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المؤلفون: NORIS, P., KLERSY, C., ZECCA, M., ARCAINI, L., PECCI, A., MELAZZINI, F., TERULLA, V., BOZZI, V., AMBAGLIO, C., PASSAMONTI, F., LOCATELLI, F., BALDUINI, C.L.

المصدر: In Journal of Thrombosis and Haemostasis December 2009 7(12):2131-2136

المؤلفون: Balduini, A. ^*, Malara, A., Pecci, A., Badalucco, S., Bozzi, V., Pallotta, I., Noris, P., Torti, M., Balduini, C.L.

المصدر: In Journal of Thrombosis and Haemostasis March 2009 7(3):478-484

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المؤلفون: Pecci, A, Klersy, C, Gresele, P, Lee, K, De Rocco, D, Bozzi, V, Russo, G, Heller, Pg, Loffredo, G, Ballmaier, M, Fabris, F, Beggiato, E, Kahr, Wha, Pujol-Moix, N, Platokouki, H, Matthijs, G, Noris, P, Yerram, P, Hermans, C, Batzios, S, De Groot, M, Zieger, B, De Candia, E, Fraticelli, V, Kersseboom, R, Piccoli, Gb, Zimmermann, S, Zaninetti, C, Nicchia, E, Baronci, C, Seri, M, Knight, Pj, Balduini, Cl, Savoia, A, Van Geet, C, Geber, B, Economou, M, Fierro, T, Glembotsky, Ac, Vianello, F, Guthner, C.

المساهمون: Pecci, A, Klersy, C, Gresele, P, Lee, Kj, De Rocco, D, Bozzi, V, Russo, G, Heller, Pg, Loffredo, G, Ballmaier, M, Fabris, F, Beggiato, E, Kahr, Wh, Pujol-Moix, N, Platokouki, H, Van Geet, C, Noris, P, Yerram, P, Hermans, C, Gerber, B, Economou, M, De Groot, M, Zieger, B, De Candia, E, Fraticelli, V, Kersseboom, R, Piccoli, Gb, Zimmermann, S, Fierro, T, Glembotsky, Ac, Vianello, F, Zaninetti, C, Nicchia, E, Güthner, C, Baronci, C, Seri, M, Knight, Pj, Balduini, Cl, Savoia, A., DE ROCCO, Daniela, Pujol Moix, N, Nicchia, Elena, Savoia, Anna, University of Zurich

المصدر: Human Mutation, 35(2), 236-247. Wiley
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

مصطلحات موضوعية: Male, Oncology, thrombocytopenia, Medicina Clínica, Disease, Malattia MYH9 associata, Myh9 related disease, MYH9 RELATED DISEASE, Myh9, MYH9, Risk Factors, purl.org/becyt/ford/3.2 [https], Genotype, Genetics(clinical), CRYSTAL-STRUCTURE, Age of Onset, IIA, Genetics (clinical), deafne, MYOSIN HEAVY-CHAIN, EPSTEIN-SYNDROME, Molecular Motor Proteins, FECHTNER SYNDROMES, Trombocitopenia, Penetrance, POWER STROKE STATE, Phenotype, Italy, nephropathy, Female, purl.org/becyt/ford/3 [https], Miosina No Muscular Iia, Adult, 2716 Genetics (clinical), medicine.medical_specialty, CIENCIAS MÉDICAS Y DE LA SALUD, MOTOR DOMAIN, Hearing Loss, Sensorineural, Genetic counseling, 610 Medicine & health, Biology, nonmuscle myosin, Article, Cataract, Nephropathy, 1311 Genetics, Internal medicine, deafness, Genetics, medicine, Humans, Hematología, Gene, Genetic Association Studies, Hereditaria, Myosin Heavy Chains, MUTATIONS, Settore MED/09 - MEDICINA INTERNA, medicine.disease, Amino Acid Substitution, Epstein Syndrome, Mutation, 10032 Clinic for Oncology and Hematology, Linear Models, SMOOTH-MUSCLE MYOSIN

وصف الملف: STAMPA; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b3202308793ba3d6d45b4fe01ee6e8
https://research.rug.nl/en/publications/8f687127-8140-4108-abe8-7c14ccda866a

المؤلفون: Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Patrizia Noris, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P, Myh, Italian Registry For -Releated Diseases

المساهمون: Pecci, A., Biino, G., Fierro, T., Bozzi, V., Mezzasoma, A., Noris, P., Ramenghi, U., Loffredo, G., Fabris, F., Momi, S., Magrini, U., Pirastu, M., Savoia, Anna, Balduini, C., Gresele, P., Italian Registry for MYH9 releated, Diseases

المصدر: Europe PubMed Central
PloS one 7 (2012). doi:10.1371/journal.pone.0035986
info:cnr-pdr/source/autori:Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P; for the Italian Registry for MYH9-releated diseases/titolo:Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome/doi:10.1371%2Fjournal.pone.0035986/rivista:PloS one/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume:7
PLoS ONE
PLoS ONE, Vol 7, Iss 4, p e35986 (2012)

مصطلحات موضوعية: MYH9, Thrombocytopenia, Male, Pathology, MYH9 Mutations, Anatomy and Physiology, Biopsy, lcsh:Medicine, Disease, Biochemistry, Liver Function Tests, may-heggly, Odds Ratio, lcsh:Science, IIA, Child, inherited thrombocytopenias, Aged, 80 and over, Multidisciplinary, medicine.diagnostic_test, Molecular Motor Proteins, Liver Diseases, Fatty liver, fechtner-syndrome, myosin heavy chain, diagnostic algorithm, epstein-syndrome, cell motility, Macrothrombocytopenia, Syndrome, Hematology, Middle Aged, Immunohistochemistry, Malattia MYH9 correlata, Enzymes, Liver, Autosomal Dominant, Child, Preschool, Medicine, Female, Research Article, Adult, Platelets, medicine.medical_specialty, Adolescent, Gastroenterology and Hepatology, Neurological System, Nephropathy, Enzyme Regulation, Young Adult, medicine, Humans, Clinical significance, Abnormalities, Multiple, Biology, Aged, Demography, Clinical Genetics, Myosin Heavy Chains, business.industry, lcsh:R, Case-control study, Infant, Odds ratio, medicine.disease, Case-Control Studies, Mutation, lcsh:Q, business, Liver function tests, Follow-Up Studies, Neuroscience

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bb1b18abda4787c7f860dc65240b568
http://hdl.handle.net/11562/1064408

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