| In vitro rescue of FGA deletion by lentiviral transduction of afibrinogenemic patient's hepatocytes | Journal of thrombosis and haemostasis |  | | 2014 | 633 | 0 |
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| Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants | Haematologica |  | | 2008 | 604 | 442 |
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| Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins | Journal of thrombosis and haemostasis | | | 2007 | 627 | 1 |
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| Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène | MS. Médecine sciences | | | 2006 | 604 | 3 |
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| Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion | Journal of medical genetics | | | 2005 | 509 | 1 |
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| Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia | Human molecular genetics | | | 2005 | 674 | 4 |
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| Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells | Blood | | | 2004 | 661 | 0 |
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| Differential expression of LMO4 protein in Alzheimer's disease | Neuropathology and applied neurobiology | | | 2004 | 571 | 1 |
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| Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family | Blood | | | 2003 | 964 | 0 |
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| Transcription regulator LMO4 interferes with neuritogenesis in human SH-SY5Y neuroblastoma cells | Molecular brain research | | | 2003 | 595 | 3 |
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| Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion | Blood | | | 2003 | 594 | 0 |
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