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Genes|May 30, 2020
Interpreting Mixture Profiles: Comparison between Precision ID GlobalFiler™ NGS STR Panel v2 and Traditional MethodsMichele Ragazzo, Stefania Carboni, Valerio Caputo, et al.
Parkinson'S Disease|July 24, 2018
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's DiseaseStefano Gambardella, Rosangela Ferese, Simona Scala, et al.
Parkinson'S Disease|October 2, 2018
Erratum to "Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease"Stefano Gambardella, Rosangela Ferese, Simona Scala, et al.
Genes|October 17, 2019
NGS Analysis for Molecular Diagnosis of Retinitis Pigmentosa (RP): Detection of a Novel Variant in PRPH2 GeneClaudia Strafella, Valerio Caputo, Giulia Pagliaroli, et al.
Neurogenetics|March 27, 2019
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS eraStefania Zampatti, Luca Colantoni, Claudia Strafella, et al.
Prenatal Diagnosis|October 11, 2018
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysisStefania Zampatti, Julia Mela, Cristina Peconi, et al.
Frontiers in Neurology|July 3, 2019
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case ReportClaudia Strafella, Giulia Campoli, Rosaria Maria Galota, et al.
Headache|January 9, 2019
Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc-HMPAO Brain SPECT StudyValentina Mancini, Giulio Mastria, Viviana Frantellizzi, et al.
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