Pisciotta L - Search Results

1

Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.

Balestrini S, Mikati MA, Álvarez-García-Rovés R, Carboni M, Hunanyan AS, Kherallah B, McLean M, Prange L, De Grandis E, Gagliardi A, Pisciotta L, Stagnaro M, Veneselli E, Campistol J, Fons C, Pias-Peleteiro L, Brashear A, Miller C, Samões R, Brankovic V, Padiath QS, Potic A, Pilch J, Vezyroglou A, Bye AME, Davis AM, Ryan MM, Semsarian C, Hollingsworth G, Scheffer IE, Granata T, Nardocci N, Ragona F, Arzimanoglou A, Panagiotakaki E, Carrilho I, Zucca C, Novy J, Dzieżyc K, Parowicz M, Mazurkiewicz-Bełdzińska M, Weckhuysen S, Pons R, Groppa S, Sinden DS, Pitt GS, Tinker A, Ashworth M, Michalak Z, Thom M, Cross JH, Vavassori R, Kaski JP, Sisodiya SM. Balestrini S, et al. Among authors: pisciotta l. Neurology. 2020 Nov 24;95(21):e2866-e2879. doi: 10.1212/WNL.0000000000010794. Epub 2020 Sep 10. Neurology. 2020. PMID: 32913013 Free PMC article.

2

[Identifying possible homozygous familial hypercholesterolemia patients: an Italian experts' opinion].

Bilato C, Zambon A, Pisciotta L, Citroni N, Carubbi F, Zambon S, Zenti MG, Vinci P, Biolo G, Bonomo K, Egalini F, Passaro A, Nascimbeni F, Negri E, D'Addato S, Averna M, Arca M, Oliva F, Colivicchi F, Catapano A. Bilato C, et al. Among authors: pisciotta l. G Ital Cardiol (Rome). 2023 Jan;24(1):5-10. doi: 10.1714/3934.39174. G Ital Cardiol (Rome). 2023. PMID: 36573504 Italian.

3

Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia.

Larrey D, D'Erasmo L, O'Brien S, Arca M; Italian Working Group on Lomitapide. Larrey D, et al. Liver Int. 2023 Feb;43(2):413-423. doi: 10.1111/liv.15497. Epub 2022 Dec 30. Liver Int. 2023. PMID: 36520008 Free PMC article. Clinical Trial.

4

Combined early treatment in hemiplegic attacks related to CACNA1A encephalopathy with brain oedema: Blocking the cascade?

Camia F, Pisciotta L, Morana G, Schiaffino MC, Renna S, Carrera P, Ferrari M, Baglietto MG, Veneselli E, Siri L, Mancardi MM. Camia F, et al. Among authors: pisciotta l. Cephalalgia. 2017 Oct;37(12):1202-1206. doi: 10.1177/0333102416668655. Epub 2016 Sep 19. Cephalalgia. 2017. PMID: 27651281

5

Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients.

Pisciotta L, Gherzi M, Stagnaro M, Calevo MG, Giannotta M, Vavassori MR, Veneselli E; I.B.AHC Consortium; De Grandis E. Pisciotta L, et al. Brain Dev. 2017 Jun;39(6):521-528. doi: 10.1016/j.braindev.2017.02.001. Epub 2017 Feb 27. Brain Dev. 2017. PMID: 28249736

6

ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases.

Stagnaro M, Pisciotta L, Gherzi M, Di Rocco M, Gurrieri F, Parrini E, Prato G, Veneselli E, De Grandis E. Stagnaro M, et al. Among authors: pisciotta l. Eur J Paediatr Neurol. 2018 Mar;22(2):264-271. doi: 10.1016/j.ejpn.2018.01.010. Epub 2018 Jan 31. Eur J Paediatr Neurol. 2018. PMID: 29396171

7

Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability.

Rosti G, Tassano E, Bossi S, Divizia MT, Ronchetto P, Servetti M, Lerone M, Pisciotta L, Mancardi MM, Veneselli E, Puliti A. Rosti G, et al. Among authors: pisciotta l. Eur J Med Genet. 2019 Sep;62(9):103555. doi: 10.1016/j.ejmg.2018.10.007. Epub 2018 Oct 22. Eur J Med Genet. 2019. PMID: 30359776

8

Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome.

Lenci G, Calevo MG, Gaggero R, Prato G, Pisciotta L, De Grandis E, Mancardi MM, Baglietto MG, Vigano' M, Veneselli E. Lenci G, et al. Among authors: pisciotta l. Brain Dev. 2019 Jun;41(6):522-530. doi: 10.1016/j.braindev.2019.02.004. Epub 2019 Feb 20. Brain Dev. 2019. PMID: 30797668

9

White matter and cerebellar involvement in alternating hemiplegia of childhood.

Severino M, Pisciotta L, Tortora D, Toselli B, Stagnaro M, Cordani R, Morana G, Zicca A, Kotzeva S, Zanaboni C, Montobbio G, Rossi A, De Grandis E; IBAHC Consortium. Severino M, et al. Among authors: pisciotta l. J Neurol. 2020 May;267(5):1300-1311. doi: 10.1007/s00415-020-09698-3. Epub 2020 Jan 16. J Neurol. 2020. PMID: 31950366

10

Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic Variant.

Giacomini T, Gamucci A, Pisciotta L, Nesti C, Fiorillo C, Doccini S, Morana G, Nobili L, Santorelli FM, Mancardi MM, De Grandis E. Giacomini T, et al. Among authors: pisciotta l. Neuropediatrics. 2020 Dec;51(6):425-429. doi: 10.1055/s-0040-1708539. Epub 2020 May 11. Neuropediatrics. 2020. PMID: 32392611

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