Corrado Mammì

Corrado Mammì

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Corrado Mammì

Corrado Mammì

Publications by authors named "Corrado Mammì"

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15Publications

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Maturity Onset Diabetes of the Young is Not Necessarily Associated with Autosomal Inheritance: Case Description of a De Novo HFN1A Mutation.

Diabetes Ther 2019 Aug 16;10(4):1543-1548. Epub 2019 May 16.

Department of Human Pathology in Adult and Developmental Age "Gaetano Barresi", University of Messina, Via Consolare Valeria 1, 98124, Messina, Italy.

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http://dx.doi.org/10.1007/s13300-019-0633-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612332PMC
August 2019

NFIX mutations affecting the DNA-binding domain cause a peculiar overgrowth syndrome (Malan syndrome): a new patients series.

Eur J Med Genet 2015 Sep 17;58(9):488-91. Epub 2015 Jul 17.

UO Genetica Medica, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2015.06.009DOI Listing
September 2015

Treatment of transient neonatal diabetes mellitus: insulin pump or insulin glargine? Our experience.

Diabetes Technol Ther 2014 Dec;16(12):880-4

1 Department of Medical and Pediatric Sciences, University of Catania , University Hospital Vittorio Emanuele, Catania, Italy .

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http://dx.doi.org/10.1089/dia.2014.0055DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241878PMC
December 2014

A peculiar mutation in the DNA-binding/dimerization domain of NFIX causes Sotos-like overgrowth syndrome: a new case.

Gene 2012 Dec 13;511(1):103-5. Epub 2012 Sep 13.

Unità Operativa di Genetica medica, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy.

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http://dx.doi.org/10.1016/j.gene.2012.08.040DOI Listing
December 2012

Absence of deletion and duplication of MLL2 and KDM6A genes in a large cohort of patients with Kabuki syndrome.

Mol Genet Metab 2012 Nov 6;107(3):627-9. Epub 2012 Jul 6.

Unita' Operativa di Genetica Medica, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy.

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http://dx.doi.org/10.1016/j.ymgme.2012.06.019DOI Listing
November 2012

High incidence of factor V Leiden and prothrombin G20210A in healthy southern Italians.

Clin Appl Thromb Hemost 2009 May-Jun;15(3):356-9. Epub 2009 Feb 11.

Centro Emofilia, Servizio Emostasi e Trombosi, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy.

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http://dx.doi.org/10.1177/1076029607310218DOI Listing
July 2009

MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.

Eur J Hum Genet 2008 May 23;16(5):565-71. Epub 2008 Jan 23.

Operative Unit of Medical Genetics, Hospital of Reggio Calabria Az. Ospedaliera Bianchi-Melacrino-Morelli, V Petrara Reggio Calabria, Reggio Calabria, Italy.

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http://dx.doi.org/10.1038/sj.ejhg.5202001DOI Listing
May 2008

Role of hyperhomocystinemia in retinal vascular occlusive disease.

Clin Appl Thromb Hemost 2007 Jan;13(1):104-7

Hemophilia Centre, Hemostasis and Thrombosis Service, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy.

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http://cat.sagepub.com/content/13/1/104.full.pdf
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http://cat.sagepub.com/cgi/doi/10.1177/1076029606296423
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http://dx.doi.org/10.1177/1076029606296423DOI Listing
January 2007

Genetic prothrombotic risk factors in women with unexplained pregnancy loss.

Thromb Res 2006 12;117(6):681-4. Epub 2005 Jul 12.

Centro Emofilia-Servizio Emostasi e Trombosi, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy.

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http://dx.doi.org/10.1016/j.thromres.2005.06.005DOI Listing
July 2006