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1 - 21 of 21
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 741 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 670 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 653 0
Zinc-induced copper deficiency in Wilson diseaseJournal of neurology, neurosurgery and psychiatry
accessLevelRestricted
2010 692 0
Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemiaEuropean journal of haematology
accessLevelRestricted
2009 675 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 703 0
Atypical presentation of acute myeloid leukemia: cardiac myeloid sarcomaInternational journal of hematology
2009 643 0
Les leucémies aiguësRevue médicale suisse
accessLevelRestricted
2008 564 2
Perioperative anaemia management: consensus statement on the role of intravenous ironBritish journal of anaesthesia
accessLevelRestricted
2008 653 0
Lentiviral PU.1 overexpression restores differentiation in myeloid leukemic blastsLeukemia
accessLevelRestricted
2007 496 0
Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosisHaematologica
accessLevelPublic
2007 204 101
Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletionEuropean journal of haematology
accessLevelRestricted
2006 259 0
Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP geneBlood
accessLevelPublic
2004 120 118
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndromeBlood
accessLevelRestricted
2003 669 0
Complete remission of pure white cell aplasia associated with thymoma, autoimmune thyroiditis and type 1 diabetesEuropean journal of haematology
accessLevelPublic
2003 722 202
Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFCTransfusion
accessLevelRestricted
2002 270 0
Hypothesis for generation of the unstable Hb Bucuresti (beta 42 Phe-->Leu) mutationHematology journal
accessLevelRestricted
2001 525 1
Prenatal diagnosis of β-thalassaemia in a twin pregnancy using transabdominal CVS samplingHaema
1998 387 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 542 1
Blood transfusion requirements in otolaryngology - head and neck surgeryActa oto-laryngologica
accessLevelPublic
1998 553 544
Hautes doses d'immunoglobulines par voie intraveineuse pour le traitement des neutropénies "auto-immunes"Schweizerische medizinische Wochenschrift
1985 660 0
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