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Items: 1 to 50 of 142

1.

Relationship of Body Composition and Urinary Incontinence in Women: A Cross-Sectional Case-Control Study.

Ferreira R, Sacramento J, Brasil C, Dias C, Plácido C, Oliveira C, Feitosa A, Januário P, Fichera M, Lordelo P.

Female Pelvic Med Reconstr Surg. 2020 Jan 25. doi: 10.1097/SPV.0000000000000834. [Epub ahead of print]

PMID:
32217921
2.

Clinical correlates in children with autism spectrum disorder and CNVs: Systematic investigation in a clinical setting.

Barone R, Gulisano M, Amore R, Domini C, Milana MC, Giglio S, Madia F, Mattina T, Casabona A, Fichera M, Rizzo R.

Int J Dev Neurosci. 2020 Mar 11. doi: 10.1002/jdn.10024. [Epub ahead of print]

PMID:
32159884
3.

Multidisciplinary management of women with pelvic organ prolapse, urinary incontinence and lower urinary tract symptoms.A clinical and psychological overview.

La Rosa VL, Ciebiera M, Lin LT, Sleiman Z, Cerentini TM, Lordelo P, Kahramanoglu I, Bruni S, Garzon S, Fichera M.

Prz Menopauzalny. 2019 Dec;18(3):184-190. doi: 10.5114/pm.2019.89496. Epub 2019 Nov 5. Review.

4.

Frataxin deficiency in Friedreich's ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival.

Tiano F, Amati F, Cherubini F, Morini E, Vancheri C, Maletta S, Fortuni S, Serio D, Quatrana A, Luffarelli R, Benini M, Alfedi G, Panarello L, Rufini A, Toschi N, Frontali M, Romano S, Marcotulli C, Casali C, Gioiosa S, Mariotti C, Mongelli A, Fichera M, Condò I, Novelli G, Testi R, Malisan F.

Hum Mol Genet. 2020 Feb 1;29(3):471-482. doi: 10.1093/hmg/ddz306.

PMID:
31943004
5.

Vitamin D, reproductive disorders and assisted reproduction: evidences and perspectives.

Fichera M, Török P, Tesarik J, Della Corte L, Rizzo G, Garzon S, Carlea A, Di Angelo Antonio S, Zito G, Panella MM.

Int J Food Sci Nutr. 2019 Sep 5:1-10. doi: 10.1080/09637486.2019.1661978. [Epub ahead of print]

PMID:
31928386
6.

Does Vaginal Wall Surgical Trauma During Hybrid Transvaginal NOTES Nephrectomy Have Traumatic Effects On Sexual Functions? A Prospective Study.

Sener TE, Sahin B, Fichera M, Panella MM, Tanidir Y, Lucan CV, Netsch C, Lunelli L.

J Invest Surg. 2020 Jan 6:1-8. doi: 10.1080/08941939.2019.1710627. [Epub ahead of print]

PMID:
31906743
7.

Vitamin D and Gestational Diabetes Mellitus: Is There a Link?

Rizzo G, Garzon S, Fichera M, Panella MM, Catena U, Schiattarella A, de Franciscis P, Vilos G, Tesarik J, Török P, Grosso G.

Antioxidants (Basel). 2019 Oct 25;8(11). pii: E511. doi: 10.3390/antiox8110511. Review.

8.

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity.

Cellini E, Vetro A, Conti V, Marini C, Doccini V, Clementella C, Parrini E, Giglio S, Della Monica M, Fichera M, Musumeci SA, Guerrini R.

Eur J Hum Genet. 2019 Jun;27(6):909-918. doi: 10.1038/s41431-019-0335-3. Epub 2019 Jan 25.

PMID:
30683929
9.

Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorder.

Scuderi C, Saccuzzo L, Vinci M, Castiglia L, Galesi O, Salemi M, Mattina T, Borgione E, Città S, Romano C, Fichera M.

Eur J Hum Genet. 2019 Apr;27(4):594-602. doi: 10.1038/s41431-018-0321-1. Epub 2019 Jan 18.

10.

Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy.

Fichera M, Failla P, Saccuzzo L, Miceli M, Salvo E, Castiglia L, Galesi O, Grillo L, Calì F, Greco D, Amato C, Romano C, Elia M.

Hum Genet. 2019 Feb;138(2):187-198. doi: 10.1007/s00439-019-01972-3. Epub 2019 Jan 17.

PMID:
30656450
11.

Use of pre-operative imaging for symptomatic uterine myomas during pregnancy: a case report and a systematic literature review.

Valenti G, Milone P, D'Amico S, Caldaci LMG, Vitagliano A, Sapia F, Fichera M.

Arch Gynecol Obstet. 2019 Jan;299(1):13-33. doi: 10.1007/s00404-018-4948-5. Epub 2018 Oct 29.

PMID:
30374647
12.

35-Week twin delivery after embryo reduction at 11 weeks and subsequent expulsion of a dead foetus at 20.

Giunta G, Fichera M, Caruso S, La Rosa B, Ferrara M, Iuculano A, Monni G, Cianci A.

J Obstet Gynaecol. 2019 May;39(4):539-540. doi: 10.1080/01443615.2018.1496075. Epub 2018 Oct 27. No abstract available.

PMID:
30370801
13.

Impedance Spectroscopic Detection of Binding and Reactions in Acid-Labile Dielectric Polymers for Biosensor Applications.

Dailey J, Fichera M, Silbergeld E, Katz H.

J Mater Chem B. 2018 May 21;6(19):2972-2981. doi: 10.1039/C7TB03171H. Epub 2018 Apr 19.

14.

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.

Pizzo L, Jensen M, Polyak A, Rosenfeld JA, Mannik K, Krishnan A, McCready E, Pichon O, Le Caignec C, Van Dijck A, Pope K, Voorhoeve E, Yoon J, Stankiewicz P, Cheung SW, Pazuchanics D, Huber E, Kumar V, Kember RL, Mari F, Curró A, Castiglia L, Galesi O, Avola E, Mattina T, Fichera M, Mandarà L, Vincent M, Nizon M, Mercier S, Bénéteau C, Blesson S, Martin-Coignard D, Mosca-Boidron AL, Caberg JH, Bucan M, Zeesman S, Nowaczyk MJM, Lefebvre M, Faivre L, Callier P, Skinner C, Keren B, Perrine C, Prontera P, Marle N, Renieri A, Reymond A, Kooy RF, Isidor B, Schwartz C, Romano C, Sistermans E, Amor DJ, Andrieux J, Girirajan S.

Genet Med. 2019 Apr;21(4):816-825. doi: 10.1038/s41436-018-0266-3. Epub 2018 Sep 7.

15.

Bi-hemispheric repetitive transcranial magnetic stimulation for upper limb motor recovery in chronic stroke: A feasibility study.

Chieffo R, Scopelliti G, Fichera M, Santangelo R, Guerrieri S, Zangen A, Comi G, Leocani L.

Brain Stimul. 2018 Jul - Aug;11(4):932-934. doi: 10.1016/j.brs.2018.03.013. Epub 2018 Mar 15. No abstract available.

PMID:
29605529
16.

Virtual Chromoendoscopy With FICE for the Classification of Polypoid and Nonpolypoid Raised Lesions in Ulcerative Colitis.

Cassinotti A, Buffoli F, Fociani P, Staiano T, Villanacci V, Nebuloni M, Duca P, Fichera M, Grassia R, Manes G, Salemme M, Molteni P, Sampietro G, Foschi D, de Franchis R, Ardizzone S.

J Clin Gastroenterol. 2019 Apr;53(4):269-276. doi: 10.1097/MCG.0000000000000974.

PMID:
29394176
17.

Weight gain after subthalamic nucleus deep brain stimulation in Parkinson's disease is influenced by dyskinesias' reduction and electrodes' position.

Balestrino R, Baroncini D, Fichera M, Donofrio CA, Franzin A, Mortini P, Comi G, Volontè MA.

Neurol Sci. 2017 Dec;38(12):2123-2129. doi: 10.1007/s10072-017-3102-7. Epub 2017 Sep 14.

PMID:
28913772
18.

Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders.

Barone R, Fichera M, De Grandi M, Battaglia M, Lo Faro V, Mattina T, Rizzo R.

Am J Med Genet A. 2017 Jun;173(6):1649-1655. doi: 10.1002/ajmg.a.38205. Epub 2017 Apr 13.

PMID:
28407444
19.

Antitumoural activity of a cytotoxic peptide of Lactobacillus casei peptidoglycan and its interaction with mitochondrial-bound hexokinase.

Fichera GA, Fichera M, Milone G.

Anticancer Drugs. 2016 Aug;27(7):609-19. doi: 10.1097/CAD.0000000000000367.

20.

Proteomic Characterization of Head and Neck Cancer Patient-Derived Xenografts.

Li H, Wheeler S, Park Y, Ju Z, Thomas SM, Fichera M, Egloff AM, Lui VW, Duvvuri U, Bauman JE, Mills GB, Grandis JR.

Mol Cancer Res. 2016 Mar;14(3):278-86. doi: 10.1158/1541-7786.MCR-15-0354. Epub 2015 Dec 18.

21.

Different Tissue-Derived Stem Cells: A Comparison of Neural Differentiation Capability.

Bonaventura G, Chamayou S, Liprino A, Guglielmino A, Fichera M, Caruso M, Barcellona ML.

PLoS One. 2015 Oct 30;10(10):e0140790. doi: 10.1371/journal.pone.0140790. eCollection 2015.

22.

MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability.

Bianciardi L, Fichera M, Failla P, Di Marco C, Grozeva D, Mencarelli MA, Spiga O, Mari F, Meloni I, Raymond L, Renieri A, Romano C, Ariani F.

J Hum Genet. 2016 Feb;61(2):95-101. doi: 10.1038/jhg.2015.118. Epub 2015 Oct 22.

23.

Recurrent duplications of 17q12 associated with variable phenotypes.

Mitchell E, Douglas A, Kjaegaard S, Callewaert B, Vanlander A, Janssens S, Yuen AL, Skinner C, Failla P, Alberti A, Avola E, Fichera M, Kibaek M, Digilio MC, Hannibal MC, den Hollander NS, Bizzarri V, Renieri A, Mencarelli MA, Fitzgerald T, Piazzolla S, van Oudenhove E, Romano C, Schwartz C, Eichler EE, Slavotinek A, Escobar L, Rajan D, Crolla J, Carter N, Hodge JC, Mefford HC.

Am J Med Genet A. 2015 Dec;167A(12):3038-45. doi: 10.1002/ajmg.a.37351. Epub 2015 Sep 30.

PMID:
26420380
24.

Drawing in Alzheimer-type dementia.

Fichera M, Bernasconi MP, Martinelli V, Comi G, Volonté MA.

Neurology. 2015 Jul 28;85(4):386-7. doi: 10.1212/WNL.0000000000001789. No abstract available.

PMID:
26215879
25.

d-chiro-Inositol and alpha lipoic acid treatment of metabolic and menses disorders in women with PCOS.

Cianci A, Panella M, Fichera M, Falduzzi C, Bartolo M, Caruso S.

Gynecol Endocrinol. 2015 Jun;31(6):483-6. doi: 10.3109/09513590.2015.1014784. Epub 2015 Apr 20.

PMID:
25893270
26.

Mongersen, an oral SMAD7 antisense oligonucleotide, and Crohn's disease.

Monteleone G, Neurath MF, Ardizzone S, Di Sabatino A, Fantini MC, Castiglione F, Scribano ML, Armuzzi A, Caprioli F, Sturniolo GC, Rogai F, Vecchi M, Atreya R, Bossa F, Onali S, Fichera M, Corazza GR, Biancone L, Savarino V, Pica R, Orlando A, Pallone F.

N Engl J Med. 2015 Mar 19;372(12):1104-13. doi: 10.1056/NEJMoa1407250.

27.

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.

van Bon BW, Coe BP, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen MH, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, Haan E, Romano C, Mefford HC, Scheffer I, Gecz J, de Vries BB, Eichler EE.

Mol Psychiatry. 2016 Jan;21(1):126-32. doi: 10.1038/mp.2015.5. Epub 2015 Feb 24.

28.

Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response.

Fichera M, Barone R, Grillo L, De Grandi M, Fiore V, Morana I, Maniscalchi T, Vinci M, Amata S, Spalletta A, Sorge G, Signorelli SS.

Mol Cytogenet. 2014 Dec 19;7(1):90. doi: 10.1186/s13039-014-0090-7. eCollection 2014.

29.

Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypes.

Snijders Blok C, Corsten-Janssen N, FitzPatrick DR, Romano C, Fichera M, Vitello GA, Willemsen MH, Schoots J, Pfundt R, van Ravenswaaij-Arts CM, Hoefsloot L, Kleefstra T.

Am J Med Genet A. 2014 Nov;164A(11):2843-8. doi: 10.1002/ajmg.a.36680. Epub 2014 Sep 22.

PMID:
25251717
30.

Refining analyses of copy number variation identifies specific genes associated with developmental delay.

Coe BP, Witherspoon K, Rosenfeld JA, van Bon BW, Vulto-van Silfhout AT, Bosco P, Friend KL, Baker C, Buono S, Vissers LE, Schuurs-Hoeijmakers JH, Hoischen A, Pfundt R, Krumm N, Carvill GL, Li D, Amaral D, Brown N, Lockhart PJ, Scheffer IE, Alberti A, Shaw M, Pettinato R, Tervo R, de Leeuw N, Reijnders MR, Torchia BS, Peeters H, O'Roak BJ, Fichera M, Hehir-Kwa JY, Shendure J, Mefford HC, Haan E, Gécz J, de Vries BB, Romano C, Eichler EE.

Nat Genet. 2014 Oct;46(10):1063-71. doi: 10.1038/ng.3092. Epub 2014 Sep 14.

31.

Sox11 is required to maintain proper levels of Hedgehog signaling during vertebrate ocular morphogenesis.

Pillai-Kastoori L, Wen W, Wilson SG, Strachan E, Lo-Castro A, Fichera M, Musumeci SA, Lehmann OJ, Morris AC.

PLoS Genet. 2014 Jul 10;10(7):e1004491. doi: 10.1371/journal.pgen.1004491. eCollection 2014 Jul.

32.

Disruptive CHD8 mutations define a subtype of autism early in development.

Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT, Schuurs-Hoeijmakers JH, Fichera M, Bosco P, Buono S, Alberti A, Failla P, Peeters H, Steyaert J, Vissers LELM, Francescatto L, Mefford HC, Rosenfeld JA, Bakken T, O'Roak BJ, Pawlus M, Moon R, Shendure J, Amaral DG, Lein E, Rankin J, Romano C, de Vries BBA, Katsanis N, Eichler EE.

Cell. 2014 Jul 17;158(2):263-276. doi: 10.1016/j.cell.2014.06.017. Epub 2014 Jul 3.

33.

Definition of minimal duplicated region encompassing the XIAP and STAG2 genes in the Xq25 microduplication syndrome.

Di Benedetto D, Musumeci SA, Avola E, Alberti A, Buono S, Scuderi C, Grillo L, Galesi O, Spalletta A, Giudice ML, Luciano D, Vinci M, Bianca S, Romano C, Fichera M.

Am J Med Genet A. 2014 Aug;164A(8):1923-30. doi: 10.1002/ajmg.a.36570. Epub 2014 Apr 14.

PMID:
24733578
34.

Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome.

Disciglio V, Lo Rizzo C, Mencarelli MA, Mucciolo M, Marozza A, Di Marco C, Massarelli A, Canocchi V, Baldassarri M, Ndoni E, Frullanti E, Amabile S, Anderlid BM, Metcalfe K, Le Caignec C, David A, Fryer A, Boute O, Joris A, Greco D, Pecile V, Battini R, Novelli A, Fichera M, Romano C, Mari F, Renieri A.

Am J Med Genet A. 2014 Jul;164A(7):1666-76. doi: 10.1002/ajmg.a.36513. Epub 2014 Apr 3.

PMID:
24700646
35.

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP.

Helsmoortel C, Vulto-van Silfhout AT, Coe BP, Vandeweyer G, Rooms L, van den Ende J, Schuurs-Hoeijmakers JH, Marcelis CL, Willemsen MH, Vissers LE, Yntema HG, Bakshi M, Wilson M, Witherspoon KT, Malmgren H, Nordgren A, Annerén G, Fichera M, Bosco P, Romano C, de Vries BB, Kleefstra T, Kooy RF, Eichler EE, Van der Aa N.

Nat Genet. 2014 Apr;46(4):380-4. doi: 10.1038/ng.2899. Epub 2014 Feb 16.

36.

Klippel-Trenaunay syndrome in a boy with concomitant ipsilateral overgrowth and undergrowth.

Ruggieri M, Pavone V, Polizzi A, Falsaperla R, Fichera M, Pavone P.

Am J Med Genet A. 2014 May;164A(5):1262-7. doi: 10.1002/ajmg.a.36414. Epub 2014 Jan 29.

PMID:
24478251
37.

TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion.

Palumbo O, Fichera M, Palumbo P, Rizzo R, Mazzolla E, Cocuzza DM, Carella M, Mattina T.

Am J Med Genet A. 2014 Mar;164A(3):828-33. doi: 10.1002/ajmg.a.36363. Epub 2014 Jan 23.

PMID:
24458984
38.

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

Lionel AC, Tammimies K, Vaags AK, Rosenfeld JA, Ahn JW, Merico D, Noor A, Runke CK, Pillalamarri VK, Carter MT, Gazzellone MJ, Thiruvahindrapuram B, Fagerberg C, Laulund LW, Pellecchia G, Lamoureux S, Deshpande C, Clayton-Smith J, White AC, Leather S, Trounce J, Melanie Bedford H, Hatchwell E, Eis PS, Yuen RK, Walker S, Uddin M, Geraghty MT, Nikkel SM, Tomiak EM, Fernandez BA, Soreni N, Crosbie J, Arnold PD, Schachar RJ, Roberts W, Paterson AD, So J, Szatmari P, Chrysler C, Woodbury-Smith M, Brian Lowry R, Zwaigenbaum L, Mandyam D, Wei J, Macdonald JR, Howe JL, Nalpathamkalam T, Wang Z, Tolson D, Cobb DS, Wilks TM, Sorensen MJ, Bader PI, An Y, Wu BL, Musumeci SA, Romano C, Postorivo D, Nardone AM, Monica MD, Scarano G, Zoccante L, Novara F, Zuffardi O, Ciccone R, Antona V, Carella M, Zelante L, Cavalli P, Poggiani C, Cavallari U, Argiropoulos B, Chernos J, Brasch-Andersen C, Speevak M, Fichera M, Ogilvie CM, Shen Y, Hodge JC, Talkowski ME, Stavropoulos DJ, Marshall CR, Scherer SW.

Hum Mol Genet. 2014 May 15;23(10):2752-68. doi: 10.1093/hmg/ddt669. Epub 2013 Dec 30.

39.

Excitatory deep repetitive transcranial magnetic stimulation with H-coil as add-on treatment of motor symptoms in Parkinson's disease: an open label, pilot study.

Spagnolo F, Volonté MA, Fichera M, Chieffo R, Houdayer E, Bianco M, Coppi E, Nuara A, Straffi L, Di Maggio G, Ferrari L, Dalla Libera D, Velikova S, Comi G, Zangen A, Leocani L.

Brain Stimul. 2014 Mar-Apr;7(2):297-300. doi: 10.1016/j.brs.2013.10.007. Epub 2013 Oct 29.

PMID:
24300835
40.

ABO histo-blood group might modulate predisposition to Crohn's disease and affect disease behavior.

Forni D, Cleynen I, Ferrante M, Cassinotti A, Cagliani R, Ardizzone S, Vermeire S, Fichera M, Lombardini M, Maconi G, de Franchis R, Asselta R, Biasin M, Clerici M, Sironi M.

J Crohns Colitis. 2014 Jun;8(6):489-94. doi: 10.1016/j.crohns.2013.10.014. Epub 2013 Nov 21.

41.

Secondary cervical dystonic tremor after Japanese encephalitis.

Spagnolo F, Scomazzoni F, Fichera M, Comi G, Volontè MA.

Neurol Sci. 2014 Mar;35(3):491-3. doi: 10.1007/s10072-013-1579-2. Epub 2013 Nov 20. No abstract available.

PMID:
24249222
42.

Striatal hand in Parkinson's disease: the re-evaluation of an old clinical sign.

Spagnolo F, Fichera M, Bucello S, Houdayer E, Baroncini D, Sarro L, Leopizzi E, Impellizzeri M, Martinelli V, Leocani L, Comi G, Volonté MA.

J Neurol. 2014 Jan;261(1):117-20. doi: 10.1007/s00415-013-7165-y. Epub 2013 Oct 25.

PMID:
24158274
43.

Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.

Schuurs-Hoeijmakers JH, Vulto-van Silfhout AT, Vissers LE, van de Vondervoort II, van Bon BW, de Ligt J, Gilissen C, Hehir-Kwa JY, Neveling K, del Rosario M, Hira G, Reitano S, Vitello A, Failla P, Greco D, Fichera M, Galesi O, Kleefstra T, Greally MT, Ockeloen CW, Willemsen MH, Bongers EM, Janssen IM, Pfundt R, Veltman JA, Romano C, Willemsen MA, van Bokhoven H, Brunner HG, de Vries BB, de Brouwer AP.

J Med Genet. 2013 Dec;50(12):802-11. doi: 10.1136/jmedgenet-2013-101644. Epub 2013 Oct 11. Erratum in: J Med Genet. 2018 May 9;:.

PMID:
24123876
44.

Increased FGF3 and FGF4 gene dosage is a risk factor for craniosynostosis.

Grillo L, Greco D, Pettinato R, Avola E, Potenza N, Castiglia L, Spalletta A, Amata S, Di Benedetto D, Luciano D, Romano C, Fichera M.

Gene. 2014 Jan 25;534(2):435-9. doi: 10.1016/j.gene.2013.09.120. Epub 2013 Oct 8.

PMID:
24120895
45.

Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions.

Nuttle X, Huddleston J, O'Roak BJ, Antonacci F, Fichera M, Romano C, Shendure J, Eichler EE.

Nat Methods. 2013 Sep;10(9):903-9. doi: 10.1038/nmeth.2572. Epub 2013 Jul 28.

46.

The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.

Curry CJ, Rosenfeld JA, Grant E, Gripp KW, Anderson C, Aylsworth AS, Saad TB, Chizhikov VV, Dybose G, Fagerberg C, Falco M, Fels C, Fichera M, Graakjaer J, Greco D, Hair J, Hopkins E, Huggins M, Ladda R, Li C, Moeschler J, Nowaczyk MJ, Ozmore JR, Reitano S, Romano C, Roos L, Schnur RE, Sell S, Suwannarat P, Svaneby D, Szybowska M, Tarnopolsky M, Tervo R, Tsai AC, Tucker M, Vallee S, Wheeler FC, Zand DJ, Barkovich AJ, Aradhya S, Shaffer LG, Dobyns WB.

Am J Med Genet A. 2013 Aug;161A(8):1833-52. doi: 10.1002/ajmg.a.35996. Epub 2013 Jun 27.

47.

Interhemispheric balance in Parkinson's disease: a transcranial magnetic stimulation study.

Spagnolo F, Coppi E, Chieffo R, Straffi L, Fichera M, Nuara A, Gonzalez-Rosa J, Martinelli V, Comi G, Volontè MA, Leocani L.

Brain Stimul. 2013 Nov;6(6):892-7. doi: 10.1016/j.brs.2013.05.004. Epub 2013 Jun 6.

PMID:
23810506
48.

Immunity, autoimmunity and inflammatory bowel disease.

Cassinotti A, Sarzi-Puttini P, Fichera M, Shoenfeld Y, de Franchis R, Ardizzone S.

Autoimmun Rev. 2014 Jan;13(1):1-2. doi: 10.1016/j.autrev.2013.06.007. Epub 2013 Jun 15. No abstract available.

PMID:
23777820
49.

[Indications and controindications of hormone replacement therapy in menopause].

Fichera M, Rinaldi N, Tarascio M, Taschetta S, Caldaci LM, Catavorello A, La Rosa B, Panella MM.

Minerva Ginecol. 2013 Jun;65(3):331-44. Review. Italian.

PMID:
23689177
50.

Intragenic ILRAPL1 deletion in a male patient with intellectual disability, mild dysmorphic signs, deafness, and behavioral problems.

Barone C, Bianca S, Luciano D, Di Benedetto D, Vinci M, Fichera M.

Am J Med Genet A. 2013 Jun;161A(6):1381-5. doi: 10.1002/ajmg.a.35860. Epub 2013 Apr 23.

PMID:
23613341

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