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2-DE and MALDI-TOF-MS for a comparative analysis of proteins expressed in different cellular models of amyotrophic lateral sclerosis

Electrophoresis, 2007-12, Vol.28 (23), p.4320-4329

2007

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Absent leptomeningeal collateralization is associated with greatest benefit from mechanical thrombectomy in the 6-24 hour time window

European stroke journal, 2024-03, p.23969873241239208-23969873241239208

2024

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Adolescents and adults affected by Cornelia de Lange syndrome: A report of 73 Italian patients

American journal of medical genetics. Part C, Seminars in medical genetics, 2016-06, Vol.172C (2), p.206-213

2016

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ALDOC- and ENO2- driven glucose metabolism sustains 3D tumor spheroids growth regardless of nutrient environmental conditions: a multi-omics analysis

Journal of experimental & clinical cancer research, 2023-03, Vol.42 (1), p.69-69, Article 69

2023

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ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usability

Neurological sciences, 2020-04, Vol.41 (4), p.835-841

2020

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Alternative Tissue Fixation Protocols Dramatically Reduce the Impact of DNA Artifacts, Unraveling the Interpretation of Clinical Comprehensive Genomic Profiling

Laboratory investigation, 2024-01, Vol.104 (1), p.100280-100280, Article 100280

2024

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Analysis and future scenarios of the SARS-CoV-2 epidemic in Tuscany Region (Central Italy)

Epidemiologia e prevenzione, 2020-09, Vol.44 (5-6 Suppl 2), p.120

2020

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Analysis of congenital heart defects in 87 consecutive patients with Brachmann-de Lange syndrome

American Journal of Medical Genetics Part A, 2009, Vol.149A (6), p.1268-1272

2009

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Analysis of congenital heart defects in 87 consecutive patients with Brachmann‐de Lange syndrome

American journal of medical genetics. Part A, 2009-06, Vol.149A (6), p.1268-1272

2009

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Analysis of predictive factors for non-adherence to organized screening for colorectal and breast cancers in the pre-pandemic period (2018-2019) in Lombardy Region (Northern Italy)

Epidemiologia e prevenzione, 2024-03, Vol.48 (2), p.118

2024

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Association between Vitamin D Serum Levels and Immune Response to the BNT162b2 Vaccine for SARS-CoV-2

Biomedicines, 2022-08, Vol.10 (8), p.1993

2022

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Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

JAMA neurology, 2021-10, Vol.78 (10), p.1236

2021

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Asymptomatic infection with clade 2.3.4.4b highly pathogenic avian influenza A(H5N1) in carnivore pets, Italy, April 2023

Euro surveillance : bulletin européen sur les maladies transmissibles, 2023-08, Vol.28 (35), p.1

2023

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Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients

Genes, 2022-07, Vol.13 (7), p.1275

2022

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Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy

American journal of medical genetics. Part A, 2018-12, Vol.176 (12), p.2867-2871

2018

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Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients

The Journal of experimental medicine, 2023-09, Vol.220 (9)

2023

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Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

Epigenetics, 2015-07, Vol.10 (7), p.643-649

2015

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Bioink Composition and Printing Parameters for 3D Modeling Neural Tissue

Cells (Basel, Switzerland), 2019-08, Vol.8 (8), p.830

2019

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Brain Organoids: Modeling in Neuroscience

2020

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Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype

Clinical epigenetics, 2016-01, Vol.89 (1), p.74-81

2016

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C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study

Journal of Alzheimer's disease, 2014-01, Vol.38 (4), p.799

2014

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Celiac disease prevalence and predisposing‐HLA in a cohort of 93 Williams‐Beuren syndrome patients

American journal of medical genetics. Part A, 2023-01, Vol.191 (1), p.84-89

2023

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Cell environment shapes TDP-43 function with implications in neuronal and muscle disease

Communications biology, 2022-04, Vol.5 (1), p.314-314, Article 314

2022

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Cervical spine malformation in cornelia de lange syndrome: A report of three patients

American journal of medical genetics. Part A, 2014-06, Vol.164A (6), p.1520-1524

2014

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2-DE and MALDI-TOF-MS for a comparative analysis of proteins expressed in different cellular models of amyotrophic lateral sclerosis

Absent leptomeningeal collateralization is associated with greatest benefit from mechanical thrombectomy in the 6-24 hour time window

Adolescents and adults affected by Cornelia de Lange syndrome: A report of 73 Italian patients

ALDOC- and ENO2- driven glucose metabolism sustains 3D tumor spheroids growth regardless of nutrient environmental conditions: a multi-omics analysis

ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usability

Alternative Tissue Fixation Protocols Dramatically Reduce the Impact of DNA Artifacts, Unraveling the Interpretation of Clinical Comprehensive Genomic Profiling

Analysis and future scenarios of the SARS-CoV-2 epidemic in Tuscany Region (Central Italy)

Analysis of congenital heart defects in 87 consecutive patients with Brachmann-de Lange syndrome

Analysis of congenital heart defects in 87 consecutive patients with Brachmann‐de Lange syndrome

Analysis of predictive factors for non-adherence to organized screening for colorectal and breast cancers in the pre-pandemic period (2018-2019) in Lombardy Region (Northern Italy)

Archaeogenomic distinctiveness of the Isthmo-Colombian area

Association between Vitamin D Serum Levels and Immune Response to the BNT162b2 Vaccine for SARS-CoV-2

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Asymptomatic infection with clade 2.3.4.4b highly pathogenic avian influenza A(H5N1) in carnivore pets, Italy, April 2023

Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients

Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy

Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients

Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

Bioink Composition and Printing Parameters for 3D Modeling Neural Tissue

Brain Organoids: Modeling in Neuroscience

Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study

Celiac disease prevalence and predisposing‐HLA in a cohort of 93 Williams‐Beuren syndrome patients

Cell environment shapes TDP-43 function with implications in neuronal and muscle disease

Cervical spine malformation in cornelia de lange syndrome: A report of three patients

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