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Items: 1 to 20 of 21

1.

Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned.

Risitano AM, Marotta S, Calzone R, Grimaldi F, Zatterale A; RIAF Contributors.

Haematologica. 2016 Mar;101(3):319-27. doi: 10.3324/haematol.2015.133520. Epub 2015 Dec 3.

2.

Current experience in testing mitochondrial nutrients in disorders featuring oxidative stress and mitochondrial dysfunction: rational design of chemoprevention trials.

Pagano G, Aiello Talamanca A, Castello G, Cordero MD, d'Ischia M, Gadaleta MN, Pallardó FV, Petrović S, Tiano L, Zatterale A.

Int J Mol Sci. 2014 Nov 5;15(11):20169-208. doi: 10.3390/ijms151120169. Review.

3.

Oxidative stress and mitochondrial dysfunction across broad-ranging pathologies: toward mitochondria-targeted clinical strategies.

Pagano G, Talamanca AA, Castello G, Cordero MD, d'Ischia M, Gadaleta MN, Pallardó FV, Petrović S, Tiano L, Zatterale A.

Oxid Med Cell Longev. 2014;2014:541230. doi: 10.1155/2014/541230. Epub 2014 May 4. Review.

4.

Bone marrow cell transcripts from Fanconi anaemia patients reveal in vivo alterations in mitochondrial, redox and DNA repair pathways.

Pagano G, Talamanca AA, Castello G, d'Ischia M, Pallardó FV, Petrović S, Porto B, Tiano L, Zatterale A.

Eur J Haematol. 2013 Aug;91(2):141-51. doi: 10.1111/ejh.12131. Epub 2013 Jun 15.

PMID:
23646927
5.

From clinical description, to in vitro and animal studies, and backward to patients: oxidative stress and mitochondrial dysfunction in Fanconi anemia.

Pagano G, Talamanca AA, Castello G, d'Ischia M, Pallardó FV, Petrović S, Porto B, Tiano L, Zatterale A.

Free Radic Biol Med. 2013 May;58:118-25. doi: 10.1016/j.freeradbiomed.2013.01.015. Epub 2013 Jan 29. Review.

PMID:
23376230
6.

Oxidative stress in Fanconi anaemia: from cells and molecules towards prospects in clinical management.

Pagano G, Talamanca AA, Castello G, Pallardó FV, Zatterale A, Degan P.

Biol Chem. 2012 Jan;393(1-2):11-21. doi: 10.1515/BC-2011-227. Review.

PMID:
22628295
7.

Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients.

Micale L, Augello B, Fusco C, Selicorni A, Loviglio MN, Silengo MC, Reymond A, Gumiero B, Zucchetti F, D'Addetta EV, Belligni E, Calcagnì A, Digilio MC, Dallapiccola B, Faravelli F, Forzano F, Accadia M, Bonfante A, Clementi M, Daolio C, Douzgou S, Ferrari P, Fischetto R, Garavelli L, Lapi E, Mattina T, Melis D, Patricelli MG, Priolo M, Prontera P, Renieri A, Mencarelli MA, Scarano G, della Monica M, Toschi B, Turolla L, Vancini A, Zatterale A, Gabrielli O, Zelante L, Merla G.

Orphanet J Rare Dis. 2011 Jun 9;6:38. doi: 10.1186/1750-1172-6-38.

8.

Confirmation of microcephaly-facio-cardio-skeletal Hadziselimovic type syndrome.

Dallapiccola B, Digilio MC, Zatterale A, Galeone R, Capolino R, Mingarelli R.

Clin Dysmorphol. 2009 Jul;18(3):135-8. doi: 10.1097/MCD.0b013e32832a9e78.

PMID:
19373080
9.

Different patterns of in vivo pro-oxidant states in a set of cancer- or aging-related genetic diseases.

Lloret A, Calzone R, Dunster C, Manini P, d'Ischia M, Degan P, Kelly FJ, Pallardó FV, Zatterale A, Pagano G.

Free Radic Biol Med. 2008 Feb 15;44(4):495-503. Epub 2007 Oct 30. Review.

PMID:
18053816
10.

Oxidative stress biomarkers in four Bloom syndrome (BS) patients and in their parents suggest in vivo redox abnormalities in BS phenotype.

Zatterale A, Kelly FJ, Degan P, d'Ischia M, Pallardó FV, Calzone R, Dunster C, Lloret A, Manini P, Coğulu O, Kavakli K, Pagano G.

Clin Biochem. 2007 Oct;40(15):1100-3. Epub 2007 Jun 30.

PMID:
17678887
11.

Glutathione levels in blood from ataxia telangiectasia patients suggest in vivo adaptive mechanisms to oxidative stress.

Degan P, d'Ischia M, Pallardó FV, Zatterale A, Brusco A, Calzone R, Cavalieri S, Kavakli K, Lloret A, Manini P, Pisanti MA, Vuttariello E, Pagano G.

Clin Biochem. 2007 Jun;40(9-10):666-70. Epub 2007 Mar 28.

PMID:
17466964
12.

The immunomodulatory protein SV-IV protects serum-deprived cells against apoptosis but not against G0/G1 arrest: possible implications for the survival of implanting embryo.

Morelli F, Peluso G, Petillo O, Giannattasio A, Filosa S, Motta CM, Tammaro S, Zatterale A, Calzone R, Budillon A, Cartenì M, de Maria S, Costanza MR, Nigro A, Petrazzuolo M, Buommino E, Rizzo M, Capasso G, Baiano S, Moscatiello F, Ravagnan G, Fuggetta MP, Tajana G, Stiuso P, Metafora BM, Metafora V, Metafora S.

J Cell Physiol. 2007 Sep;212(3):610-25.

PMID:
17458892
13.

Multiple evidence for an early age pro-oxidant state in Down Syndrome patients.

Pallardó FV, Degan P, d'Ischia M, Kelly FJ, Zatterale A, Calzone R, Castello G, Fernandez-Delgado R, Dunster C, Lloret A, Manini P, Pisanti MA, Vuttariello E, Pagano G.

Biogerontology. 2006 Aug;7(4):211-20. Epub 2006 Apr 13.

PMID:
16612664
14.

Multiple involvement of oxidative stress in Werner syndrome phenotype.

Pagano G, Zatterale A, Degan P, d'Ischia M, Kelly FJ, Pallardó FV, Kodama S.

Biogerontology. 2005;6(4):233-43.

PMID:
16333757
15.

In vivo prooxidant state in Werner syndrome (WS): results from three WS patients and two WS heterozygotes.

Pagano G, Zatterale A, Degan P, d'Ischia M, Kelly FJ, Pallardó FV, Calzone R, Castello G, Dunster C, Giudice A, Kilinç Y, Lloret A, Manini P, Masella R, Vuttariello E, Warnau M.

Free Radic Res. 2005 May;39(5):529-33.

PMID:
16036329
16.

Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy.

Pramparo T, Grosso S, Messa J, Zatterale A, Bonaglia MC, Chessa L, Balestri P, Rocchi M, Zuffardi O, Giorda R.

Hum Genet. 2005 Oct;118(1):76-81. Epub 2005 Oct 28.

PMID:
16001262
17.

Oxidative stress as a multiple effector in Fanconi anaemia clinical phenotype.

Pagano G, Degan P, d'Ischia M, Kelly FJ, Nobili B, Pallardó FV, Youssoufian H, Zatterale A.

Eur J Haematol. 2005 Aug;75(2):93-100. Review.

PMID:
16000125
18.

Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients.

Pagano G, Degan P, d'Ischia M, Kelly FJ, Pallardó FV, Zatterale A, Anak SS, Akisik EE, Beneduce G, Calzone R, De Nicola E, Dunster C, Lloret A, Manini P, Nobili B, Saviano A, Vuttariello E, Warnau M.

Carcinogenesis. 2004 Oct;25(10):1899-909. Epub 2004 Jun 10.

PMID:
15192013
19.

Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis.

Guanciali-Franchi P, Calabrese G, Morizio E, Fantasia D, Colosimo A, Rinaldi MM, Cristini L, Simonelli A, Lonardo F, Turci A, Zatterale A, Laganà C, Stuppia L, Sabatino G, Palka G.

Am J Med Genet A. 2004 Jun 1;127A(2):144-8.

PMID:
15108201
20.

Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant.

Savino M, Borriello A, D'Apolito M, Criscuolo M, Del Vecchio M, Bianco AM, Di Perna M, Calzone R, Nobili B, Zatterale A, Zelante L, Joenje H, Della Ragione F, Savoia A.

Hum Mutat. 2003 Oct;22(4):338-9.

PMID:
12955722

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