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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2004 2
2005 1
2007 1
2008 1
2009 2
2010 1
2011 2
2012 2
2013 2
2014 4
2015 3
2016 3
2017 2
2018 1
2019 7
2020 4
2022 2
2023 2
2024 1

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38 results

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Page 1
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F. Mohsenian S, et al. Among authors: menegatti m. Blood Adv. 2024 Mar 26;8(6):1392-1404. doi: 10.1182/bloodadvances.2023012186. Blood Adv. 2024. PMID: 38286442 Free PMC article.
Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for ultra-rare inherited bleeding disorders.
Nugent D, Acharya SS, Baumann KJ, Bedrosian C, Bialas R, Brown K, Corzo D, Haidar A, Hayward CPM, Marks P, Menegatti M, Miller ME, Nammacher K, Palla R, Peltier S, Pruthi RK, Recht M, Sørensen B, Tarantino M, Wolberg AS, Shapiro AD. Nugent D, et al. Among authors: menegatti m. Expert Rev Hematol. 2023 Mar;16(sup1):55-70. doi: 10.1080/17474086.2023.2175661. Expert Rev Hematol. 2023. PMID: 36920862 Free PMC article.
A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family.
Guipponi M, Masclaux F, Sloan-Béna F, Di Sanza C, Özbek N, Peyvandi F, Menegatti M, Casini A, Malbora B, Neerman-Arbez M. Guipponi M, et al. Among authors: menegatti m. Haematologica. 2022 May 1;107(5):1064-1071. doi: 10.3324/haematol.2021.278945. Haematologica. 2022. PMID: 34196169 Free PMC article.
An international registry of patients with plasminogen deficiency (HISTORY).
Shapiro AD, Menegatti M, Palla R, Boscarino M, Roberson C, Lanzi P, Bowen J, Nakar C, Janson IA, Peyvandi F. Shapiro AD, et al. Among authors: menegatti m. Haematologica. 2020 Mar;105(3):554-561. doi: 10.3324/haematol.2019.241158. Epub 2020 Jan 30. Haematologica. 2020. PMID: 32001536 Free PMC article. Review.
Management of rare acquired bleeding disorders.
Menegatti M, Biguzzi E, Peyvandi F. Menegatti M, et al. Hematology Am Soc Hematol Educ Program. 2019 Dec 6;2019(1):80-87. doi: 10.1182/hematology.2019000066. Hematology Am Soc Hematol Educ Program. 2019. PMID: 31808848 Free PMC article.
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease.
Paraboschi EM, Khera AV, Merlini PA, Gigante L, Peyvandi F, Chaffin M, Menegatti M, Busti F, Girelli D, Martinelli N, Olivieri O, Kathiresan S, Ardissino D, Asselta R, Duga S. Paraboschi EM, et al. Among authors: menegatti m. Haematologica. 2020 Jul;105(7):e365-e369. doi: 10.3324/haematol.2019.237750. Epub 2019 Nov 7. Haematologica. 2020. PMID: 31699787 Free PMC article. No abstract available.
Profiling the mutational landscape of coagulation factor V deficiency.
Paraboschi EM, Menegatti M, Rimoldi V, Borhany M, Abdelwahab M, Gemmati D, Peyvandi F, Duga S, Asselta R. Paraboschi EM, et al. Among authors: menegatti m. Haematologica. 2020 Apr;105(4):e180-e185. doi: 10.3324/haematol.2019.232587. Epub 2019 Aug 8. Haematologica. 2020. PMID: 31399523 Free PMC article. No abstract available.
38 results