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Title Published in Access level OA Policy Year Views Downloads
Identification of hemoglobin variants by top-down mass spectrometry using selected diagnostic product ionsAnalytical & bioanalytical chemistry
accessLevelRestricted
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 anaemiasEuropean journal of haematology
accessLevelRestricted
2011 662 0
Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian FamilyEuropean journal of haematology
accessLevelRestricted
2011 648 0
Zinc-induced copper deficiency in Wilson diseaseJournal of neurology, neurosurgery and psychiatry
accessLevelRestricted
2010 690 0
Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemiaEuropean journal of haematology
accessLevelRestricted
2009 672 0
Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblastsBritish journal of haematology
accessLevelRestricted
2009 701 0
Atypical presentation of acute myeloid leukemia: cardiac myeloid sarcomaInternational journal of hematology
2009 636 0
Les leucémies aiguësRevue médicale suisse
accessLevelRestricted
2008 560 2
Perioperative anaemia management: consensus statement on the role of intravenous ironBritish journal of anaesthesia
accessLevelRestricted
2008 651 0
Lentiviral PU.1 overexpression restores differentiation in myeloid leukemic blastsLeukemia
accessLevelRestricted
2007 492 0
Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosisHaematologica
accessLevelPublic
2007 200 77
Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletionEuropean journal of haematology
accessLevelRestricted
2006 253 0
Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP geneBlood
accessLevelPublic
2004 116 90
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndromeBlood
accessLevelRestricted
2003 664 0
Complete remission of pure white cell aplasia associated with thymoma, autoimmune thyroiditis and type 1 diabetesEuropean journal of haematology
accessLevelPublic
2003 718 159
Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFCTransfusion
accessLevelRestricted
2002 266 0
Hypothesis for generation of the unstable Hb Bucuresti (beta 42 Phe-->Leu) mutationHematology journal
accessLevelRestricted
2001 522 1
Prenatal diagnosis of β-thalassaemia in a twin pregnancy using transabdominal CVS samplingHaema
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 hancheSchweizerische medizinische Wochenschrift
accessLevelRestricted
1998 538 1
Blood transfusion requirements in otolaryngology - head and neck surgeryActa oto-laryngologica
accessLevelPublic
1998 550 481
Hautes doses d'immunoglobulines par voie intraveineuse pour le traitement des neutropénies "auto-immunes"Schweizerische medizinische Wochenschrift
1985 654 0
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