Enhanced carrier and prenatal diagnosis in the Italian haemophilia B population

av Goodeve, Anne
Publicerad 2007

Diagnosing von Willebrand disease: genetic analysis

av Goodeve, Anne
I publikationen Hematology Am Soc Hematol Educ Program (2016)

The molecular basis of von Willebrand disease: the under investigated, the unexpected and the overlooked

av Hampshire, Daniel J., Goodeve, Anne C.
Publicerad 2011

Principles of care for the diagnosis and treatment of von Willebrand disease

av Castaman, Giancarlo, Goodeve, Anne, Eikenboom, Jeroen
Publicerad 2013

von Willebrand Disease

av James, Paula D., Goodeve, Anne C.
Publicerad 2011

p.P2063S: a neutral VWF variant masquerading as a mutation

av Hampshire, Daniel J., Goodeve, Anne C.
Publicerad 2013

Laboratory aspects of von Willebrand disease: test repertoire and options for activity assays and genetic analysis

av Castaman, Giancarlo, Hillarp, Andreas, Goodeve, Anne
I publikationen Haemophilia (2014)

Genomics of bleeding disorders

av Goodeve, Anne C., Oldenburg, Johannes, Pavlova, Anna
I publikationen Haemophilia (2014)

Genetic Analysis of Bleeding Disorders

av Edison, Eunice, Konkle, Barbara A., Goodeve, Anne C.
I publikationen Haemophilia (2016)

Specific and global coagulation assays in the diagnosis of discrepant mild hemophilia A

av Bowyer, Annette E., Van Veen, Joost J., Goodeve, Anne C., Kitchen, Steve, Makris, Michael
Publicerad 2013

Genetic testing in bleeding disorders

av de Brasi, Carlos, El-Maarri, Osman, Perry, David J, Oldenburg, Johannes, Pezeshkpoor, Behnaz, Goodeve, Anne
I publikationen Haemophilia (2014)

Evaluation of a semi‐automated von Willebrand factor multimer assay, the Hydragel 5 von Willebrand multimer, by two European Centers

av Bowyer, Annette E., Goodfellow, Karen J., Seidel, Holger, Westhofen, Philipp, Stufano, Francesca, Goodeve, Anne, Kitchen, Stephen, Makris, Michael
I publikationen Res Pract Thromb Haemost (2018)

Somatic Mosaicism in Hemophilia A: A Fairly Common Event

av Leuer, Marco, Oldenburg, Johannes, Lavergne, Jean-Maurice, Ludwig, Michael, Fregin, Andreas, Eigel, Anton, Ljung, Rolf, Goodeve, Anne, Peake, Ian, Olek, Klaus
Publicerad 2001

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

av Naz, Arshi, Biswas, Arijit, Khan, Tehmina Nafees, Goodeve, Anne, Ahmed, Nisar, Saqlain, Nazish, Ahmed, Shariq, Ujjan, Ikram Din, Shamsi, Tahir S, Oldenburg, Johannes
I publikationen Thromb J (2017)

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

av Naz, Arshi, Biswas, Arijit, Khan, Tehmina Nafees, Goodeve, Anne, Ahmed, Nisar, Saqlain, Nazish, Ahmed, Shariq, Ujjan, Ikram Din, Shamsi, Tahir S., Oldenburg, Johannes
I publikationen Thromb J (2019)

Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD c...

av Hampshire, Daniel J., Burghel, George J., Goudemand, Jenny, Bouvet, Laura C. S., Eikenboom, Jeroen C. J., Schneppenheim, Reinhard, Budde, Ulrich, Peake, Ian R., Goodeve, Anne C.
Publicerad 2010

Assessment of the F9 genotype-specific FIX inhibitor risks and characterization of 10 novel severe F9 defects in the first molecular series of Argentine patients with haemophilia B

av Radic, Claudia Pamela, Rossetti, Liliana Carmen, Abelleyro, Miguel Martín, Candela, Miguel, Bianco, Raúl Pérez, Pinto, Miguel de Tezanos, Larripa, Irene Beatriz, Goodeve, Anne, De Brasi, Carlos Daniel
I publikationen Thromb Haemost (2012)

VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease

av Eikenboom, Jeroen, Federici, Augusto B., Dirven, Richard J., Castaman, Giancarlo, Rodeghiero, Francesco, Budde, Ulrich, Schneppenheim, Reinhard, Batlle, Javier, Canciani, Maria Teresa, Goudemand, Jenny, Peake, Ian, Goodeve, Anne, Peake, Ian, Goodeve, Anne, Rodeghiero, Francesco, Castaman, Giancarlo, Tosetto, Alberto, Federici, Augusto B., Batlle, Javier, Meyer, Dominique, Fressinaud, Edith, Mazurier, Claudine, Goudemand, Jenny, Eikenboom, Jeroen, Schneppenheim, Reinhard, Budde, Ulrich, Ingerslev, Jørgen, Vorlova, Zdena, Habart, David, Holmberg, Lars, Lethagen, Stefan, Pasi, John, Hill, Frank
Publicerad 2013

Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease

av Stockley, Jacqueline, Nisar, Shaista P., Leo, Vincenzo C., Sabi, Essa, Cunningham, Margaret R., Eikenboom, Jeroen C., Lethagen, Stefan, Schneppenheim, Reinhard, Goodeve, Anne C., Watson, Steve P., Mundell, Stuart J., Daly, Martina E.
I publikationen PLoS One (2015)

The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance

av Mufti, Ahmad H., Ogiwara, Kenichi, Swystun, Laura L., Eikenboom, Jeroen C. J., Budde, Ulrich, Hopman, Wilma M., Halldén, Christer, Goudemand, Jenny, Peake, Ian R., Goodeve, Anne C., Lillicrap, David, Hampshire, Daniel J.
I publikationen Blood Adv (2018)