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Vincenzo Leuzzi

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Mario Mastrangelo; Caterina Caputi; Serena Galosi; Maria Teresa Giannini; Vincenzo Leuzzi
Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency.
Vincenzo Leuzzi; Mario Mastrangelo; Roberta Battini; Giovanni Cioni
Inborn errors of creatine metabolism and epilepsy.
Giuseppe Marangi; Giovanni Neri; Daniela Orteschi; Vanna Pecile; Serena Lattante; Vincenzo Leuzzi; Filippo Manti; Marcella Zollino
TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotype.

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All Publications

2013: Mario Mastrangelo; Caterina Caputi; Serena Galosi; Maria Teresa Giannini; Vincenzo Leuzzi
Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency.
Movement disorders : official journal of the Movement Disorder Society 2013;28(4):556-7.
2013: Vincenzo Leuzzi; Mario Mastrangelo; Roberta Battini; Giovanni Cioni
Inborn errors of creatine metabolism and epilepsy.
Epilepsia 2013;54(2):217-27.
2013: Giuseppe Marangi; Giovanni Neri; Daniela Orteschi; Vanna Pecile; Serena Lattante; Vincenzo Leuzzi; Filippo Manti; Marcella Zollino
TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotype.
European journal of human genetics : EJHG 2013;21(2):229-32.
2013: Vincenzo Leuzzi; Italo Antonozzi; Claudia Carducci; Flavia Chiarotti; Daniela D'Agnano; Maria Teresa Giannini; Carla Carducci
Urinary neopterin and phenylalanine loading test as tools for the biochemical diagnosis of segawa disease.
JIMD reports 2013;7():67-75.
2012: Laura Libernini; Chiara Lupis; Mario Mastrangelo; Filippo Maria Santorelli; Rosalba Carrozzo; Maurizio Inghilleri; Vincenzo Leuzzi
Mitochondrial neurogastrointestinal encephalomyopathy: novel pathogenic mutations in thymidine phosphorylase gene in two Italian brothers.
Neuropediatrics 2012;43(4):201-8.
2012: Carla Giordano; Vincenzo Leuzzi; Maurizia Orlandi; Paola Papoff; Alberto Spalice; Valeria Tiranti; Carlo Viscomi; Alberto Burlina; Giulia d'Amati; Ivano Di Meo; Massimo Zeviani
Morphologic evidence of diffuse vascular damage in human and in the experimental model of ethylmalonic encephalopathy.
Journal of inherited metabolic disease 2012;35(3):451-8.
2012: Teresa Giovanniello; Federico Vigevano; Italo Antonozzi; Nenad Blau; Carla Carducci; Claudia Carducci; Dianella Claps; Vincenzo Leuzzi
A new tyrosine hydroxylase genotype associated with early-onset severe encephalopathy.
Journal of child neurology 2012;27(4):523-5.
2012: Anna Chilosi; Francesca Maria Battaglia; Roberta Battini; Manuela Casarano; Alessandro Comparini; Vincenzo Leuzzi; Margherita Maria Mancardi; Cristina Schiaffino; Michela Tosetti; Giovanni Cioni
Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency.
Orphanet journal of rare diseases 2012;7():43.
2012: Carla Carducci; Carla Carducci; Tullio Florio; Elena Gatta; Vincenzo Leuzzi; Mauro Robello; Silvia Santagata; Stefano Thellung; Enrico Adriano; Italo Antonozzi; Cristiana Artiola; Maurizio Balestrino
In vitro study of uptake and synthesis of creatine and its precursors by cerebellar granule cells and astrocytes suggests some hypotheses on the physiopathology of the inherited disorders of creatine metabolism.
BMC neuroscience 2012;13():41.
2011: Roberta Battini; Anna Chilosi; M Casarano; F Moro; A Comparini; Maria Grazia Alessandrì; Vincenzo Leuzzi; Michela Tosetti; Giovanni Cioni
Language disorder with mild intellectual disability in a child affected by a novel mutation of SLC6A8 gene.
Molecular genetics and metabolism 2011;102(2):153-6.
2011: Marcella Zollino; Fiorella Gurrieri; Daniela Orteschi; Giuseppe Marangi; Vincenzo Leuzzi; Giovanni Neri
Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndrome.
European journal of human genetics : EJHG 2011;19(2):239-42.
2010: Francesco Cali; Giuseppa Ruggeri; Mirella Vinci; Concetta Meli; Carla Carducci; Vincenzo Leuzzi; simone pozzessere; Pietro Schinocca; Alda Ragalmuto; Valeria Chiavetta; Salvatore Micciche; Valentinox Romano
Exon deletions of the phenylalanine hydroxylase gene in Italian hyperphenylalaninemics.
Experimental & molecular medicine 2010;42(2):81-6.
2009: Oliviero Bruni; Raffaele Ferri; Luana Novelli; Monica Terribili; Miriam Troianiello; Elena Finotti; Vincenzo Leuzzi; Paolo Curatolo
Sleep spindle activity is correlated with reading abilities in developmental dyslexia.
Sleep 2009;32(10):1333-40.
2009: Roberta Battini; Andrea Guzzetta; Giuseppina Sgandurra; Roberta Di Pietro; Elisa Petacchi; Eugenio Mercuri; Maria T Giannini; Vincenzo Leuzzi; Giovanni Cioni
Scale for evaluation of movement disorders in the first three years of life.
Pediatric neurology 2009;40(4):258-64.
2008: Serena Grossi; Stefano Regis; Camillo Rosano; Fabio Corsolini; Graziella Uziel; Maria Sessa; Maja Di Rocco; Giancarlo Parenti; Federica Deodato; Vincenzo Leuzzi; Roberta Biancheri; Mirella Filocamo
Molecular analysis of ARSA and PSAP genes in twenty-one Italian patients with metachromatic leukodystrophy: identification and functional characterization of 11 novel ARSA alleles.
Human mutation 2008;29(11):E220-30.
2008: Roberta Battini; Giuseppina Sgandurra; Elisa Petacchi; Andrea Guzzetta; Roberta Di Pietro; Maria T Giannini; Vincenzo Leuzzi; Eugenio Mercuri; Giovanni Cioni
Movement disorder-childhood rating scale: reliability and validity.
Pediatric neurology 2008;39(4):259-65.
2008: Giuseppe Marangi; Vincenzo Leuzzi; Daniela Orteschi; Maria E Grimaldi; Rosetta Lecce; Giovanni Neri; Marcella Zollino
Duplication of the Rubinstein-Taybi region on 16p13.3 is associated with a distinctive phenotype.
American journal of medical genetics. Part A 2008;146A(18):2313-7.
2008: Vincenzo Leuzzi; Maria G Alessandrì; Manuela Casarano; Roberta Battini; Giovanni Cioni
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts.
Analytical biochemistry 2008;375(1):153-5.
2008: Anna Chilosi; Vincenzo Leuzzi; Roberta Battini; Michela Tosetti; Giovanni Ferretti; Alessandro Comparini; Manuela Casarano; Elena Moretti; M Grazia Alessandri; Maria Cristina Bianchi; Giovanni Cioni
Treatment with L-arginine improves neuropsychological disorders in a child with creatine transporter defect.
Neurocase 2008;14(2):151-61.
2007: Teresa Giovanniello; Vincenzo Leuzzi; Carla Carducci; C Carducci; M L Di Sabato; Cristiana Artiola; S Santagata; simone pozzessere; Italo Antonozzi
Tyrosine hydroxylase deficiency presenting with a biphasic clinical course.
Neuropediatrics 2007;38(4):213-5.
2007: Roberta Battini; Anna Chilosi; Davide Mei; Manuela Casarano; Maria Grazia Alessandrì; Vincenzo Leuzzi; Giovanni Ferretti; Michela Tosetti; Maria Cristina Bianchi; Giovanni Cioni
Mental retardation and verbal dyspraxia in a new patient with de novo creatine transporter (SLC6A8) mutation.
American journal of medical genetics. Part A 2007;143A(15):1771-4.
2007: Vincenzo Leuzzi; Maria Lucia Di Sabato; Federica Deodato; Cristiano Rizzo; Sara Boenzi; Carla Carducci; Patrizia Malaspina; C Liberanome; Carlo Dionisi Vici
Vigabatrin improves paroxysmal dystonia in succinic semialdehyde dehydrogenase deficiency.
Neurology 2007;68(16):1320-1.
2007: Vincenzo Leuzzi; Michela Tosetti; Domenico Montanaro; C Carducci; Cristiana Artiola; Carla Carducci; Italo Antonozzi; M Burroni; F Carnevale; F Chiarotti; teresa popolizio; Giuseppe Maria Giannatempo; V D'Alesio; Tommaso Scarabino
The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 tesla MRI and magnetic resonance spectroscopy (1H MRS) study.
Journal of inherited metabolic disease 2007;30(2):209-16.
2007: Maria Cristina Bianchi; Michela Tosetti; Roberta Battini; Vincenzo Leuzzi; M G Alessandri'; Carla Carducci; Italo Antonozzi; Giovanni Cioni
Treatment monitoring of brain creatine deficiency syndromes: a 1H- and 31P-MR spectroscopy study.
AJNR. American journal of neuroradiology 2007;28(3):548-54.
2006: Saadet Mercimek-Mahmutoglu; Sylvia Stoeckler-Ipsiroglu; A Adami; Richard E Appleton; H Caldeira Araújo; M Duran; Regina Ensenauer; E Fernandez-Alvarez; P Garcia; C Grolik; Chike Item; Vincenzo Leuzzi; Iris Marquardt; Adolf Mühl; R A Saelke-Kellermann; Gajja S Salomons; Andreas Schulze; R Surtees; Marjo S van der Knaap; R Vasconcelos; N M Verhoeven; Laura Vilarinho; Ekkehard Wilichowski; Cornelis Jakobs
GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis.
Neurology 2006;67(3):480-4.
2006: Roberta Battini; Maria Grazia Alessandrì; Vincenzo Leuzzi; Francesca Moro; Michela Tosetti; Maria Cristina Bianchi; Giovanni Cioni
Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: early treatment can prevent phenotypic expression of the disease.
The Journal of pediatrics 2006;148(6):828-30.
2006: Valerio Carelli; Alessandro Achilli; Maria Lucia Valentino; Chiara Rengo; Ornella Semino; Maria Pala; Anna Olivieri; Marina Mattiazzi; Francesco Pallotti; Franco Carrara; Massimo Zeviani; Vincenzo Leuzzi; Carla Carducci; Giorgio Valle; Barbara Simionati; Luana Mendieta; Solange R Salomao; Rubens Belfort; Alfredo Sadun; Antonio Torroni
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.
American journal of human genetics 2006;78(4):564-74.
2006: Vincenzo Leuzzi; Carla Carducci; C Carducci; F Chiarotti; Cristiana Artiola; Teresa Giovanniello; Italo Antonozzi
The spectrum of phenylalanine variations under tetrahydrobiopterin load in subjects affected by phenylalanine hydroxylase deficiency.
Journal of inherited metabolic disease 2006;29(1):38-46.
2006: Carla Carducci; Silvia Santagata; Vincenzo Leuzzi; Carla Carducci; Cristiana Artiola; Teresa Giovanniello; Roberta Battini; Italo Antonozzi
Quantitative determination of guanidinoacetate and creatine in dried blood spot by flow injection analysis-electrospray tandem mass spectrometry.
Clinica chimica acta; international journal of clinical chemistry 2006;364(1-2):180-7.
2006: Vincenzo Leuzzi; Carla Carducci; Claudia Carducci; Maria Matricardi; Maria Cristina Bianchi; Maria Lucia Di Sabato; Cristiana Artiola; Italo Antonozzi
A mutation on exon 6 of guanidinoacetate methyltransferase (GAMT) gene supports a different function for isoform a and b of GAMT enzyme.
Molecular genetics and metabolism 2006;87(1):88-90.
2005: Elisabetta Tabolacci; Marcella Zollino; Rosetta Lecce; Eugenio Sangiorgi; Fiorella Gurrieri; Vincenzo Leuzzi; John M Opitz; Giovanni Neri
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome.
Clinical dysmorphology 2005;14(3):127-32.
2004: Vincenzo Leuzzi; Maria Lucia Di Sabato; Marcella Zollino; Maria Lucia Montanaro; Stefano Seri
Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutation.
Neurology 2004;63(10):1968-70.
2004: Maria Grazia Alessandrì; Lisa Celati; Roberta Battini; Fulvia Baldinotti; Chike Item; Vincenzo Leuzzi; Giovanni Cioni
HPLC assay for guanidinoacetate methyltransferase.
Analytical biochemistry 2004;331(1):189-91.
2004: Silvia Miano; Oliviero Bruni; Vincenzo Leuzzi; Maurizio Elia; Elisabetta Verrillo; Raffaele Ferri
Sleep polygraphy in Angelman syndrome.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2004;115(4):938-45.
2004: Vincenzo Leuzzi; M Pansini; E Sechi; F Chiarotti; Carla Carducci; G Levi; Italo Antonozzi
Executive function impairment in early-treated PKU subjects with normal mental development.
Journal of inherited metabolic disease 2004;27(2):115-25.
2003: Gaëtan Lesca; Eleonore Eymard-Pierre; Filippo M Santorelli; R Cusmai; Matteo di Capua; E M Valente; Jocelyne Attia-Sobol; Henri Plauchu; Vincenzo Leuzzi; A Ponzone; Odile Boespflug-Tanguy; Enrico Bertini
Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families.
Neurology 2003;60(4):674-82.
2002: Vincenzo Leuzzi
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment.
Journal of child neurology 2002;17 Suppl 3():3S89-97; discussion 3S97.
2002: Roberta Battini; Vincenzo Leuzzi; Carla Carducci; Michela Tosetti; Maria Cristina Bianchi; Chike Item; Sylvia Stöckler-Ipsiroglu; Giovanni Cioni
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree.
Molecular genetics and metabolism 2002;77(4):326-31.
2002: Vincenzo Leuzzi; Carla Carducci; Cl Carducci; F Cardona; Cristiana Artiola; Italo Antonozzi
Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome.
Neurology 2002;59(8):1241-3.
2002: Carla Carducci; Maurizio Birarelli; Vincenzo Leuzzi; Carla Carducci; Roberta Battini; Giovanni Cioni; Italo Antonozzi
Guanidinoacetate and creatine plus creatinine assessment in physiologic fluids: an effective diagnostic tool for the biochemical diagnosis of arginine:glycine amidinotransferase and guanidinoacetate methyltransferase deficiencies.
Clinical chemistry 2002;48(10):1772-8.
2002: Chike Item; Carmen Stromberger; Adolf Mühl; Claudia Edlinger; Olaf Bodamer; Andreas Schulze; Robert Surtees; Vincenzo Leuzzi; Gajja S Salomons; Cornelis Jakobs; Sylvia Stöckler-Ipsiroglu
Denaturing gradient gel electrophoresis for the molecular characterization of six patients with guanidinoacetate methyltransferase deficiency.
Clinical chemistry 2002;48(5):767-9.
2001: Carla Carducci; Maurizio Birarelli; P Santagata; Vincenzo Leuzzi; C Carducci; Italo Antonozzi
Automated high-performance liquid chromatographic method for the determination of guanidinoacetic acid in dried blood spots: a tool for early diagnosis of guanidinoacetate methyltransferase deficiency.
Journal of chromatography. B, Biomedical sciences and applications 2001;755(1-2):343-8.
2000: Carla Carducci; Vincenzo Leuzzi; C Carducci; Sabrina Prudente; L Mercuri; Italo Antonozzi
Two new severe mutations causing guanidinoacetate methyltransferase deficiency.
Molecular genetics and metabolism 2000;71(4):633-8.
2000: Vincenzo Leuzzi; Maria Cristina Bianchi; Michela Tosetti; Carla Carducci; C A Cerquiglini; Giovanni Cioni; Italo Antonozzi
Brain creatine depletion: guanidinoacetate methyltransferase deficiency (improving with creatine supplementation).
Neurology 2000;55(9):1407-9.
2000: Vincenzo Leuzzi; Maria Cristina Bianchi; Michela Tosetti; C L Carducci; Carla Carducci; Italo Antonozzi
Clinical significance of brain phenylalanine concentration assessed by in vivo proton magnetic resonance spectroscopy in phenylketonuria.
Journal of inherited metabolic disease 2000;23(6):563-70.
2000: Vincenzo Leuzzi; A Rinna; M Gallucci; Matteo di Capua; Carlo Dionisi Vici; Daniela Longo; Enrico Bertini
Ataxia, deafness, leukodystrophy: inherited disorder of the white matter in three related patients.
Neurology 2000;54(12):2325-8.
2000: Cristiano Rizzo; Enrico Bertini; Fiorella Piemonte; Vincenzo Leuzzi; Gaetano Sabetta; G Federici; A Luchetti; Carlo Dionisi Vici
Oxidative abnormalities in Menkes disease.
Journal of inherited metabolic disease 2000;23(4):349-51.
2000: Vincenzo Leuzzi; Stefano Seri; Antonella Cerquiglini; Carla Carducci; C Carducci; Italo Antonozzi
Derangement of the dopaminergic system in phenylketonuria: study of the event-related potential (P300).
Journal of inherited metabolic disease 2000;23(4):317-20.
2000: Carlo Dionisi Vici; Georg F Hoffmann; Vincenzo Leuzzi; H Hoffken; Christa Bräutigam; C Rizzo; G C Steebergen-Spanjers; Jan A M Smeitink; Ron A Wevers
Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapy.
The Journal of pediatrics 2000;136(4):560-2.
1999: Valerio Carelli; Anna Ghelli; Lauro Bucchi; Pasquale Montagna; Anna Maria De Negri; Vincenzo Leuzzi; Carla Carducci; Giorgio Lenaz; Elio Lugaresi; M Degli Esposti
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy.
Annals of neurology 1999;45(3):320-8.
1998: Vincenzo Leuzzi; Steno Rinalduzzi; F Chiarotti; P Garzia; G Trasimeni; Neri Accornero
Subclinical visual impairment in phenylketonuria. A neurophysiological study (VEP-P) with clinical, biochemical, and neuroradiological (MRI) correlations.
Journal of inherited metabolic disease 1998;21(4):351-64.
1997: Vincenzo Leuzzi; Carla Carducci; M Lenza; Marco Salvetti; Giovanni Ristori; Simone Di Giovanni; Antonio Torroni
LHON mutations in Italian patients affected by multiple sclerosis.
Acta neurologica Scandinavica 1997;96(3):145-8.
1997: Vincenzo Leuzzi; D Fois; Carla Carducci; Italo Antonozzi; G Trasimeni
Neuropsychological and neuroradiological (MRI) variations during phenylalanine load: protective effect of valine, leucine, and isoleucine supplementation.
Journal of child neurology 1997;12(5):338-40.
1997: Valerio Carelli; Anna Ghelli; Marina Ratta; E Bacchilega; Simonetta Sangiorgi; R Mancini; Vincenzo Leuzzi; Pietro Cortelli; Pasquale Montagna; Elio Lugaresi; M Degli Esposti
Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.
Neurology 1997;48(6):1623-32.
1997: Antonio Torroni; M Petrozzi; L D'Urbano; Daniele Sellitto; M Zeviani; F Carrara; Carla Carducci; Vincenzo Leuzzi; Valerio Carelli; Piero Barboni; Anna Maria De Negri; Rosaria Scozzari
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.
American journal of human genetics 1997;60(5):1107-21.
1996: G F De Giorgis; E Nonnis; F Crocioni; P Gregori; M P Rosini; Vincenzo Leuzzi; Alberto Loizzo
Evolution of daytime quiet sleep components in early treated phenylketonuric infants.
Brain & development 1996;18(3):201-6.
1996: Carla Carducci; M Birarelli; Vincenzo Leuzzi; G Santagata; P Serafini; Italo Antonozzi
Automated method for the measurement of amino acids in urine by high-performance liquid chromatography.
Journal of chromatography. A 1996;729(1-2):173-80.
1996: Carla Carducci; Anna Maria De Negri; Vincenzo Leuzzi; C Terregino; M Torella; Paola Pivetti-Pezzi; Italo Antonozzi
Screening of mtDNA mutations in Italian LHON pedigrees.
Journal of inherited metabolic disease 1996;19(2):127-9.
1995: Cesare Fieschi; Claudio Gasperini; Giovanni Ristori; Stefano Bastianello; F Girmenia; Vincenzo Leuzzi; Carla Buttinelli; Maurizia Rasura
Patients with clinically definite multiple sclerosis, white matter abnormalities on MRI, and normal CSF: if not multiple sclerosis, what is it?
Journal of neurology, neurosurgery, and psychiatry 1995;58(2):255-6.
1995: Vincenzo Leuzzi; G Trasimeni; G F Gualdi; Italo Antonozzi
Biochemical, clinical and neuroradiological (MRI) correlations in late-detected PKU patients.
Journal of inherited metabolic disease 1995;18(5):624-34.
1994: Vincenzo Leuzzi; F Cardona; Italo Antonozzi; Alberto Loizzo
Visual, auditory, and somatosensorial evoked potentials in early and late treated adolescents with phenylketonuria.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 1994;11(6):602-6.
1993: Vincenzo Leuzzi; G F Gualdi; F Fabbrizi; G Trasimeni; C Di Biasi; Italo Antonozzi
Neuroradiological (MRI) abnormalities in phenylketonuric subjects: clinical and biochemical correlations.
Neuropediatrics 1993;24(6):302-6.
1993: Vincenzo Leuzzi; R Elli; A Antonelli; Luciana Chessa; F Cardona; L Marcucci; P Petrinelli
Neurological and cytogenetic study in early-onset ataxia-telangiectasia patients.
European journal of pediatrics 1993;152(7):609-12.
1993: Vincenzo Leuzzi; V Ricciotti; Antonio Pelliccia
Hemiplegic dystonia associated with regional cortical dysplasia (pachygyria).
Movement disorders : official journal of the Movement Disorder Society 1993;8(2):242-4.
1992: A Antonelli; P Petrinelli; L Marcucci; D Billi; F Cardona; Vincenzo Leuzzi; R Elli
Effects of DNA-breaking agents on Cockayne syndrome cells.
Annals of the New York Academy of Sciences 1992;663():418-20.
1992: Vincenzo Leuzzi; Enrico Bertini; Anna Maria De Negri; M Gallucci; Barbara Garavaglia
Bilateral striatal necrosis, dystonia and optic atrophy in two siblings.
Journal of neurology, neurosurgery, and psychiatry 1992;55(1):16-9.
1991: Carla Carducci; Vincenzo Leuzzi; M Scuderi; Anna Maria De Negri; Corrado Balacco Gabrieli; Italo Antonozzi; Alfredo Pontecorvi
Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.
Human genetics 1991;87(6):725-7.
1991: F Cardona; Vincenzo Leuzzi; Italo Antonozzi; P Benedetti; Alberto Loizzo
The development of auditory and visual evoked potentials in early treated phenylketonuric children.
Electroencephalography and clinical neurophysiology 1991;80(1):8-15.
1990: Vincenzo Leuzzi; S Morano; Fabiola Moretti; F Fabbrizi; Italo Antonozzi
Non-ketotic hyperglycinaemia: a new case with late onset.
Journal of inherited metabolic disease 1990;13(2):238.
1989: P Vetrone; Vincenzo Leuzzi; V Zazzara; Italo Antonozzi
Psychological effects on parents of children with early detected phenylketonuria.
Journal of inherited metabolic disease 1989;12(3):345-6.
1988: Vincenzo Leuzzi; I Favatà; Stefano Seri
Bilateral striatal lesions.
Developmental medicine and child neurology 1988;30(2):252-7.
1987: I Favatà; Vincenzo Leuzzi; P Curatolo
Mental outcome in West syndrome: prognostic value of some clinical factors.
Journal of mental deficiency research 1987;31 ( Pt 1)():9-15.
1987: Italo Antonozzi; Vincenzo Leuzzi
Hyperargininaemia.
Journal of inherited metabolic disease 1987;10(2):200.