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Items: 1 to 50 of 125

1.

Understanding Childhood Neuroimmune Diseases of the Central Nervous System.

Matricardi S, Farello G, Savasta S, Verrotti A.

Front Pediatr. 2019 Dec 19;7:511. doi: 10.3389/fped.2019.00511. eCollection 2019. Review.

2.

Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients.

Giacomini T, Foiadelli T, Annovazzi P, Nosadini M, Gastaldi M, Franciotta D, Panarese C, Capris P, Camicione P, Lanteri P, De Grandis E, Prato G, Cordani R, Nobili L, Morana G, Rossi A, Pistorio A, Cellerino M, Uccelli A, Sartori S, Savasta S, Mancardi MM.

Mult Scler Relat Disord. 2019 Dec 24;39:101917. doi: 10.1016/j.msard.2019.101917. [Epub ahead of print]

PMID:
31896061
3.

Infantile spasms followed by childhood absence epilepsy: A case series.

Giordano L, Tambucci R, Cocco IE, Angriman M, Coppola G, Operto FF, Farello G, Savasta S, Belcastro V, Verrotti A.

Seizure. 2020 Jan;74:77-80. doi: 10.1016/j.seizure.2019.12.007. Epub 2019 Dec 9.

PMID:
31841970
4.

Clinical variability in children with dolichoarteriopathies of the internal carotid artery.

Foiadelli T, Ippolito R, Corbetta R, Simoncelli AM, Amariti R, Licari A, Marseglia G, Savasta S.

Childs Nerv Syst. 2019 Nov 7. doi: 10.1007/s00381-019-04395-7. [Epub ahead of print]

PMID:
31701280
5.

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.

Iapadre G, Zagaroli L, Cimini N, Belcastro V, Concolino D, Coppola G, Del Giudice E, Farello G, Iezzi ML, Margari L, Matricardi S, Orsini A, Parisi P, Piccioli M, Di Donato G, Savasta S, Siliquini S, Spalice A, Striano S, Striano P, Verrotti A.

Epilepsy Behav. 2019 Oct 31:106578. doi: 10.1016/j.yebeh.2019.106578. [Epub ahead of print]

PMID:
31680025
6.

Lower Airway Microbiota.

Pulvirenti G, Parisi GF, Giallongo A, Papale M, Manti S, Savasta S, Licari A, Marseglia GL, Leonardi S.

Front Pediatr. 2019 Sep 27;7:393. doi: 10.3389/fped.2019.00393. eCollection 2019. Review.

7.

Gradenigo's syndrome with abscess of the petrous apex in pediatric patients: what is the best treatment?

Savasta S, Canzi P, Aprile F, Michev A, Foiadelli T, Manfrin M, Benazzo M.

Childs Nerv Syst. 2019 Dec;35(12):2265-2272. doi: 10.1007/s00381-019-04352-4. Epub 2019 Aug 20.

PMID:
31432224
8.

Measurement of nitric oxide and assessment of airway diseases in children: an update.

Pappalardo MG, Parisi GF, Tardino L, Savasta S, Brambilla I, Marseglia GL, Licari A, Leonardi S.

Minerva Pediatr. 2019 Dec;71(6):524-532. doi: 10.23736/S0026-4946.19.05513-0. Epub 2019 Jul 25.

PMID:
31352766
9.

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
10.

Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature.

Savasta S, Bassanese F, Buschini C, Foiadelli T, Trabatti C, Efthymiou S, Salpietro V, Houlden H, Simoncelli A, Marseglia GL.

J Pediatr Genet. 2019 Jun;8(2):100-108. doi: 10.1055/s-0038-1676603. Epub 2018 Dec 18.

PMID:
31061755
11.

Melkersson⁻Rosenthal Syndrome in Childhood: Report of Three Paediatric Cases and a Review of the Literature.

Savasta S, Rossi A, Foiadelli T, Licari A, Elena Perini AM, Farello G, Verrotti A, Marseglia GL.

Int J Environ Res Public Health. 2019 Apr 10;16(7). pii: E1289. doi: 10.3390/ijerph16071289. Review.

12.

Absence of lingual frenulum in children with Ehlers-Danlos Syndrome: a retrospective study of forty cases and literature review of a twenty years long debate.

Savasta S, Bassanese F, Hruby C, Foiadelli T, Siri B, Gori V, Votto M, Tinelli C, Marseglia GL.

Minerva Pediatr. 2019 Apr 5. doi: 10.23736/S0026-4946.19.05530-0. [Epub ahead of print]

PMID:
30961343
13.

Acute ataxia in paediatric emergency departments: a multicentre Italian study.

Garone G, Reale A, Vanacore N, Parisi P, Bondone C, Suppiej A, Brisca G, Calistri L, Cordelli DM, Savasta S, Grosso S, Midulla F, Falsaperla R, Verrotti A, Bozzola E, Vassia C, Da Dalt L, Maggiore R, Masi S, Maltoni L, Foiadelli T, Rossetti A, Greco C, Marino S, Di Paolantonio C, Papetti L, Urbino AF, Rossi R, Raucci U.

Arch Dis Child. 2019 Aug;104(8):768-774. doi: 10.1136/archdischild-2018-315487. Epub 2019 Apr 4.

PMID:
30948362
14.

Near-field imaging of surface-plasmon vortex-modes around a single elliptical nanohole in a gold film.

Triolo C, Savasta S, Settineri A, Trusso S, Saija R, Agarwal NR, Patanè S.

Sci Rep. 2019 Mar 29;9(1):5320. doi: 10.1038/s41598-019-41781-2.

15.

Interaction of Mechanical Oscillators Mediated by the Exchange of Virtual Photon Pairs.

Di Stefano O, Settineri A, Macrì V, Ridolfo A, Stassi R, Kockum AF, Savasta S, Nori F.

Phys Rev Lett. 2019 Jan 25;122(3):030402. doi: 10.1103/PhysRevLett.122.030402.

PMID:
30735421
16.

Photodetection probability in quantum systems with arbitrarily strong light-matter interaction.

Di Stefano O, Kockum AF, Ridolfo A, Savasta S, Nori F.

Sci Rep. 2018 Dec 13;8(1):17825. doi: 10.1038/s41598-018-36056-1.

17.

Bickerstaff Brainstem Encephalitis and overlapping Guillain-Barré syndrome in children: Report of two cases and review of the literature.

Michev A, Musso P, Foiadelli T, Trabatti C, Lozza A, Franciotta D, Simoncelli AM, Savasta S.

Eur J Paediatr Neurol. 2019 Jan;23(1):43-52. doi: 10.1016/j.ejpn.2018.11.008. Epub 2018 Nov 20. Review.

PMID:
30502045
18.

West-Nile virus encephalitis in an immunocompetent pediatric patient: successful recovery.

Savasta S, Rovida F, Foiadelli T, Campana AM, Percivalle E, Marseglia GL, Baldanti F.

Ital J Pediatr. 2018 Nov 20;44(1):140. doi: 10.1186/s13052-018-0574-x.

19.

Transient symptomatic zinc deficiency in a breast-fed African infant: case report and literature review.

Barruscotti S, Vassallo C, Giorgini C, Savasta S, Licari A, Marseglia GL, Brazzelli V.

Int J Dermatol. 2019 Aug;58(8):963-965. doi: 10.1111/ijd.14206. Epub 2018 Sep 23. Review. No abstract available.

PMID:
30246396
20.

Long-term follow-up in pediatric patients with paroxysmal hypothermia (Shapiro's syndrome).

Tambasco N, Paoletti FP, Prato G, Mancardi MM, Prontera P, Giordano L, Grosso S, Romeo A, Pinto F, Savasta S, Peruzzi C, Romoli M, Striano P, Verrotti A, Belcastro V; Società Italiana Neurologia Pediatrica (SINP) Collaborative Network.

Eur J Paediatr Neurol. 2018 Nov;22(6):1081-1086. doi: 10.1016/j.ejpn.2018.08.004. Epub 2018 Aug 29.

PMID:
30195408
21.

Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications.

Verrotti A, Greco M, Varriale G, Tamborino A, Savasta S, Carotenuto M, Elia M, Operto F, Margari L, Belcastro V, Selicorni A, Freri E, Matricardi S, Granata T, Ragona F, Capovilla G, Spalice A, Coppola G, Striano P.

Acta Neurol Scand. 2018 Dec;138(6):523-530. doi: 10.1111/ane.13006. Epub 2018 Aug 14.

PMID:
30109707
22.

Clinical characteristics of headache in Italian adolescents aged 11-16 years: a cross-sectional questionnaire school-based study.

Foiadelli T, Piccorossi A, Sacchi L, De Amici M, Tucci M, Brambilla I, Marseglia GL, Savasta S, Verrotti A.

Ital J Pediatr. 2018 Apr 4;44(1):44. doi: 10.1186/s13052-018-0486-9.

23.

Efficacy of rituximab as third-line therapy in combined central and peripheral demyelination.

Savasta S, Foiadelli T, Vegezzi E, Cortese A, Lozza A, Pichiecchio A, Franciotta D, Marchioni E.

Neurol Clin Pract. 2017 Dec;7(6):534-537. doi: 10.1212/CPJ.0000000000000388. No abstract available.

24.

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
25.

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
26.

X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation.

Savasta S, Carlone G, Castagnoli R, Chiappe F, Bassanese F, Piras R, Salpietro V, Brazzelli V, Verrotti A, Marseglia GL.

Cytogenet Genome Res. 2017;152(3):111-116. doi: 10.1159/000478922. Epub 2017 Sep 7.

PMID:
28877528
27.

Frequency conversion in ultrastrong cavity QED.

Kockum AF, Macrì V, Garziano L, Savasta S, Nori F.

Sci Rep. 2017 Jul 13;7(1):5313. doi: 10.1038/s41598-017-04225-3.

28.

Unrecognised diaphragmatic hernia in a refugee child: an incidental diagnosis.

Poddighe D, Boggini T, Savasta S, Marseglia GL.

BMJ Case Rep. 2017 Jun 13;2017. pii: bcr-2017-220748. doi: 10.1136/bcr-2017-220748.

29.

Coexistence of childhood absence epilepsy and benign epilepsy with centrotemporal spikes: A case series.

Verrotti A, Casciato S, Spalice A, Carotenuto M, Striano P, Parisi P, Zamponi N, Savasta S, Rinaldi VE, D'Alonzo R, Mecarini F, Ritaccio AJ, Di Gennaro G.

Eur J Paediatr Neurol. 2017 May;21(3):570-575. doi: 10.1016/j.ejpn.2017.02.002. Epub 2017 Feb 14.

PMID:
28238620
30.

Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study.

Lisi C, Monteleone S, Tinelli C, Rinaldi B, Di Natali G, Savasta S.

Minerva Pediatr. 2017 Feb 17. doi: 10.23736/S0026-4946.17.04681-3. [Epub ahead of print]

PMID:
28211643
31.

MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome.

Vetro A, Savasta S, Russo Raucci A, Cerqua C, Sartori G, Limongelli I, Forlino A, Maruelli S, Perucca P, Vergani D, Mazzini G, Mattevi A, Stivala LA, Salviati L, Zuffardi O.

Eur J Hum Genet. 2017 May;25(5):646-650. doi: 10.1038/ejhg.2017.5. Epub 2017 Feb 15.

32.

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.

33.

Lung disease recalling paraseptal emphysema in a patient with Goltz syndrome.

Cortese R, Savasta S, Di Stasi S, Boggini T, Trabatti C, Dore R, Stella GM.

Multidiscip Respir Med. 2016 Sep 13;11(1):36. doi: 10.1186/s40248-016-0069-9. eCollection 2016.

34.

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
35.

One Photon Can Simultaneously Excite Two or More Atoms.

Garziano L, Macrì V, Stassi R, Di Stefano O, Nori F, Savasta S.

Phys Rev Lett. 2016 Jul 22;117(4):043601. doi: 10.1103/PhysRevLett.117.043601. Epub 2016 Jul 22.

PMID:
27494471
36.

Nucleotide variation in Sabin type 3 poliovirus from an Albanian infant with agammaglobulinemia and vaccine associated poliomyelitis.

Foiadelli T, Savasta S, Battistone A, Kota M, Passera C, Fiore S, Bino S, Amato C, Lozza A, Marseglia GL, Fiore L.

BMC Infect Dis. 2016 Jun 10;16:277. doi: 10.1186/s12879-016-1587-y.

37.

Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.

Pavone V, Signorelli SS, Praticò AD, Corsello G, Savasta S, Falsaperla R, Pavone P, Sessa G, Ruggieri M.

Medicine (Baltimore). 2016 Mar;95(10):e2705. doi: 10.1097/MD.0000000000002705. Erratum in: Medicine (Baltimore). 2016 Apr;95(15):e80ef. Ba, Martino Ruggieri [Corrected to Ruggieri, Martino]. Medicine (Baltimore). 2016 Apr 18;95(15):e80ef.

38.

Paediatric clinically isolated syndromes: report of seven cases, differential diagnosis and literature review.

Trabatti C, Foiadelli T, Spartà MV, Gagliardone C, Rinaldi B, Delmonte M, Lozza A, Savasta S.

Childs Nerv Syst. 2016 Jan;32(1):69-77. doi: 10.1007/s00381-015-2959-0. Epub 2015 Nov 19. Review.

PMID:
26584554
39.

Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication.

Verrotti A, Laino D, Rinaldi VE, Suppiej A, Giordano L, Toldo I, Margari L, Parisi P, Rizzo R, Matricardi S, Cusmai R, Grosso S, Gaggero R, Zamponi N, Pavone P, Capovilla G, Rauchenzauner M, Cerminara C, Di Gennaro G, Esposito M, Striano P, Savasta S, Coppola G, Siliquini S, Operto F, Belcastro V, Ragona F, Marseglia GL, Spalice A.

Eur J Neurol. 2016 Feb;23(2):241-6. doi: 10.1111/ene.12840. Epub 2015 Oct 25.

PMID:
26498733
40.

Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.

Nicita F, Garone G, Spalice A, Savasta S, Striano P, Pantaleoni C, Spartà MV, Kluger G, Capovilla G, Pruna D, Freri E, D'Arrigo S, Verrotti A.

Am J Med Genet A. 2016 Jan;170A(1):148-55. doi: 10.1002/ajmg.a.37410. Epub 2015 Oct 5.

PMID:
26437767
41.

Unilateral periventricular heterotopia and epilepsy in a girl with Ehlers-Danlos syndrome.

Savasta S, Verrotti A, Spartà MV, Foiadelli T, Villa MP, Parisi P.

Epilepsy Behav Case Rep. 2015 Jun 14;4:27-9. doi: 10.1016/j.ebcr.2015.05.004. eCollection 2015.

42.

"CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases" American Journal of Medical Genetics Part A. 164:2557-2566, 2014.

Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EH.

Am J Med Genet A. 2015 Jul;167(7):1682-3. doi: 10.1002/ajmg.a.36860. Epub 2015 May 5. No abstract available.

PMID:
26097173
43.

Stickler syndrome associated with epilepsy: report of three cases.

Savasta S, Salpietro V, Spartà MV, Foiadelli T, Laino D, Lobefalo L, Marseglia GL, Verrotti A.

Eur J Pediatr. 2015 May;174(5):697-701. doi: 10.1007/s00431-015-2514-8. Epub 2015 Mar 27.

PMID:
25809783
44.

Erratum to: Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Verrotti A, Cusmai R, Laino D, Carotenuto M, Esposito M, Falsaperla R, Margari L, Rizzo R, Savasta S, Grosso S, Striano P, Belcastro V, Franzoni E, Curatolo P, Giordano L, Freri E, Matricardi S, Pruna D, Toldo I, Tozzi E, Lobefalo L, Operto F, Altobelli E, Chiarelli F, Spalice A.

J Neurol. 2015 Jan;262(1):124-5. doi: 10.1007/s00415-014-7579-1. No abstract available.

PMID:
25428530
45.

Ultrastrong coupling of plasmons and excitons in a nanoshell.

Cacciola A, Di Stefano O, Stassi R, Saija R, Savasta S.

ACS Nano. 2014 Nov 25;8(11):11483-92. doi: 10.1021/nn504652w. Epub 2014 Oct 27.

PMID:
25337782
46.

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Verrotti A, Cusmai R, Laino D, Carotenuto M, Esposito M, Falsaperla R, Margari L, Rizzo R, Savasta S, Grosso S, Striano P, Belcastro V, Franzoni E, Curatolo P, Giordano L, Freri E, Matricardi S, Pruna D, Toldo I, Tozzi E, Lobefalo L, Operto F, Altobelli E, Chiarelli F, Spalice A.

J Neurol. 2015 Jan;262(1):116-23. doi: 10.1007/s00415-014-7542-1. Epub 2014 Oct 18. Erratum in: J Neurol. 2015 Jan;262(1):124-5. Carotenuto, Marco [added]; Esposito, Maria [added].

PMID:
25326049
47.

Clinical guidelines in pediatric headache: evaluation of quality using the AGREE II instrument.

Parisi P, Vanacore N, Belcastro V, Carotenuto M, Del Giudice E, Mariani R, Papetti L, Pavone P, Savasta S, Striano P, Toldo I, Tozzi E, Verrotti A, Raucci U; “Pediatric Headache Commission” of Società Italiana di Neurologia Pediatrica (SINP).

J Headache Pain. 2014 Sep 1;15:57. doi: 10.1186/1129-2377-15-57.

48.

CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.

Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EH.

Am J Med Genet A. 2014 Oct;164A(10):2557-66. doi: 10.1002/ajmg.a.36696. Epub 2014 Aug 14. Erratum in: Am J Med Genet A. 2015 Jul;167(7):1682-3.

PMID:
25123255
49.

Acupuncture for acute stroke, peppermint oil for irritable bowel syndrome, yoga for depression and anxiety, hypnotherapy for smoking cessation, and lime juice for sickle cell anemia.

Glickman-Simon R, Savasta S.

Explore (NY). 2014 Jul-Aug;10(4):261-4. doi: 10.1016/j.explore.2014.04.010. Epub 2014 Apr 28. No abstract available.

PMID:
25037671
50.

Gelastic epilepsy without hypothalamic hamartoma: three additional cases.

Savasta S, Budetta M, Spartà MV, Carpentieri ML, Trasimeni G, Zavras N, Villa MP, Parisi P.

Epilepsy Behav. 2014 Aug;37:87-90. doi: 10.1016/j.yebeh.2014.06.012. Epub 2014 Jul 7.

PMID:
25010321

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