نتائج البحث - "Pujol-Moix N."

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

View record at Wiley

7

Outcomes of 65 pregnancies in 34 women with 5 different forms of inherited platelet function disorders enrolled in a retrospective and multicentric study, on behalf of eha-swg on thrombocytopenias and platelet function disorders

المؤلفون: Noris, P., Civaschi, E., Catherine Klersy, Melazzini, F., Pujol-Moix, N., Santoro, C., Cattaneo, M., Lavenu-Bombled, C., Bury, L., Minuz, P., Nurden, P., Cid-Haro, A. R., Cuker, A., Latger-Cannard, V., Favier, R., Nichele, I., Balduini, C. L.

المصدر: Publons

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e2abf07f0112ca9693b17d5a2938767a
http://hdl.handle.net/11573/988434

8

Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders

المؤلفون: Civaschi E, Klersy C, Melazzini F, Pujol-Moix N, Santoro C, Cattaneo M, Lavenu-Bombled C, Bury L, Minuz P, Nurden P, Ar, Cid, Cuker A, Latger-Cannard V, Favier R, Nichele I, Patrizia Noris, European Haematology Association - Scientific Working Group on Thrombocytopenias and Platelet Function Disorders

المصدر: BRITISH JOURNAL OF HAEMATOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Europe PubMed Central

مصطلحات موضوعية: bleeding risk, inherited platelet disorders, perinatal haemostasis, bleeding diathesis, pregnancy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2b31aa3ebfce202913b36549a20391f
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2035

View record at Wiley

9

Gray Platelet Syndrome: association of NBEAL2 mutations with thrombocytopenia and absence of alpha-granules in platelets

المؤلفون: De Candia, E., Bottega, Roberta, Pecci, A., Pujol Moix, N., Heller, P., Noris, P., DE ROCCO, Daniela, Podda, G. M., Balduini, C. L., Savoia, Anna

المساهمون: '-', E., De Candia, Bottega, Roberta, A., Pecci, N., Pujol Moix, P., Heller, P., Nori, DE ROCCO, Daniela, Podda, G. M., Balduini, C. L., Savoia, Anna

مصطلحات موضوعية: platelet, GPS, mutations, mutation

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8532a750443ffdc3d8b15a86e608e405
https://hdl.handle.net/11368/2625642

10

Influence of age, gender and lifestyle in lymphocyte subsets: Report from the Spanish gait-2 study

المؤلفون: García-Dabrio M.C., Pujol-Moix N., Martinez-Perez A., Fontcuberta J., Souto J.C., Soria J.M., Nomdedéu J.F.

المصدر: ACTA HAEMATOLOGICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

مصطلحات موضوعية: Male, CD3+ T lymphocyte, cigarette smoking, physical activity, health status, genetic analysis, preschool child, Body Mass Index, human experiment, Reference Values, T-Lymphocyte Subsets, gender, CD8+ T lymphocyte, Child, fertility, Aged, 80 and over, Sex Characteristics, adult, article, Age Factors, Middle Aged, Flow Cytometry, Killer Cells, Natural, female, priority journal, Child, Preschool, idiopathic disease, lifestyle, Adolescent, Alcohol Drinking, alcohol consumption, CD56 antigen, Motor Activity, CD4 CD8 ratio, Young Adult, Humans, human, normal human, Life Style, thrombophilia, Aged, standardization, CD4+ T lymphocyte, CD19 antigen, natural killer cell, groups by age and sex, school child, body mass, Lymphocyte Subsets, Spain, lymphocyte subpopulation

URL الوصول: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::c0c05181b3152e6dbc209aa59c283da5
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84860190478&doi=10.1159/000337051&partnerID=40&md5=d7298a14f671d256fe8fdb22c9f86bed

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