, Nicchia, Elena, Moraes, Ct, Pecci, A, Salviati, L, Savoia, Anna, De Rocco, Daniela, Cerqua, Cristina, Goffrini, Paola, Russo, Giovanna, Pastore, Annalisa, Meloni, Francesca, Moraes, Carlos T., Pecci, Alessandro, Salviati, Leonardo

مصطلحات موضوعية: Male, Cellular bioenergetics, Somatic cell, DNA Mutational Analysis, Sequence Homology, Apoptosis, medicine.disease_cause, Mice, Platelet, Child, Lung, Cells, Cultured, Mutation, Cultured, Cytochrome c, Cytochromes c, Pedigree, Amino Acid, Embryo, Child, Preschool, Fibroblast, Molecular Medicine, Female, Human, Gene isoform, piastrinopenia ereditaria, Thrombocytopenia THC4, Molecular Sequence Data, Mutation, Missense, Settore BIO/11 - Biologia Molecolare, Saccharomyces cerevisiae, Biology, DNA Mutational Analysi, Oxygen Consumption, medicine, citocromo c, Animals, Humans, Amino Acid Sequence, Preschool, Gene, Molecular Biology, Family Health, Sequence Homology, Amino Acid, Base Sequence, Animal, Mammalian, Apoptosi, Fibroblasts, Embryo, Mammalian, Thrombocytopenia, Molecular biology, Molecular medicine, Cellular bioenergetic, biology.protein, Cancer research, Cell, Missense, Energy Metabolism

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e284786d80859defa08cb19fe6a21e
http://hdl.handle.net/20.500.11769/55250

المؤلفون: C. Marconi, T. Pipucci, F. Palombo, N. Bompiani, A. Pecci, P. Noris, M. Seri, C. L. Balduini, BOTTEGA, ROBERTA, FALESCHINI, MICHELA, DE ROCCO, DANIELA, SAVOIA, ANNA

المساهمون: '-', C., Marconi, Bottega, Roberta, T., Pipucci, F., Palombo, N., Bompiani, A., Pecci, P., Nori, Faleschini, Michela, DE ROCCO, Daniela, M., Seri, C. L., Balduini, Savoia, Anna

مصطلحات موضوعية: ACTN1, piastrinopenia, screening di mutazioni

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::062cb24a2dfb333c39df8e8fe4d5ade8
http://hdl.handle.net/11562/1064345

المؤلفون: Claudio Grignani, Saverio Scianguetta, Giuseppe Loffredo, Silverio Perrotta, Silvana Magrin, Anna Savoia, Momcilo Jankovic, Marco Cattaneo, Sabina Russo, Patrizia Noris, Daniela De Rocco, Carlo L. Balduini, Elisa Civaschi, Alfredo Dragani, Carlo Baronci, Roberta Bottega, Federica Melazzini, Maddalena Casale, Alessandro Pecci, V. Albano, Veronica Di Salvo, Giovanna Russo

المساهمون: Noris, P., Perrotta, S., Bottega, Roberta, Pecci, A., Melazzini, F., Civaschi, E., Russo, S., Magrin, S., Loffredo, G., Di Salvo, V., Russo, G., Casale, M., DE ROCCO, Daniela, Grignani, C., Cattaneo, M., Baronci, C., Dragani, A., Albano, V., Jankovic, M., Scianguetta, S., Savoia, Anna, Balduini, C. L., Noris, P, Perrotta, Silverio, Bottega, R, Pecci, A, Melazzini, F, Civaschi, E, Russo, S, Magrin, S, Loffredo, G, Di Salvo, V, Russo, G, Casale, Maddalena, De Rocco, D, Grignani, C, Cattaneo, M, Baronci, C, Dragani, A, Albano, V, Jankovic, M, Scianguetta, S, Savoia, A

مصطلحات موضوعية: Adult, Male, Heterozygote, Bolzano mutation, Mutazione Bolzano, Adolescent, Platelet Aggregation, Mutation, Missense, Pedigree chart, Bernard–Soulier syndrome, Young Adult, Tubulin, hemic and lymphatic diseases, Medicine, Missense mutation, Humans, Piastrinopenia ereditaria, inherited thrombocytopenia, Child, Bernard Soulier syndrome, Aged, Genetics, Aged, 80 and over, Family Health, Membrane Glycoproteins, Polymorphism, Genetic, Transition (genetics), sindrome di Bernard-Soulier, business.industry, Platelet Count, Bernard-Soulier syndrome, Haplotype, Bernard-Soulier Syndrome, Infant, Platelet Glycoprotein GPIb-IX Complex, Hematology, Original Articles, Middle Aged, medicine.disease, Thrombocytopenia, GP1BA, Italy, Thrombopoietin, Child, Preschool, Immunology, Mutation (genetic algorithm), Female, business

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc762dd7a459bf17d177179c0897787c
https://hdl.handle.net/11368/2446325

المؤلفون: Roberta Bottega, Annalisa Pastore, Valeria Bozzi, Mariateresa Di Stazio, Patrizia Noris, Daniela De Rocco, Silvana Magrin, Federica Melazzini, Elisa Civaschi, Anna Savoia, Alessandro Pecci, Carlo L. Balduini

المساهمون: Savoia, Anna, Pastore, A., DE ROCCO, Daniela, Civaschi, E., DI STAZIO, Mariateresa, Bottega, Roberta, Melazzini, F., Bozzi, V., Pecci, A., Magrin, S., Balduini, C. L., Noris, P., Savoia, A., De Rocco, D., Di Stazio, M., Bottega, R.

مصطلحات موضوعية: Male, Platelet Aggregation, GP1BB, GP1BA, geni GP1BA, Polymerase Chain Reaction, Bernard–Soulier syndrome, chemistry.chemical_compound, GP1BB and GP9 mutations, Thrombocytopathy, Child, Membrane Glycoproteins, biology, sindrome di Bernard-Soulier, Homozygote, Ristocetin-induced platelet aggregation, Platelet Glycoprotein GPIb-IX Complex, Hematology, Middle Aged, Italy, Ristocetin, Child, Preschool, Original Article, Female, Adult, Blood Platelets, Genetic Markers, Adolescent, Molecular Sequence Data, Editorials and Perspectives, Hemorrhage, Young Adult, Von Willebrand factor, von Willebrand Factor, medicine, macrothrombocytopenia, Humans, Point Mutation, Amino Acid Sequence, Cell Shape, Genetic Association Studies, Piastrinopenia, GP9, Platelet Count, Bernard-Soulier Syndrome, medicine.disease, Bernard-Soulier syndrome, Thrombocytopenia, Bleeding diathesis, chemistry, Immunology, biology.protein

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0edf98354c9f7adc2c5465e802af5f3b
http://hdl.handle.net/11562/1064369

المؤلفون: Alessandro Pecci, Carlo L. Balduini, Anna Savoia

المساهمون: Balduini, C. L., Pecci, A., Savoia, Anna

مصطلحات موضوعية: piastrinopenia ereditaria, medicine.medical_specialty, Genotype, Disease, Malattia MYH9 associata, Mice, Megakaryocyte, Cataracts, Internal medicine, medicine, Coagulopathy, Animals, Humans, Genetic Predisposition to Disease, Thrombopoietin, gene MYH9, Myosin Type II, Hematology, Myosin Heavy Chains, business.industry, Molecular Motor Proteins, miosina non muscolare IIA, medicine.disease, Thrombocytopenia, Disease Models, Animal, Phenotype, medicine.anatomical_structure, Epstein Syndrome, Mutation, Immunology, May–Hegglin anomaly, business

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fafa4da6eb67d97b344fda76f67bf69f
http://hdl.handle.net/11368/2335044

المؤلفون: De Mattia D, Del Vecchio GC, Russo G, De Santis A, Ramenghi U, Notarangelo L, Jankovic M, Molinari AC, Zecca M, Nobili B, Giordano P, AIEOP ITP Study Group, Acquaviva A, Amendola G, Baronci C, Binda S, Bisogno G, Bussetti C, Ciliberti A, Citterio M, Del Principe D, Farruggia P, Ladogana S, Magro S, Masera G, Menichelli A, Nardi M, Parodi E, Tucci F, Vimercati C., PESSION, ANDREA

المساهمون: DE MATTIA, D, DEL VECCHIO, Gc, Russo, G, DE SANTIS, A, Ramenghi, U, Notarangelo, L, Jankovic, M, Molinari, Ac, Zecca, M, Nobili, Bruno, Giordano, P, AIEOP ITP STUDY, Group, De Mattia D, Del Vecchio GC, Russo G, De Santis A, Ramenghi U, Notarangelo L, Jankovic M, Molinari AC, Zecca M, Nobili B, Giordano P, AIEOP-ITP Study Group,Acquaviva A, Amendola G, Baronci C, Binda S, Bisogno G, Bussetti C, Ciliberti A, Citterio M, Del Principe D, Farruggia P, Ladogana S, Magro S, Masera G, Menichelli A, Nardi M, Parodi E, Pession A, Tucci F, Vimercati C.

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Platelet count, Adolescent, Consensus Development Conferences as Topic, Prednisolone, Rho(D) Immune Globulin, medicine.medical_treatment, conta piastrinica, Splenectomy, Platelet Transfusion, management of pediatric thrombocytopenia, idiopathic thrombocytopenic purpura, platelet count, trattamento della piastrinopenia pediatrica, porpora trombocitopenica idiopatica, Immune system, immune system diseases, hemic and lymphatic diseases, medicine, Pediatric thrombocytopenia, Humans, Platelet, Idiopathic thrombocytopenic purpura, Management of pediatric thrombocytopenia, Thrombocytopenia, Child, Purpura, Thrombocytopenic, Idiopathic, biology, business.industry, Immunoglobulins, Intravenous, Infant, Hematology, General Medicine, medicine.disease, Thrombocytopenic purpura, Purpura, Chronic disease, Platelet transfusion, Child, Preschool, Chronic Disease, biology.protein, Antibody, medicine.symptom, business, Idiopathic thrombocytopenic purpura, Management of pediatric thrombocytopenia, Pediatric thrombocytopenia, Platelet count, Thrombocytopenia

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0562742533bb2d271ec1b4f9442feb59
http://hdl.handle.net/2318/69527