Cianciulli P - Search Results

1

Neuroacanthocytosis associated with a defect of the 4.1R membrane protein.

Orlacchio A, Calabresi P, Rum A, Tarzia A, Salvati AM, Kawarai T, Stefani A, Pisani A, Bernardi G, Cianciulli P, Caprari P. Orlacchio A, et al. Among authors: cianciulli p. BMC Neurol. 2007 Feb 13;7:4. doi: 10.1186/1471-2377-7-4. BMC Neurol. 2007. PMID: 17298666 Free PMC article.

2

Acanthocytosis as a predisposing factor for non-ketotic hyperglycaemia induced chorea-ballism.

Pisani A, Diomedi M, Rum A, Cianciulli P, Floris R, Orlacchio A, Bernardi G, Calabresi P. Pisani A, et al. Among authors: cianciulli p. J Neurol Neurosurg Psychiatry. 2005 Dec;76(12):1717-9. doi: 10.1136/jnnp.2005.067033. J Neurol Neurosurg Psychiatry. 2005. PMID: 16291901 Free PMC article.

3

Identification of G6PD Mediterranean mutation by amplification refractory mutation system.

Maffi D, Pasquino MT, Caprari P, Caforio MP, Cianciulli P, Sorrentino F, Cappabianca MP, Salvati AM. Maffi D, et al. Among authors: cianciulli p. Clin Chim Acta. 2002 Jul;321(1-2):43-7. doi: 10.1016/s0009-8981(02)00098-0. Clin Chim Acta. 2002. PMID: 12031591

4

Hereditary spherocytosis and elliptocytosis associated with prosthetic heart valve replacement: rheological study of erythrocyte modifications.

Caprari P, Tarzia A, Mojoli G, Cianciulli P, Mannella E, Martorana MC. Caprari P, et al. Among authors: cianciulli p. Int J Hematol. 2009 Apr;89(3):285-293. doi: 10.1007/s12185-009-0270-0. Epub 2009 Mar 24. Int J Hematol. 2009. PMID: 19308658

5

6-Phosphogluconate dehydrogenase deficiency in an Italian family.

Caprari P, Caforio MP, Cianciulli P, Maffi D, Pasquino MT, Tarzia A, Amadori S, Salvati AM. Caprari P, et al. Among authors: cianciulli p. Ann Hematol. 2001 Jan;80(1):41-4. doi: 10.1007/s002770000233. Ann Hematol. 2001. PMID: 11233775

6

Sickle cell anaemia: haemorheological aspects.

Martorana MC, Mojoli G, Cianciulli P, Tarzia A, Mannella E, Caprari P. Martorana MC, et al. Among authors: cianciulli p. Ann Ist Super Sanita. 2007;43(2):164-70. Ann Ist Super Sanita. 2007. PMID: 17634665

7

A new, striking morphologic feature for the human erythrocyte in hereditary spherocytosis: the blebbing pattern.

Malorni W, Iosi F, Donelli G, Caprari P, Salvati AM, Cianciulli P. Malorni W, et al. Among authors: cianciulli p. Blood. 1993 May 15;81(10):2821-2. Blood. 1993. PMID: 8490190 Free article. No abstract available.

8

[Iron accumulation in the liver of patients with thalassemia major assessed with low field strength magnetic resonance: correlation with clinico-instrumental parameters].

Di Renzi P, Cianciulli P, Preziosi P, Amadori S, Orlacchio A. Di Renzi P, et al. Among authors: cianciulli p. Radiol Med. 1996 Jun;91(6):764-8. Radiol Med. 1996. PMID: 8830363 Clinical Trial. Italian.

9

Hb Belfast (beta 15 (A 12) Trp leads to Arg) in combination with G6PD deficiency in an Italian carrier.

Giampaolo A, Salvo G, Cianciulli P, Massa A, Caprari P, Guerriero R, Cianetti L, Antimi M, Pratesi G, Tentori L. Giampaolo A, et al. Among authors: cianciulli p. Haematologica. 1982 Jun;67(3):335-40. Haematologica. 1982. PMID: 6814990 No abstract available.

10

Beta-thalassemia mutations in Rome. A high frequency of the IVSII-745 allele in subjects of latium origin.

Massa A, Cianciulli P, Cianetti L, Iazzone R, Cenci A, Sorrentino F, Franco G, Pecci G, Papa G, Peschle C. Massa A, et al. Among authors: cianciulli p. Haematologica. 1994 May-Jun;79(3):256-8. Haematologica. 1994. PMID: 7926974

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