• 1055 Citations
  • 18 h-Index
20082019
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Research Output 2008 2019

  • 1055 Citations
  • 18 h-Index
  • 103 Article
  • 12 Chapter
  • 6 Review article
  • 1 Letter
2019
1 Citation (Scopus)

Advanced MR imaging and 18F-DOPA PET characteristics of H3K27M-mutant and wild-type pediatric diffuse midline gliomas

Piccardo, A., Tortora, D., Mascelli, S., Severino, M., Piatelli, G., Consales, A., Pescetto, M., Biassoni, V., Schiavello, E., Massollo, M., Verrico, A., Milanaccio, C., Garrè, M. L., Rossi, A. & Morana, G., Jul 1 2019, In : European Journal of Nuclear Medicine and Molecular Imaging. 46, 8, p. 1685-1694 10 p.

Research output: Contribution to journalArticle

Dihydroxyphenylalanine
Glioma
Pediatrics
Cerebrovascular Circulation
Choline

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

De Mori, R., Severino, M., Mancardi, M. M., Anello, D., Tardivo, S., Biagini, T., Capra, V., Casella, A., Cereda, C., Copeland, B. R., Gagliardi, S., Gamucci, A., Ginevrino, M., Illi, B., Lorefice, E., Musaev, D., Stanley, V., Micalizzi, A., Gleeson, J. G., Mazza, T. & 2 others, Rossi, A. & Valente, E. M., 2019, In : Brain : a journal of neurology. 142, 10, p. 2965-2978 14 p.

Research output: Contribution to journalArticle

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

De Mori, R., Severino, M., Mancardi, M. M., Anello, D., Tardivo, S., Biagini, T., Capra, V., Casella, A., Cereda, C., Copeland, B. R., Gagliardi, S., Gamucci, A., Ginevrino, M., Illi, B., Lorefice, E., Musaev, D., Stanley, V., Micalizzi, A., Gleeson, J. G., Mazza, T. & 2 others, Rossi, A. & Valente, E. M., 2019, In : Brain : a journal of neurology. 142 , (10), p. 2965-78 14 p.

Research output: Contribution to journalArticle

Globus Pallidus
Homeobox Genes
Putamen
Basal Ganglia
Mutation
Sturge-Weber Syndrome
Cavernous Sinus
Port-Wine Stain
Cerebral Veins
Vascular Malformations
3 Citations (Scopus)

Hymenoptera Venom Allergy: Management of Children and Adults in Clinical Practice

Bilò, M. B., Pravettoni, V., Bignardi, D., Bonadonna, P., Mauro, M., Novembre, E., Quercia, O., Cilia, M., Cortellini, G., Costantino, M. T., Cremonte, L., Lodi Rizzini, F., Macchia, L., Marengo, F., Murzilli, F., Patella, V., Reccardini, F., Ricciardi, L., Ridolo, E., Romano, A. & 4 others, Savi, E., Schiavino, D., Severino, M. & Pastorello, E. A., Jan 1 2019, In : Journal of investigational allergology & clinical immunology. 29, 3, p. 180-205 26 p.

Research output: Contribution to journalReview article

Open Access
Hymenoptera
Venoms
Hypersensitivity
Immunotherapy
Prescriptions

Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis

Magini, P., Smits, D. J., Vandervore, L., Schot, R., Columbaro, M., Kasteleijn, E., van der Ent, M., Palombo, F., Lequin, M. H., Dremmen, M., de Wit, M. C. Y., Severino, M., Divizia, M. T., Striano, P., Ordonez-Herrera, N., Alhashem, A., Al Fares, A., Al Ghamdi, M., Rolfs, A., Bauer, P. & 32 others, Demmers, J., Verheijen, F. W., Wilke, M., van Slegtenhorst, M., van der Spek, P. J., Seri, M., Jansen, A. C., Stottmann, R. W., Hufnagel, R. B., Hopkin, R. J., Aljeaid, D., Wiszniewski, W., Gawlinski, P., Laure-Kamionowska, M., Alkuraya, F. S., Akleh, H., Stanley, V., Musaev, D., Gleeson, J. G., Zaki, M. S., Brunetti-Pierri, N., Cappuccio, G., Davidov, B., Basel-Salmon, L., Bazak, L., Shahar, N. R., Avella, A. B., Mirzaa, G. M., Dobyns, W. B., Pippucci, T., Fornerod, M. & Mancini, G. M. S., Oct 3 2019, In : American Journal of Human Genetics. 105, 4, p. 689-705 17 p.

Research output: Contribution to journalArticle

Arthrogryposis
Sphingomyelin Phosphodiesterase
Microcephaly
Nuclear Envelope
Nuclear Pore Complex Proteins
1 Citation (Scopus)

Novel homozygous TSFM pathogenic variant associated with encephalocardiomyopathy with sensorineural hearing loss and peculiar neuroradiologic findings

Scala, M., Brigati, G., Fiorillo, C., Nesti, C., Rubegni, A., Pedemonte, M., Bruno, C., Severino, M., Derchi, M., Minetti, C. & Santorelli, F. M., Aug 7 2019, In : Neurogenetics. 20, 3, p. 165-172 8 p.

Research output: Contribution to journalArticle

Mitochondrial Diseases
Sensorineural Hearing Loss
Leigh Disease
Brain Diseases
Electron Transport
2018

ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum

Gaslini Pediatric Stroke Group, Jul 2018, In : European Journal of Paediatric Neurology. 22, 4, p. 725-728 4 p.

Research output: Contribution to journalArticle

Pseudoxanthoma Elasticum
Eye Manifestations
Angioid Streaks
Stroke
Skin Manifestations
Hydrocephalus
Spinal Dysraphism
Spinal Cord
Aseptic Meningitis
Subarachnoid Space
3 Citations (Scopus)

Brain-injured survivors of monochorionic twin pregnancies complicated by single intrauterine death: MR findings in a multicenter study

Conte, G., Righini, A., Griffiths, P. D., Rustico, M., Lanna, M., Mackie, F. L., Pinelli, L., Prefumo, F., Persico, N., Igra, M. S., Parazzini, C., Doneda, C., Fichera, A., Ambrosi, C., Kilby, M., Severino, M., Triulzi, F., Rossi, A. & Skipper, N., Aug 1 2018, In : Radiology. 288, 2, p. 582-590 9 p.

Research output: Contribution to journalArticle

Twin Pregnancy
Multicenter Studies
Fetus
Magnetic Resonance Spectroscopy
Brain

Brain-injured survivors of monochorionic twin pregnancies complicated by single intrauterine death: MR findings in a multicenter study

Conte, G., Righini, A., Griffiths, P. D., Rustico, M., Lanna, M., Mackie, F. L., Pinelli, L., Prefumo, F., Persico, N., Igra, M. S., Parazzini, C., Doneda, C., Fichera, A., Ambrosi, C., Kilby, M., Severino, M., Triulzi, F., Rossi, A. & Skipper, N., 2018, In : Radiology. 288, 2, p. 582-590 9 p.

Research output: Contribution to journalArticle

Differences in subependymal vein anatomy may predispose preterm infants to GMH-IVH

Tortora, D., Severino, M., Malova, M., Parodi, A., Morana, G., Sedlacik, J., Govaert, P., Volpe, J. J., Rossi, A. & Ramenghi, L. A., Jan 2018, In : Archives of Disease in Childhood: Fetal and Neonatal Edition. 103, 1, p. F59-F65

Research output: Contribution to journalArticle

Premature Infants
Veins
Anatomy
Hemorrhage
Newborn Infant

Novel CNS malformations and skeletal anomalies in a patient with Beaulieu-boycott-Innes syndrome

Telethon Undiagnosed Diseases Program, Dec 2018, In : American Journal of Medical Genetics, Part A. 176, 12, p. 2835-2840 6 p.

Research output: Contribution to journalArticle

Hydrocephalus
Intellectual Disability
Agenesis of Corpus Callosum
Microcephaly
Mutation
8 Citations (Scopus)
Neoplasm Grading
Perfusion
Cerebrovascular Circulation
Pediatrics
Neoplasms

Quantitative susceptibility map analysis in preterm neonates with germinal matrix-intraventricular hemorrhage

Tortora, D., Severino, M., Sedlacik, J., Toselli, B., Malova, M., Parodi, A., Morana, G., Fato, M. M., Ramenghi, L. A. & Rossi, A., Nov 2018, In : Journal of Magnetic Resonance Imaging. 48, 5, p. 1199-1207 9 p.

Research output: Contribution to journalArticle

Hemorrhage
Gestational Age
Brain
Hemosiderin
Intracranial Hemorrhages
1 Citation (Scopus)

Reversible cerebral vasoconstriction complicating cerebral atherosclerotic vascular disease in Schimke immuno-osseous dysplasia

Severino, M., Giacomini, T., Verrina, E., Prato, G. & Rossi, A., Sep 1 2018, In : Neuroradiology. 60, 9, p. 885-888 4 p.

Research output: Contribution to journalLetter

Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases

Godano, E. L., Morana, G., Di Iorgi, N., Pistorio, A., Allegri, A. E. M., Napoli, F., Gastaldi, R., Calcagno, A., Patti, G., Gallizia, A., Notarnicola, S., Giaccardi, M., Noli, S., Severino, M., Tortora, D., Rossi, A. & Maghnie, M., Jun 1 2018, In : European Journal of Endocrinology. 178, 6, p. 613-622 10 p.

Research output: Contribution to journalArticle

Pituitary Diseases
Gadolinium
Pituitary Gland
Posterior Pituitary Gland
Contrast Media
3 Citations (Scopus)

Spinal motor neuron involvement in a patient with homozygous PRUNE mutation

Iacomino, M., Fiorillo, C., Torella, A., Severino, M., Broda, P., Romano, C., Falsaperla, R., Pozzolini, G., Minetti, C., Striano, P., Nigro, V. & Zara, F., May 1 2018, In : European Journal of Paediatric Neurology. 22, 3, p. 541-543 3 p.

Research output: Contribution to journalArticle

Motor Neurons
Mutation
Exome
Phenotype
Spinal Muscular Atrophy

Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study

Whelan, C. D., Altmann, A., Botía, J. A., Jahanshad, N., Hibar, D. P., Absil, J., Alhusaini, S., Alvim, M. K. M., Auvinen, P., Bartolini, E., Bergo, F. P. G., Bernardes, T., Blackmon, K., Braga, B., Caligiuri, M. E., Calvo, A., Carr, S. J., Chen, J., Chen, S., Cherubini, A. & 30 others, David, P., Domin, M., Foley, S., França, W., Haaker, G., Isaev, D., Keller, S. S., Kotikalapudi, R., Kowalczyk, M. A., Kuzniecky, R., Langner, S., Lenge, M., Leyden, K. M., Liu, M., Loi, R. Q., Martin, P., Mascalchi, M., Morita, M. E., Pariente, J. C., Rodríguez-Cruces, R., Rummel, C., Saavalainen, T., Semmelroch, M. K., Severino, M., Tortora, D., Bernasconi, A., Gambardella, A., Guerrini, R., Striano, P. & Vezzani, A., 2018, In : Brain. 141, 2, p. 391-408 18 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)
Germ Cell and Embryonal Neoplasms
Germinoma
Basal Ganglia
Pediatrics
5 Citations (Scopus)
Newborn Infant
Hemorrhage
Gestational Age
Anisotropy
White Matter

Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations

Severino, M., Lualdi, S., Fiorillo, C., Striano, P., De Toni, T., Peluso, S., De Michele, G., Rossi, A., Filocamo, M. & Bruno, C., Jun 1 2018, In : Journal of Neurology. 265, 6, p. 1419-1425 7 p.

Research output: Contribution to journalArticle

Cerebellar Nuclei
Mutation
Brain
Frameshift Mutation
Atrophy
2017
52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., Oct 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

Polyarteritis Nodosa
Adenosine Deaminase
Multicenter Studies
Stroke
Mutation
52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., Oct 1 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

Polyarteritis Nodosa
Adenosine Deaminase
Multicenter Studies
Stroke
Mutation
52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)

Added value of diffusion weighted imaging in pediatric central nervous system embryonal tumors surveillance

Morana, G., Alves, C. A., Tortora, D., Severino, M., Nozza, P., Cama, A., Ravegnani, M., D'Apolito, G., Raso, A., Milanaccio, C., da Costa Leite, C., Garrè, M. L. & Rossi, A., Sep 1 2017, In : Oncotarget. 8, 36, p. 60401-60413 13 p.

Research output: Contribution to journalArticle

Central Nervous System Neoplasms
Pediatrics
Recurrence
Radiation
Medulloblastoma

Characterization of the Phenotype Associated with Microduplication Reciprocal to NF1 Microdeletion Syndrome

Tassano, E., Giacomini, T., Severino, M., Gamucci, A., Fiorio, P., Gimelli, G. & Ronchetto, P., 2017, In : Cytogenetic and Genome Research. 152, 1, p. 22-28 7 p.

Research output: Contribution to journalArticle

Phenotype
Neurofibromatosis 1
Intellectual Disability
Genes
NF1 Microdeletion Syndrome
11 Citations (Scopus)

Cryopyrin-associated periodic syndromes in Italian Patients: Evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., Nov 1 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

Cryopyrin-Associated Periodic Syndromes
Mosaicism
Mutation
High-Throughput Nucleotide Sequencing
Rheumatology
11 Citations (Scopus)

Cryopyrin-associated Periodic Syndromes in Italian Patients: Evaluation of the Rate of Somatic NLRP3 Mosaicism and Phenotypic Characterization

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., Nov 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

Cryopyrin-Associated Periodic Syndromes
Mosaicism
Mutation
High-Throughput Nucleotide Sequencing
Neurologic Manifestations
11 Citations (Scopus)

Cryopyrin-associated Periodic Syndromes in Italian Patients

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., Nov 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

Cryopyrin-Associated Periodic Syndromes
Mosaicism
Mutation
High-Throughput Nucleotide Sequencing
Neurologic Manifestations
11 Citations (Scopus)

Cryopyrin-associated periodic syndromes in Italian Patients: Evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

Early impairment of somatosensory evoked potentials in very young children with achondroplasia with foramen magnum stenosis

Fornarino, S., Rossi, D. P., Severino, M., Pistorio, A., Allegri, A. E. M., Martelli, S., Doria Lamba, L. & Lanteri, P., Feb 2017, In : Developmental Medicine and Child Neurology. 59, 2, p. 192-198 7 p.

Research output: Contribution to journalArticle

Achondroplasia
Foramen Magnum
Somatosensory Evoked Potentials
Pathologic Constriction
Sensitivity and Specificity
17 Citations (Scopus)
Dihydroxyphenylalanine
Perfusion
Pediatrics
Cerebrovascular Circulation
Neoplasms
8 Citations (Scopus)
Diffusion Magnetic Resonance Imaging
Diffusion Tensor Imaging
Pediatrics
Age Groups
Color
Very Low Birth Weight Infant
Incidental Findings
Premature Infants
Magnetic Resonance Imaging
Brain
5 Citations (Scopus)

Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature

Tortora, D., Severino, M., Accogli, A., Martinetti, C., Vercellino, N., Capra, V., Rossi, A. & Pavanello, M., Dec 2017, In : World Neurosurgery. 108, p. 291-302 12 p.

Research output: Contribution to journalReview article

Moyamoya Disease
Eye Abnormalities
Hemangioma
Natural History
Neurocutaneous Syndromes
4 Citations (Scopus)

MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly

Severino, M., Righini, A., Tortora, D., Pinelli, L., Parazzini, C., Morana, G., Accorsi, P., Capra, V., Paladini, D. & Rossi, A., Aug 2017, In : American Journal of Neuroradiology. 38, 8, p. 1643-1646 4 p.

Research output: Contribution to journalArticle

Butterflies
Fetus
Hydrocephalus
Mesencephalon
Diencephalon
11 Citations (Scopus)

Neuroimaging changes in menkes disease, part 1

Manara, R., D'Agata, L., Rocco, M. C., Cusmai, R., Freri, E., Pinelli, L., Darra, F., Procopio, E., Mardari, R., Zanus, C., Di Rosa, G., Soddu, C., Severino, M., Ermani, M., Longo, D. & Sartori, S., 2017, In : American Journal of Neuroradiology. 38, 10, p. 1850-1857 8 p.

Research output: Contribution to journalArticle

11 Citations (Scopus)

Neuroimaging changes in menkes disease, part 1

Manara, R., D'Agata, L., Rocco, M. C., Cusmai, R., Freri, E., Pinelli, L., Darra, F., Procopio, E., Mardari, R., Zanus, C., Di Rosa, G., Soddu, C., Severino, M., Ermani, M., Longo, D. & Sartori, S., Oct 1 2017, In : American Journal of Neuroradiology. 38, 10, p. 1850-1857 8 p.

Research output: Contribution to journalReview article

Menkes Kinky Hair Syndrome
Neuroimaging
Blood Vessels
Brain
Brain Injuries
11 Citations (Scopus)

Neuroimaging Changes in Menkes Disease, Part 1

Manara, R., D'Agata, L., Rocco, M. C., Cusmai, R., Freri, E., Pinelli, L., Darra, F., Procopio, E., Mardari, R., Zanus, C., Di Rosa, G., Soddu, C., Severino, M., Ermani, M., Longo, D., Sartori, S. & Diseases, M. W. G. I. T. I. N. N. F. R., Oct 2017, In : American Journal of Neuroradiology. 38, 10, p. 1850-1857 8 p.

Research output: Contribution to journalArticle

Menkes Kinky Hair Syndrome
Neuroimaging
Blood Vessels
Brain
Brain Injuries
11 Citations (Scopus)

Neuroimaging Changes in Menkes Disease, Part 1

Manara, R., D'Agata, L., Rocco, M. C., Cusmai, R., Freri, E., Pinelli, L., Darra, F., Procopio, E., Mardari, R., Zanus, C., Di Rosa, G., Soddu, C., Severino, M., Ermani, M., Longo, D., Sartori, S. & Menkes Working Group in the Italian Neuroimaging Network for Rare Diseases, Oct 2017, In : American Journal of Neuroradiology. 38, 10, p. 1850-1857 8 p.

Research output: Contribution to journalReview article

Menkes Kinky Hair Syndrome
Neuroimaging
Blood Vessels
Brain
Brain Injuries
3 Citations (Scopus)

Structural Connectivity Analysis in Children with Segmental Callosal Agenesis

Severino, M., Tortora, D., Toselli, B., Uccella, S., Traverso, M., Morana, G., Capra, V., Veneselli, E., Fato, M. M. & Rossi, A., Mar 2017, In : American Journal of Neuroradiology. 38, 3, p. 639-647 9 p.

Research output: Contribution to journalArticle

Agenesis of Corpus Callosum
Corpus Callosum
Connectome
Brain Fornix
Parietal Lobe
1 Citation (Scopus)
2 Citations (Scopus)

Torcular pseudomass: a potential diagnostic pitfall in infants and young children

Sampaio, L., Morana, G., Severino, M., Tortora, D., Leão, M. & Rossi, A., Feb 2017, In : Pediatric Radiology. 47, 2, p. 227-234 8 p.

Research output: Contribution to journalArticle

Confidence Intervals
Brain
Facilitated Diffusion
Pediatric Hospitals
Incidental Findings
2016
10 Citations (Scopus)

Ability of 18F-DOPA PET/CT and fused 18F-DOPA PET/MRI to assess striatal involvement in paediatric glioma

Morana, G., Puntoni, M., Garrè, M. L., Massollo, M., Gallucci, M., Naseri, M., Severino, M., Tortora, D., Rossi, A. & Piccardo, A., Feb 25 2016, (Accepted/In press) In : European Journal Of Nuclear Medicine. p. 1-9 9 p.

Research output: Contribution to journalArticle

Corpus Striatum
Glioma
Pediatrics
Multivariate Analysis
Sensitivity and Specificity

Ability of 18F-DOPA PET/CT and fused 18F-DOPA PET/MRI to assess striatal involvement in paediatric glioma

Morana, G., Puntoni, M., Garre', M. L., Massollo, M., Lopci, E., Naseri, M., Severino, M., Tortora, D., Rossi, A. & Piccardo, A., Feb 25 2016, (Accepted/In press) In : European Journal of Nuclear Medicine and Molecular Imaging. p. 1-9 9 p.

Research output: Contribution to journalArticle

Corpus Striatum
Glioma
Pediatrics
Multivariate Analysis
Sensitivity and Specificity
8 Citations (Scopus)

Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2

Fiorillo, C., Moro, F., Brisca, G., Accogli, A., Trucco, F., Trovato, R., Pedemonte, M., Severino, M., Catala, M., Capra, V., Santorelli, F. M., Bruno, C., Rossi, A. & Minetti, C., Apr 1 2016, In : European Journal of Neurology. 23, 4, p. e19-e21

Research output: Contribution to journalArticle

Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2

Fiorillo, C., Moro, F., Brisca, G., Accogli, A., Trucco, F., Trovato, R., Pedemonte, M., Severino, M., Catala, M., Capra, V., Santorelli, F. M., Bruno, C., Rossi, A. & Minetti, C., Apr 1 2016, In : European Journal of Neurology. 23, 4, p. e19-e21

Research output: Contribution to journalArticle