CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 5.560
EU - Europa 5.252
AS - Asia 3.253
SA - Sud America 513
AF - Africa 40
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 14.627
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Nazione #
US - Stati Uniti d'America 5.494
RU - Federazione Russa 1.664
GB - Regno Unito 1.473
CN - Cina 1.243
SG - Singapore 1.223
BR - Brasile 454
SE - Svezia 358
DE - Germania 351
FR - Francia 332
FI - Finlandia 326
HK - Hong Kong 321
IT - Italia 269
IE - Irlanda 235
VN - Vietnam 140
UA - Ucraina 122
KR - Corea 114
TR - Turchia 50
IN - India 36
CA - Canada 34
BE - Belgio 32
AR - Argentina 23
JP - Giappone 22
MX - Messico 21
NL - Olanda 21
BD - Bangladesh 18
ID - Indonesia 18
PL - Polonia 16
ES - Italia 15
ZA - Sudafrica 14
CL - Cile 10
IQ - Iraq 10
PK - Pakistan 9
AT - Austria 6
EG - Egitto 6
IL - Israele 6
PE - Perù 6
AZ - Azerbaigian 5
EC - Ecuador 5
KE - Kenya 5
UY - Uruguay 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
PT - Portogallo 4
PY - Paraguay 4
AL - Albania 3
CO - Colombia 3
CZ - Repubblica Ceca 3
IR - Iran 3
KG - Kirghizistan 3
LB - Libano 3
LT - Lituania 3
MA - Marocco 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
HU - Ungheria 2
JM - Giamaica 2
JO - Giordania 2
LU - Lussemburgo 2
LV - Lettonia 2
OM - Oman 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 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
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
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PS - Palestinian Territory 1
RO - Romania 1
SC - Seychelles 1
SI - Slovenia 1
Totale 14.622
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Città #
Southend 1.290
Jacksonville 838
Dallas 738
Chandler 605
Woodbridge 558
Moscow 554
Singapore 500
Hong Kong 320
Ann Arbor 318
Ashburn 307
Dublin 234
Houston 232
Beijing 205
New York 137
Munich 123
Lawrence 111
Princeton 111
Wilmington 111
Jinan 105
Los Angeles 102
Verona 101
Nanjing 99
Helsinki 91
Shenyang 87
The Dalles 60
Columbus 55
Hebei 54
Tianjin 46
Buffalo 45
Ho Chi Minh City 44
Sindelfingen 44
Dearborn 40
Changsha 37
Taiyuan 37
Taizhou 36
Santa Clara 35
Nanchang 34
Milan 33
São Paulo 33
Haikou 32
Hangzhou 32
Hanoi 32
Ningbo 32
Guangzhou 31
Lancaster 30
Brussels 27
Zhengzhou 26
Boardman 25
Jiaxing 24
Redondo Beach 24
Seattle 23
Turku 22
Seoul 19
Tokyo 19
Chicago 18
Norwalk 18
Fuzhou 17
Council Bluffs 16
Auburn Hills 15
Brooklyn 15
Warsaw 15
Chennai 14
Atlanta 13
Belo Horizonte 13
Denver 13
Lanzhou 13
Riva 13
San Francisco 13
London 12
Phoenix 12
Falls Church 11
Johannesburg 11
Montreal 11
Orem 11
Poplar 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
Amsterdam 7
Brasília 7
Caxias do Sul 7
Detroit 7
Istanbul 7
Manchester 7
Mumbai 7
Porto Alegre 7
Rome 7
Cairo 6
Jyväskylä 6
Redwood City 6
San Mateo 6
Stockholm 6
Totale 9.388
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 283
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 235
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 216
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 201
AZT-induced mitochondrial myopathy 198
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 196
Bortezomib-induced muscle toxicity in multiple myeloma 192
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 191
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 189
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 186
Oral zinc sulphate treatment in Wilson's disease 184
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 184
Acute reversible paralysis in critically ill patients 182
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 182
Autophagy, inflammation and innate immunity in inflammatory myopathies. 179
[Myopathy with lipid accumulation and type-II glutaric aciduria] 177
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 173
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 173
Hypokalemic periodic paralysis: a single fiber electromyographic study 173
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 172
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 168
McArdle disease and sporadic inclusion-body myositis. 165
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 161
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 159
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 158
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 157
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 157
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 154
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 153
Two and half years of oral zinc sulphate therapy in an adult patient with Wilson's disease. 152
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 150
Calpain 3 deficiency presenting as fiber type disproportion. 150
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 150
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 149
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 148
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 145
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 144
Polymyositis in solid organ transplant recipients receiving tacrolimus. 143
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 142
The role of muscle biopsy in investigating isolated muscle pain 142
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 142
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 140
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 139
T-cell anti-apoptotic mechanisms in inflammatory myopathies 139
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 139
Human skeletal muscle as a target organ of trichloroethylene toxicity. 138
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 138
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 138
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 136
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 135
Critical illness myopathy and neuropathy 132
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 132
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] 131
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 131
Current options in the treatment of mitochondrial diseases. 131
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 130
A case of persistent thyrotoxic myopathy 130
Sarcoidosis and inclusion body myositis. 129
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 128
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. 128
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 127
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 123
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 123
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers 122
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 120
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 120
Malattia del motoneurone 118
Protein expression of canine and feline muscular dystrophies 118
Reversible upper limb muscle weakness with selective loss of thick filaments 118
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 117
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 117
Neuropathology of mitochondrial diseases 117
Miotoniche, sindromi 114
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 114
The role of mitochondria in neurodegenerative diseases. 112
Relapsing-remitting painful masses of the skeletal muscle 111
Critically ill patients: immunological evidence of inflammation in muscle biopsy 110
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 108
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] 107
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 105
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 105
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 103
Chronic alcoholic and corticosteroid myopathy 100
Dermatomyositis and retroperitoneal germ cell cancer 99
Transitory L-carnitine depletion in rat skeletal muscle by D-carnitine 98
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 98
Sporadic adult onset distal myopathy 97
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 97
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 97
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 96
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 95
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 94
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 93
Polyglucosan body myopathy: a new case 93
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 93
Paraplegia spastica familiare 92
Progression of carotid atheromatous involvement in cerebrovascular patients. 92
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 91
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function 90
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 89
Totale 13.832
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Categoria #
all - tutte 48.529
article - articoli 45.266
book - libri 0
conference - conferenze 1.778
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.485
Totale 97.058
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021577 0 0 0 0 114 119 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
2025/20263.952 446 643 482 988 1.393 0 0 0 0 0 0 0
Totale 14.722