CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 7.678
EU - Europa 5.765
AS - Asia 4.050
SA - Sud America 586
Continente sconosciuto - Info sul continente non disponibili 99
AF - Africa 77
OC - Oceania 7
Totale 18.262
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Nazione #
US - Stati Uniti d'America 7.547
RU - Federazione Russa 1.878
SG - Singapore 1.564
GB - Regno Unito 1.504
CN - Cina 1.323
BR - Brasile 497
IT - Italia 444
DE - Germania 369
SE - Svezia 360
HK - Hong Kong 352
FR - Francia 343
FI - Finlandia 329
VN - Vietnam 315
IE - Irlanda 239
KR - Corea 141
UA - Ucraina 130
BD - Bangladesh 77
CA - Canada 74
TR - Turchia 58
IN - India 52
NL - Olanda 36
BE - Belgio 33
MX - Messico 33
JP - Giappone 31
AR - Argentina 26
IQ - Iraq 21
ID - Indonesia 20
PK - Pakistan 20
PL - Polonia 20
NG - Nigeria 19
ES - Italia 18
ZA - Sudafrica 16
CL - Cile 14
CO - Colombia 14
AT - Austria 10
UZ - Uzbekistan 10
EC - Ecuador 9
MY - Malesia 9
PE - Perù 8
AZ - Azerbaigian 7
EG - Egitto 7
IL - Israele 7
AE - Emirati Arabi Uniti 6
AU - Australia 6
CR - Costa Rica 6
KE - Kenya 6
MA - Marocco 6
CZ - Repubblica Ceca 5
JM - Giamaica 5
JO - Giordania 5
LT - Lituania 5
PY - Paraguay 5
UY - Uruguay 5
VE - Venezuela 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
GT - Guatemala 3
HR - Croazia 3
IR - Iran 3
KG - Kirghizistan 3
KZ - Kazakistan 3
LB - Libano 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
AO - Angola 2
CG - Congo 2
DZ - Algeria 2
EE - Estonia 2
EU - Europa 2
HN - Honduras 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
TT - Trinidad e Tobago 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
Totale 18.149
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Città #
Southend 1.290
Jacksonville 847
Singapore 805
Dallas 755
Ashburn 745
San Jose 677
Moscow 613
Chandler 606
Woodbridge 560
Hong Kong 349
Ann Arbor 319
Dublin 238
Houston 234
Beijing 217
Verona 215
Council Bluffs 194
The Dalles 192
New York 163
Los Angeles 125
Munich 124
Lawrence 111
Princeton 111
Wilmington 111
Ho Chi Minh City 106
Jinan 105
Nanjing 99
Helsinki 94
Shenyang 87
Hanoi 74
Santa Clara 69
Columbus 56
Hebei 54
Buffalo 52
São Paulo 50
Tianjin 46
Sindelfingen 44
Dearborn 41
Milan 41
Changsha 37
Taiyuan 37
Taizhou 36
Nanchang 34
Guangzhou 33
Haikou 32
Hangzhou 32
Ningbo 32
Lancaster 30
Las Vegas 29
Brussels 28
Zhengzhou 27
Tokyo 26
Boardman 25
Seattle 25
Jiaxing 24
Redondo Beach 24
Orem 22
Toronto 22
Turku 22
Atlanta 21
Brooklyn 20
Chicago 20
Norwalk 19
Seoul 19
Warsaw 19
Amsterdam 18
Annandale 18
Denver 18
Montreal 18
Phoenix 18
Abuja 17
Chennai 17
Fuzhou 17
London 17
Frankfurt am Main 16
San Francisco 16
Auburn Hills 15
Poplar 15
Haiphong 14
Belo Horizonte 13
Da Nang 13
Lanzhou 13
Rio de Janeiro 13
Riva 13
Johannesburg 12
Washington 12
Falls Church 11
Philadelphia 11
Rome 11
Boston 10
Clearwater 10
Fairfield 10
Jakarta 10
Kent 10
Manchester 10
Tashkent 10
Baghdad 9
Catania 9
Detroit 9
Istanbul 9
Mumbai 9
Totale 11.785
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 331
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 282
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 257
AZT-induced mitochondrial myopathy 246
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 242
Bortezomib-induced muscle toxicity in multiple myeloma 237
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 234
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 233
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 232
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 231
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 230
Acute reversible paralysis in critically ill patients 228
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 227
[Myopathy with lipid accumulation and type-II glutaric aciduria] 226
Autophagy, inflammation and innate immunity in inflammatory myopathies. 226
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 225
Oral zinc sulphate treatment in Wilson's disease 209
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 206
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 204
Hypokalemic periodic paralysis: a single fiber electromyographic study 201
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 199
McArdle disease and sporadic inclusion-body myositis. 199
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 199
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 197
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 197
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 194
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 192
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 189
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 189
Two and half years of oral zinc sulphate therapy in an adult patient with Wilson's disease. 187
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 184
Calpain 3 deficiency presenting as fiber type disproportion. 183
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 183
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 183
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 181
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 178
Polymyositis in solid organ transplant recipients receiving tacrolimus. 178
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 177
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 176
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 175
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 175
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 175
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function 174
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 173
T-cell anti-apoptotic mechanisms in inflammatory myopathies 173
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 171
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 170
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 170
Human skeletal muscle as a target organ of trichloroethylene toxicity. 169
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 169
The role of muscle biopsy in investigating isolated muscle pain 168
Current options in the treatment of mitochondrial diseases. 165
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. 164
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 162
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 160
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 160
Critical illness myopathy and neuropathy 159
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 159
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 158
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 158
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] 157
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 154
A case of persistent thyrotoxic myopathy 154
Sarcoidosis and inclusion body myositis. 152
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 152
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 151
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers 151
Neuropathology of mitochondrial diseases 147
Malattia del motoneurone 145
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 145
Protein expression of canine and feline muscular dystrophies 145
Relapsing-remitting painful masses of the skeletal muscle 144
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 143
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 143
Reversible upper limb muscle weakness with selective loss of thick filaments 143
The role of mitochondria in neurodegenerative diseases. 140
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 137
Critically ill patients: immunological evidence of inflammation in muscle biopsy 135
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] 134
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 134
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 132
Miotoniche, sindromi 130
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 129
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 129
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 128
Progression of carotid atheromatous involvement in cerebrovascular patients. 128
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 127
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 125
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 124
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 123
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 121
Phenotype modulators in myophosphorylase deficiency 121
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 121
Sporadic adult onset distal myopathy 119
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 119
Chronic alcoholic and corticosteroid myopathy 118
Dermatomyositis and retroperitoneal germ cell cancer 117
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions. 117
Paraplegia spastica familiare 115
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 114
Totale 17.142
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Categoria #
all - tutte 61.100
article - articoli 57.019
book - libri 0
conference - conferenze 2.222
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.859
Totale 122.200
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022512 0 0 0 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
2025/20266.625 446 643 482 988 1.622 419 581 263 559 336 135 151
2026/2027867 52 150 195 470 0 0 0 0 0 0 0 0
Totale 18.262