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Items: 26

1.

Disordered Eating Behaviors Among Italian Adolescents with Type 1 Diabetes: Exploring Relationships with Parents' Eating Disorder Symptoms, Externalizing and Internalizing Behaviors, and Body Image Problems.

Troncone A, Chianese A, Zanfardino A, Cascella C, Confetto S, Piscopo A, Loffredo G, Golino A, Iafusco D.

J Clin Psychol Med Settings. 2019 Oct 5. doi: 10.1007/s10880-019-09665-9. [Epub ahead of print]

PMID:
31587133
2.

A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.

Noris P, Marconi C, De Rocco D, Melazzini F, Pippucci T, Loffredo G, Giangregorio T, Pecci A, Seri M, Savoia A.

Br J Haematol. 2018 Jun;181(5):698-701. doi: 10.1111/bjh.14694. Epub 2017 May 3. No abstract available.

PMID:
28466964
3.

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia.

Melazzini F, Palombo F, Balduini A, De Rocco D, Marconi C, Noris P, Gnan C, Pippucci T, Bozzi V, Faleschini M, Barozzi S, Doubek M, Di Buduo CA, Kozubik KS, Radova L, Loffredo G, Pospisilova S, Alfano C, Seri M, Balduini CL, Pecci A, Savoia A.

Haematologica. 2016 Nov;101(11):1333-1342. Epub 2016 Jun 30.

4.

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.

Noris P, Biino G, Pecci A, Civaschi E, Savoia A, Seri M, Melazzini F, Loffredo G, Russo G, Bozzi V, Notarangelo LD, Gresele P, Heller PG, Pujol-Moix N, Kunishima S, Cattaneo M, Bussel J, De Candia E, Cagioni C, Ramenghi U, Barozzi S, Fabris F, Balduini CL.

Blood. 2014 Aug 7;124(6):e4-e10. doi: 10.1182/blood-2014-03-564328. Epub 2014 Jul 2.

5.

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.

Noris P, Schlegel N, Klersy C, Heller PG, Civaschi E, Pujol-Moix N, Fabris F, Favier R, Gresele P, Latger-Cannard V, Cuker A, Nurden P, Greinacher A, Cattaneo M, De Candia E, Pecci A, Hurtaud-Roux MF, Glembotsky AC, Muñiz-Diaz E, Randi ML, Trillot N, Bury L, Lecompte T, Marconi C, Savoia A, Balduini CL, Bayart S, Bauters A, Benabdallah-Guedira S, Boehlen F, Borg JY, Bottega R, Bussel J, De Rocco D, de Maistre E, Faleschini M, Falcinelli E, Ferrari S, Ferster A, Fierro T, Fleury D, Fontana P, James C, Lanza F, Le Cam Duchez V, Loffredo G, Magini P, Martin-Coignard D, Menard F, Mercier S, Mezzasoma A, Minuz P, Nichele I, Notarangelo LD, Pippucci T, Podda GM, Pouymayou C, Rigouzzo A, Royer B, Sie P, Siguret V, Trichet C, Tucci A, Saposnik B, Veneri D; European Hematology Association – Scientific Working Group on Thrombocytopenias and Platelet Function Disorders.

Haematologica. 2014 Aug;99(8):1387-94. doi: 10.3324/haematol.2014.105924. Epub 2014 Apr 24.

6.

MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.

Pecci A, Klersy C, Gresele P, Lee KJ, De Rocco D, Bozzi V, Russo G, Heller PG, Loffredo G, Ballmaier M, Fabris F, Beggiato E, Kahr WH, Pujol-Moix N, Platokouki H, Van Geet C, Noris P, Yerram P, Hermans C, Gerber B, Economou M, De Groot M, Zieger B, De Candia E, Fraticelli V, Kersseboom R, Piccoli GB, Zimmermann S, Fierro T, Glembotsky AC, Vianello F, Zaninetti C, Nicchia E, Güthner C, Baronci C, Seri M, Knight PJ, Balduini CL, Savoia A.

Hum Mutat. 2014 Feb;35(2):236-47. doi: 10.1002/humu.22476. Epub 2013 Dec 12.

7.

Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study.

Noris P, Klersy C, Gresele P, Giona F, Giordano P, Minuz P, Loffredo G, Pecci A, Melazzini F, Civaschi E, Mezzasoma A, Piedimonte M, Semeraro F, Veneri D, Menna F, Ciardelli L, Balduini CL; Italian Gruppo di Studio delle Piastrine.

Br J Haematol. 2013 Jul;162(1):112-9. doi: 10.1111/bjh.12349. Epub 2013 Apr 25.

8.

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes.

Marletta C, Valli R, Pressato B, Mare L, Montalbano G, Menna G, Loffredo G, Bernardo ME, Vinti L, Ferrari S, Di Cesare-Merlone A, Zecca M, Lo Curto F, Locatelli F, Pasquali F, Maserati E.

Mol Cytogenet. 2012 Oct 1;5(1):39. doi: 10.1186/1755-8166-5-39.

9.

Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.

Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P; Italian Registry for MYH9-releated diseases.

PLoS One. 2012;7(4):e35986. doi: 10.1371/journal.pone.0035986. Epub 2012 Apr 25.

10.

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation).

Noris P, Perrotta S, Bottega R, Pecci A, Melazzini F, Civaschi E, Russo S, Magrin S, Loffredo G, Di Salvo V, Russo G, Casale M, De Rocco D, Grignani C, Cattaneo M, Baronci C, Dragani A, Albano V, Jankovic M, Scianguetta S, Savoia A, Balduini CL.

Haematologica. 2012 Jan;97(1):82-8. doi: 10.3324/haematol.2011.050682. Epub 2011 Sep 20.

11.

Needs and challenges of daily life for people with Down syndrome residing in the city of Rome, Italy.

Bertoli M, Biasini G, Calignano MT, Celani G, De Grossi G, Digilio MC, Fermariello CC, Loffredo G, Luchino F, Marchese A, Mazotti S, Menghi B, Razzano C, Tiano C, Zambon Hobart A, Zampino G, Zuccalà G.

J Intellect Disabil Res. 2011 Aug;55(8):801-20. doi: 10.1111/j.1365-2788.2011.01432.x. Epub 2011 Jun 13.

12.

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.

Noris P, Perrotta S, Seri M, Pecci A, Gnan C, Loffredo G, Pujol-Moix N, Zecca M, Scognamiglio F, De Rocco D, Punzo F, Melazzini F, Scianguetta S, Casale M, Marconi C, Pippucci T, Amendola G, Notarangelo LD, Klersy C, Civaschi E, Balduini CL, Savoia A.

Blood. 2011 Jun 16;117(24):6673-80. doi: 10.1182/blood-2011-02-336537. Epub 2011 Apr 5.

PMID:
21467542
13.

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.

Pippucci T, Savoia A, Perrotta S, Pujol-Moix N, Noris P, Castegnaro G, Pecci A, Gnan C, Punzo F, Marconi C, Gherardi S, Loffredo G, De Rocco D, Scianguetta S, Barozzi S, Magini P, Bozzi V, Dezzani L, Di Stazio M, Ferraro M, Perini G, Seri M, Balduini CL.

Am J Hum Genet. 2011 Jan 7;88(1):115-20. doi: 10.1016/j.ajhg.2010.12.006.

14.

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.

Savoia A, De Rocco D, Panza E, Bozzi V, Scandellari R, Loffredo G, Mumford A, Heller PG, Noris P, De Groot MR, Giani M, Freddi P, Scognamiglio F, Riondino S, Pujol-Moix N, Fabris F, Seri M, Balduini CL, Pecci A.

Thromb Haemost. 2010 Apr;103(4):826-32. doi: 10.1160/TH09-08-0593. Epub 2010 Feb 19.

PMID:
20174760
15.

Palonosetron to prevent nausea and vomiting in children undergoing BMT: efficacy and safety.

Ripaldi M, Parasole R, De Simone G, D'Amico MR, Migliorati R, Zanotta G, Loffredo G, Petruzziello F, Poggi V.

Bone Marrow Transplant. 2010 Nov;45(11):1663-4. doi: 10.1038/bmt.2010.23. Epub 2010 Feb 22. No abstract available.

PMID:
20173793
16.

Comparison of different biochemical and molecular methods for the identification of Vibrio parahaemolyticus.

Croci L, Suffredini E, Cozzi L, Toti L, Ottaviani D, Pruzzo C, Serratore P, Fischetti R, Goffredo E, Loffredo G, Mioni R; Vibrio parahaemolyticus Working Group.

J Appl Microbiol. 2007 Jan;102(1):229-37.

17.

The relationship between immune thrombocytopenic purpura and Helicobacter pylori infection in children: where is the truth?

Loffredo G, Marzano MG, Migliorati R, Miele E, Menna F, Poggi V, Staiano A.

Eur J Pediatr. 2007 Oct;166(10):1067-8. Epub 2006 Nov 29. No abstract available.

PMID:
17136353
18.

Splenectomy in children with chronic ITP: long-term efficacy and relation between its outcome and responses to previous treatments.

Ramenghi U, Amendola G, Farinasso L, Giordano P, Loffredo G, Nobili B, Perrotta S, Russo G, Zecca M.

Pediatr Blood Cancer. 2006 Oct 15;47(5 Suppl):742-5.

PMID:
16933239
19.

von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets.

Loffredo G, Baronciani L, Noris P, Menna F, Federici AB, Balduini CL.

Platelets. 2006 May;17(3):149-52.

PMID:
16702040
20.

Verocytotoxin-producing Escherichia coli O157 in minced beef and dairy products in Italy.

Conedera G, Dalvit P, Martini M, Galiero G, Gramaglia M, Goffredo E, Loffredo G, Morabito S, Ottaviani D, Paterlini F, Pezzotti G, Pisanu M, Semprini P, Caprioli A.

Int J Food Microbiol. 2004 Oct 1;96(1):67-73.

PMID:
15358507
21.

Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis.

Balduini CL, Pecci A, Loffredo G, Izzo P, Noris P, Grosso M, Bergamaschi G, Rosti V, Magrini U, Ceresa IF, Conti V, Poggi V, Savoia A.

Thromb Haemost. 2004 Jan;91(1):129-40.

PMID:
14691578
22.

Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases.

DeFranco S, Bonissoni S, Cerutti F, Bona G, Bottarel F, Cadario F, Brusco A, Loffredo G, Rabbone I, Corrias A, Pignata C, Ramenghi U, Dianzani U.

Diabetes. 2001 Mar;50(3):483-8.

23.

The spleen in the Wiskott-Aldrich syndrome: histopathologic abnormalities of the white pulp correlate with the clinical phenotype of the disease.

Vermi W, Blanzuoli L, Kraus MD, Grigolato P, Donato F, Loffredo G, Marino CE, Alberti D, Notarangelo LD, Facchetti F.

Am J Surg Pathol. 1999 Feb;23(2):182-91.

PMID:
9989845
24.

Inefficacy of immunosuppressive treatment in HBSAg-positive, delta-negative, moderate chronic active hepatitis in children.

Vajro P, Orso G, D'Antonio A, Greco L, Fontanella A, Loffredo G, Oggero V, Buffolano W.

J Pediatr Gastroenterol Nutr. 1985 Feb;4(1):26-31.

PMID:
3884766
25.

[Iron content of colostrum and human transition milk and its distribution in samples from women tested].

Greco AM, Sticchi R, Loffredo G, Boschi V.

Minerva Pediatr. 1984 Apr 30;36(8):413-6. Italian. No abstract available.

PMID:
6472223
26.

[Feeding of the low birth weight newborn infant: personal experience in 28 cases].

Saitta F, Loffredo G, Sorrentino F, Paone MC, Fiore MR.

Pediatria (Napoli). 1983 Jun-Sep;91(2-3):173-8. Italian. No abstract available.

PMID:
6664728

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