C M Kessler
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Explore the profile of C M Kessler including associated specialties, affiliations and a list of published articles.
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Articles
145
Citations
1472
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Recent Articles
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Kessler C, Benchikh El Fegoun S, Worster A
Haemophilia
. 2018 May;
24(4):536-547.
PMID: 29741299
Aims: To systematically review the effectiveness of on-demand treatment with recombinant coagulation factor VIIa (rFVIIa) in congenital haemophilia with inhibitors and, if feasible, perform a meta-analysis of the data. Materials...
3.
Khatri N, Patel B, Kohli D, Solomon S, Bull-Henry K, Kessler C
Haemophilia
. 2018 Feb;
24(2):278-282.
PMID: 29446520
Introduction: Lenalidomide is a thalidomide analog with anti-angiogenic properties. Previous case reports suggest its efficacy in preventing gastrointestinal bleeding (GIB) secondary to angiodysplasia (AD) in hereditary haemorrhagic telangiectasia and potentially...
4.
Zozulya N, Kessler C, Klukowska A, von Depka M, Hampton K, Hay C, et al.
Haemophilia
. 2017 Oct;
24(1):70-76.
PMID: 29048712
Introduction: Haemophilia A patients are at a high risk of excess bleeding during surgeries. The aim of haemostatic therapy during the perioperative period is to normalize FVIII level perioperatively and...
5.
Napolitano M, Siragusa S, Mancuso S, Kessler C
Haemophilia
. 2017 Sep;
24(1):43-56.
PMID: 28960809
Aim: There is a paucity of data on the clinical presentation and management of cancer patients with acquired haemophilia (AH), we here report a systematic literature review on acquired haemophilia...
6.
Humphries T, Mathew P, Kessler C
Haemophilia
. 2017 Jun;
23(4):e380-e382.
PMID: 28574634
No abstract available.
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Witkop M, Neff A, Buckner T, Wang M, Batt K, Kessler C, et al.
Haemophilia
. 2017 Apr;
23(4):556-565.
PMID: 28419637
Introduction: Haemophilia is characterized by frequent haemarthrosis, leading to acute/chronic joint pain. Aim: To assess self-reported prevalence, description and management of pain in adult males with mild-to-severe haemophilia and history...
9.
Srivastava A, Serban M, Werner S, Schwartz B, Kessler C
Haemophilia
. 2016 Dec;
23(2):264-272.
PMID: 28026130
Introduction: Surgical procedures in von Willebrand disease (VWD) patients may require prophylactic treatment with exogenous von Willebrand factor (VWF) and coagulation factor VIII (FVIII) to prevent excessive bleeding. Wilate is...
10.
Ragni M, Yabes J, Fogarty P, Josephson N, Kessler C, Neff A, et al.
Haemophilia
. 2016 Dec;
23(1):e43-e46.
PMID: 27943502
No abstract available.