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Items: 1 to 20 of 22

1.

Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis.

Prandini P, De Logu F, Fusi C, Provezza L, Nassini R, Montagner G, Materazzi S, Munari S, Gilioli E, Bezzerri V, Finotti A, Lampronti I, Tamanini A, Dechecchi MC, Lippi G, Ribeiro CM, Rimessi A, Pinton P, Gambari R, Geppetti P, Cabrini G.

Am J Respir Cell Mol Biol. 2016 Nov;55(5):645-656.

PMID:
27281024
2.

A survey of clinical features of allergic rhinitis in adults.

Frati F, Dell'Albani I, Passalacqua G, Bonini S, Rossi O, Senna G, Incorvaia C; Adult SURF Study Group.

Med Sci Monit. 2014 Nov 4;20:2151-6. doi: 10.12659/MSM.891206.

3.

Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs.

Prandini P, Zusi C, Malerba G, Itan, Pignatti PF, Trabetti E.

Mol Cell Probes. 2014 Oct-Dec;28(5-6):242-5. doi: 10.1016/j.mcp.2014.05.001. Epub 2014 Jun 3.

PMID:
24938762
4.

The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families.

Prandini P, Pasquali A, Malerba G, Marostica A, Zusi C, Xumerle L, Muglia P, Da Ros L, Ratti E, Trabetti E, Pignatti PF; Italian Autism Network (ITAN).

Psychiatr Genet. 2012 Aug;22(4):177-81. doi: 10.1097/YPG.0b013e32835185c9.

PMID:
22739633
5.

Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease.

Angiolillo DJ, Bernardo E, Zanoni M, Vivas D, Capranzano P, Malerba G, Capodanno D, Prandini P, Pasquali A, Trabetti E, Sabaté M, Jimenez-Quevedo P, Ferreiro JL, Ueno M, Bass TA, Pignatti PF, Fernandez-Ortiz A, Macaya C.

J Am Coll Cardiol. 2011 Jun 28;58(1):30-9. doi: 10.1016/j.jacc.2011.02.040.

6.

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.

Curran S, Bolton P, Rozsnyai K, Chiocchetti A, Klauck SM, Duketis E, Poustka F, Schlitt S, Freitag CM, Lee I, Muglia P; ITAN, Poot M, Staal W, de Jonge MV, Ophoff RA, Lewis C, Skuse D, Mandy W, Vassos E, Fossdal R, Magnusson P, Hreidarsson S, Saemundsen E, Stefansson H, Stefansson K, Collier D.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):633-9. doi: 10.1002/ajmg.b.31201. Epub 2011 Jun 8.

PMID:
21656903
7.

A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype.

Costantini S, Prandini P, Corradi M, Pasquali A, Contreas G, Pignatti PF, Pinelli L, Trabetti E, Maffeis C.

Diabetes Res Clin Pract. 2011 Apr;92(1):e23-6. doi: 10.1016/j.diabres.2011.01.014. Epub 2011 Feb 1.

PMID:
21288587
8.

Adherence issues related to sublingual immunotherapy as perceived by allergists.

Scurati S, Frati F, Passalacqua G, Puccinelli P, Hilaire C, Incorvaia C; Italian Study Group on SLIT Compliance.

Patient Prefer Adherence. 2010 Jun 24;4:141-5.

9.

A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome.

Pereira PL, Magnol L, Sahún I, Brault V, Duchon A, Prandini P, Gruart A, Bizot JC, Chadefaux-Vekemans B, Deutsch S, Trovero F, Delgado-García JM, Antonarakis SE, Dierssen M, Herault Y.

Hum Mol Genet. 2009 Dec 15;18(24):4756-69. doi: 10.1093/hmg/ddp438. Epub 2009 Sep 26.

10.

Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.

Lyle R, Prandini P, Osoegawa K, ten Hallers B, Humphray S, Zhu B, Eyras E, Castelo R, Bird CP, Gagos S, Scott C, Cox A, Deutsch S, Ucla C, Cruts M, Dahoun S, She X, Bena F, Wang SY, Van Broeckhoven C, Eichler EE, Guigo R, Rogers J, de Jong PJ, Reymond A, Antonarakis SE.

Genome Res. 2007 Nov;17(11):1690-6. Epub 2007 Sep 25.

11.

Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance.

Prandini P, Deutsch S, Lyle R, Gagnebin M, Delucinge Vivier C, Delorenzi M, Gehrig C, Descombes P, Sherman S, Dagna Bricarelli F, Baldo C, Novelli A, Dallapiccola B, Antonarakis SE.

Am J Hum Genet. 2007 Aug;81(2):252-63. Epub 2007 Jun 20.

12.

Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I.

Boito CA, Melacini P, Vianello A, Prandini P, Gavassini BF, Bagattin A, Siciliano G, Angelini C, Pegoraro E.

Arch Neurol. 2005 Dec;62(12):1894-9.

PMID:
16344347
13.

Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy.

Brockington M, Torelli S, Prandini P, Boito C, Dolatshad NF, Longman C, Brown SC, Muntoni F.

Hum Mol Genet. 2005 Mar 1;14(5):657-65. Epub 2005 Jan 20.

PMID:
15661757
14.

A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E.

Andrigo C, Boito C, Prandini P, Mostacciuolo ML, Siciliano G, Angelini C, Pegoraro E.

Neurogenetics. 2005 Feb;6(1):49-50. Epub 2005 Jan 15. No abstract available.

PMID:
15654615
15.

LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy.

Prandini P, Berardinelli A, Fanin M, Morello F, Zardini E, Pichiecchio A, Uggetti C, Lanzi G, Angelini C, Pegoraro E.

Neurology. 2004 Sep 28;63(6):1118-21.

PMID:
15452315
16.

Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency.

Tezak Z, Prandini P, Boscaro M, Marin A, Devaney J, Marino M, Fanin M, Trevisan CP, Park J, Tyson W, Finkel R, Garcia C, Angelini C, Hoffman EP, Pegoraro E.

Hum Mutat. 2003 Feb;21(2):103-11.

PMID:
12552556
17.

Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology.

Pegoraro E, Cepollaro F, Prandini P, Marin A, Fanin M, Trevisan CP, El-Messlemani AH, Tarone G, Engvall E, Hoffman EP, Angelini C.

Am J Pathol. 2002 Jun;160(6):2135-43.

18.

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.

Brockington M, Yuva Y, Prandini P, Brown SC, Torelli S, Benson MA, Herrmann R, Anderson LV, Bashir R, Burgunder JM, Fallet S, Romero N, Fardeau M, Straub V, Storey G, Pollitt C, Richard I, Sewry CA, Bushby K, Voit T, Blake DJ, Muntoni F.

Hum Mol Genet. 2001 Dec 1;10(25):2851-9.

PMID:
11741828
19.

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, Voit T, Sewry CA, Guicheney P, Muntoni F.

Am J Hum Genet. 2001 Dec;69(6):1198-209. Epub 2001 Oct 8.

20.

[IgE-mediated allergy to ethylene oxide in hemodialyzed patients].

Tosoni C, Prandini P, Carabellese N, Cattaneo R, Campanini M, Ranzini C, Soldati F.

Minerva Urol Nefrol. 1991 Apr-Jun;43(2):97-100. Italian.

PMID:
1957238

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