RUSSO, Antonella
 Distribuzione geografica
Continente #
NA - Nord America 4.870
EU - Europa 2.137
AS - Asia 1.762
SA - Sud America 270
AF - Africa 218
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 4
Totale 9.266
Nazione #
US - Stati Uniti d'America 4.606
SG - Singapore 964
IE - Irlanda 745
CN - Cina 707
UA - Ucraina 690
CA - Canada 258
BR - Brasile 242
IT - Italia 226
RU - Federazione Russa 184
CI - Costa d'Avorio 124
DE - Germania 92
SN - Senegal 85
SE - Svezia 32
GB - Regno Unito 30
CH - Svizzera 28
FR - Francia 24
IN - India 19
FI - Finlandia 14
PL - Polonia 14
UZ - Uzbekistan 14
GR - Grecia 13
NL - Olanda 12
TR - Turchia 10
AR - Argentina 9
AT - Austria 8
EC - Ecuador 6
IR - Iran 6
BD - Bangladesh 5
BE - Belgio 5
BG - Bulgaria 5
EU - Europa 5
CO - Colombia 4
CZ - Repubblica Ceca 4
IQ - Iraq 4
JO - Giordania 4
JP - Giappone 4
LB - Libano 4
AU - Australia 3
IL - Israele 3
MA - Marocco 3
CL - Cile 2
DZ - Algeria 2
EE - Estonia 2
GE - Georgia 2
KZ - Kazakistan 2
MX - Messico 2
MY - Malesia 2
NG - Nigeria 2
NP - Nepal 2
PA - Panama 2
PE - Perù 2
PY - Paraguay 2
VE - Venezuela 2
AL - Albania 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
EG - Egitto 1
ES - Italia 1
HK - Hong Kong 1
HU - Ungheria 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
LV - Lettonia 1
MC - Monaco 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PK - Pakistan 1
PS - Palestinian Territory 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 9.266
Città #
Santa Clara 844
Dublin 737
Jacksonville 681
Chandler 587
Singapore 548
Boardman 305
Nanjing 246
Chicago 228
Toronto 207
Andover 206
Lawrence 202
Cambridge 200
San Mateo 131
Abidjan 124
Ashburn 120
Des Moines 104
Nanchang 87
Dakar 85
Wilmington 77
Shenyang 69
Catania 55
Bremen 52
Hebei 52
Saint Petersburg 52
Changsha 50
Ottawa 49
Tianjin 47
Jiaxing 40
Los Angeles 26
São Paulo 19
Moscow 18
Beijing 17
Norwalk 17
Civitanova Marche 15
Seattle 15
Palermo 14
Liberty Lake 13
Pune 13
Jinan 12
Munich 12
Zhengzhou 11
Helsinki 10
Rome 10
Council Bluffs 8
Den Haag 8
Princeton 8
Washington 8
Porto Alegre 7
Ann Arbor 6
Belo Horizonte 6
Guangzhou 6
Hefei 6
Ludwigshafen 6
Ningbo 6
Ardabil 5
Augusta 5
Brussels 5
Edinburgh 5
Goiânia 5
Pedara 5
Rio de Janeiro 5
The Dalles 5
Amman 4
Campinas 4
Fuzhou 4
Hangzhou 4
Houston 4
Kiev 4
Leawood 4
Phoenix 4
Santo André 4
Scandicci 4
Sorocaba 4
Tashkent 4
Brasília 3
Campo Grande 3
Caxias do Sul 3
Curitiba 3
Frankfurt Am Main 3
Guarulhos 3
Jundiaí 3
Niterói 3
Redwood City 3
Reggio Calabria 3
Stockholm 3
Tokyo 3
Turku 3
Abuja 2
Almirante Tamandaré 2
Asunción 2
Baghdad 2
Bloomsbury 2
Bogotá 2
Cagliari 2
Carapicuíba 2
Cavallino 2
Contagem 2
Dallas 2
Guayaquil 2
Hamburg 2
Totale 6.635
Nome #
Proiezioni al talamo ventrobasale ed al nucleo fastigiale del cervelletto originate dai medesimi neuroni del nucleo del tratto spinale del trigemino. 87
Olfactory Ensheathing Cells express both Ghrelin and Ghrelin Receptor in vitro: a new hypothesis in favor of a neurotrophic effect 87
Involvement of HSP70 in resveratrol apoptosis of human prostate cancer 84
5-HTr Expression in Primary Trigeminal Neurons Following Injury 81
Activation of metabotropic glutamate receptor protects cultured neurons against apoptosis induced by beta-amyloid peptide 80
. Branching projections from Subcoeruleus area neurons to medial preoptic area and cervical spinal cord revealed by double retrograde neuronal labeling 79
Branching axons from subcoeruleus area project to the nucleus raphe pontis and hypothalamic zona incerta, as studied with the double fluorescent retrograde tracing technique. 77
[Afferent projections to the raphe pontis and zona incerta. Study using using fluorescent dye markers]. 77
Role of the ventromedial hypothalamus in the regulation of adenohypophyseal immunoreactive dynorphin in the rat. 75
Activation of metabotropic glutamate receptors protects cultured neurons against apoptosis induced by beta-amyloid peptide. 75
Bilateral Trigeminal projections to the cerebellar nuclei. 75
28. Projections to the Ventrobasal Thalamus and to cerebellar nuclei originate from the same neurons of the n.of the spinal tract of the Trigeminal nerve. 72
Effects of different musical frequencies on NPY and Ghrelin secretion in the rat hypothalamus 72
"In vitro" postnatal expression of 5-HT7 receptors in the rat hypothalamus: an immunohistochemical analysis 70
Evidence for a trigeminal mesencephalic-hypoglossal nuclei loop involved in controlling vibrissae movements in the rat 70
[Direct interamygdaloid connections demonstrated by the technic of retrograde transport of peroxidase enzyme]. 70
[Afferent connections in the ventromedial hypothalamus of rats demonstrated by retrograde transport of horseradish peroxidase]. 69
[Projections to the supraoptic and paraventricular nuclei studied in the rat by means of retrograde fluorescent tracers (fast blue, nuclear yellow)]. 69
Branching neurons in Pontine Raphe Nuclei Pontis and Magnus project to Preoptic area and cervical spinal cord. 68
Olfactory ensheathing cells exert a trophic effect on the hypothalamic neurons in vitro 66
[Afferent and efferent connections between the hypothalamus and raphe. Study using the technic of retrograde transport of peroxidases]. 66
Branching neurons of Subcoeruleus area project to preoptic area and cervical spinal cord. 65
Proiezioni trigeminali al nucleo dentato del cervelletto, nel ratto. 64
Ghrelin peptide improves glial conditioned medium effects on neuronal differentiation of human adipose mesenchymal stem cells 64
Primary afferent plasticity following deafferentation of the trigeminal brainstem nuclei in the adult rat 63
[Injection of horseradish peroxidase in the superior colliculus of the rate: afferent connections]. 63
Different musical frequencies increase the neuronal and serum expression of Ghrelin hormone, in the rat. 63
The Schwann Cell: a source of neurotrophic activity on cortical glutamatergic neurons in culture 63
Trophic effect of olfactory ensheating cells on the hypothalamic neurons “in vitro” 62
Barrington’s nucleus: direct serotoninergic projection. 62
Connessioni dirette interamigdaloidee dimostrate attraverso la tecnica del trasporto retrogrado dell'enzima perossidasi (HRP) 61
[Injections of peroxidase in the ventrobasal complex of the amygdala: afferent connections]. 61
Behavioral effects of medial-dorsal thalamic, mediobasal hypothalamic and amygdaloid lesions in the rat]. 61
Hypoglossal nucleus projections to the rat masseter muscle. Brain Res 61
Branching axons from SubCoeruleus area neurons project to preoptic area and thoracic spinal cord. 61
Effects of hypothalamic lesions on the content of dynorphin immunoreactivity in pituitary. 61
Ghrelin-containing neurons in the olfactory bulb send collateralized projections into medial amygdaloid and arcuate hypothalamic nuclei: neuroanatomical study 61
[Functional significance of trigeminal projections to the fastigial nucleus of the cerebellum]. 60
The "Locus Coeruleus": branching axons project to the "Nucleus Raphe Pontis" and hypothalamic "Zona Incerta", as studied in the rat with fluorescent retrograde double labeling. 60
Hypoglossal nuclei participation in rat mystacial pad control 60
[Afferent projections to "nucleus dorsalis raphes": a study done by the technic of retrograde peroxidase transport]. 60
Metabotropic glutamate receptors mGluR1 and mGluR2 are co-located with serotonergic 5-HT1A and 5-HT2A receptors in Secondary Vestibular Neurons of the rat 59
Projections to cerebellar nuclei and ventrobasal thalamus originate from the same neurons of the nucleus tractus spinalis nervi trigemini (NTST). 59
The efferent collateral pathways from the Subcoeruleus to medial preoptic area and lumbar spinal cord. 59
Afferent and efferent branching axons from the rat lumbo-sacral spinal cord project either to the urinary bladder and urethra as demonstrated by double retrograde neuronal labeling 59
Branching projections of ventrolateral reticular neurons to the medial preoptic area and lumbo-sacral spinal cord 58
Role of the trigeminal nerve on regrowth of hypoglossal motoneurons after hypoglossal facial anastomosis 57
Iniezioni di perossidasi nel complesso ventrobasale dell'amigdala: connessioni afferenti. 57
Branching axons from the rat sacral cord projecting to the urinary bladder and urethra: neuroanatomical evidence. 57
Branching neurons in Subcoeruleus area: projections to preoptic area and cervical spinal cord. 57
Behavioral analysis performed on TRH-T treated rats after spinal cord injury: a pre¬liminary approach. 57
12. Trigeminal afferents to the Fastigial N. and Paleocerebellar modulation of hypoglossal motoneurons: evidence for a trans-cerebellar loop involved in tongue muscle activity regulation 57
Functional significance of trigeminal projections to the dentate nucleus of the cerebellum 57
Hippocampal ghreline- containing neurons, modulate food-intake behavior by direct patways to ventrobasal hypothalamus and basolateral amygdala. 57
Neuroendocrine phenotype of human Leydig cells 56
Projections to the Ventrobasal Thalamus and to the cerebellar fastigial n. originate from the same neurons of the n.of the spinal tract of the Trigeminal Nerve. 56
Olfactory Ensheathing Cells: a source of growth factors promoting hippocampal neuronal survival 56
Olfactory Ensheathing Cells: morpho-funzional features 56
Hippocampal Ghrelin-positive neurons directly project to arcuate hypothalamic and medial amygdaloid nuclei. Could they modulate food-intake? 56
Hypoglossal projection to mimetic facial muscle in adult rat: functional hypothesis 55
Branching neurons in Pontine Raphe Nuclei Pontis and Magnus project to Preoptic area and cervical spinal cord. 55
Cortical projection to the hipoglossal neurons in the rat 54
Immunohistochemical investigation of expression of 5-HT7 receptors in the rat hypothalamus. A study in vitro 53
Neuroni "branching" nel "Subcoeruleus": proiezioni all'area preottica ed al midollo spinale. 53
Studio degli effetti del bFGF sui neuroni serotoninergici dei nuclei del raphe coltivati "in vitro". 53
Selettività delle proiezioni trigeminali al nucleo fastigiale del cervelletto. 52
The effect of selective hypothalamic lesions on pituitary immunoreactive Dynorphin. 52
Significato funzionale delle proiezioni trigeminali al nucleo fastigiale del cervelletto. 52
Proiezioni afferenti al "nucleus dorsalis raphes": studio effettuato mediante la tecnica del trasporto retrogrado dell'enzima perossidasi. 51
Involvement of trigeminal mesencephalic nucleus in kinetic encoding of whisker movements. 51
Sistemi di regolazione delle Dinorfine ipofisarie. 51
Trigeminal afferents to the Fastigial N. and Paleocerebellar modulation of hypoglossal motoneurons: evidence for a trans-cerebellar loop involved in tongue muscle activity regulation. 51
Cortical motor control of the tongue motor nucleus in the rat. 51
Trigeminal afferents to the Interpositus N.: neuroanatomical study suggesting a trans-cerebellar loop for tongue muscle activity regulation. 51
Medio-lateral gradient of Trigeminal projections to the cerebellar Fastigial, Interpositus and Dentate nuclei, in the rat. 51
Effetti del “basic Fibroblast Growth Factor” (b-FGF) sui neuroni glutamatergici embrionali di ratto, coltivati “in vitro” 51
Collateralized hypoglossal projections on to fastigial cerebellar nucleus and tongue. 51
Effects of lesions in the ventromedial hypothalamus, basolateral complex of amygdala and dorsal raphe on serum luteinizing hormone level in the rat. 50
Regulation of immunoreactive dynorphin in rat anterior pituitary lobe. 50
Organization of trigeminal projections of the cerebellar nuclei. 50
Mechanical deflection of macrovibrissae induces in rats activation of trigeminal mesencephalic nucleus neurons 50
Metabotropic glutamate receptors mGLUR1 and mGLUR2 are co-located with serotoninergic 5-HT1A and 5-HT2A receptors in secondary vestibular neurons of the rat 50
Branching projections to medial preoptic area and lumbar spinal cord arise from serotoninergic and non-serotoninergic raphe neurones 50
Olfactory-hypoglossal connections 49
Connessioni afferenti ed efferenti tra ipotalamo e rafe. Studio effettuato mediante la tecnica del trasporto retrogrado dell' enzima perossidasi. 49
Trigemino-cerebellar nuclei and Trigemino-ventrobasal complex projections: a double retrograde neuronal labeling through divergent axon collaterals. 48
The "Locus Coeruleus": projections to "Nucleus Raphe Pontis" and "Zona Incerta". Study with retrograde fluorescent substances. 48
Branching projections to medial preoptic area and lumbar spinal cord arise from serotoninergic and non-serotoninergic raphe neurones. 48
Noradrenergic modulation of n-methyl-d-aspartate receptors in the vestibular complex 48
Immunoreactive Dynorphin-like material in rat pituitary after ovariectomy. 47
Trigeminal afferents to the fastigial n. and paleocerebellar modulation of hypoglossal motoneurons: neuroanatomical and electrophysiological study suggesting a transcerebellar loop for tongue muscle activity regulation. 47
The "Locus Coeruleus": projections to "Nucleus Raphe Pontis" and "Zona Incerta". Study with retrograde fluorescent substances 47
Bilateral Trigeminal projections to the cerebellar nuclei 47
Proiezioni trigeminali al nucleo Interposito del cervelletto, nel ratto. 47
Effects of Ghrelin on Olfactory Ensheathing Cell Viability and Neural Marker Expression 46
Hypoglossal innervation to the rat masseter muscle 46
Projections to the Ventrobasal Thalamus and to cerebellar nuclei originate from the same neurons of the n.of the spinal tract of the Trigeminal nerve. 46
Different pathways contribute to modify the content of immunoreactive dynorphin in pituitary and hypothalamus. 45
[Injections of horseradish peroxidase into median raphe nuclei: afferent connections]. 45
Catecholaminergic phenotype of human Leydig cells 44
Totale 5.870
Categoria #
all - tutte 35.197
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 35.197


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020185 0 0 0 0 0 0 0 0 0 0 133 52
2020/2021946 2 127 132 3 344 8 106 4 104 2 101 13
2021/20221.472 220 208 15 7 212 4 215 41 161 5 54 330
2022/20232.131 218 73 26 191 189 372 2 385 549 23 60 43
2023/2024699 42 61 21 42 30 185 1 29 1 28 165 94
2024/20252.775 38 512 209 48 843 294 72 119 279 338 23 0
Totale 9.507