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Ilaria Taglia

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 25, 2016
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular geneticsCarmen Stabile, Ilaria Taglia, Carla Battisti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 18, 2015
Primary familial brain calcification: update on molecular geneticsIlaria Taglia, Vincenzo Bonifati, Andrea Mignarri, et al.
Journal of Cellular Physiology|July 20, 2017
Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localizationIlaria Taglia, Patrizia Formichi, Carla Battisti, et al.
Journal of the Neurological Sciences|August 8, 2012
Hereditary cerebral small vessel diseases: a reviewAntonio Federico, Ilaria Di Donato, Silvia Bianchi, et al.
Journal of Cellular Physiology|February 5, 2020
HTRA1 expression profile and activity on TGF-β signaling in HTRA1 mutation carriersAlessandro Fasano, Patrizia Formichi, Ilaria Taglia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 8, 2015
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance?Paola Da Pozzo, Anna Rubegni, Alessandra Rufa, et al.
Journal of Neurology|February 18, 2014
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R geneCarla Battisti, Ilaria Di Donato, Silvia Bianchi, et al.
Journal of Alzheimer'S Disease : JAD|September 25, 2015
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal SpheroidsIlaria Di Donato, Carmen Stabile, Silvia Bianchi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2014
Primary familial brain calcification: Genetic analysis and clinical spectrumIlaria Taglia, Andrea Mignarri, Simone Olgiati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 7, 2020
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletionsPatrizia Formichi, Nastasia Cardone, Ilaria Taglia, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 25, 2016
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular geneticsCarmen Stabile, Ilaria Taglia, Carla Battisti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 18, 2015
Primary familial brain calcification: update on molecular geneticsIlaria Taglia, Vincenzo Bonifati, Andrea Mignarri, et al.
Journal of Cellular Physiology|July 20, 2017
Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localizationIlaria Taglia, Patrizia Formichi, Carla Battisti, et al.
Journal of the Neurological Sciences|August 8, 2012
Hereditary cerebral small vessel diseases: a reviewAntonio Federico, Ilaria Di Donato, Silvia Bianchi, et al.
Journal of Cellular Physiology|February 5, 2020
HTRA1 expression profile and activity on TGF-β signaling in HTRA1 mutation carriersAlessandro Fasano, Patrizia Formichi, Ilaria Taglia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 8, 2015
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance?Paola Da Pozzo, Anna Rubegni, Alessandra Rufa, et al.
Journal of Neurology|February 18, 2014
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R geneCarla Battisti, Ilaria Di Donato, Silvia Bianchi, et al.
Journal of Alzheimer'S Disease : JAD|September 25, 2015
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal SpheroidsIlaria Di Donato, Carmen Stabile, Silvia Bianchi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2014
Primary familial brain calcification: Genetic analysis and clinical spectrumIlaria Taglia, Andrea Mignarri, Simone Olgiati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 7, 2020
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletionsPatrizia Formichi, Nastasia Cardone, Ilaria Taglia, et al.
Pageof 2