CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 6.897
EU - Europa 5.725
AS - Asia 4.026
SA - Sud America 560
AF - Africa 77
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 17.296
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Nazione #
US - Stati Uniti d'America 6.800
RU - Federazione Russa 1.878
SG - Singapore 1.561
GB - Regno Unito 1.489
CN - Cina 1.314
BR - Brasile 480
IT - Italia 422
DE - Germania 369
SE - Svezia 360
HK - Hong Kong 349
FR - Francia 343
FI - Finlandia 329
VN - Vietnam 315
IE - Irlanda 239
KR - Corea 141
UA - Ucraina 129
BD - Bangladesh 73
TR - Turchia 57
IN - India 51
CA - Canada 50
NL - Olanda 36
BE - Belgio 33
MX - Messico 32
JP - Giappone 31
AR - Argentina 26
IQ - Iraq 21
ID - Indonesia 20
NG - Nigeria 19
PK - Pakistan 19
PL - Polonia 19
ES - Italia 18
ZA - Sudafrica 16
CL - Cile 11
AT - Austria 10
CO - Colombia 10
UZ - Uzbekistan 10
EC - Ecuador 9
MY - Malesia 8
PE - Perù 8
AZ - Azerbaigian 7
EG - Egitto 7
IL - Israele 7
AE - Emirati Arabi Uniti 6
AU - Australia 6
KE - Kenya 6
MA - Marocco 6
CZ - Repubblica Ceca 5
JO - Giordania 5
LT - Lituania 5
PY - Paraguay 5
UY - Uruguay 5
AL - Albania 4
HU - Ungheria 4
NP - Nepal 4
PH - Filippine 4
PT - Portogallo 4
BO - Bolivia 3
CH - Svizzera 3
CR - Costa Rica 3
ET - Etiopia 3
IR - Iran 3
JM - Giamaica 3
KG - Kirghizistan 3
LB - Libano 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
VE - Venezuela 3
AO - Angola 2
CG - Congo 2
DZ - Algeria 2
EE - Estonia 2
EU - Europa 2
GT - Guatemala 2
HR - Croazia 2
KZ - Kazakistan 2
LU - Lussemburgo 2
LV - Lettonia 2
MT - Malta 2
NI - Nicaragua 2
NO - Norvegia 2
OM - Oman 2
RO - Romania 2
RS - Serbia 2
SA - Arabia Saudita 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 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
GA - Gabon 1
GR - Grecia 1
Totale 17.279
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Città #
Southend 1.290
Jacksonville 838
Singapore 805
Dallas 748
Moscow 613
Chandler 605
Ashburn 604
San Jose 577
Woodbridge 558
Hong Kong 346
Ann Arbor 318
Dublin 238
Houston 233
Verona 214
Beijing 211
The Dalles 192
New York 157
Munich 124
Los Angeles 121
Lawrence 111
Princeton 111
Wilmington 111
Ho Chi Minh City 106
Jinan 105
Nanjing 99
Helsinki 94
Council Bluffs 93
Shenyang 87
Hanoi 74
Columbus 56
Hebei 54
Santa Clara 53
Buffalo 51
Tianjin 46
Sindelfingen 44
Dearborn 40
São Paulo 38
Changsha 37
Milan 37
Taiyuan 37
Taizhou 36
Nanchang 34
Guangzhou 33
Haikou 32
Hangzhou 32
Ningbo 32
Lancaster 30
Brussels 28
Zhengzhou 27
Tokyo 26
Boardman 25
Jiaxing 24
Redondo Beach 24
Seattle 24
Orem 22
Turku 22
Seoul 19
Amsterdam 18
Chicago 18
Denver 18
Montreal 18
Norwalk 18
Warsaw 18
Abuja 17
Chennai 17
Fuzhou 17
Brooklyn 16
Frankfurt am Main 16
London 16
Atlanta 15
Auburn Hills 15
Poplar 15
San Francisco 15
Toronto 15
Haiphong 14
Belo Horizonte 13
Da Nang 13
Lanzhou 13
Rio de Janeiro 13
Riva 13
Johannesburg 12
Phoenix 12
Falls Church 11
Washington 11
Boston 10
Clearwater 10
Fairfield 10
Jakarta 10
Kent 10
Manchester 10
Tashkent 10
Baghdad 9
Mumbai 9
Nuremberg 9
Rome 9
Biên Hòa 8
Istanbul 8
Redmond 8
Stockholm 8
Brasília 7
Totale 11.298
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 324
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 271
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 249
AZT-induced mitochondrial myopathy 238
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 236
Bortezomib-induced muscle toxicity in multiple myeloma 232
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 225
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 224
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 223
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 222
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 221
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 220
[Myopathy with lipid accumulation and type-II glutaric aciduria] 218
Autophagy, inflammation and innate immunity in inflammatory myopathies. 218
Acute reversible paralysis in critically ill patients 215
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 213
Oral zinc sulphate treatment in Wilson's disease 200
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 199
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 199
Hypokalemic periodic paralysis: a single fiber electromyographic study 193
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 192
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 192
McArdle disease and sporadic inclusion-body myositis. 189
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 188
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 186
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 186
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 184
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 182
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 179
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 179
Two and half years of oral zinc sulphate therapy in an adult patient with Wilson's disease. 178
Calpain 3 deficiency presenting as fiber type disproportion. 175
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 174
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 172
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 172
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 172
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 171
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 170
Polymyositis in solid organ transplant recipients receiving tacrolimus. 168
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 166
T-cell anti-apoptotic mechanisms in inflammatory myopathies 166
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function 166
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 165
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 164
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 163
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 163
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 162
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 161
The role of muscle biopsy in investigating isolated muscle pain 161
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 160
Human skeletal muscle as a target organ of trichloroethylene toxicity. 158
Current options in the treatment of mitochondrial diseases. 157
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 156
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 155
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. 154
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 153
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 152
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 151
Critical illness myopathy and neuropathy 150
A case of persistent thyrotoxic myopathy 150
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 149
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 148
Sarcoidosis and inclusion body myositis. 147
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 146
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] 144
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 142
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers 142
Malattia del motoneurone 141
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 139
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 138
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 138
Protein expression of canine and feline muscular dystrophies 138
Relapsing-remitting painful masses of the skeletal muscle 137
Reversible upper limb muscle weakness with selective loss of thick filaments 137
Neuropathology of mitochondrial diseases 136
The role of mitochondria in neurodegenerative diseases. 130
Critically ill patients: immunological evidence of inflammation in muscle biopsy 128
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 127
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 126
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] 124
Miotoniche, sindromi 124
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 122
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 122
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 119
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 118
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 117
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 116
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 115
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 115
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 114
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 113
Phenotype modulators in myophosphorylase deficiency 112
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 112
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions. 112
Progression of carotid atheromatous involvement in cerebrovascular patients. 112
Chronic alcoholic and corticosteroid myopathy 111
Dermatomyositis and retroperitoneal germ cell cancer 111
Sporadic adult onset distal myopathy 110
Paraplegia spastica familiare 109
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 109
Totale 16.332
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Categoria #
all - tutte 56.424
article - articoli 52.664
book - libri 0
conference - conferenze 2.048
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.712
Totale 112.848
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202125 0 0 0 0 0 0 0 0 0 0 0 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
2025/20266.621 446 643 482 988 1.622 419 581 263 559 336 135 147
Totale 17.391