Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2001 1
2002 2
2003 1
2006 3
2007 2
2008 2
2009 3
2010 2
2011 1
2012 7
2013 8
2014 4
2015 2
2016 4
2017 4
2018 2
2019 3
2020 2
2021 2
2022 3
2023 3
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

52 results

Results by year

Filters applied: . Clear all
Page 1
Thrombotic thrombocytopenic purpura.
Kremer Hovinga JA, Coppo P, Lämmle B, Moake JL, Miyata T, Vanhoorelbeke K. Kremer Hovinga JA, et al. Nat Rev Dis Primers. 2017 Apr 6;3:17020. doi: 10.1038/nrdp.2017.20. Nat Rev Dis Primers. 2017. PMID: 28382967 Review.
Ultra-large vWF strings remain uncleaved after endothelial cell secretion and anchorage, bind to platelets and form microthrombi, leading to the clinical manifestations of TTP. Congenital TTP (Upshaw-Schulman syndrome) is the result of homozygous or compound …
Ultra-large vWF strings remain uncleaved after endothelial cell secretion and anchorage, bind to platelets and form microthrombi, leading to …
Upshaw-Schulman Syndrome.
Ahmad R, Natiq M, Aziz M. Ahmad R, et al. J Coll Physicians Surg Pak. 2015 Oct;25 Suppl 2:S97-9. doi: 10.2015/JCPSP.S9799. J Coll Physicians Surg Pak. 2015. PMID: 26522217
On the basis of history, physical examination and extensive investigations, patient was diagnosed as Upshaw-Schulman syndrome, a rare case of congenital Thrombotic Thrombocytopenic Purpura (TTP). ...
On the basis of history, physical examination and extensive investigations, patient was diagnosed as Upshaw-Schulman syndro …
Hereditary Thrombotic Thrombocytopenic Purpura.
Nusrat S, Beg K, Khan O, Sinha A, George J. Nusrat S, et al. Genes (Basel). 2023 Oct 18;14(10):1956. doi: 10.3390/genes14101956. Genes (Basel). 2023. PMID: 37895305 Free PMC article. Review.
Hereditary thrombotic thrombocytopenic purpura (hTTP), also known as Upshaw-Schulman syndrome, is a rare genetic disorder caused by mutations in the ADAMTS13 gene that leads to decreased or absent production of the plasma von Willebrand factor (VWF)-cleaving …
Hereditary thrombotic thrombocytopenic purpura (hTTP), also known as Upshaw-Schulman syndrome, is a rare genetic disord …
Upshaw-Schulman syndrome diagnosed during pregnancy complicated by reversible cerebral vasoconstriction syndrome.
Tsuda M, Shiratsuchi M, Nakashima Y, Ikeda M, Muta H, Narazaki T, Masuda T, Kimura D, Takamatsu A, Matsumoto M, Fujimura Y, Kokame K, Matsushima T, Ogawa Y. Tsuda M, et al. Transfus Apher Sci. 2018 Dec;57(6):790-792. doi: 10.1016/j.transci.2018.10.023. Epub 2018 Nov 16. Transfus Apher Sci. 2018. PMID: 30471945
Upshaw-Schulman syndrome (USS) is an inherited type of thrombotic thrombocytopenic purpura (TTP) that is extremely rare, but often diagnosed during pregnancy. ...
Upshaw-Schulman syndrome (USS) is an inherited type of thrombotic thrombocytopenic purpura (TTP) that is extremely rare …
Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.
Pérez-Rodríguez A, Lourés E, Rodríguez-Trillo Á, Costa-Pinto J, García-Rivero A, Batlle-López A, Batlle J, López-Fernández MF. Pérez-Rodríguez A, et al. Thromb Res. 2014 Dec;134(6):1171-5. doi: 10.1016/j.thromres.2014.09.004. Epub 2014 Sep 10. Thromb Res. 2014. PMID: 25242241 Review.
Congenital thrombotic thrombocytopenic purpura (TTP), also known as Upshaw-Schulman syndrome, is associated with an inherited deficiency of ADAMTS13, a von Willebrand factor-cleaving protease. ...The prevalence of this entity is probably underestimated becaus …
Congenital thrombotic thrombocytopenic purpura (TTP), also known as Upshaw-Schulman syndrome, is associated with an inh …
Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome.
Fujimura Y, Matsumoto M, Yagi H, Yoshioka A, Matsui T, Titani K. Fujimura Y, et al. Int J Hematol. 2002 Jan;75(1):25-34. doi: 10.1007/BF02981975. Int J Hematol. 2002. PMID: 11843286 Review.
Furthermore, a congenital deficiency of this enzyme activity has been shown to cause Upshaw-Schulman syndrome, a complex constitutional bleeding diathesis. ...
Furthermore, a congenital deficiency of this enzyme activity has been shown to cause Upshaw-Schulman syndrome, a comple …
Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan.
Fujimura Y, Matsumoto M, Isonishi A, Yagi H, Kokame K, Soejima K, Murata M, Miyata T. Fujimura Y, et al. J Thromb Haemost. 2011 Jul;9 Suppl 1:283-301. doi: 10.1111/j.1538-7836.2011.04341.x. J Thromb Haemost. 2011. PMID: 21781265 Free article. Review.
Upshaw-Schulman syndrome (USS) is an extremely rare hereditary deficiency of ADAMTS13 activity, termed congenital TTP. ...
Upshaw-Schulman syndrome (USS) is an extremely rare hereditary deficiency of ADAMTS13 activity, termed congenital TTP. …
Hereditary TTP/Upshaw-Schulman syndrome: the ductus arteriosus controls newborn survival.
Fujimura Y. Fujimura Y. Int J Hematol. 2024 May;119(5):532-540. doi: 10.1007/s12185-024-03731-1. Epub 2024 Mar 27. Int J Hematol. 2024. PMID: 38536644 Review.
Hereditary TTP (hTTP), termed Upshaw-Schulman syndrome, is an ultra-rare disorder caused by a severe deficiency of plasma ADAMTS13 activity that allows circulation of ultra-large von Willebrand factor (UL-VWF) multimers. ...
Hereditary TTP (hTTP), termed Upshaw-Schulman syndrome, is an ultra-rare disorder caused by a severe deficiency of plas …
Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry.
Mansouri Taleghani M, von Krogh AS, Fujimura Y, George JN, Hrachovinová I, Knöbl PN, Quist-Paulsen P, Schneppenheim R, Lämmle B, Kremer Hovinga JA. Mansouri Taleghani M, et al. Hamostaseologie. 2013 May 29;33(2):138-43. doi: 10.5482/HAMO-13-04-0026. Hamostaseologie. 2013. PMID: 23715103 Review.
Hereditary thrombotic thrombocytopenic purpura, Upshaw-Schulman syndrome, ADAMTS13 Hereditary thrombotic thrombocytopenic purpura (TTP), also known as Upshaw-Schulman syndrome, is a rare recessively inherited disease. ...Through the hered …
Hereditary thrombotic thrombocytopenic purpura, Upshaw-Schulman syndrome, ADAMTS13 Hereditary thrombotic thrombocytopen …
Pregnancy in Upshaw-Schulman syndrome.
Kentouche K, Voigt A, Schleussner E, Schneppenheim R, Budde U, Beck JF, Stefańska-Windyga E, Windyga J. Kentouche K, et al. Hamostaseologie. 2013 May 29;33(2):144-8. doi: 10.5482/HAMO-13-04-0025. Hamostaseologie. 2013. PMID: 23715104
The Upshaw Schulman syndrome (MIM #274150) is a hereditary deficiency of the von Willebrand factor cleaving protease (ADAMTS13) due to homozygous or compound heterozygous mutations in the ADAMTS13 gene. ...
The Upshaw Schulman syndrome (MIM #274150) is a hereditary deficiency of the von Willebrand factor cleaving protease (A …
52 results