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Items: 1 to 50 of 78

1.

Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent.

Chiriaco M, Casciano F, Di Matteo G, Gentner B, Claps A, Di Cesare S, Cotugno N, D'Argenio P, Rossi P, Aiuti A, Finocchi A.

Clin Immunol. 2018 Feb 3. pii: S1521-6616(17)30242-5. doi: 10.1016/j.clim.2018.01.010. [Epub ahead of print]

PMID:
29410324
2.

Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells.

Cifaldi C, Chiriaco M, Di Matteo G, Di Cesare S, Alessia S, De Angelis P, Rea F, Angelino G, Pastore M, Ferradini V, Pagliara D, Cancrini C, Rossi P, Bertaina A, Finocchi A.

Front Immunol. 2017 Dec 22;8:1893. doi: 10.3389/fimmu.2017.01893. eCollection 2017.

3.

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Dobbs K, Tabellini G, Calzoni E, Patrizi O, Martinez P, Giliani SC, Moratto D, Al-Herz W, Cancrini C, Cowan M, Bleesing J, Booth C, Buchbinder D, Burns SO, Chatila TA, Chou J, Daza-Cajigal V, Ott de Bruin LM, de la Morena MT, Di Matteo G, Finocchi A, Geha R, Goyal RK, Hayward A, Holland S, Huang CH, Kanariou MG, King A, Kaplan B, Kleva A, Kuijpers TW, Lee BW, Lougaris V, Massaad M, Meyts I, Morsheimer M, Neven B, Pai SY, Parvaneh N, Plebani A, Prockop S, Reisli I, Soh JY, Somech R, Torgerson TR, Kim YJ, Walter JE, Gennery AR, Keles S, Manis JP, Marcenaro E, Moretta A, Parolini S, Notarangelo LD.

Front Immunol. 2017 Oct 10;8:1244. doi: 10.3389/fimmu.2017.01244. eCollection 2017.

4.

Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience.

Angelino G, De Angelis P, Faraci S, Rea F, Romeo EF, Torroni F, Tambucci R, Claps A, Francalanci P, Chiriaco M, Di Matteo G, Cancrini C, Palma P, D'Argenio P, Dall'Oglio L, Rossi P, Finocchi A.

Pediatr Allergy Immunol. 2017 Dec;28(8):801-809. doi: 10.1111/pai.12814.

PMID:
28981976
5.

Characterization of T and B cell repertoire diversity in patients with RAG deficiency.

Lee YN, Frugoni F, Dobbs K, Tirosh I, Du L, Ververs FA, Ru H, Ott de Bruin L, Adeli M, Bleesing JH, Buchbinder D, Butte MJ, Cancrini C, Chen K, Choo S, Elfeky RA, Finocchi A, Fuleihan RL, Gennery AR, El-Ghoneimy DH, Henderson LA, Al-Herz W, Hossny E, Nelson RP, Pai SY, Patel NC, Reda SM, Soler-Palacin P, Somech R, Palma P, Wu H, Giliani S, Walter JE, Notarangelo LD.

Sci Immunol. 2016 Dec 16;1(6). pii: eaah6109. doi: 10.1126/sciimmunol.aah6109. Epub 2016 Dec 16.

6.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Dobbs K, Tabellini G, Calzoni E, Patrizi O, Martinez P, Giliani SC, Moratto D, Al-Herz W, Cancrini C, Cowan M, Bleesing J, Booth C, Buchbinder D, Burns SO, Chatila TA, Chou J, Daza-Cajigal V, Ott de Bruin LM, de la Morena M, Di Matteo G, Finocchi A, Geha R, Goyal RK, Hayward A, Holland S, Huang CH, Kanariou MG, King A, Kaplan B, Kleva A, Kuijpers TW, Lee BW, Lougaris V, Massaad M, Meyts I, Morsheimer M, Neven B, Pai SY, Plebani A, Prockop S, Reisli I, Soh JY, Somech R, Torgerson TR, Kim YJ, Walter JE, Gennery AR, Keles S, Manis JP, Marcenaro E, Moretta A, Parolini S, Notarangelo LD.

Front Immunol. 2017 Jul 17;8:798. doi: 10.3389/fimmu.2017.00798. eCollection 2017. Erratum in: Front Immunol. 2017 Oct 10;8:1244.

7.

Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry.

Farruggia P, Puccio G, Fioredda F, Lanza T, Porretti L, Ramenghi U, Barone A, Bonanomi S, Finocchi A, Ghilardi R, Ladogana S, Marra N, Martire B, Notarangelo LD, Onofrillo D, Pillon M, Russo G, Lo Valvo L, Serafinelli J, Tucci F, Zunica F, Verzegnassi F, Dufour C.

Am J Hematol. 2017 Sep;92(9):E546-E549. doi: 10.1002/ajh.24803. Epub 2017 Jul 7. No abstract available.

PMID:
28567966
8.

Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders.

Slack J, Albert MH, Balashov D, Belohradsky BH, Bertaina A, Bleesing J, Booth C, Buechner J, Buckley RH, Ouachée-Chardin M, Deripapa E, Drabko K, Eapen M, Feuchtinger T, Finocchi A, Gaspar HB, Ghosh S, Gillio A, Gonzalez-Granado LI, Grunebaum E, Güngör T, Heilmann C, Helminen M, Higuchi K, Imai K, Kalwak K, Kanazawa N, Karasu G, Kucuk ZY, Laberko A, Lange A, Mahlaoui N, Meisel R, Moshous D, Muramatsu H, Parikh S, Pasic S, Schmid I, Schuetz C, Schulz A, Schultz KR, Shaw PJ, Slatter MA, Sykora KW, Tamura S, Taskinen M, Wawer A, Wolska-Kuśnierz B, Cowan MJ, Fischer A, Gennery AR; Inborn Errors Working Party of the European Society for Blood and Marrow Transplantation and the European Society for Immunodeficiencies; Stem Cell Transplant for Immunodeficiencies in Europe (SCETIDE); Center for International Blood and Marrow Transplant Research; Primary Immunodeficiency Treatment Consortium.

J Allergy Clin Immunol. 2018 Jan;141(1):322-328.e10. doi: 10.1016/j.jaci.2017.02.036. Epub 2017 Apr 7.

PMID:
28392333
9.

Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies.

Canessa C, Iacopelli J, Pecoraro A, Spadaro G, Matucci A, Milito C, Vultaggio A, Agostini C, Cinetto F, Danieli MG, Gambini S, Marasco C, Trizzino A, Vacca A, De Mattia D, Martire B, Plebani A, Di Gioacchino M, Gatta A, Finocchi A, Licciardi F, Martino S, De Carli M, Moschese V, Azzari C.

Int J Immunopathol Pharmacol. 2017 Mar;30(1):73-82. doi: 10.1177/0394632016681577. Epub 2016 Dec 7.

10.

Late-onset combined immune deficiency due to LIGIV mutations in a 12-year-old patient.

Cifaldi C, Angelino G, Chiriaco M, Di Cesare S, Claps A, Serafinelli J, Rossi P, Antoccia A, Di Matteo G, Cancrini C, De Villartay JP, Finocchi A.

Pediatr Allergy Immunol. 2017 Mar;28(2):203-206. doi: 10.1111/pai.12684. No abstract available.

PMID:
27893162
11.

Noncanonical Fungal Autophagy Inhibits Inflammation in Response to IFN-γ via DAPK1.

Oikonomou V, Moretti S, Renga G, Galosi C, Borghi M, Pariano M, Puccetti M, Palmerini CA, Amico L, Carotti A, Prezioso L, Spolzino A, Finocchi A, Rossi P, Velardi A, Aversa F, Napolioni V, Romani L.

Cell Host Microbe. 2016 Dec 14;20(6):744-757. doi: 10.1016/j.chom.2016.10.012. Epub 2016 Nov 23.

12.

Human B-cell memory is shaped by age- and tissue-specific T-independent and GC-dependent events.

Aranburu A, Piano Mortari E, Baban A, Giorda E, Cascioli S, Marcellini V, Scarsella M, Ceccarelli S, Corbelli S, Cantarutti N, De Vito R, Inserra A, Nicolosi L, Lanfranchi A, Porta F, Cancrini C, Finocchi A, Carsetti R.

Eur J Immunol. 2017 Feb;47(2):327-344. doi: 10.1002/eji.201646642. Epub 2016 Dec 14.

13.

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

Speckmann C, Doerken S, Aiuti A, Albert MH, Al-Herz W, Allende LM, Scarselli A, Avcin T, Perez-Becker R, Cancrini C, Cant A, Di Cesare S, Finocchi A, Fischer A, Gaspar HB, Ghosh S, Gennery A, Gilmour K, González-Granado LI, Martinez-Gallo M, Hambleton S, Hauck F, Hoenig M, Moshous D, Neven B, Niehues T, Notarangelo L, Picard C, Rieber N, Schulz A, Schwarz K, Seidel MG, Soler-Palacin P, Stepensky P, Strahm B, Vraetz T, Warnatz K, Winterhalter C, Worth A, Fuchs S, Uhlmann A, Ehl S; P-CID study of the Inborn Errors Working Party of the EBMT.

J Allergy Clin Immunol. 2017 Apr;139(4):1302-1310.e4. doi: 10.1016/j.jaci.2016.07.040. Epub 2016 Sep 19.

PMID:
27658761
14.

Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection.

Brigida I, Chiriaco M, Di Cesare S, Cittaro D, Di Matteo G, Giannelli S, Lazarevic D, Zoccolillo M, Stupka E, Jenkner A, Francalanci P, Livadiotti S, Morawski A, Ravell J, Lenardo M, Cancrini C, Aiuti A, Finocchi A.

J Clin Immunol. 2017 Jan;37(1):32-35. doi: 10.1007/s10875-016-0341-y. Epub 2016 Oct 21. No abstract available.

15.

Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy.

Cifaldi C, Scarselli A, Petricone D, Di Cesare S, Chiriaco M, Claps A, Rossi P, Calzoni E, Yamazaki Y, Notarangelo LD, Di Matteo G, Cancrini C, Finocchi A.

Clin Immunol. 2016 Dec;173:121-123. doi: 10.1016/j.clim.2016.09.013. Epub 2016 Oct 3.

PMID:
27713031
16.

Fungal infections of the lung in children.

Toma P, Bertaina A, Castagnola E, Colafati GS, D'Andrea ML, Finocchi A, Lucidi V, Mastronuzzi A, Granata C.

Pediatr Radiol. 2016 Dec;46(13):1856-1865. Epub 2016 Sep 23. Review.

PMID:
27663906
17.

Waning of vaccine-induced immunity to measles in kidney transplanted children.

Rocca S, Santilli V, Cotugno N, Concato C, Manno EC, Nocentini G, Macchiarulo G, Cancrini C, Finocchi A, Guzzo I, Dello Strologo L, Palma P.

Medicine (Baltimore). 2016 Sep;95(37):e4738. doi: 10.1097/MD.0000000000004738.

18.

The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment.

Chiriaco M, Brigida I, Ariganello P, Di Cesare S, Di Matteo G, Taus F, Cittaro D, Lazarevic D, Scarselli A, Santilli V, Attardi E, Stupka E, Giannelli S, Fraziano M, Finocchi A, Rossi P, Aiuti A, Palma P, Cancrini C.

Clin Immunol. 2017 May;178:20-28. doi: 10.1016/j.clim.2015.12.008. Epub 2015 Dec 28.

PMID:
26732860
19.

Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects.

Chiriaco M, Salfa I, Di Matteo G, Rossi P, Finocchi A.

Pediatr Allergy Immunol. 2016 May;27(3):242-53. doi: 10.1111/pai.12527. Epub 2016 Jan 21. Review.

PMID:
26680691
20.

Celiac Disease in an Adoptive Child with Recurrent Giardia Infection.

Tchidjou HK, De Matteis A, Di Iorio L, Finocchi A.

Int J Health Sci (Qassim). 2015 Apr;9(2):193-7.

21.

Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia.

Leuzzi V, Micheli R, D'Agnano D, Molinaro A, Venturi T, Plebani A, Soresina A, Marini M, Ferremi Leali P, Quinti I, Pietrogrande MC, Finocchi A, Fazzi E, Chessa L, Magnani M.

Neurol Neuroimmunol Neuroinflamm. 2015 Apr 9;2(3):e98. doi: 10.1212/NXI.0000000000000098. eCollection 2015 Jun.

22.

Multi-drugs resistant acne rosacea in a child affected by Ataxia-Telangiectasia: successful treatment with Isotretinoin.

Cantarutti N, Claps A, Angelino G, Chessa L, Callea F, El Hachem M, Diociaiuti A, Finocchi A.

Ital J Pediatr. 2015 Mar 28;41:23. doi: 10.1186/s13052-015-0125-7.

23.

Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency.

Scarselli A, Di Cesare S, Capponi C, Cascioli S, Romiti ML, Di Matteo G, Simonetti A, Palma P, Finocchi A, Lucarelli B, Pinto RM, Rana I, Palumbo G, Caniglia M, Rossi P, Carsetti R, Cancrini C, Aiuti A.

J Clin Immunol. 2015 May;35(4):373-83. doi: 10.1007/s10875-015-0154-4. Epub 2015 Apr 15.

PMID:
25875698
24.

Immunization status of internationally adopted children in Rome, Italy.

Tchidjou HK, Gargiullo L, Vescio F, Giampaolo R, Nicolosi L, Finocchi A, Rossi P.

Niger J Clin Pract. 2015 May-Jun;18(3):307-11. doi: 10.4103/1119-3077.151714.

25.

Subcutaneous immunoglobulin replacement therapy in patients with primary immunodeficiency in routine clinical practice: the VISPO prospective multicenter study.

Vultaggio A, Azzari C, Milito C, Finocchi A, Toppino C, Spadaro G, Trizzino A, Baldassarre M, Paganelli R, Moschese V, Soresina A, Matucci A.

Clin Drug Investig. 2015 Mar;35(3):179-85. doi: 10.1007/s40261-015-0270-1.

26.

Gene therapy for chronic granulomatous disease: current status and future perspectives.

Kaufmann KB, Chiriaco M, Siler U, Finocchi A, Reichenbach J, Stein S, Grez M.

Curr Gene Ther. 2014;14(6):447-60. Review.

PMID:
25245086
27.

Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease.

Cotugno N, Finocchi A, Cagigi A, Di Matteo G, Chiriaco M, Di Cesare S, Rossi P, Aiuti A, Palma P, Douagi I.

J Allergy Clin Immunol. 2015 Mar;135(3):753-61.e2. doi: 10.1016/j.jaci.2014.07.012. Epub 2014 Aug 29.

PMID:
25175493
28.

Consanguinity and polygenic diseases: a model for antibody deficiencies.

Di Pierro V, Zuntini R, Cancrini C, Finocchi A, Angelino G, Rossi P, Ferrari S.

Hum Hered. 2014;77(1-4):144-9. doi: 10.1159/000362364. Epub 2014 Jul 29.

29.

How should eosinophilic cystitis be treated in patients with chronic granulomatous disease?

Claps A, Della Corte M, Gerocarni Nappo S, Francalanci P, Palma P, Finocchi A.

Pediatr Nephrol. 2014 Nov;29(11):2229-33. doi: 10.1007/s00467-014-2883-7. Epub 2014 Jul 19.

PMID:
25037864
30.

Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease.

Carnevale R, Loffredo L, Sanguigni V, Plebani A, Rossi P, Pignata C, Martire B, Finocchi A, Pietrogrande MC, Azzari C, Soresina AR, Martino S, Cirillo E, Martino F, Pignatelli P, Violi F.

J Am Heart Assoc. 2014 Jun 27;3(3):e000920. doi: 10.1161/JAHA.114.000920.

31.

HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders.

Bertaina A, Merli P, Rutella S, Pagliara D, Bernardo ME, Masetti R, Pende D, Falco M, Handgretinger R, Moretta F, Lucarelli B, Brescia LP, Li Pira G, Testi M, Cancrini C, Kabbara N, Carsetti R, Finocchi A, Moretta A, Moretta L, Locatelli F.

Blood. 2014 Jul 31;124(5):822-6. doi: 10.1182/blood-2014-03-563817. Epub 2014 May 28.

32.

Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis.

Chiriaco M, Farinelli G, Capo V, Zonari E, Scaramuzza S, Di Matteo G, Sergi LS, Migliavacca M, Hernandez RJ, Bombelli F, Giorda E, Kajaste-Rudnitski A, Trono D, Grez M, Rossi P, Finocchi A, Naldini L, Gentner B, Aiuti A.

Mol Ther. 2014 Aug;22(8):1472-1483. doi: 10.1038/mt.2014.87. Epub 2014 May 29.

33.

A 13-year-old girl with recurrent inguinal lymphadenopathy.

Del Bufalo F, Salfa I, Pardi V, Colafati GS, De Ioris MA, De Vito R, Finocchi A.

Pediatr Ann. 2014 Apr;43(4):136-8. doi: 10.3928/00904481-20140325-04. No abstract available.

PMID:
24716556
34.

Clinical features and follow-up in patients with 22q11.2 deletion syndrome.

Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EM, Cardinale F, Finocchi A, Romiti ML, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MC, Marino B, Ugazio AG, Plebani A, Rossi P; Italian Network for Primary Immunodeficiencies.

J Pediatr. 2014 Jun;164(6):1475-80.e2. doi: 10.1016/j.jpeds.2014.01.056. Epub 2014 Mar 20.

PMID:
24657119
35.

Chronic granulomatous disease presenting with salmonella brain abscesses.

Finocchi A, Claps A, Serafinelli J, Salfa I, Longo D, Di Matteo G, Aiuti A, Rossi P.

Pediatr Infect Dis J. 2014 May;33(5):525-8. doi: 10.1097/INF.0000000000000270.

PMID:
24445825
36.

Intra-erythrocyte infusion of dexamethasone reduces neurological symptoms in ataxia teleangiectasia patients: results of a phase 2 trial.

Chessa L, Leuzzi V, Plebani A, Soresina A, Micheli R, D'Agnano D, Venturi T, Molinaro A, Fazzi E, Marini M, Ferremi Leali P, Quinti I, Cavaliere FM, Girelli G, Pietrogrande MC, Finocchi A, Tabolli S, Abeni D, Magnani M.

Orphanet J Rare Dis. 2014 Jan 9;9:5. doi: 10.1186/1750-1172-9-5.

37.

Immunotherapy with an HIV-DNA Vaccine in Children and Adults.

Palma P, Gudmundsdotter L, Finocchi A, Eriksson LE, Mora N, Santilli V, Aquilani A, Manno EC, Zangari P, Romiti ML, Montesano C, Grifoni A, Brave A, Ljungberg K, Blomberg P, Bernardi S, Sandström E, Hejdeman B, Rossi P, Wahren B.

Vaccines (Basel). 2014 Jul 17;2(3):563-80. doi: 10.3390/vaccines2030563.

38.

Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases.

Angelino G, Caruso R, D'Argenio P, Calò Carducci FI, Pascone R, Lanciotti M, Cancrini C, Palma P, Aiuti A, Rossi P, Finocchi A.

Pediatr Allergy Immunol. 2014 May;25(3):283-9. doi: 10.1111/pai.12177. Epub 2013 Dec 10.

PMID:
24325465
39.

Serum soluble ST2 as diagnostic marker of systemic inflammatory reactive syndrome of bacterial etiology in children.

Calò Carducci FI, Aufiero LR, Folgori L, Vittucci AC, Amodio D, De Luca M, Li Pira G, Bergamini A, Pontrelli G, Finocchi A, D'Argenio P.

Pediatr Infect Dis J. 2014 Feb;33(2):199-203. doi: 10.1097/INF.0000000000000030.

PMID:
23989103
40.

Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging.

Montella S, Mollica C, Finocchi A, Pession A, Pietrogrande MC, Trizzino A, Ranucci G, Maglione M, Giardino G, Salvatore M, Santamaria F, Pignata C.

J Clin Immunol. 2013 Oct;33(7):1185-91. doi: 10.1007/s10875-013-9933-y. Epub 2013 Aug 24.

PMID:
23975689
41.

Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia.

Ariganello P, Angelino G, Scarselli A, Salfa I, Della Corte M, De Matteis A, D'Argenio P, Livadiotti S, Manno EC, Russo C, Finocchi A, Cancrini C.

Case Rep Pediatr. 2013;2013:735108. doi: 10.1155/2013/735108. Epub 2013 Jun 3.

42.

Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome.

Aiuti A, Biasco L, Scaramuzza S, Ferrua F, Cicalese MP, Baricordi C, Dionisio F, Calabria A, Giannelli S, Castiello MC, Bosticardo M, Evangelio C, Assanelli A, Casiraghi M, Di Nunzio S, Callegaro L, Benati C, Rizzardi P, Pellin D, Di Serio C, Schmidt M, Von Kalle C, Gardner J, Mehta N, Neduva V, Dow DJ, Galy A, Miniero R, Finocchi A, Metin A, Banerjee PP, Orange JS, Galimberti S, Valsecchi MG, Biffi A, Montini E, Villa A, Ciceri F, Roncarolo MG, Naldini L.

Science. 2013 Aug 23;341(6148):1233151. doi: 10.1126/science.1233151. Epub 2013 Jul 11.

43.

Familial hemophagocytic lymphohistiocytosis type 3 diagnosed at school age: a case report.

Manno EC, Salfa I, Palma P, Bertaina A, Lombardi A, Moretta F, Coniglio ML, Sieni E, Aricò M, Finocchi A.

J Pediatr Hematol Oncol. 2014 Mar;36(2):e128-30. doi: 10.1097/MPH.0b013e318292bc7c.

PMID:
23669735
44.

Serratia marcescens osteomyelitis in a newborn with chronic granulomatous disease.

Salfa I, Cantarutti N, Angelino G, Di Matteo G, Capo V, Farinelli G, Cancrini C, Aiuti A, Palma P, Finocchi A.

Pediatr Infect Dis J. 2013 Aug;32(8):926. doi: 10.1097/INF.0b013e31828f682a. No abstract available.

PMID:
23518820
45.

Reduced atherosclerotic burden in subjects with genetically determined low oxidative stress.

Violi F, Pignatelli P, Pignata C, Plebani A, Rossi P, Sanguigni V, Carnevale R, Soresina A, Finocchi A, Cirillo E, Catasca E, Angelico F, Loffredo L.

Arterioscler Thromb Vasc Biol. 2013 Feb;33(2):406-12. doi: 10.1161/ATVBAHA.112.300438. Epub 2013 Jan 3.

46.

Does NADPH oxidase deficiency cause artery dilatation in humans?

Loffredo L, Carnevale R, Sanguigni V, Plebani A, Rossi P, Pignata C, De Mattia D, Finocchi A, Martire B, Pietrogrande MC, Martino S, Gambineri E, Giardino G, Soresina AR, Martino F, Pignatelli P, Violi F.

Antioxid Redox Signal. 2013 Apr 20;18(12):1491-6. doi: 10.1089/ars.2012.4987. Epub 2012 Dec 7.

PMID:
23216310
47.

A 2-month-old male with pyuria and persistent fever.

Cotugno N, Aquilani A, Manno EC, Salfa I, Castelluzzo MA, Finocchi A, Palma P.

Pediatr Ann. 2012 Oct;41(10):405-7. doi: 10.3928/00904481-20120924-06. No abstract available.

PMID:
23052143
48.

A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia.

Zannolli R, Buoni S, Betti G, Salvucci S, Plebani A, Soresina A, Pietrogrande MC, Martino S, Leuzzi V, Finocchi A, Micheli R, Rossi LN, Brusco A, Misiani F, Fois A, Hayek J, Kelly C, Chessa L.

Mov Disord. 2012 Sep 1;27(10):1312-6. doi: 10.1002/mds.25126. Epub 2012 Aug 23.

PMID:
22927201
49.

Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency.

Hassan A, Booth C, Brightwell A, Allwood Z, Veys P, Rao K, Hönig M, Friedrich W, Gennery A, Slatter M, Bredius R, Finocchi A, Cancrini C, Aiuti A, Porta F, Lanfranchi A, Ridella M, Steward C, Filipovich A, Marsh R, Bordon V, Al-Muhsen S, Al-Mousa H, Alsum Z, Al-Dhekri H, Al Ghonaium A, Speckmann C, Fischer A, Mahlaoui N, Nichols KE, Grunebaum E, Al Zahrani D, Roifman CM, Boelens J, Davies EG, Cavazzana-Calvo M, Notarangelo L, Gaspar HB; Inborn Errors Working Party of the European Group for Blood and Marrow Transplantation and European Society for Immunodeficiency.

Blood. 2012 Oct 25;120(17):3615-24; quiz 3626. doi: 10.1182/blood-2011-12-396879. Epub 2012 Jul 12.

50.

Fulminant Fusobacterium necrophorum meningitis in an immunocompetent adolescent.

Angelino G, Cantarutti N, Chiurchiù S, Amodio D, De Luca M, Lancella L, Coltella L, Russo C, Finocchi A.

Pediatr Emerg Care. 2012 Jul;28(7):703-4. doi: 10.1097/PEC.0b013e31825d23fb.

PMID:
22766589

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