CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 6.692
EU - Europa 5.693
AS - Asia 3.969
SA - Sud America 556
AF - Africa 77
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 16.998
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Nazione #
US - Stati Uniti d'America 6.604
RU - Federazione Russa 1.878
SG - Singapore 1.557
GB - Regno Unito 1.489
CN - Cina 1.309
BR - Brasile 478
IT - Italia 391
DE - Germania 369
SE - Svezia 360
HK - Hong Kong 347
FR - Francia 343
FI - Finlandia 329
VN - Vietnam 315
IE - Irlanda 239
KR - Corea 141
UA - Ucraina 129
TR - Turchia 57
IN - India 50
CA - Canada 45
NL - Olanda 35
BE - Belgio 33
JP - Giappone 31
MX - Messico 31
BD - Bangladesh 28
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
UZ - Uzbekistan 10
CO - Colombia 9
EC - Ecuador 9
MY - Malesia 8
AZ - Azerbaigian 7
EG - Egitto 7
IL - Israele 7
PE - Perù 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
ET - Etiopia 3
IR - Iran 3
KG - Kirghizistan 3
LB - Libano 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
VE - Venezuela 3
AO - Angola 2
CG - Congo 2
CR - Costa Rica 2
DZ - Algeria 2
EE - Estonia 2
EU - Europa 2
HR - Croazia 2
JM - Giamaica 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
GT - Guatemala 1
Totale 16.981
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Città #
Southend 1.290
Jacksonville 838
Singapore 803
Dallas 744
Moscow 613
Chandler 605
Ashburn 577
Woodbridge 558
San Jose 557
Hong Kong 344
Ann Arbor 318
Dublin 238
Houston 233
Verona 214
Beijing 211
The Dalles 192
New York 151
Munich 124
Los Angeles 118
Lawrence 111
Princeton 111
Wilmington 111
Ho Chi Minh City 106
Jinan 105
Nanjing 99
Helsinki 94
Shenyang 87
Hanoi 74
Columbus 55
Hebei 54
Buffalo 47
Santa Clara 46
Tianjin 46
Sindelfingen 44
Dearborn 40
São Paulo 38
Changsha 37
Taiyuan 37
Taizhou 36
Milan 35
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 23
Turku 22
Orem 21
Seoul 19
Amsterdam 18
Chicago 18
Montreal 18
Norwalk 18
Warsaw 18
Abuja 17
Chennai 17
Denver 17
Fuzhou 17
Brooklyn 16
Council Bluffs 16
Frankfurt am Main 16
Auburn Hills 15
London 15
Poplar 15
San Francisco 15
Atlanta 14
Haiphong 14
Belo Horizonte 13
Da Nang 13
Lanzhou 13
Rio de Janeiro 13
Riva 13
Johannesburg 12
Phoenix 12
Toronto 12
Falls Church 11
Washington 11
Fairfield 10
Jakarta 10
Kent 10
Manchester 10
Tashkent 10
Baghdad 9
Boston 9
Clearwater 9
Nuremberg 9
Biên Hòa 8
Istanbul 8
Mumbai 8
Redmond 8
Rome 8
Stockholm 8
Brasília 7
Totale 11.131
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 317
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
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 236
Bortezomib-induced muscle toxicity in multiple myeloma 228
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 224
AZT-induced mitochondrial myopathy 224
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 223
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 222
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 221
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 217
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 217
[Myopathy with lipid accumulation and type-II glutaric aciduria] 216
Autophagy, inflammation and innate immunity in inflammatory myopathies. 214
Acute reversible paralysis in critically ill patients 213
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 212
Oral zinc sulphate treatment in Wilson's disease 200
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 198
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 194
Hypokalemic periodic paralysis: a single fiber electromyographic study 193
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 192
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 189
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 187
McArdle disease and sporadic inclusion-body myositis. 185
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 185
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 184
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 183
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 178
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 178
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. 171
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 171
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 171
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 169
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 169
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 169
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 168
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 168
Polymyositis in solid organ transplant recipients receiving tacrolimus. 167
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 165
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 165
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 163
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 163
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 162
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 160
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 160
The role of muscle biopsy in investigating isolated muscle pain 160
T-cell anti-apoptotic mechanisms in inflammatory myopathies 158
Human skeletal muscle as a target organ of trichloroethylene toxicity. 157
Current options in the treatment of mitochondrial diseases. 157
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 155
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 155
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 155
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 151
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. 151
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 150
A case of persistent thyrotoxic myopathy 150
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 150
Critical illness myopathy and neuropathy 149
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 148
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 147
Sarcoidosis and inclusion body myositis. 145
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
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 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
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 138
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 137
Neuropathology of mitochondrial diseases 136
Relapsing-remitting painful masses of the skeletal muscle 135
Protein expression of canine and feline muscular dystrophies 135
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 133
Reversible upper limb muscle weakness with selective loss of thick filaments 133
The role of mitochondria in neurodegenerative diseases. 128
Critically ill patients: immunological evidence of inflammation in muscle biopsy 126
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 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
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 123
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 119
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 117
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 117
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 116
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 116
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 115
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 114
Chronic alcoholic and corticosteroid myopathy 111
Dermatomyositis and retroperitoneal germ cell cancer 111
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 111
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 110
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions. 110
Paraplegia spastica familiare 109
Sporadic adult onset distal myopathy 109
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 109
Progression of carotid atheromatous involvement in cerebrovascular patients. 108
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 106
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function 106
Transitory L-carnitine depletion in rat skeletal muscle by D-carnitine 104
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 104
Totale 16.060
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Categoria #
all - tutte 53.425
article - articoli 49.853
book - libri 0
conference - conferenze 1.948
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.624
Totale 106.850
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021168 0 0 0 0 0 0 0 0 0 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
2025/20266.323 446 643 482 988 1.622 419 581 263 559 320 0 0
Totale 17.093