Zobrazeno 1 - 10 of 31 pro vyhledávání: '"Claudia Djambas Khayat"'
1
Akademický článek
The added value of WES reanalysis in the field of genetic diagnosis: lessons learned from 200 exomes in the Lebanese population
Autor: Nadine Jalkh, Sandra Corbani, Zahraa Haidar, Nadine Hamdan, Elias Farah, Joelle Abou Ghoch, Rouba Ghosn, Nabiha Salem, Ali Fawaz, Claudia Djambas Khayat, Mariam Rajab, Chebl Mourani, Adib Moukarzel, Simon Rassi, Bernard Gerbaka, Hicham Mansour, Malek Baassiri, Rawane Dagher, David Breich, André Mégarbané, Jean Pierre Desvignes, Valérie Delague, Cybel Mehawej, Eliane Chouery
Publikováno v: BMC Medical Genomics, Vol 12, Iss 1, Pp 1-7 (2019)
Abstract Background The past few decades have witnessed a tremendous development in the field of genetics. The implementation of next generation sequencing (NGS) technologies revolutionized the field of molecular biology and made the genetic informat
Externí odkaz: https://doaj.org/article/05a422e6778046b28f3efa5646c21d80
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2
Akademický článek
Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome
Autor: Alain Chebly, Claudia Djambas Khayat, Tony Yammine, Rima Korban, Warde Semaan, Jessica Bou Zeid, Chantal Farra
Publikováno v: Leukemia Research Reports, Vol 16, Iss , Pp 100277- (2021)
Acute myeloid leukemia (AML) patients with MLL-SEPT6 fusion represent a small subset of AML. The uncommon MLL-SEPT6 rearrangement results from t(X;11) or other variants like ins(X;11), and it is usually associated with complex cytogenetic abnormaliti
Externí odkaz: https://doaj.org/article/3751b9d1ef464ed5aecf299d32bc705e
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4
Pharmacokinetics, efficacy and safety of a novel fibrinogen concentrate in pediatric patients with congenital afibrinogenemia
Autor: Claudia Djambas Khayat, Jordi Navarro-Puerto, Cecil Reuben Ross, Kannan Subramanian, Nijalingappa K. Kalappanavar, Karen Rucker, Wei Liang, Elsa Mondou
Publikováno v: Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis.
Congenital afibrinogenemia treatment with plasma-derived fibrinogen concentrates in pediatric patients is limited. This study investigated the pharmacokinetics, surrogate efficacy, and safety of a plasma-derived fibrinogen concentrate (FIB Grifols) i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a54db8639239cff960419bcbbc3cdfe2
https://pubmed.ncbi.nlm.nih.gov/36484281
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5
Efficacy, Safety and Pharmacokinetic Results of a Phase III, Open-Label, Multicenter Study with a Plasma-Derived Von Willebrand Factor (VWF)/Factor VIII (FVIII) Concentrate in Pediatric Patients
Autor: Wilfried Seifert, Claudia Djambas Khayat, Genadi Iosava, Tobias Rogosch, Marta Julia Lopez, Irina Romashevskaya, Oleksandra Stasyshyn, Maria Teresa Pompa
Publikováno v: Journal of Blood Medicine. 12:483-495
Background: Plasma-derived von Willebrand factor/factor VIII (pdVWF/FVIII; VONCENTO®, CSL Behring) is a high-concentration, low-volume, high-purity concentrate, with a high level of VWF high-molecular-weight multimers and a VWF/FVIII ratio of ∼ 2.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5837d207439c9702924d1976ac870e1f
https://doi.org/10.2147/jbm.s299130
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6
Analysis of fibrinogen concentrate pharmacokinetics and dosing for bleeds and surgery in adults, adolescents, and children with congenital afibrinogenaemia and hypofibrinogenaemia
Autor: Claudia Djambas Khayat, Sunil D. Lohade, Omid R. Zekavat, Irina Kruzhkova, Cristina Solomon, Sigurd Knaub, Flora Peyvandi
Publikováno v: Haemophilia : the official journal of the World Federation of HemophiliaREFERENCES. 28(6)
Congenital afibrinogenaemia and hypofibrinogenaemia are rare coagulation disorders where clotting is impaired due to a lack of fibrinogen. Consequent bleeding episodes (BEs) are treated using human fibrinogen concentrate (HFC).This post-hoc analysis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af1eafef31e1abba211eda7a5eabc4bd
https://pubmed.ncbi.nlm.nih.gov/35925493
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7
Efficacy and safety of fibrinogen concentrate for perioperative prophylaxis of bleeding in adult, adolescent, and pediatric patients with congenital fibrinogen deficiency: FORMA-02 and FORMA-04 clinical trials
Autor: Claudia Djambas, Khayat, Sunil, Lohade, Omid Reza, Zekavat, Irina, Kruzhkova, Cristina, Solomon, Flora, Peyvandi
Publikováno v: Transfusion. 62(9)
Congenital fibrinogen deficiency (CFD) is a rare coagulation disorder placing patients at increased bleeding risk. Human fibrinogen concentrate (HFC) represents current standard of care for fibrinogen replacement in CFD, however, limited data are ava
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::429e9ea3256f9bbbe629431f7889b854
https://pubmed.ncbi.nlm.nih.gov/35932202
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8
Pharmacokinetics, Efficacy and Safety of a Plasma-Derived VWF/FVIII Concentrate (Formulation V) in Pediatric Patients with von Willebrand Disease (SWIFTLY-VWD Study)
Autor: Irina Romashevskaya, Guenter Auerswald, Marta Julia Lopez, Oleksandra Stasyshyn, Claudia Djambas Khayat, Wilfried Seifert, Tobias Rogosch, Genadi Iosava
Publikováno v: Journal of Blood Medicine
Guenter Auerswald,1 Claudia Djambas Khayat,2 Oleksandra Stasyshyn,3 Genadi Iosava,4 Irina Romashevskaya,5 Marta Julia López,6 Wilfried Seifert,7 Tobias Rogosch7 1Hess Kinderklinik, Klinikum Bremen-Mitte, Bremen, Germany; 2Hotel Dieu de France Hospit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e918752567451f25323b1e004ca1fc63
http://europepmc.org/articles/PMC7319533
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9
Heavy menstrual bleeding in women with inherited bleeding disorders
Autor: Rezan A. Kadir, Sylvia von Mackensen, Claudia Djambas Khayat, Emna Gouider
Publikováno v: Haemophilia. 26:16-19
Heavy menstrual bleeding (HMB) is the commonest bleeding symptom among women with inherited bleeding disorders (IBD). Since HMB starts at the very onset of menarche and continues throughout the reproductive life, the health related quality of life of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056750111db9a5b40d3eb323344d1e7d
https://doi.org/10.1111/hae.13888
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10
Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome
Autor: Claudia Djambas Khayat, Tony Yammine, Warde Semaan, Rima Korban, Alain Chebly, Jessica Bou Zeid, Chantal Farra
Publikováno v: Leukemia Research Reports, Vol 16, Iss, Pp 100277-(2021)
Leukemia Research Reports
Acute myeloid leukemia (AML) patients with MLL-SEPT6 fusion represent a small subset of AML. The uncommon MLL-SEPT6 rearrangement results from t(X;11) or other variants like ins(X;11), and it is usually associated with complex cytogenetic abnormaliti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34009468cd1946eed720bd48cbacf754
http://www.sciencedirect.com/science/article/pii/S2213048921000443
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