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Research Output 2010 2019

  • 281 Citations
  • 9 h-Index
  • 23 Article
  • 1 Letter
  • 1 Review article
2019
Lipid Metabolism
Antipsychotic Agents
Cholesterol
Obesity
HDL Lipoproteins

Broadening the spectrum of adulthood X-linked adrenoleukodystrophy: A report of two atypical cases

Foschi, M., Vacchiano, V., Avoni, P., Incensi, A., Battaglia, S., Donadio, V., Panzeri, E., Bassi, M. T., Liguori, R. & Rizzo, G., Jan 1 2019, In : Frontiers in Neurology. 10, FEB, 70.

Research output: Contribution to journalArticle

Open Access
Adrenoleukodystrophy
Spastic Paraparesis
Spinal Cord Diseases
Phenotype
Addison Disease
Hereditary Spastic Paraplegia
Mutation
Brain
Magnetic Resonance Imaging
Phenotype
Hereditary Spastic Paraplegia
Mutation
Brain
Magnetic Resonance Imaging
Phenotype
Epilepsy
Genes
Tubulin
Brain
Mutation

Naringenin Ameliorates Drosophila ReepA Hereditary Spastic Paraplegia-Linked Phenotypes

Napoli, B., Gumeni, S., Forgiarini, A., Fantin, M., De Filippis, C., Panzeri, E., Vantaggiato, C. & Orso, G., Nov 19 2019, In : Frontiers in Neuroscience. 13, 1202.

Research output: Contribution to journalArticle

Open Access

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

Vantaggiato, C., Panzeri, E., Castelli, M., Citterio, A., Arnoldi, A., Santorelli, F. M., Liguori, R., Scarlato, M., Musumeci, O., Toscano, A., Clementi, E. & Bassi, M. T., 2019, In : Autophagy.

Research output: Contribution to journalArticle

Hereditary Spastic Paraplegia
Autophagy
Endocytosis
Spastic Paraparesis
Mutation
2018
Open Access
Hereditary Spastic Paraplegia
Amyotrophic Lateral Sclerosis
Fathers
Spastic Paraparesis
Nerve Degeneration
2017

Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21

Scarlato, M., Citterio, A., Barbieri, A., Godi, C., Panzeri, E. & Bassi, M. T., Sep 1 2017, In : Journal of Neurology. 264, 9, p. 2021-2023 3 p.

Research output: Contribution to journalLetter

Tubulin-related cerebellar dysplasia

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, R., D'Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M. M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., Dec 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin
Malformations of Cortical Development
Neuroimaging
Genes
Cysts

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, M., D’Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin
Malformations of Cortical Development
Neuroimaging
Genes
Cysts

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, R., D’Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, R., D’Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin
Malformations of Cortical Development
Neuroimaging
Genes
Cysts

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, M., D'Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tuettelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., Dec 1 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

2015

A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype

Romaniello, R., Saettini, F., Panzeri, E., Arrigoni, F., Bassi, M. T. & Borgatti, R., Mar 15 2015, In : NeuroReport. 26, 5, p. 254-257 4 p.

Research output: Contribution to journalArticle

Qa-SNARE Proteins
Rett Syndrome
Carrier Proteins
Phenotype
Mutation

Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis

Citterio, A., Arnoldi, A., Panzeri, E., Merlini, L., D’Angelo, M. G., Musumeci, O., Toscano, A., Bondi, A., Martinuzzi, A., Bresolin, N. & Bassi, M. T., Dec 1 2015, In : Journal of Neurology. 262, 12, p. 2684-2690 7 p.

Research output: Contribution to journalArticle

Spastic Paraparesis
Dominant Genes
Hereditary Sensory and Autonomic Neuropathies
Kinesin
Neurodegenerative Diseases
2014

Chromosomal imbalances in human bladder urothelial carcinoma: Similarities and differences between biopsy samples and cancer stem-like cells

Conconi, D., Panzeri, E., Redaelli, S., Bovo, G., Viganò, P., Strada, G., Dalprà, L. & Bentivegna, A., Sep 1 2014, In : BMC Cancer. 14, 1, 646.

Research output: Contribution to journalArticle

Neoplastic Stem Cells
Urinary Bladder
Carcinoma
Biopsy
Neoplasms

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

Citterio, A., Arnoldi, A., Panzeri, E., D'Angelo, M. G., Filosto, M., Dilena, R., Arrigoni, F., Castelli, M., Maghini, C., Germiniasi, C., Menni, F., Martinuzzi, A., Bresolin, N. & Bassi, M. T., 2014, In : Journal of Neurology. 261, 2, p. 373-381 9 p.

Research output: Contribution to journalArticle

Hereditary Spastic Paraplegia
Spastic Paraparesis
Mutation
Genes
Mutation Rate

Mutations in MAPT give rise to aneuploidy in animal models of tauopathy

Rossi, G., Conconi, D., Panzeri, E., Paoletta, L., Piccoli, E., Ferretti, M. G., Mangieri, M., Ruggerone, M., Dalprà, L. & Tagliavini, F., 2014, In : Neurogenetics. 15, 1, p. 31-40 10 p.

Research output: Contribution to journalArticle

Tauopathies
Microtubule-Associated Proteins
Aneuploidy
Animal Models
Chromosomal Instability
2013

Mutations in MAPT gene cause chromosome instability and introduce copy number variations widely in the genome

Rossi, G., Conconi, D., Panzeri, E., Redaelli, S., Piccoli, E., Paoletta, L., Dalprà, L. & Tagliavini, F., 2013, In : Journal of Alzheimer's Disease. 33, 4, p. 969-982 14 p.

Research output: Contribution to journalArticle

Chromosomal Instability
Microtubule-Associated Proteins
Genomic Instability
Aneuploidy
DNA Repair
2012

DNA copy number alterations and PPARG amplification in a patient with multifocal bladder urothelial carcinoma

Conconi, D., Panzeri, E., Redaelli, S., Bovo, G., Volante, M., Viganò, P., Strada, G., Dalprà, L. & Bentivegna, A., 2012, In : BMC Research Notes. 5, 607.

Research output: Contribution to journalArticle

Amplification
Tumors
Urinary Bladder
Urinary Bladder Neoplasms
Carcinoma

Investigating the role of X chromosome breakpoints in premature ovarian failure

Baronchelli, S., Villa, N., Redaelli, S., Lissoni, S., Saccheri, F., Panzeri, E., Conconi, D., Bentivegna, A., Crosti, F., Sala, E., Bertola, F., Marozzi, A., Pedicini, A., Ventruto, M., Police, M. A. & Dalprá, L., 2012, In : Molecular Cytogenetics. 5, 1, 32.

Research output: Contribution to journalArticle

Chromosome Breakpoints
Primary Ovarian Insufficiency
X Chromosome
Chromosomes
Chromosome Aberrations
2011

Chromosomal aberrations in bladder cancer: Fresh versus formalin fixed paraffin embedded tissue and targeted FISH versus wide microarray-based CGH analysis

Panzeri, E., Conconi, D., Antolini, L., Redaelli, S., Valsecchi, M. G., Bovo, G., Pallotti, F., Viganò, P., Strada, G., Dalprà, L. & Bentivegna, A., Sep 1 2011, In : PLoS One. 6, 9, e24237.

Research output: Contribution to journalArticle

chromosome aberrations
Microarrays
Chromosomes
Aberrations
formalin

Cytogenetics of premature ovarian failure: An investigation on 269 affected women

Dalpr, L., Baronchelli, S., Conconi, D., Panzeri, E., Bentivegna, A., Redaelli, S., Lissoni, S., Saccheri, F., Villa, N., Crosti, F., Sala, E., Martinoli, E., Volontè, M., Marozzi, A. & Dalprà, L., 2011, In : Journal of Biomedicine and Biotechnology. 2011, 370195.

Research output: Contribution to journalArticle

Primary Ovarian Insufficiency
X Chromosome
Cytogenetics
Mosaicism
Sex Chromosomes
2010

Biological heterogeneity of putative bladder cancer stem-like cell populations from human bladder transitional cell carcinoma samples

Bentivegna, A., Conconi, D., Panzeri, E., Sala, E., Bovo, G., Viganò, P., Brunelli, S., Bossi, M., Tredici, G., Strada, G. & Dalprà, L., Feb 2010, In : Cancer Science. 101, 2, p. 416-424 9 p.

Research output: Contribution to journalArticle

Neoplastic Stem Cells
Transitional Cell Carcinoma
Urinary Bladder Neoplasms
Urinary Bladder
Stem Cells