Publications by authors named "Alex Felice"

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Spatiotemporal expression and control of haemoglobin in space.
Josef Borg, Conor Loy, JangKeun Kim, Alfred Buhagiar, Christopher Chin, Alex Felice

Nat Commun· June 2024

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Decentralized energy in flexible energy system: Life cycle environmental impacts in Belgium.
Dominik Huber, Daniele Costa, Alex Felice, Pieter Valkering, Thierry Coosemans

Sci Total Environ· August 2023

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A comparative profile of total protein and six angiogenically-active growth factors in three platelet products.
Scott Custo, Byron Baron, Alex Felice, Elisa Seria

GMS Interdiscip Plast Reconstr Surg DGPW· July 2022

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Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.
Steven Heshusius, Laura Grech, Nynke Gillemans, Rutger W W Brouwer, Xander T den Dekker, Alex E Felice

Sci Rep· January 2022

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Immunoglobulin G in Platelet-Derived Wound Healing Factors.
Elisa Seria, Sarah Samut Tagliaferro, Doreen Cutajar, Ruth Galdies, Alex Felice

Biomed Res Int· May 2021

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GYNOCARE Update: Modern Strategies to Improve Diagnosis and Treatment of Rare Gynecologic Tumors—Current Challenges and Future Directions.
Riccardo Di Fiore, Sherif Suleiman, Bridget Ellul, Sharon A O'Toole, Charles Savona-Ventura, Alex Felice

Cancers (Basel)· January 2021

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Identification of an p.Gly292fs Frameshift Mutation Presenting as Diabetes During Pregnancy in a Maltese Family.
Nikolai Paul Pace, Christopher Rizzo, Alexia Abela, Mark Gruppetta, Stephen Fava, Alex Felice

Clin Med Insights Case Rep· February 2019

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Case Report: Identification of an HNF1B p.Arg527Gln mutation in a Maltese patient with atypical early onset diabetes and diabetic nephropathy.
Nikolai Paul Pace, Johann Craus, Alex Felice, Josanne Vassallo

BMC Endocr Disord· May 2018

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Genetic causes of Parkinson's disease in the Maltese: a study of selected mutations in LRRK2, MTHFR, QDPR and SPR.
Charmaine Zahra, Christine Tabone, Graziella Camilleri, Alex E Felice, Rosienne Farrugia

BMC Med Genet· September 2016

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The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases.
Marina Mora, Corrado Angelini, Fabrizia Bignami, Anne-Mary Bodin, Marco Crimi, Alex Felice

Eur J Hum Genet· September 2015

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Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy.
Jennifer Friedman, Emmanuel Roze, Jose E Abdenur, Richard Chang, Serena Gasperini, Alex Felice

Ann Neurol· April 2012

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Erythroid phenotypes associated with KLF1 mutations.
Joseph Borg, George P Patrinos, Alex E Felice, Sjaak Philipsen

Haematologica· May 2011

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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
Belinda Giardine, Joseph Borg, Douglas R Higgs, Kenneth R Peterson, Sjaak Philipsen, Alex E Felice

Nat Genet· March 2011

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Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.
George P Patrinos, Jumana Al Aama, Aida Al Aqeel, Fahd Al-Mulla, Joseph Borg, Alex E Felice

Hum Mutat· January 2011

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Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.
Joseph Borg, Petros Papadopoulos, Marianthi Georgitsi, Laura Gutiérrez, Godfrey Grech, Alex E Felice

Nat Genet· September 2010

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An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.
Carsten W Lederer, A Nazli Basak, Yesim Aydinok, Soteroula Christou, Amal El-Beshlawy, Alex E Felice

Hemoglobin· February 2010

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Hb Valletta [beta87(F3)Thr-->Pro] and Hb Marseille/Long Island [beta2(NA2)His-->Pro; (-1)Met-(+1)Val-(+2)Pro-Leu], in a unique compound heterozygote with a normal hemoglobin phenotype.
Ruth Galdies, Wilhelmina Cassar, Monica Pizzuto, Christian A Scerri, Nicholas Felice, Alex E Felice

Hemoglobin· January 2010

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A review of cis-trans interplay between DNA sequences 5' to the (G)gamma- and beta-globin genes among Hb F-Malta-I heterozygotes/homozygotes and beta-thalassemia homozygotes/compound heterozygotes, and the effects of hydroxyurea on the Hb F/F-erythrocyte; the need for large multicenter trials.
Alex E Felice, Joseph Borg, Monica Pizzuto, Wilhelmina Cassar, Ruth Galdies

Hemoglobin· July 2007

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Developmental effect of the XmnI site on Ggamma-globin gene expression among newborn Hb F-Malta-I [Ggamma117(G19)His-->Arg, CAT-->CGT] heterozygotes and adult beta+ -Thalassemia homozygotes.
Svetlana Pulis, Christian A Scerri, Pierre Schembri Wismayer, Ruth Galdies, Stephanie Bezzina Wettinger, Alex E Felice

Hemoglobin· May 2007

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Molecular genetics of tetrahydrobiopterin (BH4) deficiency in the Maltese population.
Rosienne Farrugia, Christian A Scerri, Simon Attard Montalto, Raymond Parascandolo, Brian G R Neville, Alex E Felice

Mol Genet Metab· March 2007

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Novel polymorphisms influencing transcription of the human CHRM2 gene in airway smooth muscle.
Anthony G Fenech, Charlotte K Billington, Caroline Swan, Susan Richards, Therese Hunter, Alex E Felice

Am J Respir Cell Mol Biol· May 2004

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