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S-02-05 Integration of data across toxicity endpoints for improved safety assessment of chemicals: key characteristics and other approaches to cancer hazard evaluation

Toxicology letters, 2022-09, Vol.368, p.S16

Madia, F.

2022

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A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability

Scientific reports, 2018-09, Vol.8 (1), p.13382-8, Article 13382

2018

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Natural history of young-adult amyotrophic lateral sclerosis

Neurology, 2008-09, Vol.71 (12), p.876-881

2008

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SARS-CoV-2 was already circulating in Italy, in early December 2019

European review for medical and pharmacological sciences, 2021-04, Vol.25 (8), p.3342

2021

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Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations

European journal of paediatric neurology, 2020-09, Vol.28, p.110-119

2020

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Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

Neurology, 2003-06, Vol.60 (12), p.1961-1967

2003

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Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy

Neurology, 2006-10, Vol.67 (7), p.1230-1235

2006

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S-18-02 Fifty years of IARC Monographs leading to a modernized approach for synthesizing epidemiological and experimental data on carcinogenicity

Toxicology letters, 2022-09, Vol.368, p.S47

2022

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Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy

Journal of the neurological sciences, 2012-08, Vol.319 (1), p.75-80

2012

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A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype

Journal of the neurological sciences, 2010-11, Vol.298 (1), p.114-117

2010

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PO-097 Integration of data across toxicity endpoints to explore new ways for carcinogenicity safety assessment of chemicals

ESMO open, 2018-07, Vol.3 (Suppl 2), p.A264-A264

2018

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Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia

Journal of the neurological sciences, 2010-04, Vol.291 (1), p.89-91

2010

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D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation

Journal of the neurological sciences, 2011-10, Vol.309 (1), p.31-33

2011

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Pure motor chronic inflammatory demyelinating polyneuropathy

Journal of neurology, 2001-09, Vol.248 (9), p.772-777

2001

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A simple model system for age-dependent DNA damage and cancer

Mechanisms of ageing and development, 2007-01, Vol.128 (1), p.45-49

2007

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SEIPIN S90L Mutation in an Italian family with CMT2/dHMN and pyramidal signs

Muscle & nerve, 2010-09, Vol.42 (3), p.448-451

2010

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P03-14: Cancer Hazard Identification in the IARC Monographs: Recent evaluations for which cancer in experimental animals and toxicological evidence was influential

Toxicology letters, 2023-09, Vol.384, p.S90-S91

2023

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OS02-04Advancing the evaluation of mechanistic evidence in cancer hazard identification: update on the IARC key characteristic (KCs) of carcinogens framework

Toxicology letters, 2023-09, Vol.384, p.S63-S64

2023

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P03-14: Cancer Hazard Identification in theIARC Monographs: Recent evaluations for which cancer in experimental animals and toxicological evidence was influential

Toxicology letters, 2023-09, Vol.384, p.S88-S88

2023

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OS02-04: Advancing the evaluation of mechanistic evidence in cancer hazard identification: update on the IARC key characteristic (KCs) of carcinogens framework

Toxicology letters, 2023-09, Vol.384, p.S65

2023

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P13-17 Assessment of the efficiency of the literature search of the ten key characteristics of carcinogens in the IARC Monographs evaluation process

Toxicology letters, 2024-09, Vol.399, p.S216-S216

2024

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P93 – 2953: Identification of a new mutation of the SCL1A gene in a patient with GLUT1-DS

European journal of paediatric neurology, 2015-05, Vol.19, p.S120-S120

2015

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Chronic autoimmune autonomic neuropathy responsive to immunosuppressive therapy

Neurology, 2007-01, Vol.68 (2), p.161-162

2007

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Triple A syndrome: A novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency

Journal of the neurological sciences, 2010-03, Vol.290 (1), p.150-152

2010

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Neurologic improvement after peripheral blood stem cell transplantation in poems

Neurology, 2009-10, Vol.73 (14), p.1165; author reply 1165-1166

2009

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S-02-05 Integration of data across toxicity endpoints for improved safety assessment of chemicals: key characteristics and other approaches to cancer hazard evaluation

A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability

Natural history of young-adult amyotrophic lateral sclerosis

SARS-CoV-2 was already circulating in Italy, in early December 2019

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy

S-18-02 Fifty years of IARC Monographs leading to a modernized approach for synthesizing epidemiological and experimental data on carcinogenicity

Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy

A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype

PO-097 Integration of data across toxicity endpoints to explore new ways for carcinogenicity safety assessment of chemicals

Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia

D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation

Pure motor chronic inflammatory demyelinating polyneuropathy

A simple model system for age-dependent DNA damage and cancer

SEIPIN S90L Mutation in an Italian family with CMT2/dHMN and pyramidal signs

P03-14: Cancer Hazard Identification in the IARC Monographs: Recent evaluations for which cancer in experimental animals and toxicological evidence was influential

OS02-04Advancing the evaluation of mechanistic evidence in cancer hazard identification: update on the IARC key characteristic (KCs) of carcinogens framework

P03-14: Cancer Hazard Identification in theIARC Monographs: Recent evaluations for which cancer in experimental animals and toxicological evidence was influential

OS02-04: Advancing the evaluation of mechanistic evidence in cancer hazard identification: update on the IARC key characteristic (KCs) of carcinogens framework

P13-17 Assessment of the efficiency of the literature search of the ten key characteristics of carcinogens in the IARC Monographs evaluation process

P93 – 2953: Identification of a new mutation of the SCL1A gene in a patient with GLUT1-DS

Chronic autoimmune autonomic neuropathy responsive to immunosuppressive therapy

Triple A syndrome: A novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency

Neurologic improvement after peripheral blood stem cell transplantation in poems

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