Search Results - "Miclea, D."

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  1. 1

    Role of Glycosylation in Conformational Stability, Activity, Macromolecular Interaction and Immunogenicity of Recombinant Human Factor VIII by Kosloski, Matthew P., Miclea, Razvan D., Balu-Iyer, Sathy V.

    Published in The AAPS journal (01-09-2009)
    “…Factor VIII (FVIII) is a multi-domain glycoprotein that is an essential cofactor in the blood coagulation cascade. Its deficiency or dysfunction causes…”
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    Journal Article
  2. 2

    Lipid binding region (2303-2332) is involved in aggregation of recombinant human FVIII (rFVIII) by Ramani, Karthik, Purohit, Vivek S, Miclea, Razvan D, Middaugh, C Russell, Balasubramanian, Sathyamangalam V

    Published in Journal of pharmaceutical sciences (01-06-2005)
    “…Factor VIII (FVIII) is a multi-domain protein that is important in the clotting cascade. Its deficiency causes Hemophilia A, a bleeding disorder. The unfolding…”
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    Journal Article
  3. 3

    Phosphatidylserine containing liposomes reduce immunogenicity of recombinant human factor VIII (rFVIII) in a murine model of hemophilia A by Ramani, Karthik, Miclea, Razvan D, Purohit, Vivek S, Mager, Donald E, Straubinger, Robert M, Balu-Iyer, Sathy V

    Published in Journal of pharmaceutical sciences (01-04-2008)
    “…Factor VIII (FVIII) is a multidomain protein that is deficient in hemophilia A, a clinically important bleeding disorder. Replacement therapy using recombinant…”
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    Journal Article
  4. 4

    Effect of route of administration of human recombinant factor VIII on its immunogenicity in Hemophilia A mice by Peng, Aaron, Gaitonde, Puneet, Kosloski, Matthew P, Miclea, Razvan D, Varma, Prashant, Balu-Iyer, Sathy V

    Published in Journal of pharmaceutical sciences (01-12-2009)
    “…Factor VIII is a multi-domain glycoprotein and is an essential cofactor in the blood coagulation cascade. Its deficiency or dysfunction causes Hemophilia A, a…”
    Get more information
    Journal Article
  5. 5

    Development and characterization of lipidic cochleate containing recombinant factor VIII by Miclea, Razvan D., Varma, Prashant R., Peng, Aaron, Balu-Iyer, Sathy V.

    Published in Biochimica et biophysica acta (01-11-2007)
    “…Hemophilia A, a life-threatening bleeding disorder, is caused by deficiency of factor VIII (FVIII). Replacement therapy using rFVIII is the first line therapy…”
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    Journal Article
  6. 6

    Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review by Lazea, Cecilia, Al-Khzouz, Camelia, Sufana, Crina, Miclea, Diana, Asavoaie, Carmen, Filimon, Ioana, Fufezan, Otilia

    Published in Therapeutics and clinical risk management (31-03-2022)
    “…Middle aortic syndrome (MAS) is a rare vascular disease representing an important cause of severe hypertension in children. MAS is characterized by segmental…”
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    Journal Article
  7. 7

    O-phospho-L-serine, multi-functional excipient for B domain deleted recombinant factor VIII by Miclea, Razvan D, Purohit, Vivek S, Balu-Iyer, Sathy V

    Published in The AAPS journal (29-06-2007)
    “…Factor VIII (FVIII) is an important cofactor in the blood coagulation cascade. A deficiency or dysfunction of FVIII causes hemophilia A, a life-threatening…”
    Get full text
    Journal Article
  8. 8

    Immunogenicity and pharmacokinetic studies of recombinant factor VIII containing lipid cochleates by Kosloski, Matthew P, Peng, Aaron, Varma, Prashant R, Fathallah, Anas M, Miclea, Razvan D, Mager, Donald E, Balu-iyer, Sathy V

    Published in Drug delivery (01-05-2011)
    “…Replacement therapy using recombinant factor VIII (rFVIII) is currently the most common therapy for hemophilia A, a bleeding disorder caused by the deficiency…”
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    Journal Article
  9. 9

    Comparison of the haemodynamic actions of desflurane/N2O and isoflurane/N2O anaesthesia in vascular surgical patients by Zubicki, A., Gostin, X., Miclea, D., Rrou, B., Buy, E., Richer, C., Coriat, P.

    Published in Acta anaesthesiologica Scandinavica (01-10-1998)
    “…Background: The purpose of this study was to compare heart rate and arterial blood pressure response to desflurane/N2O vs isoflurane/N2O anaesthesia in a…”
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    Journal Article
  10. 10

    Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study) by Bucerzan, Simona, Miclea, Diana, Popp, Radu, Alkhzouz, Camelia, Lazea, Cecilia, Pop, Ioan Victor, Grigorescu-Sido, Paula

    Published in Therapeutics and clinical risk management (01-01-2017)
    “…Recent years have seen a shift in perspective on Turner syndrome, as it is no longer considered a significant disability due to therapeutic advances. The delay…”
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    Journal Article
  11. 11

    Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients by Alkhzouz, Camelia, Cabau, Georgiana, Lazea, Cecilia, Asavoaie, Carmen, Bucerzan, Simona, Mirea, Andreea Manuela, Farcas, Marius, Miclaus Jnr, Maria, Popp, Radu, Miclea, Diana

    Published in Pharmacogenomics and personalized medicine (01-01-2021)
    “…Articular and bone damage, which is so disabling in Mucopolysaccharidosis (MPS), requires attention as to the explanatory bias of the pathogenetic mechanisms…”
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    Journal Article
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  15. 15

    Comparison of the haemodynamic actions of desflurane/N 2 O and isoflurane/N 2 O anaesthesia in vascular surgical patients by Zubicki, A., Gostin, X., Miclea, D., Rrou, B., Buy, E., Richer, C., Coriat, P.

    Published in Acta anaesthesiologica Scandinavica (01-10-1998)
    “…Background: The purpose of this study was to compare heart rate and arterial blood pressure response to desflurane/N 2 O vs isoflurane/N 2 O anaesthesia in a…”
    Get full text
    Journal Article
  16. 16

    Phosphatidylserine mediated enhancement of the therapeutic efficacy of B domain deleted recombinant factor VIII by Miclea, Razvan D

    Published 01-01-2007
    “…Factor VIII (FVIII) is an important cofactor in the blood coagulation cascade. Deficiency or dysfunction of FVIII causes hemophilia A, a life threatening…”
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    Dissertation