CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 5.164
EU - Europa 3.790
AS - Asia 2.779
SA - Sud America 365
AF - Africa 28
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 12.135
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Nazione #
US - Stati Uniti d'America 5.122
GB - Regno Unito 1.450
CN - Cina 1.125
SG - Singapore 1.059
SE - Svezia 354
DE - Germania 347
BR - Brasile 340
FR - Francia 331
FI - Finlandia 326
HK - Hong Kong 315
RU - Federazione Russa 265
IT - Italia 262
IE - Irlanda 235
UA - Ucraina 122
KR - Corea 98
TR - Turchia 47
BE - Belgio 32
VN - Vietnam 28
IN - India 22
CA - Canada 21
NL - Olanda 20
MX - Messico 13
BD - Bangladesh 11
JP - Giappone 11
ES - Italia 10
IQ - Iraq 9
ZA - Sudafrica 8
CL - Cile 7
PK - Pakistan 7
AR - Argentina 6
AT - Austria 6
IL - Israele 6
AZ - Azerbaigian 5
UZ - Uzbekistan 5
AU - Australia 4
ID - Indonesia 4
KE - Kenya 4
UY - Uruguay 4
AL - Albania 3
CZ - Repubblica Ceca 3
EC - Ecuador 3
EG - Egitto 3
IR - Iran 3
LB - Libano 3
PL - Polonia 3
PT - Portogallo 3
CH - Svizzera 2
DZ - Algeria 2
EU - Europa 2
HU - Ungheria 2
JM - Giamaica 2
JO - Giordania 2
KG - Kirghizistan 2
LU - Lussemburgo 2
LV - Lettonia 2
MA - Marocco 2
MY - Malesia 2
NP - Nepal 2
OM - Oman 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 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
BO - Bolivia 1
CM - Camerun 1
CO - Colombia 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 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
PE - Perù 1
PH - Filippine 1
PS - Palestinian Territory 1
PY - Paraguay 1
RO - Romania 1
SC - Seychelles 1
SI - Slovenia 1
SN - Senegal 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
Totale 12.134
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Città #
Southend 1.290
Jacksonville 838
Dallas 698
Chandler 605
Woodbridge 558
Singapore 488
Ann Arbor 318
Hong Kong 314
Dublin 234
Houston 227
Ashburn 198
Beijing 174
Munich 122
Lawrence 111
Princeton 111
Wilmington 111
Jinan 105
New York 100
Verona 100
Nanjing 98
Helsinki 91
Shenyang 87
Los Angeles 76
The Dalles 60
Columbus 55
Hebei 54
Sindelfingen 44
Dearborn 40
Tianjin 40
Taiyuan 37
Buffalo 36
Changsha 36
Taizhou 36
Nanchang 34
Haikou 32
Ningbo 32
Guangzhou 31
Hangzhou 31
Milan 31
Lancaster 30
Brussels 27
Zhengzhou 26
Boardman 25
Santa Clara 24
Jiaxing 23
Turku 22
Seattle 19
Norwalk 18
Chicago 17
Fuzhou 17
Redondo Beach 17
Seoul 17
Council Bluffs 16
Auburn Hills 15
Belo Horizonte 13
Lanzhou 13
Moscow 13
Riva 13
São Paulo 13
San Francisco 12
Falls Church 11
Brooklyn 10
Fairfield 10
Kent 10
Washington 10
Clearwater 9
Ho Chi Minh City 9
Nuremberg 9
Hanoi 8
Redmond 8
Rio de Janeiro 8
Tokyo 8
Boston 7
Detroit 7
Istanbul 7
Phoenix 7
Rome 7
Toronto 7
Amsterdam 6
Brasília 6
Caxias do Sul 6
Chennai 6
Johannesburg 6
Jyväskylä 6
London 6
Porto Alegre 6
Redwood City 6
San Mateo 6
Atlanta 5
Baku 5
Chiusdino 5
Düsseldorf 5
Frankfurt am Main 5
Gangdong-gu 5
Madrid 5
Montreal 5
Mumbai 5
Novokuznetsk 5
Tashkent 5
Buk-gu 4
Totale 8.344
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 251
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 190
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 187
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 165
Oral zinc sulphate treatment in Wilson's disease 161
AZT-induced mitochondrial myopathy 161
Hypokalemic periodic paralysis: a single fiber electromyographic study 161
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 157
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 152
Acute reversible paralysis in critically ill patients 152
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 150
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 148
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 145
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 143
[Myopathy with lipid accumulation and type-II glutaric aciduria] 143
Autophagy, inflammation and innate immunity in inflammatory myopathies. 140
Bortezomib-induced muscle toxicity in multiple myeloma 140
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 137
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 137
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 136
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 135
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 134
Two and half years of oral zinc sulphate therapy in an adult patient with Wilson's disease. 131
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 131
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 131
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 130
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 130
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 128
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 127
Human skeletal muscle as a target organ of trichloroethylene toxicity. 123
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] 122
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 122
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 122
Calpain 3 deficiency presenting as fiber type disproportion. 122
The role of muscle biopsy in investigating isolated muscle pain 122
T-cell anti-apoptotic mechanisms in inflammatory myopathies 121
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 118
McArdle disease and sporadic inclusion-body myositis. 118
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 117
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 117
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 117
Polymyositis in solid organ transplant recipients receiving tacrolimus. 117
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 115
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 115
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 114
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 114
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers 112
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 112
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 112
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 111
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 111
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 111
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 111
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 111
Critical illness myopathy and neuropathy 110
Malattia del motoneurone 109
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 109
Reversible upper limb muscle weakness with selective loss of thick filaments 109
Miotoniche, sindromi 107
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 105
A case of persistent thyrotoxic myopathy 105
Sarcoidosis and inclusion body myositis. 105
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 104
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] 103
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 103
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. 102
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 100
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 98
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 98
Current options in the treatment of mitochondrial diseases. 97
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 95
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 94
Chronic alcoholic and corticosteroid myopathy 93
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 92
Transitory L-carnitine depletion in rat skeletal muscle by D-carnitine 91
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 91
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 91
The role of mitochondria in neurodegenerative diseases. 91
Sporadic adult onset distal myopathy 90
Critically ill patients: immunological evidence of inflammation in muscle biopsy 90
Dermatomyositis and retroperitoneal germ cell cancer 90
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 88
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 88
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 87
Neuropathology of mitochondrial diseases 87
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 86
Paraplegia spastica familiare 86
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 86
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 86
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 84
Polyglucosan body myopathy: a new case 83
Progression of carotid atheromatous involvement in cerebrovascular patients. 83
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 81
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 80
Relapsing-remitting painful masses of the skeletal muscle 80
Protein expression of canine and feline muscular dystrophies 78
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 77
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 75
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions. 75
Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutation 74
Totale 11.476
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Categoria #
all - tutte 42.688
article - articoli 39.747
book - libri 0
conference - conferenze 1.591
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.350
Totale 85.376
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021726 0 0 44 105 114 119 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
2025/20261.460 446 643 371 0 0 0 0 0 0 0 0 0
Totale 12.230