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Research Output 1990 2019

  • 2644 Citations
  • 30 h-Index
  • 87 Article
  • 2 Chapter
2019

Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?

Benzoni, C., Farina, L., Pensato, V., Marotta, G., Kuqo, A., Mauro, E., Pareyson, D. & Salsano, E., Nov 1 2019, In : The neurologist. 24, 6, p. 194-197 4 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Leukoencephalopathies
Mutation
Brain Stem
Phenotype

Microwave thermal ablation using CT-scanner for predicting the variation of ablated region over time: advantages and limitations

Strigari, L., Minosse, S., D'Alessio, D., Farina, L., Cavagnaro, M., Cassano, B., Pinto, R., Vallati, G. & Lopresto, V., Apr 17 2019, In : Physics in Medicine and Biology.

Research output: Contribution to journalArticle

X-Ray Computed Tomography Scanners
Microwaves
Hot Temperature
Temperature
Multivariate Analysis
2018

Efficacy of bendamustine and rituximab as first salvage treatment in chronic lymphocytic leukemia and indirect comparison with ibrutinib: A GIMEMA, ERIC and UK CLL FORUM study

Cuneo, A., Follows, G., Rigolin, G. M., Piciocchi, A., Tedeschi, A., Trentin, L., Perez, A. M., Coscia, M., Laurenti, L., Musuraca, G., Farina, L., Delgado, A. R., Orlandi, E. M., Galieni, P., Mauro, F. R., Visco, C., Amendola, A., Billio, A., Marasca, R., Chiarenza, A. & 24 others, Meneghini, V., Ilariucci, F., Marchetti, M., Molica, S., Re, F., Gaidano, G., Gonzalez, M., Forconi, F., Ciolli, S., Cortelezzi, A., Montillo, M., Smolej, L., Schuh, A., Eyre, T. A., Kennedy, B., Bowles, K. M., Vignetti, M., De La Serna, J., Moreno, C., Foà, R., Ghia, P., Party, GIMEMA., (ERIC), E. R. I. O. CLL. & forum, UK. CLL., 2018, In : Haematologica. 103, 7, p. 1209-1217 9 p.

Research output: Contribution to journalArticle

Efficacy of bendamustine and rituximab as first salvage treatment in chronic lymphocytic leukemia and indirect comparison with ibrutinib: A GIMEMA, ERIC and UK CLL FORUM study

Cuneo, A., Follows, G., Rigolin, G. M., Piciocchi, A., Tedeschi, A., Trentin, L., Perez, A. M., Coscia, M., Laurenti, L., Musuraca, G., Farina, L., Delgado, A. R., Orlandi, E. M., Galieni, P., Mauro, F. R., Visco, C., Amendola, A., Billio, A., Marasca, R., Chiarenza, A. & 24 others, Meneghini, V., Ilariucci, F., Marchetti, M., Molica, S., Re, F., Gaidano, G., Gonzalez, M., Forconi, F., Ciolli, S., Cortelezzi, A., Montillo, M., Smolej, L., Schuh, A., Eyre, T. A., Kennedy, B., Bowles, K. M., Vignetti, M., De La Serna, J., Moreno, C., Foà, R., Ghia, P., Party, GIMEMA., (ERIC), E. R. I. O. CLL. & forum, UK. CLL., 2018, In : Haematologica. 103, 7, p. 1209-1217 9 p.

Research output: Contribution to journalArticle

Leukoencephalopathies
Brain Stem
Spinal Cord
Phenotype
Mitochondrial Diseases
7 Citations (Scopus)
Leukoencephalopathies
Brain Stem
Spinal Cord
Phenotype
Mitochondrial Diseases
2017
3 Citations (Scopus)

A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-Lom

Piscosquito, G., Magri, S., Saveri, P., Milani, M., Ciano, C., Farina, L., Taroni, F. & Pareyson, D., Mar 1 2017, In : Journal of the Peripheral Nervous System. 22, 1, p. 47-50 4 p.

Research output: Contribution to journalArticle

Hereditary Sensory and Motor Neuropathy
Roma
Mutation
Genes
Medulla Oblongata
2016

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings

Sagnelli, A., Magri, S., Farina, L., Chiapparini, L., Marotta, G., Tonduti, D., Consonni, M., Scigliuolo, G., Benti, R., Pareyson, D., Taroni, F., Salsano, E. & Di Bella, D., Mar 1 2016, In : Journal of Neurology. 263, 3, p. 591-593 3 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings

Sagnelli, A., Magri, S., Farina, L., Chiapparini, L., Marotta, G., Tonduti, D., Consonni, M., Scigliuolo, G. M., Benti, R., Pareyson, D., Taroni, F., Salsano, E. & Di Bella, D., Mar 1 2016, In : Journal of Neurology. 263, 3, p. 591-593 3 p.

Research output: Contribution to journalArticle

14 Citations (Scopus)

Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes

Torraco, A., Ardissone, A., Invernizzi, F., Rizza, T., Fiermonte, G., Niceta, M., Zanetti, N., Martinelli, D., Vozza, A., Verrigni, D., Di Nottia, M., Lamantea, E., Diodato, D., Tartaglia, M., Dionisi-Vici, C., Moroni, I., Farina, L., Bertini, E., Ghezzi, D. & Carrozzo, R., Oct 26 2016, (Accepted/In press) In : Journal of Neurology. p. 1-10 10 p.

Research output: Contribution to journalArticle

Phenotype
Mutation
Glycine Decarboxylase Complex H-Protein
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Ketoglutarate Dehydrogenase Complex
1 Citation (Scopus)
Alexander Disease
Mutation
Cerebrum
Phenotype
2015
20 Citations (Scopus)

A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders

Ardissone, A., Piscosquito, G., Legati, A., Langella, T., Lamantea, E., Garavaglia, B., Salsano, E., Farina, L., Moroni, I., Pareyson, D. & Ghezzi, D., May 26 2015, In : Neurology. 84, 21, p. 2193-2195 3 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
Leukoencephalopathies
Mitochondrial Diseases
Penetrance
Mitochondrial Encephalomyopathies
Mutation
21 Citations (Scopus)
Cerebral Amyloid Angiopathy
Amyloid
Autoantibodies
Cerebrospinal Fluid
Alzheimer Disease
6 Citations (Scopus)

Simultaneous overexpression of functional human HO-1, E5NT and ENTPD1 protects murine fibroblasts against TNF-α-induced injury in vitro

Cinti, A., De Giorgi, M., Chisci, E., Arena, C., Galimberti, G., Farina, L., Bugarin, C., Rivolta, I., Gaipa, G., Smolenski, R. T., Cerrito, M. G., Lavitrano, M. & Giovannoni, R., Oct 29 2015, In : PLoS One. 10, 10, e0141933.

Research output: Contribution to journalArticle

Fibroblasts
tumor necrosis factor-alpha
fibroblasts
Tumor Necrosis Factor-alpha
Genes
2014
5 Citations (Scopus)

Adult Polyglucosan Body Disease: Clinical and histological heterogeneity of a large Italian family

Colombo, I., Pagliarani, S., Testolin, S., Salsano, E., Napoli, L. M., Bordoni, A., Salani, S., D'Adda, E., Morandi, L., Farina, L., Magri, F., Riva, M., Prelle, A., Sciacco, M., Comi, G. P. & Moggio, M., Sep 15 2014, In : Neuromuscular Disorders. 25, 5, p. 423-428 6 p.

Research output: Contribution to journalArticle

Polyneuropathies
Spine
Biopsy
Leukoencephalopathies
Muscles
7 Citations (Scopus)

Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease

Sagnelli, A., Savoiardo, M., Marchesi, C., Morandi, L., Mora, M., Morbin, M., Farina, L., Mazzeo, A., Toscano, A., Pagliarani, S., Lucchiari, S., Comi, G. P., Salsano, E. & Pareyson, D., Mar 2014, In : Neuromuscular Disorders. 24, 3, p. 272-276 5 p.

Research output: Contribution to journalArticle

Fabry Disease
1,4-alpha-Glucan Branching Enzyme
Galactosidases
Mutation
Genes
12 Citations (Scopus)

A new mutation in gjc2 associated with subclinical leukodystrophy

Abrams, C. K., Flores-Obando, R., Scherer, S. S., Wong, S., Freidin, M. M., Lamantea, E., Farina, L., Scaioli, V., Pareyson, D. & Salsano, E., 2014, In : Journal of Neurology. 261, 1, p. 1929-1938 10 p.

Research output: Contribution to journalArticle

Mutation
Oligodendroglia
Phenotype
Hereditary Spastic Paraplegia
Gap Junctions
9 Citations (Scopus)

Brain fluorodeoxyglucose PET in adrenoleukodystrophy

Salsano, E., Marotta, G., Manfredi, V., Giovagnoli, A. R., Farina, L., Savoiardo, M., Pareyson, D., Benti, R. & Uziel, G., Sep 1 2014, In : Neurology. 83, 11, p. 981-989 9 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Brain
Glucose
Millon Clinical Multiaxial Inventory
Compulsive Personality Disorder
27 Citations (Scopus)

Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations

Invernizzi, F., Ardissone, A., Lamantea, E., Garavaglia, B., Zeviani, M., Farina, L., Ghezzi, D. & Moroni, I., 2014, In : Frontiers in Genetics. 5, NOV, 412.

Research output: Contribution to journalArticle

Leukoencephalopathies
Lactic Acidosis
Pyruvate Dehydrogenase Complex Deficiency Disease
Pyruvate Dehydrogenase Complex
Mitochondrial Diseases
21 Citations (Scopus)

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

Di Bella, D., Pareyson, D., Savoiardo, M., Farina, L., Ciano, C., Caldarazzo, S., Sagnelli, A., Bonato, S., Nava, S., Bresolin, N., Tedeschi, G., Taroni, F. & Salsano, E., Sep 1 2014, In : Neurology. 83, 13, p. 1217-1218 2 p.

Research output: Contribution to journalArticle

33 Citations (Scopus)
Substantia Nigra
Parkinson Disease
Anisotropy
Diffusion Tensor Imaging
Disease Progression
2013
11 Citations (Scopus)

Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant

Melchionda, L., Fang, M., Wang, H., Fugnanesi, V., Morbin, M., Liu, X., Li, W., Ceccherini, I., Farina, L., Savoiardo, M., D'Adamo, P., Zhang, J., Costa, A., Ravaglia, S., Ghezzi, D. & Zeviani, M., 2013, In : Orphanet Journal of Rare Diseases. 8, 1, 66.

Research output: Contribution to journalArticle

Alexander Disease
Exome
Siblings
Motor Neuron Disease
Mutation
4 Citations (Scopus)

Adult-onset leukodystrophies from respiratory chain disorders: Do they exist?

Salsano, E., Farina, L., Lamperti, C., Piscosquito, G., Salerno, F., Morandi, L., Carrara, F., Lamantea, E., Zeviani, M., Uziel, G., Savoiardo, M. & Pareyson, D., Jun 2013, In : Journal of Neurology. 260, 6, p. 1617-1623 7 p.

Research output: Contribution to journalArticle

Electron Transport
Mitochondrial Diseases
Differential Diagnosis
Ataxia
Basal Ganglia
9 Citations (Scopus)

An autoinflammatory neurological disease due to interleukin 6 hypersecretion

Salsano, E., Rizzo, A., Bedini, G., Bernard, L., Dallolio, V., Volorio, S., Lazzaroni, M., Ceccherini, I., Lazarevic, D., Cittaro, D., Stupka, E., Paterra, R., Farina, L., Savoiardo, M., Pareyson, D. & Sciacca, F. L., Feb 21 2013, (Accepted/In press) In : Journal of Neuroinflammation. p. 29 1 p.

Research output: Contribution to journalArticle

Interleukin-6
Mutation
Interleukin-1
Hearing Loss
Meningitis
2012
14 Citations (Scopus)
Brain Neoplasms
Tomography
Neuroimaging
Magnetic Resonance Imaging
Diffusion Tensor Imaging
1 Citation (Scopus)

Effectiveness of valproate for the treatment of manic-like behavior in X-linked adrenoleukodystrophy

Salsano, E., Gambini, O., Giovagnoli, A. R., Farina, L., Uziel, G. & Pareyson, D., Oct 2012, In : Neurological Sciences. 33, 5, p. 1197-1199 3 p.

Research output: Contribution to journalArticle

16 Citations (Scopus)

Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease

Saredi, S., Ardissone, A., Ruggieri, A., Mottarelli, E., Farina, L., Rinaldi, R., Silvestri, E., Gandioli, C., D'Arrigo, S., Salerno, F., Morandi, L., Grammatico, P., Pantaleoni, C., Moroni, I. & Mora, M., Jul 15 2012, In : Journal of the Neurological Sciences. 318, 1-2, p. 45-50 6 p.

Research output: Contribution to journalArticle

Walker-Warburg Syndrome
Point Mutation
Dystroglycans
Glycosylation
Exons
2010
5 Citations (Scopus)

Childhood-onset HAM/TSP with progressive cognitive impairment

Zorzi, G., Mancuso, R., Nardocci, N., Farina, L., Guerini, F. R. & Ferrante, P., Apr 2010, In : Neurological Sciences. 31, 2, p. 209-212 4 p.

Research output: Contribution to journalArticle

HTLV-I Infections
Tropical Spastic Paraparesis
Paraparesis
Human T-lymphotropic virus 1
Spinal Cord Diseases
17 Citations (Scopus)

Congenital muscular dystrophies with cognitive impairment: A population study

Messina, S., Bruno, C., Moroni, I., Pegoraro, E., D'Amico, A., Biancheri, R., Berardinelli, A., Boffi, P., Cassandrini, D., Farina, L., Minetti, C., Moggio, M., Mongini, T., Mottarelli, E., Pane, M., Pantaleoni, C., Pichiecchio, A., Pini, A., Ricci, E., Saredi, S. & 10 others, Sframeli, M., Tortorella, G., Toscano, A., Trevisan, C. P., Uggetti, C., Vasco, G., Comi, G. P., Santorelli, F. M., Bertini, E. & Mercuri, E., Sep 7 2010, In : Neurology. 75, 10, p. 898-903 6 p.

Research output: Contribution to journalArticle

Muscular Dystrophies
Laminin
Population
Muscles
Biopsy
2 Citations (Scopus)

Sagging and swelling of the midbrain suggest spontaneous intracranial hypotension rather than a malformation

Savoiardo, M., Farina, L. & Chiapparini, L., Aug 2010, In : Brain. 133, 8

Research output: Contribution to journalArticle

2009
7 Citations (Scopus)

Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement

Saredi, S., Ruggieri, A., Mottarelli, E., Ardissone, A., Zanotti, S., Farina, L., Morandi, L., Mora, M. & Moroni, I., Jun 2009, In : Muscle and Nerve. 39, 6, p. 845-848 4 p.

Research output: Contribution to journalArticle

Walker-Warburg Syndrome
Dystroglycans
Muscular Dystrophies
Central Nervous System
Mutation
56 Citations (Scopus)

Identification of novel mutations in five patients with mitochondrial encephalomyopathy

Valente, L., Piga, D., Lamantea, E., Carrara, F., Uziel, G., Cudia, P., Zani, A., Farina, L., Morandi, L., Mora, M., Spinazzola, A., Zeviani, M. & Tiranti, V., May 2009, In : Biochimica et Biophysica Acta - Bioenergetics. 1787, 5, p. 491-501 11 p.

Research output: Contribution to journalArticle

Mitochondrial Encephalomyopathies
Mitochondrial DNA
Mutation
Mitochondrial Diseases
Genes
2008
105 Citations (Scopus)

Adult-onset Alexander disease: A series of eleven unrelated cases with review of the literature

Pareyson, D., Fancellu, R., Mariotti, C., Romano, S., Salmaggi, A., Carella, F., Girotti, F., Gattellaro, G., Carriero, M. R., Farina, L., Ceccherini, I. & Savoiardo, M., Sep 2008, In : Brain. 131, 9, p. 2321-2331 11 p.

Research output: Contribution to journalArticle

Alexander Disease
Glial Fibrillary Acidic Protein
Cerebellar Ataxia
Myoclonus
Missense Mutation
68 Citations (Scopus)

Can MR imaging diagnose adult-onset Alexander disease?

Farina, L., Pareyson, D., Minati, L., Ceccherini, I., Chiapparini, L., Romano, S., Gambaro, P., Fancellu, R. & Savoiardo, M., Jun 2008, In : American Journal of Neuroradiology. 29, 6, p. 1190-1196 7 p.

Research output: Contribution to journalArticle

Alexander Disease
Glial Fibrillary Acidic Protein
Genes
Medulla Oblongata
Inositol
27 Citations (Scopus)

Classification of childhood white matter disorders using proton MR spectroscopic imaging

Bizzi, A., Castelli, G., Bugiani, M., Barker, P. B., Herskovits, E. H., Danesi, U., Erbetta, A., Moroni, I., Farina, L. & Uziel, G., Aug 2008, In : American Journal of Neuroradiology. 29, 7, p. 1270-1275 6 p.

Research output: Contribution to journalArticle

Creatine
Protons
Leukoencephalopathies
Discriminant Analysis
Choline
46 Citations (Scopus)

Haemato-oncology and burnout: An Italian survey

Bressi, C., Manenti, S., Porcellana, M., Cevales, D., Farina, L., Felicioni, I., Meloni, G., Milone, G., Miccolis, I. R., Pavanetto, M., Pescador, L., Poddigue, M., Scotti, L., Zambon, A., Corrao, G., Lambertenghi-Deliliers, G. & Invernizzi, G., Mar 25 2008, In : British Journal of Cancer. 98, 6, p. 1046-1052 7 p.

Research output: Contribution to journalArticle

Psychiatry
Logistic Models
Nurses
Depersonalization
Delivery of Health Care
30 Citations (Scopus)

POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study

Messina, S., Mora, M., Pegoraro, E., Pini, A., Mongini, T., D'Amico, A., Pane, M., Aiello, C., Bruno, C., Biancheri, R., Berardinelli, A., Boito, C., Farina, L., Morandi, L., Moroni, I., Pezzani, R., Pichiecchio, A., Ricci, E., Ruggieri, A., Saredi, S. & 9 others, Scuderi, C., Tessa, A., Toscano, A., Tortorella, G., Trevisan, C. P., Uggetti, C., Santorelli, F. M., Bertini, E. & Mercuri, E., Jul 2008, In : Neuromuscular Disorders. 18, 7, p. 565-571 7 p.

Research output: Contribution to journalArticle

Muscular Dystrophies
Mutation
Phenotype
Walker-Warburg Syndrome
Dystroglycans
30 Citations (Scopus)

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome

Rossi, G., Marelli, C., Farina, L., Laurà, M., Basile, A. M., Ciano, C., Tagliavini, F. & Pareyson, D., Apr 30 2008, In : Movement Disorders. 23, 6, p. 893-896 4 p.

Research output: Contribution to journalArticle

Microtubule-Associated Proteins
Frontotemporal Dementia
Mutation
Genes
Pyramidal Tracts
2007
96 Citations (Scopus)

Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy

Fernandez-Vizarra, E., Bugiani, M., Goffrini, P., Carrara, F., Farina, L., Procopio, E., Donati, A., Uziel, G., Ferrero, I. & Zeviani, M., May 2007, In : Human Molecular Genetics. 16, 10, p. 1241-1252 12 p.

Research output: Contribution to journalArticle

Electron Transport Complex III
Mutation
Genes
Lactic Acidosis
Mitochondrial Proteins
38 Citations (Scopus)

Non-accidental brain trauma in infants: diffusion imaging, contributions to understanding the injury process

Zimmerman, R. A., Bilaniuk, L. T. & Farina, L., May 2007, In : Journal of Neuroradiology. 34, 2, p. 109-114 6 p.

Research output: Contribution to journalArticle

Diffuse Axonal Injury
Diffusion Magnetic Resonance Imaging
Contusions
Wounds and Injuries
Infarction
78 Citations (Scopus)

Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy

Malfatti, E., Bugiani, M., Invernizzi, F., De Souza, C. F. M., Farina, L., Carrara, F., Lamantea, E., Antozzi, C., Confalonieri, P., Sanseverino, M. T., Giugliani, R., Uziel, G. & Zeviani, M., Jul 2007, In : Brain. 130, 7, p. 1894-1904 11 p.

Research output: Contribution to journalArticle

Mutation
Genes
Mitochondrial DNA
MELAS Syndrome
Leigh Disease
63 Citations (Scopus)

Spontaneous intracranial hypotension with deep brain swelling

Savoiardo, M., Minati, L., Farina, L., De Simone, T., Aquino, D., Mea, E., Filippini, G., Bussone, G. & Chiapparini, L., Jul 2007, In : Brain. 130, 7, p. 1884-1893 10 p.

Research output: Contribution to journalArticle

Intracranial Hypotension
Cerebral Veins
Brain Edema
Brain
Coma
2005
8 Citations (Scopus)

Familial frontotemporal dementia associated with the novel MAPT mutation T427M [4]

Giaccone, G., Rossi, G., Farina, L., Marcon, G., Di Fede, G., Catania, M., Morbin, M., Sacco, L., Bugiani, O. & Tagliavini, F., Dec 2005, In : Journal of Neurology. 252, 12, p. 1543-1545 3 p.

Research output: Contribution to journalArticle

44 Citations (Scopus)

Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency.

Bugiani, M., Tiranti, V., Farina, L., Uziel, G. & Zeviani, M., May 2005, In : Journal of Medical Genetics. 42, 5

Research output: Contribution to journalArticle

Cytochrome-c Oxidase Deficiency
Leigh Disease
Oxidoreductases
Mutation
Heme
27 Citations (Scopus)

Wallerian degeneration of the pontocerebellar fibers

De Simone, T., Regna-Gladin, C., Carriero, M. R., Farina, L. & Savoiardo, M., 2005, In : American Journal of Neuroradiology. 26, 5, p. 1062-1065 4 p.

Research output: Contribution to journalArticle

Wallerian Degeneration
Anatomy
White Matter
2004
42 Citations (Scopus)

Acute diffusion abnormalities in the hippocampus of children with new-onset seizures: The development of mesial temporal sclerosis

Farina, L., Bergqvist, C., Zimmerman, R. A., Haselgrove, J., Hunter, J. V. & Bilaniuk, L. T., Apr 2004, In : Neuroradiology. 46, 4, p. 251-257 7 p.

Research output: Contribution to journalArticle

Sclerosis
Hippocampus
Seizures
Head
Atrophy
182 Citations (Scopus)

Clinical and molecular findings in children with complex I deficiency

Bugiani, M., Invernizzi, F., Alberio, S., Briem, E., Lamantea, E., Carrara, F., Moroni, I., Farina, L., Spada, M., Donati, M. A., Uziel, G. & Zeviani, M., Dec 6 2004, In : Biochimica et Biophysica Acta - Bioenergetics. 1659, 2-3, p. 136-147 12 p.

Research output: Contribution to journalArticle

Mitochondrial DNA
Genes
Leigh Disease
Leukoencephalopathies
Mutation
89 Citations (Scopus)

Operative findings and outcomes of microvascular decompression for trigeminal neuralgia in 35 patients affected by multiple sclerosis

Broggi, G., Ferroli, P., Franzini, A., Nazzi, V., Farina, L., La Mantia, L., Milanese, C., Ciric, I. S., Jannetta, P. J., Casey, K. F., Rhoton, A. L., Morgan, C. J. & Tew, J. M., Oct 2004, In : Neurosurgery. 55, 4, p. 830-839 10 p.

Research output: Contribution to journalArticle

Microvascular Decompression Surgery
Trigeminal Neuralgia
Multiple Sclerosis
Magnetic Resonance Imaging
Blood Vessels