IRIS
ABBRUZZESE, MICHELE
 Distribuzione geografica
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Continente #
EU - Europa 5.498
Totale 5.498
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Nazione #
IT - Italia 5.498
Totale 5.498
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Città #
Genova 4.092
Rapallo 618
Genoa 404
Vado Ligure 373
Bordighera 11
Totale 5.498
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Nome #
New subcorti-cal components of the cerebral somatosensory evoked potential in man. 180
A reassessment of sensory evoked potential parameters in multiple sclerosis: a discriminant analysis approach. 172
Investigations on the nervous mechanisms underlying the somatosensory cervical response in man. 171
Conduction time of the lemniscal pathway in males and females. 165
Experimental Charcot-Marie-Tooth type 1A: A cDNA microarrays analysis 158
Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases 158
Electrophysio-logical assessment of the central lemniscal pathway in man. 156
Spinal components of the cerebral somatosensory evoked response in normal man: the "S wave". 154
Organic brain syndrome: diagnostic value of the EEG. 154
The effect of hand muscle vibration on the somatosensory evoked potential in man: an interaction between lemniscal and spinocerebellar inputs? 153
17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1 150
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers. 149
Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease. 144
Granulocyte-macrophage colony-stimulating factor activity in cerebrospinal fluid 143
Short-latency somatosensory evoked potentials in degenerative and vascular dementia. 141
Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies 140
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families. 137
Sonography of the median nerve in Charcot-Marie-Tooth disease 135
A restricted T cell response to myelin basic protein (MBP) is stable in multiple sclerosis (MS) patients. 133
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A. 132
Progressive sensory-motor polyneuropathy with tomaculous changes is associated to 17p11.2 deletion. 132
Acute axonal form of Guillain-Barre syndrome in a multiple sclerosis patient: chance association or linked disorders? 131
Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease. 127
Multifocal motor neuropathy with conduction block after Campylobacter jejuni enteritis. 127
Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patients. 126
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients. 124
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients. 120
Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease 120
Impaired expression of ciliary neurotrophic factor in Charcot-Marie-Tooth type 1A neuropathy 120
Intermediate components of the somatosensory evoked potential (SEP) in man. 117
Early electophysiological changes in transgenic rat model of charcot-marie-tooth. 117
Different movement disorders responsive to carbamazepine in patients with brainstem focal lesions 113
Risposte cervicali evocate da stimoli somestesici: nuovi dati nel soggetto normale. 111
Case 11-1997: critical-illness myopathy. 108
A study of lactoferrin and antibodies against lactoferrin in neurological diseases. 108
Analisi e studio longitudinale della fine specificità di linee linfocitarie T specifiche per la proteina basica della mielina (MBP) in pazienti con sclerosi multipla e in controlli normali. 107
De novo duplication in Charcot-Marie Tooth type 1A. 106
Due nuove componenti del potenziale evocato corticale somestesico. Osservazioni preliminari nel soggetto normale. 97
Ricerche sulle componenti encefaliche del potenziale spinale evocato da stimolazione del nervo mediano nell'uomo. 96
Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding 92
Nuove osservazioni sulla risposta "primaria" somestesica nell'uomo. Risultati preliminari. 88
Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies 80
Guillain barré syndrome of axonal type in a multple sclerosis patient: Fortuitous association or linked disorders? 14
Totale 5.506
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Categoria #
all - tutte 14.488
article - articoli 13.912
book - libri 0
conference - conferenze 576
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 28.976
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020805 0 0 0 0 0 0 195 72 123 200 161 54
2020/2021440 72 28 54 75 34 15 45 32 18 31 14 22
2021/2022739 34 61 40 144 47 26 53 118 27 91 18 80
2022/2023710 58 72 7 70 111 112 2 44 142 8 82 2
2023/2024288 20 30 4 33 23 72 20 24 25 5 10 22
2024/2025409 36 53 51 69 109 90 1 0 0 0 0 0
Totale 5.506