Immacolata Andolfo

Immacolata Andolfo

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Immacolata Andolfo

Immacolata Andolfo

Publications by authors named "Immacolata Andolfo"

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The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant.

Am J Hematol 2019 Nov 30;94(11):1227-1235. Epub 2019 Aug 30.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples, Italy.

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http://dx.doi.org/10.1002/ajh.25613DOI Listing
November 2019

Advances in understanding the pathogenesis of red cell membrane disorders.

Br J Haematol 2019 Oct 31;187(1):13-24. Epub 2019 Jul 31.

Department of Molecular Medicine and Medical Biotechnologies, Federico II" University of Naples, Naples, Italy.

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http://dx.doi.org/10.1111/bjh.16126DOI Listing
October 2019

Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.

Am J Hematol 2018 12 2;93(12):1509-1517. Epub 2018 Oct 2.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples, Italy.

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http://dx.doi.org/10.1002/ajh.25276DOI Listing
December 2018

Label-Free Optical Marker for Red-Blood-Cell Phenotyping of Inherited Anemias.

Anal Chem 2018 06 4;90(12):7495-7501. Epub 2018 Jun 4.

Institute of Applied Sciences and Intelligent Systems, ISASI, "E. Caianiello" , CNR , Via Campi Flegrei 34 , 80078 Pozzuoli , NA , Italy.

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http://dx.doi.org/10.1021/acs.analchem.8b01076DOI Listing
June 2018

Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.

Am J Hematol 2018 05 24;93(5):672-682. Epub 2018 Feb 24.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli, Italy.

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http://dx.doi.org/10.1002/ajh.25058DOI Listing
May 2018

Hereditary stomatocytosis: An underdiagnosed condition.

Am J Hematol 2018 01 23;93(1):107-121. Epub 2017 Oct 23.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli, Italy.

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http://dx.doi.org/10.1002/ajh.24929DOI Listing
January 2018

Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis.

Am J Hematol 2017 10 29;92(10):E607-E609. Epub 2017 Jul 29.

Department of Molecular Medicine and Medical Biotechnology, University Federico II, Naples, Italy.

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http://dx.doi.org/10.1002/ajh.24853DOI Listing
October 2017

New insights on hereditary erythrocyte membrane defects.

Haematologica 2016 11 18;101(11):1284-1294. Epub 2016 Oct 18.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Italy

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http://dx.doi.org/10.3324/haematol.2016.142463DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394881PMC
November 2016

Increased levels of ERFE-encoding in patients with congenital dyserythropoietic anemia type II.

Blood 2016 10 18;128(14):1899-1902. Epub 2016 Aug 18.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli, Italy.

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http://dx.doi.org/10.1182/blood-2016-06-724328DOI Listing
October 2016

Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia.

Haematologica 2016 08 5;101(8):909-17. Epub 2016 May 5.

Department of Molecular Medicine and Medical Biotechnologies, "Federico II" University of Naples, Italy CEINGE, Biotecnologie Avanzate, Naples, Italy.

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http://dx.doi.org/10.3324/haematol.2016.142372DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967569PMC
August 2016

Next generation research and therapy in red blood cell diseases.

Haematologica 2016 05;101(5):515-7

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Italy CEINGE Biotecnologie Avanzate, Napoli, Italy

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http://dx.doi.org/10.3324/haematol.2015.139238DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004366PMC
May 2016

Diagnosis and management of congenital dyserythropoietic anemias.

Expert Rev Hematol 2016 Mar 6;9(3):283-96. Epub 2016 Jan 6.

a Dipartimento di Medicina Molecolare e Biotecnologie Mediche , Università degli Studi di Napoli Federico II , Napoli , Italy.

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http://dx.doi.org/10.1586/17474086.2016.1131608DOI Listing
March 2016

Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).

Am J Hematol 2015 Oct;90(10):921-6

Department Of Molecular Medicine And Medical Biotechnologies, "Federico II" University Of Naples, Naples, Italy.

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http://dx.doi.org/10.1002/ajh.24117DOI Listing
October 2015

Inhibition of hypoxia inducible factors combined with all-trans retinoic acid treatment enhances glial transdifferentiation of neuroblastoma cells.

Sci Rep 2015 Jun 9;5:11158. Epub 2015 Jun 9.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli "Federico II", Naples, Italy.

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http://dx.doi.org/10.1038/srep11158DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460899PMC
June 2015

Red cells in post-genomic era: impact of personalized medicine in the treatment of anemias.

Haematologica 2015 Jan;100(1):3-6

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli; and CEINGE Biotecnologie Avanzate, Napoli, Italy.

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http://dx.doi.org/10.3324/haematol.2014.120733DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281306PMC
January 2015

Hereditary xerocytosis revisited.

Am J Hematol 2014 Dec 21;89(12):1142-6. Epub 2014 Jul 21.

Division of Hematology and Oncology, Boston Children's Hospital, Boston, Massachusetts; Dana-Farber Cancer Center, Boston, Massachusetts.

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http://dx.doi.org/10.1002/ajh.23799DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237618PMC
December 2014

Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.

Am J Hematol 2014 Oct 22;89(10):E169-75. Epub 2014 Jul 22.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli, Italy; CEINGE Biotecnologie Avanzate, Napoli, Italy.

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http://dx.doi.org/10.1002/ajh.23800DOI Listing
October 2014

Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model.

Neurosci Res 2013 Nov 17;77(3):121-7. Epub 2013 Sep 17.

CEINGE, Biotecnologie Avanzate, Naples, Italy; Department of Biochemistry and Medical Biotechnologies, "Federico II" University of Naples, Naples, Italy.

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http://dx.doi.org/10.1016/j.neures.2013.09.003DOI Listing
November 2013

MicroRNA 199b-5p delivery through stable nucleic acid lipid particles (SNALPs) in tumorigenic cell lines.

Naunyn Schmiedebergs Arch Pharmacol 2013 Apr 26;386(4):287-302. Epub 2013 Jan 26.

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Federico II University of Naples, Naples, Italy.

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http://dx.doi.org/10.1007/s00210-013-0837-4DOI Listing
April 2013

Identification of ALK germline mutation (3605delG) in pediatric anaplastic medulloblastoma.

J Hum Genet 2012 Oct 19;57(10):682-4. Epub 2012 Jul 19.

Translational Oncopathology, Department of Pathology, IRCCS A.O.U. San Martino-IST, National Cancer Research Institute, Genoa, Italy.

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http://dx.doi.org/10.1038/jhg.2012.87DOI Listing
October 2012

The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastoma.

Cell Cycle 2012 Feb 1;11(3):569-81. Epub 2012 Feb 1.

CEINGE, Biotecnologie Avanzate; Naples, Italy and Department of Biochemistry and Medical Biotechnology; 'Federico II' University of Naples; Naples, Italy.

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http://dx.doi.org/10.4161/cc.11.3.19063DOI Listing
February 2012