Zobrazeno 1 - 10
of 1 015
pro vyhledávání: '"Pujol-Moix N."'
Autor:
Pujol-Moix N; Platelet Pathology Unit, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. npujolmoix@gmail.com.; Medicine Department, Universitat Autònoma de Barcelona, Barcelona, Spain. npujolmoix@gmail.com., Muñiz-Díaz E; Immunohematology Laboratory, Banc de Sang i Teixits de Catalunya, Barcelona, Spain., Español I; Platelet Pathology Unit, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; Medicine Department, Universitat Autònoma de Barcelona, Barcelona, Spain.; Hematology Department, Hospital Clínico Universitario Virgen de la Arrixaca., Murcia, Spain., Mojal S; Thrombosis and Haemostasis Research, Institut d'Investigació Biomèdica Sant Pau (IIB Sant Pau), Barcelona, Spain., Soler A; Platelet Pathology Unit, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; Hematology Department, Hospital Universitari Parc Taulí. Sabadell, Barcelona, Spain., Souto JC; Thrombosis and Haemostasis Research, Institut d'Investigació Biomèdica Sant Pau (IIB Sant Pau), Barcelona, Spain.; Unitat d'Hemostàsia i Trombosi., Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Publikováno v:
Annals of hematology [Ann Hematol] 2023 Jun; Vol. 102 (6), pp. 1363-1374. Date of Electronic Publication: 2023 Mar 31.
Autor:
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.
Publikováno v:
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
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
MYH9-related disease (MYH9-RD) is a rare autosomal-dominant disorder caused by mutations in the gene for nonmuscle myosin heavy chain IIA (NMMHC-IIA). MYH9-RD is characterized by a considerable variability in clinical evolution: patients present at b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b3202308793ba3d6d45b4fe01ee6e8
https://research.rug.nl/en/publications/8f687127-8140-4108-abe8-7c14ccda866a
https://research.rug.nl/en/publications/8f687127-8140-4108-abe8-7c14ccda866a
Autor:
Chang, Syuan-Ting1 (AUTHOR), Chuang, Yi-Fang2,3 (AUTHOR), Li, Ai-Hsien4,5 (AUTHOR), Fan, Yang-Teng4 (AUTHOR), Liao, Man-Ru4,5 (AUTHOR), Chen, I-Yu6 (AUTHOR), Hung, Ruo-Wei6 (AUTHOR), Yang, Tienyu Owen7 (AUTHOR), Chiu, Yen-Ling4,6 (AUTHOR) yenling.chiu@saturn.yzu.edu.tw
Publikováno v:
Immunity & Ageing. 10/29/2024, Vol. 21 Issue 1, p1-12. 12p.
Autor:
Yusoff, Halianis1, Hami, Rohayu1, Mokhti, Fauzana A.2, Hussin, Hasmah3, Ghazali, Mohamad Bazli4, Mohamad, Siti Mardhiana1 mardhiana@usm.my
Publikováno v:
Malaysian Journal of Medicine & Health Sciences. 2024 Supplement, Vol. 20, p86-92. 7p.
Autor:
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.
Publikováno v:
Publons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e2abf07f0112ca9693b17d5a2938767a
http://hdl.handle.net/11573/988434
http://hdl.handle.net/11573/988434
Autor:
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
Publikováno v:
BRITISH JOURNAL OF HAEMATOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Europe PubMed Central
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Europe PubMed Central
This study evaluated 65 pregnancies in 34 women with five different inherited platelet function disorders. Gestation was similar to that of the general population. Severe bleeds requiring blood transfusions were observed in 50% of deliveries in Glanz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2b31aa3ebfce202913b36549a20391f
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2035
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2035
Autor:
Rio-Machin A; Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK. a.rio-machin@qmul.ac.uk., Vulliamy T; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK. t.vulliamy@qmul.ac.uk., Hug N; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK., Walne A; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK., Tawana K; Department of Haematology, Addenbrooke's Hospital, Cambridge, UK., Cardoso S; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK., Ellison A; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK., Pontikos N; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK., Wang J; Centre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK., Tummala H; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK., Al Seraihi AFH; Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK., Alnajar J; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK., Bewicke-Copley F; Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK., Armes H; Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK., Barnett M; The Leukemia/BMT Program of British Columbia, Division of Hematology, Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada., Bloor A; Department of Haematology, Christie Hospital, Manchester, UK., Bödör C; MTA-SE Lendulet Molecular Oncohematology Research Group, 1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary., Bowen D; Department of Haematology, St James's University Hospital, Leeds, UK., Fenaux P; Service d'hématologie Séniors, Hôpital St Louis/Université Paris, Paris, France., Green A; National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland., Hallahan A; Children's Health Queensland Hospital and Health Service, Queensland Children's Hospital, South Brisbane, QLD, Australia., Hjorth-Hansen H; Department of Hematology, St Olavs Hospital and Institute of Cancer Research and Molecular Medicine (IKM) Norwegian University of Science and Technology (NTNU), Trondheim, Norway., Hossain U; Department of Haematology, Whipps Cross Hospital, Barts NHS Trust, London, UK., Killick S; Department of Haematology, The Royal Bournemouth Hospital NHS Foundation Trust, Bournemouth, UK., Lawson S; Department of Haematology, Birmingham Children's Hospital, Birmingham, UK., Layton M; Centre for Haematology, Imperial College London, Hammersmith Hospital, London, UK., Male AM; Clinic Genetics Unit, Great Ormond Street Hospital, London, UK., Marsh J; Department of Haematological Medicine, Haematology Institute, King's College Hospital, London, UK., Mehta P; Bristol Haematology Unit, University Hospitals Bristol NHS Foundation Trust, Bristol, UK., Mous R; UMC Utrecht Cancer Center, Universitair Medisch Centrum Utrecht, Huispostnummer, Utrecht, Netherlands., Nomdedéu JF; Laboratori d´Hematologia, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain., Owen C; Division of Hematology and Hematological Malignancies, Foothills Medical Centre, Calgary, AB, Canada., Pavlu J; Centre for Haematology, Imperial College London, Hammersmith Hospital, London, UK., Payne EM; Department of Haematology, UCL Cancer Institute, University College London, London, UK., Protheroe RE; Bristol Haematology Unit, University Hospitals Bristol NHS Foundation Trust, Bristol, UK., Preudhomme C; Laboratory of Hematology, Biology and Pathology Center, Centre Hospitalier Regional Universitaire de Lille, Lille, France.; Jean-Pierre Aubert Research Center, INSERM, Universitaire de Lille, Lille, France., Pujol-Moix N; Laboratori d´Hematologia, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain., Renneville A; Broad Institute of Harvard and MIT, Cambridge, MA, USA., Russell N; Centre for Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK., Saggar A; Clinical Genetics, St George's Hospital Medical School, London, UK., Sciuccati G; Servicio de Hematologia y Oncologia, Hospital de Pediatría 'Prof. Dr. Juan P. Garrahan', Ciudad Autonoma de Buenos Aires, Argentina., Taussig D; Haemato-oncology Department, Royal Marsden Hospital, Sutton, UK., Toze CL; The Leukemia/BMT Program of British Columbia, Division of Hematology, Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada., Uyttebroeck A; Department of Hematology, University Hospitals Leuven, Leuven, Belgium., Vandenberghe P; Department of Hematology, University Hospitals Leuven, Leuven, Belgium., Schlegelberger B; Institut für Humangenetik, Medizinische Hochschule Hannover, Hannover, Germany., Ripperger T; Institut für Humangenetik, Medizinische Hochschule Hannover, Hannover, Germany., Steinemann D; Institut für Humangenetik, Medizinische Hochschule Hannover, Hannover, Germany., Wu J; British Columbia Children's Hospital, Vancouver, BC, Canada., Mason J; West Midlands Regional Genetics Laboratory, Birmingham Women's NHS Foundation Trust, Birmingham, UK., Page P; West Midlands Regional Genetics Laboratory, Birmingham Women's NHS Foundation Trust, Birmingham, UK., Akiki S; Department of Laboratory Medicine & Pathology, Qatar Rehabilitation Institute, Hamad Bin Khalifa Medical City (HBKM), Doha, Qatar., Reay K; West Midlands Regional Genetics Laboratory, Birmingham Women's NHS Foundation Trust, Birmingham, UK., Cavenagh JD; Department of Haematology, St Bartholomew's Hospital, Barts NHS Trust, London, UK., Plagnol V; Genetics Institute, University College London, London, UK., Caceres JF; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK., Fitzgibbon J; Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK. j.fitzgibbon@qmul.ac.uk., Dokal I; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, UK. i.dokal@qmul.ac.uk.; Barts Health NHS Trust, London, UK. i.dokal@qmul.ac.uk.
Publikováno v:
Nature communications [Nat Commun] 2020 Feb 25; Vol. 11 (1), pp. 1044. Date of Electronic Publication: 2020 Feb 25.
Autor:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8532a750443ffdc3d8b15a86e608e405
https://hdl.handle.net/11368/2625642
https://hdl.handle.net/11368/2625642
Autor:
García-Dabrio M.C., Pujol-Moix N., Martinez-Perez A., Fontcuberta J., Souto J.C., Soria J.M., Nomdedéu J.F.
Publikováno v:
ACTA HAEMATOLOGICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Introduction: Flow cytometry analysis of lymphocyte subsets in peripheral blood is a common technique in diagnostic laboratories. Abnormal values have been identified in prevalent infections, autoimmune disorders and neoplastic diseases. Reference ra
Externí odkaz:
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
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84860190478&doi=10.1159/000337051&partnerID=40&md5=d7298a14f671d256fe8fdb22c9f86bed
Autor:
Feroz, Wasim1 (AUTHOR) ferozwm@mail.uc.edu, Park, Briley SoYoung1,2 (AUTHOR) sarahpark0806@gmail.com, Siripurapu, Meghna1 (AUTHOR) meghna.siripurapu24@ihsd.us, Ntim, Nicole1 (AUTHOR) ntimne@mail.uc.edu, Kilroy, Mary Kate1 (AUTHOR) kilroymk@mail.uc.edu, Sheikh, Arwah Mohammad Ali3 (AUTHOR) sheikhaw@ucmail.uc.edu, Mishra, Rosalin1 (AUTHOR) rosalin.mishra@cchmc.org, Garrett, Joan T.1 (AUTHOR) garrejn@ucmail.uc.edu
Publikováno v:
International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9435. 45p.