Stallone Raffaella

Analisi SNP Array e profilo di espressione genica a livello genico e di micro RNA.

Informazioni aggiuntive

  • Pubblicazioni Scientifiche:

    Totale pubblicazioni a partire dal 2011: 22


    Anno

    2018; 61(5): 248-252

    Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders.

    Palumbo O, Accadia M, Palumbo P, Leone MP, Scorrano A, Palladino T, Stallone R, Bonaglia MC, Carella M


    2018; 176(2): 391-398

    Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome.

    Palumbo P, Accadia M, Leone MP, Palladino T, Stallone R, Carella M, Palumbo O


    2017; ():

    Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.

    Leone MP, Palumbo P, Ortore R, Castellana S, Palumbo O, Melchionda S, Palladino T, Stallone R, Mazza T, Cocchi R, Carella M


    Molecular syndromology 2016; 7(5): 282-286

    PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature.

    Palumbo O, Palumbo P, Leone MP, Stallone R, Palladino T, Vendemiale M, Palladino S, Papadia F, Carella M, Fischetto R


    Molecular Syndromology 2016; :

    PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature

    Palumbo O., Palumbo P., Leone M.P., Stallone R., Palladino T., Vendemiale M., Palladino S., Papadia F., Carella M., FIschetto R:

    2016; 9(): 40

    Clinical and molecular characterization of a de novo 19p13.3 microdeletion.

    Palumbo P, Palumbo O, Leone MP, Stallone R, Palladino T, Zelante L, Carella M


    2016; ():

    Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancer.

    Mazza T, Mazzoccoli G, Fusilli C, Capocefalo D, Panza A, Biagini T, Castellana S, Gentile A, De Cata A, Palumbo O, Stallone R, Rubino R, Carella M, Piepoli A


    2015; ():

    Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay.

    Palumbo P, Palumbo O, Leone MP, Stallone R, Palladino T, Zelante L, Carella M


    2014; ():

    Microdeletion of 12q24.31: Report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms.

    Palumbo O, Palumbo P, Delvecchio M, Palladino T, Stallone R, Crisetti M, Zelante L, Carella M


    Società Italiana di Genetica Umana - XVI Congresso Nazionale 2013; : P280

    Microdeletion of chromosome 12Q24.31 in a girl with intellectual disabilities, overgrowth and facial dysmorphisms

    Palumbo O., Palumbo P., Delvecchio M., Palladino T., Stallone R., Zelante L., Carella M.

    Società Italiana di Genetica Umana - XVI Congresso Nazionale 2013; : P276

    Clinical and molecular description of a patient with a de novo 6Q16.1Q16.2 microdeletion: three candidate genes for the observed phenotype

    Palumbo P., Palumbo O., Palladino T., Stallone R., Zelante L., Carella M.

    2012; 5(1): 1

    A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report.

    Palumbo O, Palumbo P, Palladino T, Stallone R, Zelante L, Carella M


    2012; ():

    3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.

    Palumbo O, D'Agruma L, Minenna AF, Palumbo P, Stallone R, Palladino T, Zelante L, Carella M


    2012; 513(1): 209-13

    8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: Case report and critical review of the literature.

    Palumbo O, Palumbo P, Stallone R, Palladino T, Zelante L, Carella M


    2012; 55(12): 747-52

    Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlation.

    Mattina T, Palumbo O, Stallone R, Pulvirenti RM, Di Dio L, Pavone P, Carella M, Pavone L


    2012; 83(1): 83-7

    MODY type 2 P59S GCK mutant: founder effect in South of Italy.

    Delvecchio M, Ludovico O, Bellacchio E, Stallone R, Palladino T, Mastroianno S, Zelante L, Sacco M, Trischitta V, Carella M


    2012; 158A(12): 3182-9

    An emerging phenotype of interstitial 15q25.2 microdeletions: clinical report and review.

    Palumbo O, Palumbo P, Palladino T, Stallone R, Miroballo M, Piemontese MR, Zelante L, Carella M


    XIV Congresso Nazionale della Società Italiana di Genetica Umana 2011; SIGU: cod. 161

    Due casi di sindrome da microdelezione 17q21.31

    Cassisi G, Praticò E, Pitta R, Palumbo O, Ferrara A, Stallone R, Carella M, Mattina T

    XIV Congresso Nazionale della Società Italiana di Genetica Umana 2011; SIGU: cod. 144

    Un caso di sindrome da duplicazione 16p13 con falangi distali di forma conica

    Di Dio L, Pavone P, Pulvirenti R, Stallone R, Palumbo O, Carella M, Mattina T

    XIV Congresso Nazionale della Società Italiana di Genetica Umana 2011; SIGU: cod. 084

    8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of charge syndrome

    Palumbo O, Palumbo P, Palladino T, Stallone R, Zelante L, Carella M

    XIV Congresso Nazionale della Società Italiana di Genetica Umana 2011; SIGU: cod. 083

    Identification of a FOXP1 deletion in a patient with autism, developmental verbal dyspraxia (DVD) and deficit of motor cordination

    Palumbo O, D'Agruma L, Minenna AF, Palumbo P, Palladino T, Stallone R, Zelante L, Carella M

    2011; 17(): 2482-94

    Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.

    De Bonis P, Laborante A, Pizzicoli C, Stallone R, Barbano R, Longo C, Mazzilli E, Zelante L, Bisceglia L


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