CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 5.686
EU - Europa 5.475
AS - Asia 3.487
SA - Sud America 524
AF - Africa 45
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 15.226
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Nazione #
US - Stati Uniti d'America 5.613
RU - Federazione Russa 1.877
GB - Regno Unito 1.474
SG - Singapore 1.394
CN - Cina 1.257
BR - Brasile 458
SE - Svezia 360
DE - Germania 351
FR - Francia 332
FI - Finlandia 326
HK - Hong Kong 323
IT - Italia 270
IE - Irlanda 235
VN - Vietnam 170
UA - Ucraina 122
KR - Corea 121
TR - Turchia 50
IN - India 37
CA - Canada 35
BE - Belgio 32
MX - Messico 26
AR - Argentina 25
JP - Giappone 23
NL - Olanda 21
BD - Bangladesh 19
ID - Indonesia 18
ES - Italia 16
PL - Polonia 16
ZA - Sudafrica 14
IQ - Iraq 12
PK - Pakistan 11
CL - Cile 10
AT - Austria 9
AE - Emirati Arabi Uniti 6
CO - Colombia 6
EC - Ecuador 6
EG - Egitto 6
IL - Israele 6
PE - Perù 6
UZ - Uzbekistan 6
AZ - Azerbaigian 5
KE - Kenya 5
MA - Marocco 5
UY - Uruguay 5
AU - Australia 4
PT - Portogallo 4
PY - Paraguay 4
AL - Albania 3
CZ - Repubblica Ceca 3
HU - Ungheria 3
IR - Iran 3
KG - Kirghizistan 3
LB - Libano 3
LT - Lituania 3
MY - Malesia 3
NP - Nepal 3
BO - Bolivia 2
CH - Svizzera 2
CR - Costa Rica 2
DZ - Algeria 2
EE - Estonia 2
EU - Europa 2
JM - Giamaica 2
JO - Giordania 2
LU - Lussemburgo 2
LV - Lettonia 2
NI - Nicaragua 2
OM - Oman 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TN - Tunisia 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BG - Bulgaria 1
BJ - Benin 1
BN - Brunei Darussalam 1
CD - Congo 1
CI - Costa d'Avorio 1
CM - Camerun 1
DK - Danimarca 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GR - Grecia 1
GT - Guatemala 1
HN - Honduras 1
IS - Islanda 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
MK - Macedonia 1
MU - Mauritius 1
MZ - Mozambico 1
NZ - Nuova Zelanda 1
PH - Filippine 1
Totale 15.219
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Città #
Southend 1.290
Jacksonville 838
Dallas 738
Singapore 671
Moscow 613
Chandler 605
Woodbridge 558
Ashburn 337
Hong Kong 322
Ann Arbor 318
Dublin 234
Houston 233
Beijing 205
New York 138
Munich 123
The Dalles 119
Lawrence 111
Princeton 111
Wilmington 111
Jinan 105
Los Angeles 103
Verona 101
Nanjing 99
Helsinki 91
Shenyang 87
Columbus 55
Hebei 54
Ho Chi Minh City 54
Tianjin 46
Buffalo 45
Sindelfingen 44
Dearborn 40
Changsha 37
Hanoi 37
Taiyuan 37
Taizhou 36
Santa Clara 35
Nanchang 34
Guangzhou 33
Milan 33
São Paulo 33
Haikou 32
Hangzhou 32
Ningbo 32
Lancaster 30
Brussels 27
Zhengzhou 27
Boardman 25
Jiaxing 24
Redondo Beach 24
Seattle 23
Turku 22
Tokyo 20
Seoul 19
Chicago 18
Norwalk 18
Fuzhou 17
Council Bluffs 16
Auburn Hills 15
Brooklyn 15
Warsaw 15
Chennai 14
Denver 14
Atlanta 13
Belo Horizonte 13
Lanzhou 13
Orem 13
Riva 13
San Francisco 13
London 12
Montreal 12
Phoenix 12
Poplar 12
Falls Church 11
Johannesburg 11
Fairfield 10
Jakarta 10
Kent 10
Toronto 10
Washington 10
Boston 9
Clearwater 9
Nuremberg 9
Rio de Janeiro 9
Haiphong 8
Redmond 8
San Jose 8
Stockholm 8
Amsterdam 7
Brasília 7
Caxias do Sul 7
Detroit 7
Istanbul 7
Manchester 7
Mumbai 7
Porto Alegre 7
Rome 7
Cairo 6
Guarulhos 6
Jyväskylä 6
Totale 9.740
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 291
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 245
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 223
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 211
AZT-induced mitochondrial myopathy 205
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 203
Bortezomib-induced muscle toxicity in multiple myeloma 199
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 198
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 198
[Myopathy with lipid accumulation and type-II glutaric aciduria] 195
Acute reversible paralysis in critically ill patients 195
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 195
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 192
Oral zinc sulphate treatment in Wilson's disease 191
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 191
Autophagy, inflammation and innate immunity in inflammatory myopathies. 185
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 184
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 177
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 176
Hypokalemic periodic paralysis: a single fiber electromyographic study 176
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 175
McArdle disease and sporadic inclusion-body myositis. 168
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 166
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 166
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 165
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 165
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 165
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 160
Two and half years of oral zinc sulphate therapy in an adult patient with Wilson's disease. 158
Calpain 3 deficiency presenting as fiber type disproportion. 158
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 158
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 157
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 156
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 153
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 150
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 150
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 149
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 148
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 147
Polymyositis in solid organ transplant recipients receiving tacrolimus. 147
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 147
The role of muscle biopsy in investigating isolated muscle pain 146
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 145
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 145
T-cell anti-apoptotic mechanisms in inflammatory myopathies 144
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 143
Human skeletal muscle as a target organ of trichloroethylene toxicity. 143
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 143
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 142
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 141
Miopatia distale sporadica: descrizione di un caso in un soggetto femminile [Sporadic distal myopathy. Description of a case in a patient of the female sex] 138
Critical illness myopathy and neuropathy 138
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 138
Current options in the treatment of mitochondrial diseases. 137
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 135
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 135
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 133
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 133
A case of persistent thyrotoxic myopathy 133
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers 132
Sarcoidosis and inclusion body myositis. 132
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 131
An Italian multicentre randomized study on early treatment of Parkinson disease: Comparison of L-dopa, L-deprenyl and dopamine-agonists. Study design and preliminary results. 131
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 127
Malattia del motoneurone 126
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 126
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 125
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 125
Reversible upper limb muscle weakness with selective loss of thick filaments 122
Protein expression of canine and feline muscular dystrophies 121
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 120
Neuropathology of mitochondrial diseases 120
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 119
Miotoniche, sindromi 118
Relapsing-remitting painful masses of the skeletal muscle 117
The role of mitochondria in neurodegenerative diseases. 115
Distrofia muscolare oculo-faringea. Descrizione di un caso con interessamento del Sistema Nervoso Centrale [Oculopharyngeal muscular dystrophy. Description of a case with involvement of the central nervous system] 113
Critically ill patients: immunological evidence of inflammation in muscle biopsy 113
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 111
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 110
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 110
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 105
Chronic alcoholic and corticosteroid myopathy 104
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 103
Dermatomyositis and retroperitoneal germ cell cancer 102
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 102
Paraplegia spastica familiare 101
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 101
Sporadic adult onset distal myopathy 100
Transitory L-carnitine depletion in rat skeletal muscle by D-carnitine 100
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 99
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 98
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 97
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 96
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions. 96
Progression of carotid atheromatous involvement in cerebrovascular patients. 96
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 95
Polyglucosan body myopathy: a new case 95
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 95
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 94
Totale 14.393
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Categoria #
all - tutte 49.753
article - articoli 46.405
book - libri 0
conference - conferenze 1.824
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.524
Totale 99.506
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021463 0 0 0 0 0 119 11 94 71 15 128 25
2021/20221.055 140 399 4 98 17 18 15 46 29 20 78 191
2022/20231.784 151 164 173 294 175 379 23 117 230 6 43 29
2023/2024746 41 56 65 90 85 142 19 63 9 36 90 50
2024/20252.356 126 135 59 344 133 100 175 135 360 128 197 464
2025/20264.551 446 643 482 988 1.622 370 0 0 0 0 0 0
Totale 15.321