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Enrico Parano
Enrico Parano
Primo Ricercatore, Responsabile IRIB sede di Catania, Consiglio Nazionale delle Ricerche, CNR
Email verificata su cnr.it - Home page
Titolo
Citata da
Citata da
Anno
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
RE Tanzi, K Petrukhin, I Chernov, JL Pellequer, W Wasco, B Ross, ...
Nature genetics 5 (4), 344-350, 1993
16751993
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
K Petrukhin, SG Fischer, M Pirastu, RE Tanzi, I Chernov, M Devoto, ...
Nature genetics 5 (4), 338-343, 1993
6181993
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses
AB Shah, I Chernov, HT Zhang, BM Ross, K Das, S Lutsenko, E Parano, ...
The American Journal of Human Genetics 61 (2), 317-328, 1997
4581997
A genomewide screen for autism susceptibility loci
J Liu, DR Nyholt, P Magnussen, E Parano, P Pavone, D Geschwind, ...
The American Journal of Human Genetics 69 (2), 327-340, 2001
4092001
Neuropsychological assessment in children with absence epilepsy
P Pavone, R Bianchini, RR Trifiletti, G Incorpora, A Pavone, E Parano
Neurology 56 (8), 1047-1051, 2001
2232001
TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa
P Banerjee, PW Kleyn, JA Knowles, CA Lewis, BM Ross, E Parano, ...
Nature genetics 18 (2), 177-179, 1998
1761998
Worldwide distribution and broader clinical spectrum of muscle–eye–brain disease
K Taniguchi, K Kobayashi, K Saito, H Yamanouchi, A Ohnuma, ...
Human molecular genetics 12 (5), 527-534, 2003
1682003
Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection
P Pavone, R Bianchini, E Parano, G Incorpora, R Rizzo, L Mazzone, ...
Pediatric neurology 30 (2), 107-110, 2004
1632004
Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood
E Parano, A Uncini, DC De Vivo, RE Lovelace
Journal of child neurology 8 (4), 336-338, 1993
1131993
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions
TA Carter, CG Bönnemann, CH Wang, S Obici, E Parano, ...
Human molecular genetics 6 (2), 229-236, 1997
1061997
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis
P Pavone, M Pettoello-Mantovano, A Le Pira, I Giardino, A Pulvirenti, ...
Neuropediatrics 41 (06), 246-255, 2010
1042010
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles
P Pavone, AD Praticò, G Vitaliti, M Ruggieri, R Rizzo, E Parano, L Pavone, ...
Italian journal of pediatrics 40, 1-8, 2014
1022014
Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity
M Ruggieri, G Incorpora, A Polizzi, E Parano, M Spina, P Pavone
The Journal of pediatrics 152 (2), 244-249. e1, 2008
992008
Epilepsy is not a prominent feature of primary autism
P Pavone, G Incorpora, A Fiumara, E Parano, RR Trifiletti, M Ruggieri
Neuropediatrics 35 (04), 207-210, 2004
992004
Topical review: autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants
P Pavone, E Parano, R Rizzo, RR Trifiletti
Journal of Child Neurology 21 (9), 727-736, 2006
972006
Congenital muscular dystrophy: from muscle to brain
R Falsaperla, AD Praticò, M Ruggieri, E Parano, R Rizzo, G Corsello, ...
Italian journal of pediatrics 42, 1-11, 2016
962016
Limb reduction defects in humans associated with prenatal isotretinoin exposure
R Rizzo, EJ Lammer, E Parano, L Pavone, JC Argyle
Teratology 44 (6), 599-604, 1991
761991
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment
P Pavone, AD Praticò, R Rizzo, G Corsello, M Ruggieri, E Parano, ...
Medicine 96 (26), e6814, 2017
732017
Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood
E Parano, E Falcidia, A Grillo, P Pavone, N Cutuli, H Takabayashi, ...
American journal of medical genetics 101 (3), 262-267, 2001
622001
Aicardi syndrome with multiple tumors: a case report with literature review
RR Trifiletti, G Incorpora, A Polizzi, MD Cocuzza, EA Bolan, E Parano
Brain and Development 17 (4), 283-285, 1995
551995
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
Articoli 1–20