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Research Output 1990 2019

  • 2656 Citations
  • 30 h-Index
  • 87 Article
  • 2 Chapter
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
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
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
6 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

Alterazioni del polo temporale in 16 casi di epilessia temporale farmaco resistente

Translated title of the contribution: Temporal lobe changes in 16 cases of drug-resistant temporal lobe epilepsyD'Incerti, L., Farina, L., Maccagnano, C. & Villani, F., 2001, In : Rivista di Neuroradiologia. 14, SUPPL. 3, p. 77-80 4 p.

Research output: Contribution to journalArticle

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
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
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
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

45 Citations (Scopus)

Ataxia-telangiectasia: Mr and ct findings

Farina, L., Uggetti, C., Ottolini, A., Martelli, A., Bergamaschi, R., Sibilla, L., Zappoli, F., Egitto, M. G. & Lanzi, G., 1994, In : Journal of Computer Assisted Tomography. 18, 5, p. 724-727 4 p.

Research output: Contribution to journalArticle

Ataxia Telangiectasia
Cisterna Magna
Chromosomes, Human, Pair 14
Cerebellar Ataxia
Chromosomal Instability
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
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
28 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
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
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
47 Citations (Scopus)

Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduria

Moroni, I., D'Incerti, L., Farina, L., Rimoldi, M. & Uziel, G., 2000, In : Neurological Sciences. 21, 2, p. 103-108 6 p.

Research output: Contribution to journalArticle

Magnetic Resonance Imaging
Cerebellar Diseases
Inborn Errors Metabolism
Vascular Dementia
Prenatal Diagnosis
184 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
18 Citations (Scopus)

Clinical correlations in 16 patients with total or partial laminin α2 deficiency characterized using antibodies against 2 fragments of the protein

Morandi, L., Di Blasi, C., Farina, L., Sorokin, L., Uzlcl, G., Azan, G., Pini, A., Toscfliio, A., Lanfossi, A., Galbiaü, S., Cornelio, F. & Mora, M., Feb 1999, In : Archives of Neurology. 56, 2, p. 209-215 7 p.

Research output: Contribution to journalArticle

Laminin
Antibodies
Proteins
Phenotype
Biopsy
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
24 Citations (Scopus)

Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients

Farina, L., Morandi, L., Milanesi, I., Ciceri, E., Mora, M., Moroni, I., Pantaleoni, C. & Savoiardo, M., 1998, In : Neuroradiology. 40, 12, p. 807-811 5 p.

Research output: Contribution to journalArticle

Muscular Dystrophies
Laminin
Signs and Symptoms
Central Nervous System
White Matter
14 Citations (Scopus)
Brain Neoplasms
Tomography
Neuroimaging
Magnetic Resonance Imaging
Diffusion Tensor Imaging
7 Citations (Scopus)

Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease [1]

Selleri, S., Torchiana, E., Pareyson, D., Lulli, L., Bertagnolio, B., Savoiardo, M., Farina, L., Carrara, F., Filocamo, M., Gatti, R., Sghirlanzoni, A., Uziel, G. & Finocchiaro, G., 2000, In : Journal of Neurology. 247, 11, p. 875-877 3 p.

Research output: Contribution to journalArticle

90 Citations (Scopus)

Diagnostic imaging in 13 cases of Rasmussen's encephalitis: Can early MRI suggest the diagnosis?

Chiapparini, L., Granata, T., Farina, L., Ciceri, E., Erbetta, A., Ragona, F., Freri, E., Fusco, L., Gobbi, G., Capovilla, G., Tassi, L., Giordano, L., Viri, M., Dalla Bernardina, B., Spreafico, R. & Savoiardo, M., Mar 1 2003, In : Neuroradiology. 45, 3, p. 171-183 13 p.

Research output: Contribution to journalArticle

Encephalitis
Diagnostic Imaging
Atrophy
Single-Photon Emission-Computed Tomography
Positron-Emission Tomography

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

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

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

1 Citation (Scopus)

Encefalomiopatie mitocondriali in età pediatrica: Incidenza dell'accumulo di acido lattico documentato con immagini di spettroscopia rm del protone

Translated title of the contribution: Mitochondrial encephalomyopathy in childhood: Incidence of lactic acid accumulation documented with proton MR spectroscopic imagingBizzi, A., Danesi, U., Moroni, I., Castelli, M., Bugiani, M., Erbetta, A., Farina, L., Uziel, G. & Savoiardo, M., 2001, In : Rivista di Neuroradiologia. 14, SUPPL. 3, p. 149-152 4 p.

Research output: Contribution to journalArticle

129 Citations (Scopus)

Epileptic phenotypes associated with mitochondrial disorders

Canafoglia, L., Franceschetti, S., Antozzi, C., Carrara, F., Farina, L., Granata, T., Lamantea, E., Savoiardo, M., Uziel, G., Villani, F., Zeviani, M. & Avanzini, G., May 22 2001, In : Neurology. 56, 10, p. 1340-1346 7 p.

Research output: Contribution to journalArticle

Mitochondrial Diseases
Phenotype
Electroencephalography
MERRF Syndrome
Seizures
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

126 Citations (Scopus)

Familial schizencephaly associated with EMX2 mutation

Granata, T., Farina, L., Faiella, A., Cardini, R., D'Incerti, L., Boncinelli, E. & Battaglia, G., May 1997, In : Neurology. 48, 5, p. 1403-1406 4 p.

Research output: Contribution to journalArticle

Homeobox Genes
Mutation
Brain
Neurologic Manifestations
Point Mutation
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
19 Citations (Scopus)

Ganglioneuroblastoma of the spinal cord

Sibilla, L., Martelli, A., Farina, L., Uggetti, C., Zappoli, F., Sessa, F., Rodriguez y Baena, R. & Gaeltani, P., 1995, In : American Journal of Neuroradiology. 16, SUPPL., p. 875-877 3 p.

Research output: Contribution to journalArticle

Ganglioneuroblastoma
Spinal Cord
Neoplasms
47 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
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
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
54 Citations (Scopus)

Infantile neuroaxonal dystrophy: Neuroradiological studies in 11 patients

Farina, L., Nardocci, N., Bruzzone, M. G., D'Incerti, L., Zorzi, G., Verga, L., Morbin, M. & Savoiardo, M., May 1999, In : Neuroradiology. 41, 5, p. 376-380 5 p.

Research output: Contribution to journalArticle

Neuroaxonal Dystrophies
Pantothenate Kinase-Associated Neurodegeneration
Globus Pallidus
Optic Chiasm
Cerebellar Nuclei
79 Citations (Scopus)

Infantile neuroaxonal dystrophy: Clinical spectrum and diagnostic criteria

Nardocci, N., Zorzi, G., Farina, L., Binelli, S., Scaioli, W., Ciano, C., Verga, L., Angelini, L., Savoiardo, M. & Bugiani, O., Apr 22 1999, In : Neurology. 52, 7, p. 1472-1478 7 p.

Research output: Contribution to journalArticle

Neuroaxonal Dystrophies
Cerebellar Cortex
Visual Evoked Potentials
Denervation
Substantia Nigra
7 Citations (Scopus)

KARS-related diseases: Progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature

Ardissone, A., Tonduti, D., Legati, A., Lamantea, E., Barone, R., Dorboz, I., Boespflug-Tanguy, O., Nebbia, G., Maggioni, M., Garavaglia, B., Moroni, I., Farina, L., Pichiecchio, A., Orcesi, S., Chiapparini, L. & Ghezzi, D., Apr 4 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 45.

Research output: Contribution to journalArticle

Leukoencephalopathies
Brain Stem
Spinal Cord
Phenotype
Mitochondrial Diseases

KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature

Ardissone, A., Tonduti, D., Legati, A., Lamantea, E., Barone, R., Dorboz, I., Boespflug-Tanguy, O., Nebbia, G., Maggioni, M., Garavaglia, B., Moroni, I., Farina, L., Pichiecchio, A., Orcesi, S., Chiapparini, L. & Ghezzi, D., Apr 4 2018, In : Orphanet Journal of Rare Diseases. 13, 1, p. 45

Research output: Contribution to journalArticle

Leukoencephalopathies
Brain Stem
Spinal Cord
Phenotype
Mitochondrial Diseases
54 Citations (Scopus)

L-2-Hydroxyglutaric aciduria: MRI in seven cases

D'Incerti, L., Farina, L., Moroni, I., Uziel, G. & Savoiardo, M., 1998, In : Neuroradiology. 40, 11, p. 727-733 7 p.

Research output: Contribution to journalArticle

Basal Ganglia
Cerebellar Nuclei
Atrophy
2-Hydroxyglutaricaciduria

LA TOMOGRAFIA COMPUTERIZZATA NELLO STUDIO DELLE MALATTIE NEUROMUSCOLARI. PARTE I

Translated title of the contribution: Computer-assisted tomography in the study of neuromuscular diseases. Part IOttolini, A., Gozzoli, L., Farina, L., Martelli, A., Valenti, A., Uggetti, C. & Lanzi, G., 1990, Rivista di Neuroradiologia. 2 ed. Vol. 3. p. 215-221 7 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

3 Citations (Scopus)

Le acidure organiche. Le ceroidolipofuscinosi

Translated title of the contribution: Organic acidurias. CeroidolipofuscinosisD'Incerti, L., Farina, L., Moroni, I., Uziel, G. & Savoiardo, M., 1996, In : Rivista di Neuroradiologia. 9, 6, p. 769-774 6 p.

Research output: Contribution to journalArticle

Brain Diseases
Chronic Brain Damage
Urine
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Muscle Hypotonia
1 Citation (Scopus)

Le encefalomiopatie mitocondriali in eta pediatrica

Translated title of the contribution: Mitochondrial encephalomyopathies in childhoodFarina, L., Moroni, I., Ciceri, E., Uziel, G. & Savoiardo, M., 1999, In : Rivista di Neuroradiologia. 12, 1, p. 113-117 5 p.

Research output: Contribution to journalArticle

Letter to the editor

Savoiardo, M. & Farina, L., Jul 2003, In : Journal of Computer Assisted Tomography. 27, 4, p. 552 1 p.

Research output: Contribution to journalArticle