PB
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Identification of hemoglobin variants by top-down mass spectrometry using selected diagnostic product ions | Analytical & bioanalytical chemistry | 2015 | 738 | 3 | |||
| Response of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemias | European journal of haematology | 2011 | 662 | 0 | |||
| Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian Family | European journal of haematology | 2011 | 648 | 0 | |||
| Zinc-induced copper deficiency in Wilson disease | Journal of neurology, neurosurgery and psychiatry | 2010 | 690 | 0 | |||
| Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemia | European journal of haematology | 2009 | 672 | 0 | |||
| Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblasts | British journal of haematology | 2009 | 701 | 0 | |||
| Atypical presentation of acute myeloid leukemia: cardiac myeloid sarcoma | International journal of hematology | 2009 | 636 | 0 | |||
| Les leucémies aiguës | Revue médicale suisse | 2008 | 560 | 2 | |||
| Perioperative anaemia management: consensus statement on the role of intravenous iron | British journal of anaesthesia | 2008 | 651 | 0 | |||
| Lentiviral PU.1 overexpression restores differentiation in myeloid leukemic blasts | Leukemia | 2007 | 492 | 0 | |||
| Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosis | Haematologica | 2007 | 200 | 77 | |||
| Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion | European journal of haematology | 2006 | 253 | 0 | |||
| Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP gene | Blood | 2004 | 116 | 90 | |||
| Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome | Blood | 2003 | 664 | 0 | |||
| Complete remission of pure white cell aplasia associated with thymoma, autoimmune thyroiditis and type 1 diabetes | European journal of haematology | 2003 | 718 | 159 | |||
| Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFC | Transfusion | 2002 | 266 | 0 | |||
| Hypothesis for generation of the unstable Hb Bucuresti (beta 42 Phe-->Leu) mutation | Hematology journal | 2001 | 522 | 1 | |||
| Prenatal diagnosis of β-thalassaemia in a twin pregnancy using transabdominal CVS sampling | Haema | 1998 | 382 | 0 | |||
| Effet de l'administration de la r-HuEpo associée a l'hémodilution normovolémique aigüe sur les besoins transfusionnels lors d'interventions pour prothèse totale de hanche | Schweizerische medizinische Wochenschrift | 1998 | 538 | 1 | |||
| Blood transfusion requirements in otolaryngology - head and neck surgery | Acta oto-laryngologica | 1998 | 550 | 481 | |||
| Hautes doses d'immunoglobulines par voie intraveineuse pour le traitement des neutropénies "auto-immunes" | Schweizerische medizinische Wochenschrift | 1985 | 654 | 0 |
