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Author/Creator Stagnaro, Michela

1. ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases. (March 2018)

Authors:
Stagnaro, Michela; Pisciotta, Livia; Gherzi, Marcella; Di Rocco, Maja; Gurrieri, Fiorella; Parrini, Elena; Prato, Giulia; Veneselli, Edvige; De Grandis, Elisa
Journal:
European journal of paediatric neurology
Issue:
Volume 22:Number 2(2018:Mar.)
Page Start:
264
Record Type:
Journal Article
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2. Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study. (24th November 2020)

Authors:
Balestrini, Simona; Mikati, Mohamad A.; Álvarez-García-Rovés, Reyes; Carboni, Michael; Hunanyan, Arsen S.; Kherallah, Bassil; McLean, Melissa; Prange, Lyndsey; De Grandis, Elisa; Gagliardi, Alessandra; Pisciotta, Livia; Stagnaro, Michela; Veneselli, Edvige; Campistol, Jaume; Fons, Carmen; Pias-Pe...
Journal:
Neurology
Issue:
Volume 95:Number 21(2020)
Page Start:
Record Type:
Journal Article
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3. Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients. Issue 1 (December 2015)

Authors:
Panagiotakaki, Eleni; De Grandis, Elisa; Stagnaro, Michela; Heinzen, Erin; Fons, Carmen; Sisodiya, Sanjay; de Vries, Boukje; Goubau, Christophe; Weckhuysen, Sarah; Kemlink, David; Scheffer, Ingrid; Lesca, Gaëtan; Rabilloud, Muriel; Klich, Amna; Ramirez-Camacho, Alia; Ulate-Campos, Adriana; Campis...
Journal:
Orphanet journal of rare diseases
Issue:
Volume 9:Issue 1(2014)
Page Start:
1
Record Type:
Journal Article
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