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Items: 1 to 50 of 139

1.

Homocysteine and education but not lipoprotein (a) predict estimated 10-year risk of cardiovascular disease in blood donors: a community based cross-sectional study.

Vadini F, Santilli F, Casalini G, dell'Isola M, Iuliani O, D'Ardes D, Lattanzio L, Di Nicola M, Di Iorio G, Accorsi P.

BMC Cardiovasc Disord. 2019 Jul 26;19(1):177. doi: 10.1186/s12872-019-1157-5.

2.

Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study.

Di Pisa V, Provini F, Ubertiello S, Bonetti S, Ricci E, Ivanovski I, Caraffi SG, Giordano L, Accorsi P, Savasta S, Raviglione F, Boni A, Grioni D, Graziano C, Garavelli L, Cordelli DM.

Sleep Med. 2019 Sep;61:44-51. doi: 10.1016/j.sleep.2019.04.011. Epub 2019 Apr 26.

PMID:
31285160
3.

The spectrum of intermediate SCN8A-related epilepsy.

Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS.

Epilepsia. 2019 May;60(5):830-844. doi: 10.1111/epi.14705. Epub 2019 Apr 10.

PMID:
30968951
4.

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study.

Trivisano M, Pietrafusa N, Terracciano A, Marini C, Mei D, Darra F, Accorsi P, Battaglia D, Caffi L, Canevini MP, Cappelletti S, Cesaroni E, de Palma L, Costa P, Cusmai R, Giordano L, Ferrari A, Freri E, Fusco L, Granata T, Martino T, Mastrangelo M, Bova SM, Parmeggiani L, Ragona F, Sicca F, Striano P, Specchio LM, Tondo I, Zambrelli E, Zamponi N, Zanus C, Boniver C, Vecchi M, Avolio C, Dalla Bernardina B, Bertini E, Guerrini R, Vigevano F, Specchio N.

Epilepsia. 2018 Dec;59(12):2260-2271. doi: 10.1111/epi.14600. Epub 2018 Nov 19.

5.

Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature.

Agostini A, Marchetti D, Izzi C, Cocco I, Pinelli L, Accorsi P, Iascone Maria R, Giordano L.

Am J Med Genet B Neuropsychiatr Genet. 2018 Dec;177(8):687-690. doi: 10.1002/ajmg.b.32677. Epub 2018 Oct 22. Review.

PMID:
30345598
6.

Response to "Questions arising on phlebotomy in polycythemia vera: prophylactic measures to reduce thromboembolic events require patient-focused decisions" by Heidel et al.

Barosi G, Passamonti F, Accorsi P, Pane F, Vannucchi AM, Velati C, Gale RP, Tura S, Barbui T.

Leukemia. 2018 Dec;32(12):2727-2728. doi: 10.1038/s41375-018-0259-x. Epub 2018 Sep 28. No abstract available.

PMID:
30267006
7.

Apheresis treatment of cryoglobulinemic vasculitis: A multicentre cohort study of 159 patients.

Marson P, Monti G, Montani F, Riva A, Mascia MT, Castelnovo L, Filippini D, Capuzzo E, Moretto M, D'Alessandri G, Marenchino D, Zani R, Fraticelli P, Ferri C, Quartuccio L, De Silvestro G, Oreni L, Accorsi P, Galli M.

Transfus Apher Sci. 2018 Oct;57(5):639-645. doi: 10.1016/j.transci.2018.06.005. Epub 2018 Jun 26.

PMID:
30228046
8.

NOTCH and Graft-Versus-Host Disease.

Di Ianni M, Del Papa B, Baldoni S, Di Tommaso A, Fabi B, Rosati E, Natale A, Santarone S, Olioso P, Papalinetti G, Giancola R, Accorsi P, Di Bartolomeo P, Sportoletti P, Falzetti F.

Front Immunol. 2018 Aug 10;9:1825. doi: 10.3389/fimmu.2018.01825. eCollection 2018. Review.

9.

Etiology and Prognosis of Severe Ventriculomegaly Diagnosed at Late Gestation.

Dall'Asta A, van Oostrum NHM, Basheer SN, Paramasivam G, Ghi T, Galli L, Groenenberg IA, Tangi A, Accorsi P, Echevarria M, Angeles Rodríguez Perez M, Albaiges Baiget G, Prefumo F, Frusca T, Go AT, Lees CC.

Ultraschall Med. 2018 Dec;39(6):675-689. doi: 10.1055/a-0627-7173. Epub 2018 Jul 5.

10.

Evidence- and consensus-based recommendations for phlebotomy in polycythemia vera.

Barbui T, Passamonti F, Accorsi P, Pane F, Vannucchi AM, Velati C, Gale RP, Tura S, Barosi G.

Leukemia. 2018 Sep;32(9):2077-2081. doi: 10.1038/s41375-018-0199-5. Epub 2018 Jun 28. No abstract available.

PMID:
29955128
11.

NOTCH1 Is Aberrantly Activated in Chronic Lymphocytic Leukemia Hematopoietic Stem Cells.

Di Ianni M, Baldoni S, Del Papa B, Aureli P, Dorillo E, De Falco F, Albi E, Varasano E, Di Tommaso A, Giancola R, Accorsi P, Rotta G, Rompietti C, Silva Barcelos EC, Campese AF, Di Bartolomeo P, Screpanti I, Rosati E, Falzetti F, Sportoletti P.

Front Oncol. 2018 Apr 20;8:105. doi: 10.3389/fonc.2018.00105. eCollection 2018.

12.

Disposal of the residual autologous HSC units: Results of a survey carried out two years after the publication of a national policy in Italy.

Perseghin P, Laszlò D, Bonifazi F, Introna M, Accorsi P, Petrini C, Lombardini L.

Transfus Apher Sci. 2018 Apr;57(2):197-200. doi: 10.1016/j.transci.2018.01.007. Epub 2018 Jan 31. No abstract available.

PMID:
29402635
13.

Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15).

Matricardi S, Darra F, Spalice A, Basti C, Fontana E, Dalla Bernardina B, Elia M, Giordano L, Accorsi P, Cusmai R, De Liso P, Romeo A, Ragona F, Granata T, Concolino D, Carotenuto M, Pavone P, Pruna D, Striano P, Savasta S, Verrotti A.

Acta Neurol Scand. 2018 Jun;137(6):575-581. doi: 10.1111/ane.12902. Epub 2018 Jan 23.

PMID:
29363096
14.

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.

Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Ajmone PF, Badura-Stronka M, Baldo C, Baldi M, Bayat A, Bigoni S, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, De Brasi D, Devriendt K, Dinulos MB, Hjortshøj TD, Epifanio R, Faravelli F, Fiumara A, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Kuburovic V, Kutkowska-Kazmierczak A, Lacombe D, Lo Rizzo C, Luchetti A, Malbora B, Mammi I, Mari F, Montorsi G, Moutton S, Møller RS, Muschke P, Nielsen JEK, Obersztyn E, Pantaleoni C, Pellicciari A, Pisanti MA, Prpic I, Poch-Olive ML, Raviglione F, Renieri A, Ricci E, Rivieri F, Santen GW, Savasta S, Scarano G, Schanze I, Selicorni A, Silengo M, Smigiel R, Spaccini L, Sorge G, Szczaluba K, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zenker M, Conidi A, Zollino M, Rauch A, Zweier C, Garavelli L.

Genet Med. 2018 Sep;20(9):965-975. doi: 10.1038/gim.2017.221. Epub 2018 Jan 4.

PMID:
29300384
15.

Did you know that your animals have consciousness?

Accorsi PA, Mondo E, Cocchi M.

J Integr Neurosci. 2017;16(s1):S3-S11. doi: 10.3233/JIN-170061.

PMID:
29154287
16.

Pyridoxine responsiveness in pyridox(am)ine-5-phosphate oxidase deficiency: The importance of early treatment.

Accorsi P, Cellini E, Paolantonio CD, Panzarino G, Verrotti A, Giordano L.

Clin Neurol Neurosurg. 2017 Dec;163:90-93. doi: 10.1016/j.clineuro.2017.10.019. Epub 2017 Oct 23. No abstract available.

PMID:
29080399
17.

Secondary solid cancer following hematopoietic cell transplantation in patients with thalassemia major.

Santarone S, Pepe A, Meloni A, Natale A, Pistoia L, Olioso P, Papalinetti G, Cuccia L, Spasiano A, Lisi R, Di Ianni M, Bonfini T, Accorsi P, Salvadori S, Papola F, Angelini S, Di Bartolomeo P.

Bone Marrow Transplant. 2018 Jan;53(1):39-43. doi: 10.1038/bmt.2017.214. Epub 2017 Oct 9.

PMID:
28991245
18.

Treg-protected donor lymphocyte infusions: a new tool to address the graft-versus-leukemia effect in the absence of graft-versus-host disease in patients relapsed after HSCT.

Di Ianni M, Olioso P, Giancola R, Santarone S, Natale A, Papalinetti G, Villanova I, Baldoni S, Di Tommaso A, Bonfini T, Accorsi P, Di Bartolomeo P.

Int J Hematol. 2017 Dec;106(6):860-864. doi: 10.1007/s12185-017-2292-3. Epub 2017 Jul 18.

PMID:
28721499
19.

MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly.

Severino M, Righini A, Tortora D, Pinelli L, Parazzini C, Morana G, Accorsi P, Capra V, Paladini D, Rossi A.

AJNR Am J Neuroradiol. 2017 Aug;38(8):1643-1646. doi: 10.3174/ajnr.A5245. Epub 2017 Jun 8.

20.

Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories.

Perricone M, Palandri F, Ottaviani E, Angelini M, Bagli L, Bellesia E, Donati M, Gemmati D, Zucchini P, Mancini S, Marchica V, Trubini S, De Matteis G, Di Zacomo S, Favarato M, Fioroni A, Bolzonella C, Maccari G, Navaglia F, Gatti D, Toffolatti L, Orlandi L, Laloux V, Manfrini M, Galieni P, Giannini B, Tieghi A, Barulli S, Serino ML, Maccaferri M, Scortechini AR, Giuliani N, Vallisa D, Bonifacio M, Accorsi P, Salbe C, Fazio V, Gusella M, Toffoletti E, Salvucci M, Svaldi M, Gherlinzoni F, Cassavia F, Orsini F, Martinelli G.

Oncotarget. 2017 May 16;8(20):32608-32617. doi: 10.18632/oncotarget.15940.

21.

Development of the Platelet Efficacy Score (PEscore) to predict the efficacy of platelet transfusion in oncohematologic patients.

Quaglietta A, Di Saverio M, Lucisano G, Accorsi P, Nicolucci A.

Transfusion. 2017 Apr;57(4):905-912. doi: 10.1111/trf.13997. Epub 2017 Feb 24.

PMID:
28236299
22.

Overstocking dairy cows during the dry period affects dehydroepiandrosterone and cortisol secretion.

Fustini M, Galeati G, Gabai G, Mammi LE, Bucci D, Baratta M, Accorsi PA, Formigoni A.

J Dairy Sci. 2017 Jan;100(1):620-628. doi: 10.3168/jds.2016-11293. Epub 2016 Nov 9.

23.

Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.

Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR.

Genet Med. 2017 Jun;19(6):691-700. doi: 10.1038/gim.2016.176. Epub 2016 Nov 10.

24.

Neurodevelopmental profile in Angelman syndrome: more than low intelligence quotient.

Micheletti S, Palestra F, Martelli P, Accorsi P, Galli J, Giordano L, Trebeschi V, Fazzi E.

Ital J Pediatr. 2016 Oct 21;42(1):91.

25.

Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities.

Matricardi S, Spalice A, Salpietro V, Di Rosa G, Balistreri MC, Grosso S, Parisi P, Elia M, Striano P, Accorsi P, Cusmai R, Specchio N, Coppola G, Savasta S, Carotenuto M, Tozzi E, Ferrara P, Ruggieri M, Verrotti A.

Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):288-95. doi: 10.1002/ajmg.c.31513. Epub 2016 Aug 13.

PMID:
27519909
26.

Spinal lipoma as a dysembryogenetic anomaly: Four unusual cases of ectopic iliac rib within the spinal lipoma.

Accogli A, Pavanello M, Accorsi P, De Marco P, Merello E, Pacetti M, Nozza P, Fiorillo C, Pinelli L, Cama A, Rossi A, Catala M, Capra V.

Birth Defects Res A Clin Mol Teratol. 2016 Jul;106(7):530-5. doi: 10.1002/bdra.23489. Epub 2016 Apr 18.

PMID:
27087621
27.

LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance.

Dallabona C, Abbink TE, Carrozzo R, Torraco A, Legati A, van Berkel CG, Niceta M, Langella T, Verrigni D, Rizza T, Diodato D, Piemonte F, Lamantea E, Fang M, Zhang J, Martinelli D, Bevivino E, Dionisi-Vici C, Vanderver A, Philip SG, Kurian MA, Verma IC, Bijarnia-Mahay S, Jacinto S, Furtado F, Accorsi P, Ardissone A, Moroni I, Ferrero I, Tartaglia M, Goffrini P, Ghezzi D, van der Knaap MS, Bertini E.

Brain. 2016 Mar;139(Pt 3):782-94. doi: 10.1093/brain/awv392. Epub 2016 Jan 29. Erratum in: Brain. 2018 Nov 1;141(11):e82.

PMID:
26912632
28.

STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.

Stamberger H, Nikanorova M, Willemsen MH, Accorsi P, Angriman M, Baier H, Benkel-Herrenbrueck I, Benoit V, Budetta M, Caliebe A, Cantalupo G, Capovilla G, Casara G, Courage C, Deprez M, Destrée A, Dilena R, Erasmus CE, Fannemel M, Fjær R, Giordano L, Helbig KL, Heyne HO, Klepper J, Kluger GJ, Lederer D, Lodi M, Maier O, Merkenschlager A, Michelberger N, Minetti C, Muhle H, Phalin J, Ramsey K, Romeo A, Schallner J, Schanze I, Shinawi M, Sleegers K, Sterbova K, Syrbe S, Traverso M, Tzschach A, Uldall P, Van Coster R, Verhelst H, Viri M, Winter S, Wolff M, Zenker M, Zoccante L, De Jonghe P, Helbig I, Striano P, Lemke JR, Møller RS, Weckhuysen S.

Neurology. 2016 Mar 8;86(10):954-62. doi: 10.1212/WNL.0000000000002457. Epub 2016 Feb 10. Review.

29.

High seroprevalence of HCV in the Abruzzo Region, Italy: results on a large sample from opt-out pre-surgical screening.

Polilli E, Tontodonati M, Flacco ME, Ursini T, Striani P, Di Giammartino D, Paoloni M, Vallarola L, Pressanti GL, Fragassi G, Accorsi P, Manzoli L, Parruti G.

Infection. 2016 Feb;44(1):85-91. doi: 10.1007/s15010-015-0841-3. Epub 2015 Sep 12.

PMID:
26363567
30.

The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.

Cellini E, Vignoli A, Pisano T, Falchi M, Molinaro A, Accorsi P, Bontacchio A, Pinelli L, Giordano L, Guerrini R; FOXG1 Syndrome Study Group.

Dev Med Child Neurol. 2016 Jan;58(1):93-7. doi: 10.1111/dmcn.12894. Epub 2015 Sep 6.

31.

CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures.

Trivisano M, Striano P, Sartorelli J, Giordano L, Traverso M, Accorsi P, Cappelletti S, Claps DJ, Vigevano F, Zara F, Specchio N.

Epilepsy Behav. 2015 Oct;51:53-6. doi: 10.1016/j.yebeh.2015.06.029. Epub 2015 Aug 7.

PMID:
26262932
32.

Refractory absence seizures: An Italian multicenter retrospective study.

Franzoni E, Matricardi S, Di Pisa V, Capovilla G, Romeo A, Tozzi E, Pruna D, Salerno GG, Zamponi N, Accorsi P, Giordano L, Coppola G, Cerminara C, Curatolo P, Nicita F, Spalice A, Grosso S, Pavone P, Striano P, Parisi P, Boni A, Gobbi G, Carotenuto M, Esposito M, Cottone C, Verrotti A.

Eur J Paediatr Neurol. 2015 Nov;19(6):660-4. doi: 10.1016/j.ejpn.2015.07.008. Epub 2015 Jul 18.

PMID:
26239083
33.

Pediatric epilepsy following neonatal seizures symptomatic of stroke.

Suppiej A, Mastrangelo M, Mastella L, Accorsi P, Grazian L, Casara G, Peruzzi C, Carpanelli ML, Janes A, Traverso A, Dalla Bernardina B.

Brain Dev. 2016 Jan;38(1):27-31. doi: 10.1016/j.braindev.2015.05.010. Epub 2015 Jun 6.

PMID:
26058328
34.

A modified prediction model for VBAC, in a European population.

Annessi E, Del Giovane C, Magnani L, Carossino E, Baldoni G, Battagliarin G, Accorsi P, Fabio F.

J Matern Fetal Neonatal Med. 2016;29(3):435-9. doi: 10.3109/14767058.2014.1002767. Epub 2015 Jan 14.

PMID:
25586316
35.

Do pure absence seizures occur in myoclonic epilepsy of infancy? A case series.

Belcastro V, Giordano L, Pruna D, Peruzzi C, Madeddu F, Accorsi P, Gobbi G, Verrotti A, Striano P.

Seizure. 2015 Jan;24:8-11. doi: 10.1016/j.seizure.2014.11.002. Epub 2014 Nov 15. Erratum in: Seizure. 2015 Aug;30:138.

36.

Non-epileptic myoclonic attacks in infancy: three cases.

Vignoli A, Giordano L, Guerra D, La Briola F, Accorsi P, Savini MN, Iodice A, Molinaro A, Canevini MP.

Epileptic Disord. 2014 Dec;16(4):433-8. doi: 10.1684/epd.2014.0713.

37.

Thyroid hormones increase collagen I and cartilage oligomeric matrix protein (COMP) expression in vitro human tenocytes.

Berardi AC, Oliva F, Berardocco M, la Rovere M, Accorsi P, Maffulli N.

Muscles Ligaments Tendons J. 2014 Nov 17;4(3):285-91. eCollection 2014 Jul.

38.

Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?

Romani M, Mancini F, Micalizzi A, Poretti A, Miccinilli E, Accorsi P, Avola E, Bertini E, Borgatti R, Romaniello R, Ceylaner S, Coppola G, D'Arrigo S, Giordano L, Janecke AR, Lituania M, Ludwig K, Martorell L, Mazza T, Odent S, Pinelli L, Poo P, Santucci M, Signorini S, Simonati A, Spiegel R, Stanzial F, Steinlin M, Tabarki B, Wolf NI, Zibordi F, Boltshauser E, Valente EM.

Hum Genet. 2015 Jan;134(1):123-6. doi: 10.1007/s00439-014-1508-3. Epub 2014 Nov 19.

39.

Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.

Verrotti A, Cusmai R, Darra F, Martelli P, Accorsi P, Bergamo S, Bevivino E, Coppola G, Freri E, Grosso S, Matricardi S, Parisi P, Sartori S, Spalice A, Specchio N, Carelli A, Zini D, Dalla Bernardina B, Giordano L.

Epilepsy Res. 2014 Nov;108(9):1597-603. doi: 10.1016/j.eplepsyres.2014.08.006. Epub 2014 Aug 30.

PMID:
25218893
40.

Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies.

Grosso S, Coppola G, Dontin SD, Gobbi G, Pruna D, Accorsi P, Verrotti A, Parisi P, Balestri P.

Eur J Paediatr Neurol. 2014 Sep;18(5):641-5. doi: 10.1016/j.ejpn.2014.05.001. Epub 2014 May 15. Erratum in: Eur J Paediatr Neurol. 2015 May;19(3):388.

PMID:
24912730
41.

Fecal concentrations of cortisol, testosterone, and progesterone in cotton-top tamarins housed in different zoological parks: relationships among physiological data, environmental conditions, and behavioral patterns.

Fontani S, Vaglio S, Beghelli V, Mattioli M, Bacci S, Accorsi PA.

J Appl Anim Welf Sci. 2014;17(3):228-52. doi: 10.1080/10888705.2014.916173. Epub 2014 May 16.

PMID:
24836597
42.

A policy for the disposal of autologous hematopoietic progenitor cells: report from an Italian consensus panel.

Perseghin P, Marchetti M, Pierelli L, Olivieri A, Introna M, Lombardini L, Accorsi P, Petrini C, Risso M, Bosi A; Società Italiana di Emaferesi e Manipolazione Cellulare,; Gruppo Italiano Trapianto Midollo Osseo; Centro Nazionale Trapianti.

Transfusion. 2014 Sep;54(9):2353-60. doi: 10.1111/trf.12619. Epub 2014 Mar 24.

PMID:
24654567
43.

Central venous catheter insertion in peripheral blood hematopoietic stem cell sibling donors: the SIdEM (Italian Society of Hemapheresis and Cell Manipulation) point of view.

Vacca M, Perseghin P, Accorsi P, Pierelli L; SIdEM Board.

Transfus Apher Sci. 2014 Apr;50(2):200-6. doi: 10.1016/j.transci.2014.02.001. Epub 2014 Feb 14. Review.

PMID:
24569005
44.

17p13.1 microdeletion: genetic and clinical findings in a new patient with epilepsy and comparison with literature.

Giordano L, Palestra F, Giuffrida MG, Molinaro A, Iodice A, Bernardini L, La Boria P, Accorsi P, Novelli A.

Am J Med Genet A. 2014 Jan;164A(1):225-30. Review.

PMID:
24501763
45.

Setleis syndrome: genetic and clinical findings in a new case with epilepsy.

Giordano L, Desnick RJ, Molinaro A, Uliana V, Forzano F, Edelmann L, Nazarenko I, Pinelli L, Accorsi P, Faravelli F.

Pediatr Neurol. 2014 Apr;50(4):389-91. doi: 10.1016/j.pediatrneurol.2013.12.009. Epub 2013 Dec 14.

PMID:
24486222
46.

Hyperventilation and seizures in an adolescent female.

Nicosia F, Giordano L, Bonini L, Corda L, Bolzon M, Bettinzoli M, Braghini A, Accorsi P, Tantucci C.

Monaldi Arch Chest Dis. 2013 Jun;79(2):93-5.

47.

Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.

Liegel RP, Handley MT, Ronchetti A, Brown S, Langemeyer L, Linford A, Chang B, Morris-Rosendahl DJ, Carpanini S, Posmyk R, Harthill V, Sheridan E, Abdel-Salam GM, Terhal PA, Faravelli F, Accorsi P, Giordano L, Pinelli L, Hartmann B, Ebert AD, Barr FA, Aligianis IA, Sidjanin DJ.

Am J Hum Genet. 2013 Dec 5;93(6):1001-14. doi: 10.1016/j.ajhg.2013.10.011. Epub 2013 Nov 14.

48.

Kinetics of the use of cryopreserved autologous stem cell grafts: a GITMO-SIDEM survey.

Olivieri J, Pierelli L, Introna M, Accorsi P, Bosi A, Perseghin P, Risso M, Pandolfi A, Mancini S, Marchetti M, Dal Pozzo S, Gotti E, Rambaldi A, Leoni P, Olivieri A; Gitmo (Gruppo Italiano Trapianto di Midollo Osseo)–SIDEM (Società Italiana di Emaferesi e Manipolazione Cellulare) Working Group on SCU Disposal.

Cytotherapy. 2014 Jan;16(1):101-10. doi: 10.1016/j.jcyt.2013.07.001. Epub 2013 Oct 26.

PMID:
24169075
49.

Early onset absence epilepsy with onset in the first year of life: a multicenter cohort study.

Giordano L, Vignoli A, Cusmai R, Parisi P, Mastrangelo M, Coppola G, Cordelli DM, Accorsi P, Milito G, Darra F, Pruna D, Belcastro V, Verrotti A, Striano P.

Epilepsia. 2013 Oct;54 Suppl 7:66-9. doi: 10.1111/epi.12311.

50.

Clinical dissection of early onset absence epilepsy in children and prognostic implications.

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