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L. Farina · SciRah

Researcher profile · Semantic Scholar

L. Farina

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L. Farina — researcher profile on SciRah

h-index: 36
Works: 95
Citations: 3,923

Most-cited papers

Clinical and molecular findings in children with complex I deficiency.
M. Bugiani, F. Invernizzi, Simona Alberio, Egill Briem +8 more
2004Biochimica et Biophysica Acta276 citations Open access
Semantic Scholar
Tetracyclines affect prion infectivity
G. Forloni, S. Iussich, T. Awan, L. Colombo +14 more
2002Proceedings of the National Academy of Sciences of the United States of America204 citations Open access
Semantic Scholar
Operative Findings and Outcomes of Microvascular Decompression for Trigeminal Neuralgia in 35 Patients Affected by Multiple Sclerosis
G. Broggi, P. Ferroli, A. Franzini, V. Nazzi +3 more
2004Neurosurgery182 citations
Semantic Scholar
Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy.
E. Fernández-Vizarra, M. Bugiani, P. Goffrini, F. Carrara +6 more
2007Human Molecular Genetics173 citations
Semantic Scholar
Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy.
E. Malfatti, M. Bugiani, F. Invernizzi, C. F. D. de Souza +9 more
2007Brain : a journal of neurology168 citations
Semantic Scholar
Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.
D. Pareyson, R. Fancellu, C. Mariotti, S. Romano +8 more
2008Brain : a journal of neurology164 citations
Semantic Scholar
Epileptic phenotypes associated with mitochondrial disorders
L. Canafoglia, S. Franceschetti, C. Antozzi, F. Carrara +8 more
2001Neurology157 citations
Semantic Scholar
Familial schizencephaly associated with EMX2 mutation
T. Granata, L. Farina, A. Faiella, R. Cardini +3 more
1997Neurology150 citations
Semantic Scholar
Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?
L. Chiapparini, T. Granata, L. Farina, E. Ciceri +12 more
2003Neuroradiology136 citations
Semantic Scholar
Spinal radiological findings in nine patients with spontaneous intracranial hypotension
L. Chiapparini, L. Farina, L. D'Incerti, A. Erbetta +3 more
2002Neuroradiology132 citations
Semantic Scholar
Spontaneous intracranial hypotension with deep brain swelling.
M. Savoiardo, L. Minati, L. Farina, T. De Simone +5 more
2007Brain : a journal of neurology112 citations Open access
Semantic Scholar
MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.
L. Farina, L. Chiapparini, G. Uziel, M. Bugiani +2 more
2002AJNR. American journal of neuroradiology108 citations
Semantic Scholar
Can MR Imaging Diagnose Adult-Onset Alexander Disease?
L. Farina, D. Pareyson, L. Minati, I. Ceccherini +5 more
2008American Journal of Neuroradiology104 citations Open access
Semantic Scholar
Identification of novel mutations in five patients with mitochondrial encephalomyopathy.
L. Valente, D. Piga, E. Lamantea, F. Carrara +9 more
2009Biochimica et Biophysica Acta97 citations Open access
Semantic Scholar
MR imaging and proton MR spectroscopy in adult Krabbe disease.
L. Farina, A. Bizzi, G. Finocchiaro, D. Pareyson +6 more
2000AJNR. American journal of neuroradiology82 citations
Semantic Scholar
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
M. Bugiani, V. Tiranti, L. Farina, G. Uziel +1 more
2005Journal of Medical Genetics79 citations Open access
Semantic Scholar
Periventricular Nodular Heterotopia: Epileptogenic Findings
Giorgio Battaglia, T. Granata, L. Farina, L. D'Incerti +2 more
1997Epilepsia76 citations Open access
Semantic Scholar
Positive response to immunomodulatory therapy in an adult patient with Rasmussen’s encephalitis
F. Villani, R. Spreafico, L. Farina, A. Giovagnoli +3 more
2001Neurology71 citations
Semantic Scholar
Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients
L. Farina, N. Nardocci, M. Bruzzone, L. D'Incerti +4 more
1999Neuroradiology63 citations
Semantic Scholar
Non-accidental brain trauma in infants: diffusion imaging, contributions to understanding the injury process.
Robert A. Zimmerman, L. Bilaniuk, L. Farina
2007Journal of neuroradiology. Journal de neuroradiologie62 citations
Semantic Scholar
L-2-Hydroxyglutaric aciduria: MRI in seven cases
L. D'Incerti, L. Farina, I. Moroni, Graziella Uziel +1 more
1998Neuroradiology60 citations
Semantic Scholar
Substantia nigra in Parkinson’s disease: a multimodal MRI comparison between early and advanced stages of the disease
D. Aquino, V. Contarino, A. Albanese, L. Minati +5 more
2014Neurological Sciences59 citations
Semantic Scholar
Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities.
M. Mora, I. Moroni, G. Uziel, C. Di Blasi +3 more
1996Neuromuscular Disorders56 citations
Semantic Scholar
A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders
A. Ardissone, G. Piscosquito, A. Legati, T. Langella +7 more
2015Neurology54 citations Open access
Semantic Scholar
Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduria
I. Moroni, L. D'Incerti, L. Farina, M. Rimoldi +1 more
2000Neurological Sciences54 citations
Semantic Scholar
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations
F. Invernizzi, A. Ardissone, E. Lamantea, B. Garavaglia +4 more
2014Frontiers in Genetics53 citations Open access
Semantic Scholar
Ataxia‐Telangiectasia: MR and CT Findings
L. Farina, C. Uggetti, A. Ottolini, A. Martelli +5 more
1994Journal of computer assisted tomography52 citations
Semantic Scholar
Classification of Childhood White Matter Disorders Using Proton MR Spectroscopic Imaging
A. Bizzi, G. Castelli, M. Bugiani, P. Barker +6 more
2008American Journal of Neuroradiology50 citations Open access
Semantic Scholar
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome
G. Rossi, C. Marelli, L. Farina, M. Laurá +4 more
2008Movement Disorders49 citations
Semantic Scholar
Acute diffusion abnormalities in the hippocampus of children with new-onset seizures: the development of mesial temporal sclerosis
L. Farina, C. Bergqvist, R. Zimmerman, J. Haselgrove +2 more
2004Neuroradiology49 citations
Semantic Scholar
Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes
A. Torraco, A. Ardissone, F. Invernizzi, T. Rizza +16 more
2016Journal of Neurology47 citations
Semantic Scholar
Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation
D. Di Bella, D. Pareyson, M. Savoiardo, L. Farina +9 more
2014Neurology45 citations Open access
Semantic Scholar
Prodromal Alzheimer's Disease Presenting as Cerebral Amyloid Angiopathy-Related Inflammation with Spontaneous Amyloid-Related Imaging Abnormalities and High Cerebrospinal Fluid Anti-Aβ Autoantibodies
G. Boncoraglio, F. Piazza, M. Savoiardo, L. Farina +5 more
2015Journal of Alzheimer's Disease44 citations
Semantic Scholar
Wallerian degeneration of the pontocerebellar fibers.
T. De Simone, C. Regna-Gladin, M. Carriero, L. Farina +1 more
2005AJNR. American journal of neuroradiology43 citations
Semantic Scholar
KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature
A. Ardissone, D. Tonduti, A. Legati, E. Lamantea +12 more
2018Orphanet Journal of Rare Diseases41 citations Open access
Semantic Scholar
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study.
S. Messina, M. Mora, E. Pegoraro, A. Pini +25 more
2008Neuromuscular Disorders39 citations
Semantic Scholar
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients
L. Farina, L. Morandi, I. Milanesi, E. Ciceri +4 more
1998Neuroradiology34 citations
Semantic Scholar
Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant
L. Melchionda, M. Fang, Hairong Wang, V. Fugnanesi +12 more
2013Orphanet Journal of Rare Diseases29 citations Open access
Semantic Scholar
Ganglioneuroblastoma of the spinal cord.
L. Sibilla, A. Martelli, L. Farina, C. Uggetti +4 more
1995AJNR. American journal of neuroradiology29 citations
Semantic Scholar
Partial laminin α2 chain deficiency in a patient with myopathy resembling inclusion body myositis
C. Di Blasi, M. Mora, D. Pareyson, L. Farina +6 more
200027 citations
Semantic Scholar
MRI in Leigh syndrome with SURF1 gene mutation
M. Savoiardo, M. Zeviani, G. Uziel, L. Farina
2002Annals of Neurology24 citations
Semantic Scholar
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease
S. Saredi, A. Ardissone, A. Ruggieri, E. Mottarelli +11 more
2012Journal of Neurological Sciences22 citations Open access
Semantic Scholar
Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the protein.
L. Morandi, C. Di Blasi, L. Farina, L. Sorokin +8 more
1999Archives of Neurology22 citations Open access
Semantic Scholar
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance
A. Ardissone, F. Invernizzi, A. Nasca, I. Moroni +2 more
2015Molecular Genetics and Metabolism Reports21 citations Open access
Semantic Scholar
Hypomyelinating leukodystrophies in adults: Clinical and genetic features
D. Di Bella, S. Magri, C. Benzoni, L. Farina +12 more
2020European Journal of Neurology20 citations
Semantic Scholar
A New Mutation in Gjc2 Associated with Subclinical Leukodystrophy
C. Abrams, S. Scherer, Rafael E. Flores-Obando, M. Freidin +6 more
2014Journal of Neurology20 citations Open access
Semantic Scholar
The effects of wallerian degeneration of the optic radiations demonstrated by MRI
M. Savoiardo, Davide Pareyson, M. Grisoli, M. Forester +2 more
2004Neuroradiology19 citations
Semantic Scholar
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family.
I. Colombo, S. Pagliarani, S. Testolin, E. Salsano +12 more
2015Neuromuscular Disorders18 citations
Semantic Scholar
An autoinflammatory neurological disease due to interleukin 6 hypersecretion
E. Salsano, Ambra Rizzo, G. Bedini, L. Bernard +12 more
2013Journal of Neuroinflammation18 citations Open access
Semantic Scholar
Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings
A. Sagnelli, S. Magri, L. Farina, L. Chiapparini +9 more
2016Journal of Neurology16 citations
Semantic Scholar

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M. Savoiardo×18
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M. Savoiardo — researcher profile on SciRah
D. Pareyson×11
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D. Pareyson — researcher profile on SciRah
G. Uziel×10
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G. Uziel — researcher profile on SciRah
E. Lamantea×9
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E. Lamantea — researcher profile on SciRah

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I. Moroni — researcher profile on SciRah

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M. Zeviani — researcher profile on SciRah

L. Chiapparini×8

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L. Chiapparini — researcher profile on SciRah

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E. Salsano — researcher profile on SciRah

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M. Bugiani — researcher profile on SciRah

L. D'Incerti×6

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L. D'Incerti — researcher profile on SciRah

A. Ardissone×6

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A. Ardissone — researcher profile on SciRah

F. Invernizzi×5

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F. Invernizzi — researcher profile on SciRah