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Items: 1 to 20 of 65


Genetic polymorphisms and retinal vein occlusion in an Italian population.

De Polo L, Maltese PE, Rigoni E, Bertelli M, Cecchin S, Staurenghi G, Stoppa G.

Genet Mol Res. 2015 Oct 27;14(4):13337-41. doi: 10.4238/2015.October.26.30.


Polymorphism of UGT1A1*28 (TA)7 and liver damage in hepatitis B virus-positive patients in Albania.

Marku E, Maltese PE, Koni M, Capodicasa N, Qendro IS, Rigoni E, Cecchin S, Bertelli M.

Genet Mol Res. 2015 May 18;14(2):5221-8. doi: 10.4238/2015.May.18.13.


Choroidal Thickness Analysis in Patients with Usher Syndrome Type 2 Using EDI OCT.

Colombo L, Sala B, Montesano G, Pierrottet C, De Cillà S, Maltese P, Bertelli M, Rossetti L.

J Ophthalmol. 2015;2015:189140. doi: 10.1155/2015/189140. Epub 2015 May 17.


Multimodal Approach to Monitoring and Investigating Cone Structure and Function in an Inherited Macular Dystrophy.

Ziccardi L, Giannini D, Lombardo G, Serrao S, Dell'Omo R, Nicoletti A, Bertelli M, Lombardo M.

Am J Ophthalmol. 2015 Aug;160(2):301-312.e6. doi: 10.1016/j.ajo.2015.04.024. Epub 2015 Apr 20.


Training on intellectual disability in health sciences: the European perspective.

Salvador-Carulla L, Martínez-Leal R, Heyler C, Alvarez-Galvez J, Veenstra MY, García-Ibáñez J, Carpenter S, Bertelli M, Munir K, Torr J, Van Schrojenstein Lantman-de Valk HM.

Int J Dev Disabil. 2015 Jan;61(1):20-31.


Syndromic and non-syndromic forms of retinitis pigmentosa: a comprehensive Italian clinical and molecular study reveals new mutations.

Pierrottet CO, Zuntini M, Digiuni M, Bazzanella I, Ferri P, Paderni R, Rossetti LM, Cecchin S, Orzalesi N, Bertelli M.

Genet Mol Res. 2014 Oct 27;13(4):8815-33. doi: 10.4238/2014.October.27.23.


Moving beyond intelligence in the revision of ICD-10: specific cognitive functions in intellectual developmental disorders.

Bertelli MO, Salvador-Carulla L, Scuticchio D, Varrucciu N, Martinez-Leal R, Cooper SA, Simeonsson RJ, Deb S, Weber G, Jung R, Munir K, Adnams C, Akoury-Dirani L, Girimaji SC, Katz G, Kwok H, Walsh C.

World Psychiatry. 2014 Feb;13(1):93-4. doi: 10.1002/wps.20094. No abstract available.


Polymorphisms of alpha-actinin-3 and ciliary neurotrophic factor in national-level Italian athletes.

Persi A, Maltese PE, Bertelli M, Cecchin S, Ciaghi M, Guarnieri MC, Agnello L, Maggioni MA, Merati G, Veicsteinas A.

Panminerva Med. 2013 Jun;55(2):217-24.


Is it normal to be a principal mindreader? Revising theories of social cognition on the basis of schizophrenia and high functioning autism-spectrum disorders.

Froese T, Stanghellini G, Bertelli MO.

Res Dev Disabil. 2013 May;34(5):1376-87. doi: 10.1016/j.ridd.2013.01.005. Epub 2013 Mar 5.


Clinical and molecular genetic study of 12 Italian families with autosomal recessive Stargardt disease.

Oldani M, Marchi S, Giani A, Cecchin S, Rigoni E, Persi A, Podavini D, Guerrini A, Nervegna A, Staurenghi G, Bertelli M.

Genet Mol Res. 2012 Dec 17;11(4):4342-50. doi: 10.4238/2012.October.9.3.


Clinical and genetic study of 46 Italian patients with primary lymphedema.

Michelini S, Degiorgio D, Cestari M, Corda D, Ricci M, Cardone M, Mander A, Famoso L, Contini E, Serrani R, Pinelli L, Cecchin S, Bertelli M.

Lymphology. 2012 Mar;45(1):3-12. Erratum in: Lymphology. 2012 Jun;45(2):87.


Prediction of arterial pressure increase after fluid challenge.

Natalini G, Rosano A, Militano CR, Di Maio A, Ferretti P, Bertelli M, de Giuli F, Bernardini A.

BMC Anesthesiol. 2012 Mar 5;12:3. doi: 10.1186/1471-2253-12-3.


Reliability and validity of the SPAID-G checklist for detecting psychiatric disorders in adults with intellectual disability.

Bertelli M, Scuticchio D, Ferrandi A, Lassi S, Mango F, Ciavatta C, Porcelli C, Bianco A, Monchieri S.

Res Dev Disabil. 2012 Mar-Apr;33(2):382-90. doi: 10.1016/j.ridd.2011.08.020. Epub 2011 Nov 24.


Intellectual developmental disorders: towards a new name, definition and framework for "mental retardation/intellectual disability" in ICD-11.

Salvador-Carulla L, Reed GM, Vaez-Azizi LM, Cooper SA, Martinez-Leal R, Bertelli M, Adnams C, Cooray S, Deb S, Akoury-Dirani L, Girimaji SC, Katz G, Kwok H, Luckasson R, Simeonsson R, Walsh C, Munir K, Saxena S.

World Psychiatry. 2011 Oct;10(3):175-80.


Relationship between individual quality of life and family quality of life for people with intellectual disability living in Italy.

Bertelli M, Bianco A, Rossi M, Scuticchio D, Brown I.

J Intellect Disabil Res. 2011 Dec;55(12):1136-50. doi: 10.1111/j.1365-2788.2011.01464.x. Epub 2011 Aug 30.


Neurological disorders of purine and pyrimidine metabolism.

Micheli V, Camici M, Tozzi MG, Ipata PL, Sestini S, Bertelli M, Pompucci G.

Curr Top Med Chem. 2011;11(8):923-47. Review.


Remifentanil improves breathing pattern and reduces inspiratory workload in tachypneic patients.

Natalini G, Di Maio A, Rosano A, Ferretti P, Bertelli M, Bernardini A.

Respir Care. 2011 Jun;56(6):827-33. doi: 10.4187/respcare.01014. Epub 2011 Feb 11.


Olanzapine vs. risperidone in treating aggressive behaviours in adults with intellectual disability: a single blind study.

Amore M, Bertelli M, Villani D, Tamborini S, Rossi M.

J Intellect Disabil Res. 2011 Feb;55(2):210-8. doi: 10.1111/j.1365-2788.2010.01352.x. Epub 2010 Dec 3.


Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation.

Micheli V, Massarino F, Jacomelli G, Bertelli M, Corradi MR, Guerrini A, Cucchiara A, Ravetti JL, Negretti L, Cannella G.

NDT Plus. 2010 Oct;3(5):436-8. doi: 10.1093/ndtplus/sfq096. Epub 2010 Jun 2.


International guide to prescribing psychotropic medication for the management of problem behaviours in adults with intellectual disabilities.

Deb S, Kwok H, Bertelli M, Salvador-Carulla L, Bradley E, Torr J, Barnhill J; Guideline Development Group of the WPA Section on Psychiatry of Intellectual Disability.

World Psychiatry. 2009 Oct;8(3):181-6.

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