Works by Felice, Alex E.
Results: 13
Treatment of leg ulcers with platelet-derived wound healing factor (pdwhfs) in a patient with beta thalassaemia intermedia.
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- British Journal of Haematology, 2001, v. 112, n. 2, p. 528, doi. 10.1046/j.1365-2141.2001.02540-2.x
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- Article
Novel Polymorphisms Influencing Transcription of the Human CHRM2 Gene in Airway Smooth Muscle.
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- American Journal of Respiratory Cell & Molecular Biology, 2004, v. 30, n. 5, p. 678, doi. 10.1165/rcmb.2003-0011OC
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- Article
Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.
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- Human Mutation, 2011, v. 32, n. 1, p. 2, doi. 10.1002/humu.21397
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- Article
Two new missense mutations (P134T and A244V) in the coagulation factor VII gene.
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- Human Mutation, 1998, v. 11, p. S189, doi. 10.1002/humu.1380110161
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- Article
A Twenty-Five Year Prospective Clinical Review and Family Studies Revealed New Globin Gene Regulators for Hb F Induction.
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- 2019
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- Abstract
Hb Valletta [β87(F3)Thr→Pro] and Hb Marseille/Long Island [β2(NA2)His→Pro; (–1)Met-(+1)Val-(+2)Pro-Leu], in a Unique Compound Heterozygote with a Normal Hemoglobin Phenotype.
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- Hemoglobin, 2010, v. 34, n. 2, p. 169, doi. 10.3109/03630261003673675
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- Article
An Electronic Infrastructure for Research and Treatment of the Thalassemias and Other Hemoglobinopathies: The Euro-Mediterranean Ithanet Project.
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- Hemoglobin, 2009, v. 33, n. 3/4, p. 163, doi. 10.1080/03630260903089177
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- Article
A Review of Cis-Trans Interplay Between DNA Sequences 5' to the Gγ- and β-Globin Genes Among Hb F-Malta-I Heterozygotes/Homozygotes and β-Thalassemia Homozygotes/Compound Heterozygotes, and the Effects of Hydroxyurea on the Hb F/F-Erythrocyte; the Need for Large Multicenter Trials
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- Hemoglobin, 2007, v. 31, n. 2, p. 279, doi. 10.1080/03630260701297261
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- Article
Developmental Effect of the XmnI Site on Gγ-Globin Gene Expression Among Newborn Hb F-Malta-I [Gγ117(G19)Hi(s)→Arg, CA(T)→CGT] Heterozygotes and Adult β -Thalassemia Homozygotes.
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- Hemoglobin, 2007, v. 31, n. 1, p. 71, doi. 10.1080/03630260601057187
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- Article
Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04126-6
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- Article
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
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- Nature Genetics, 2011, v. 43, n. 4, p. 295, doi. 10.1038/ng.785
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- Article
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.
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- Nature Genetics, 2010, v. 42, n. 9, p. 801, doi. 10.1038/ng.630
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- Article
Genetic causes of Parkinson's disease in the Maltese: a study of selected mutations in LRRK2, MTHFR, QDPR and SPR.
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- BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0327-x
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- Article