Dell'Edera D - Search Results

1

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.

Dell'Edera D, Allegretti A, Ventura M, Mercuri L, Mitidieri A, Cuscianna G, Epifania AA, Morizio E, Alfonsi M, Guanciali-Franchi P. Dell'Edera D, et al. J Med Case Rep. 2021 Apr 21;15(1):208. doi: 10.1186/s13256-021-02716-6. J Med Case Rep. 2021. PMID: 33883018 Free PMC article.

2

Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies.

Dell'Edera D, Malvasi A, Vitullo E, Epifania AA, Tinelli A, Laterza F, Novelli A, Pacella E, Mazzone E, Novelli G. Dell'Edera D, et al. Eur Rev Med Pharmacol Sci. 2010 Nov;14(11):947-57. Eur Rev Med Pharmacol Sci. 2010. PMID: 21284344

3

Importance of molecular biology in the characterization of beta-thalassemia carriers.

Dell'Edera D, Pacella E, Epifania AA, Benedetto M, Tinelli A, Mazzone E, Laterza F, Malvasi A. Dell'Edera D, et al. Eur Rev Med Pharmacol Sci. 2011 Jan;15(1):79-86. Eur Rev Med Pharmacol Sci. 2011. PMID: 21381502

4

[Importance of the molecular diagnosis in the screening of alpha-thalassemia].

Dell'Edera D, Malvasi A, Tinelli A, Mazzone E, Leo M, Monti V, Epifania AA. Dell'Edera D, et al. Recenti Prog Med. 2011 Jul-Aug;102(7-8):302-6. doi: 10.1701/913.10050. Recenti Prog Med. 2011. PMID: 21779123 Italian.

5

Study of a family in the province of Matera presenting with glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome.

Dell'edera D, Epifania AA, Tinelli A, Leo M, Novelli A, Di Trani A, Barrano G, Bertoli M, Mazzone E, Benedetto M, Simona D, Malvasi A. Dell'edera D, et al. Mol Med Rep. 2012 Jun;5(6):1521-5. doi: 10.3892/mmr.2012.830. Epub 2012 Mar 8. Mol Med Rep. 2012. PMID: 22407023

6

Incidence of β-thalassemia carrier on 1495 couples in preconceptional period.

Dell'Edera D, Epifania AA, Malvasi A, Pacella E, Tinelli A, Capalbo A, Lioi MB, Di Renzo G. Dell'Edera D, et al. J Matern Fetal Neonatal Med. 2013 Mar;26(5):445-8. doi: 10.3109/14767058.2012.735998. Epub 2012 Oct 30. J Matern Fetal Neonatal Med. 2013. PMID: 23039078 Free article.

7

Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report.

Dell'edera D, Tinelli A, Capozzi O, Epifania AA, Malvasi A, Lofrese D, Pacella E, Milazzo GN, Mazzone E, Leo M, Rocchi M. Dell'edera D, et al. J Med Case Rep. 2012 Oct 29;6:368. doi: 10.1186/1752-1947-6-368. J Med Case Rep. 2012. PMID: 23107510 Free PMC article.

8

Effect of multivitamins on plasma homocysteine in patients with the 5,10 methylenetetrahydrofolate reductase C677T homozygous state.

Dell'edera D, Tinelli A, Milazzo GN, Malvasi A, Domenico C, Pacella E, Pierluigi C, Giuseppe T, Marcello G, Francesco L, Epifania AA. Dell'edera D, et al. Mol Med Rep. 2013 Aug;8(2):609-12. doi: 10.3892/mmr.2013.1563. Epub 2013 Jun 28. Mol Med Rep. 2013. PMID: 23818036

9

Identification of patients with defects in the globin genes.

Dell'edera D, Epifania AA, Milazzo GN, Leo M, Santacesaria C, Allegretti A, Mazzone E, Panetta P, Iammarino G, Lupo MG, Barbieri R, Lioi MB. Dell'edera D, et al. J Prenat Med. 2013 Oct;7(4):47-50. J Prenat Med. 2013. PMID: 24611095 Free PMC article.

10

Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: a research study.

Dell'Edera D, Benedetto M, Gadaleta G, Carone D, Salvatore D, Angione A, Gallo M, Milo M, Pisaturo ML, Di Pierro G, Mazzone E, Epifania AA. Dell'Edera D, et al. J Med Case Rep. 2014 Oct 10;8:339. doi: 10.1186/1752-1947-8-339. J Med Case Rep. 2014. PMID: 25304080 Free PMC article.

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