Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

83 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.
Iolascon A, Russo R, Esposito MR, Asci R, Piscopo C, Perrotta S, Fénéant-Thibault M, Garçon L, Delaunay J. Iolascon A, et al. Among authors: piscopo c. Haematologica. 2010 May;95(5):708-15. doi: 10.3324/haematol.2009.014985. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015893 Free PMC article.
[New types of microcytic anemia].
Iolascon A, De Falco L, Boschetto L, Piscopo C, Pirolo C, Di Noce F. Iolascon A, et al. Among authors: piscopo c. Minerva Pediatr. 2007 Oct;59(5):525-7. Minerva Pediatr. 2007. PMID: 17947902 Italian. No abstract available.
Natural history of recessive inheritance of DMT1 mutations.
Iolascon A, Camaschella C, Pospisilova D, Piscopo C, Tchernia G, Beaumont C. Iolascon A, et al. Among authors: piscopo c. J Pediatr. 2008 Jan;152(1):136-9. doi: 10.1016/j.jpeds.2007.08.041. J Pediatr. 2008. PMID: 18154916
Red cell membrane disorders in pediatrics.
Iolascon A, Piscopo C, Boschetto L. Iolascon A, et al. Among authors: piscopo c. Pediatr Ann. 2008 May;37(5):295-301. doi: 10.3928/00904481-20080501-05. Pediatr Ann. 2008. PMID: 18543540 No abstract available.
Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA).
De Falco L, Totaro F, Nai A, Pagani A, Girelli D, Silvestri L, Piscopo C, Campostrini N, Dufour C, Al Manjomi F, Minkov M, Van Vuurden DG, Feliu A, Kattamis A, Camaschella C, Iolascon A. De Falco L, et al. Among authors: piscopo c. Hum Mutat. 2010 May;31(5):E1390-405. doi: 10.1002/humu.21243. Hum Mutat. 2010. PMID: 20232450
Hereditary spherocytosis.
Iolascon A, Avvisati RA, Piscopo C. Iolascon A, et al. Among authors: piscopo c. Transfus Clin Biol. 2010 Sep;17(3):138-42. doi: 10.1016/j.tracli.2010.05.006. Epub 2010 Jul 23. Transfus Clin Biol. 2010. PMID: 20655264
Congenital dyserythropoietic anaemias: new acquisitions.
Iolascon A, Russo R, Esposito MR, Piscopo C, Asci R, De Falco L, Di Noce F. Iolascon A, et al. Among authors: piscopo c. Blood Transfus. 2011 Jul;9(3):278-80. doi: 10.2450/2010.0085-10. Epub 2010 Dec 13. Blood Transfus. 2011. PMID: 21251457 Free PMC article. Review. No abstract available.
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research.
Daga S, Fallerini C, Baldassarri M, Fava F, Valentino F, Doddato G, Benetti E, Furini S, Giliberti A, Tita R, Amitrano S, Bruttini M, Meloni I, Pinto AM, Raimondi F, Stella A, Biscarini F, Picchiotti N, Gori M, Pinoli P, Ceri S, Sanarico M, Crawley FP, Birolo G; GEN-COVID Multicenter Study; Renieri A, Mari F, Frullanti E. Daga S, et al. Eur J Hum Genet. 2021 May;29(5):745-759. doi: 10.1038/s41431-020-00793-7. Epub 2021 Jan 17. Eur J Hum Genet. 2021. PMID: 33456056 Free PMC article. Clinical Trial.
83 results