0000000000449869

AUTHOR

F Gagliano

showing 12 related works from this author

Così la pratica dell'inerbimento migliora la qualità del vino

2008

cover crops vigneto qualità uva
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LA MALATTIA DI KAWASAKI: LA CASISTICA DELLA CLINICA PEDIATRICA DI PALERMO

2010

Settore MED/38 - Pediatria Generale E SpecialisticaMALATTIA DI KAWASAKI
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ENDOCRINE PROFILE, BMD EVALUATION, ESTROPROGESTINIC TREATMENT IN THE FOLLOW UP OF GIRLS WITH CONGENITAL COAGULOPATHIES

2011

Settore MED/38 - Pediatria Generale E SpecialisticaBMDESTROPROGESTINICCONGENITAL COAGULOPATHIES
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Deficit di G6PD: diagnosi fenotipica e genetica. Prevalenza e caratterizzazione molecolare delle varianti genetiche nella popolazione pediatrica sici…

2015

Settore MED/38 - Pediatria Generale E SpecialisticaG6PD
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Gene symbol: f9.

2007

Factor IXSettore MED/38 - Pediatria Generale E SpecialisticaCodon NonsenseMutationCodon TerminatorHumansHemophilia B/genetics.CodonHemophilia BSicilyProtein Structure TertiaryHuman genetics
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L’ADOLESCENTE CON PATOLOGIA DELL’EMOSTASI E MENOMETRORRAGIA: DALLA PROFILASSI AL FOLLOW-UP ENDOCRINO

2011

ADOLESCENTEMENOMETRORRAGIA
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PROFILO ENDOCRINO E DENSITA’ MINERALE OSSEA IN ADOLESCENTI CON COAGULOPATIE CONGENITE IN TERAPIA CON ESTROPROGESTINICI

2011

Settore MED/38 - Pediatria Generale E SpecialisticaESTROPROGESTINICIDENSITA’ MINERALE OSSEACOAGULOPATIE CONGENITEPROFILO ENDOCRINO
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Vitigni autoctoni siciliani, un valore aggiunto che cresce

2008

Settore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeVitigni autoctoni vitis vinifera valore aggiunto
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Tailoring haemophilia A prophylaxis with BAY 81-8973: A case series

2020

BAY 81-8973 is an unmodified, full-length third generation recombinant factor VIII (rFVIII) which offers a more favorable pharmacokinetic (PK) profile, compared to its predecessor sucrose-formulated rFVIII (rFVIII-FS). We here report on a retrospective case series of nine patients affected by hemophilia A (HA), with variable disease severity, bleeding phenotype and comorbidities, to underline our clinical practice on prophylaxis with a recently introduced standard hall-life recombinant Factor VIII. The current case series highlights how the current clinical management of hemophilia is able to personalize treatment in several specific conditions like concomitant illnesses with thrombotic ris…

AdultMalemedicine.medical_specialtyAdolescentHemophilia A HemarthrosisHemophilic arthropathyrFVIIIPharmacokineticProphylaxisHaemophilia A030204 cardiovascular system & hematologyHemophilia ARecombinant factor viii03 medical and health sciencesYoung Adult0302 clinical medicinehemic and lymphatic diseasesInternal medicineMedicineHumansChildVariable disease severityAgedRetrospective StudiesThrombotic riskFactor VIIIbusiness.industryHematologyHemarthrosisMiddle Agedmedicine.diseaseThird generationClinical PracticeTreatment OutcomeConcomitantbusiness030215 immunology
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A novel nonsense mutation in exon 2 of the factor IX gene resulting in severe haemophilia B

2006

GeneticsCalciphylaxismedicine.diagnostic_testbusiness.industrymedia_common.quotation_subjectNonsense mutationNonsensemedicine.diseaseExonEmergency MedicineInternal MedicineMedicineHaemophilia BbusinessGeneGenetic testingFactor IXmedicine.drugmedia_commonInternal and Emergency Medicine
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Le adolescenti con coagulopatie congenite: dalla terapia con estroprogestinici al follow-up endocrino.

2012

Settore MED/38 - Pediatria Generale E Specialisticacoagulopatie congeniteestroprogestinici complicanze endocrine
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Ottenere cloni moderni

2008

Settore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeSelezione clonale vitis vinifera
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