CATALOGO DEI PRODOTTI DELLA RICERCA

TOMELLERI, Giuliano
 Distribuzione geografica
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Continente #
NA - Nord America 4.030
EU - Europa 3.560
AS - Asia 1.616
SA - Sud America 47
AF - Africa 9
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 3
Totale 9.270
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Nazione #
US - Stati Uniti d'America 4.016
GB - Regno Unito 1.431
CN - Cina 1.061
SG - Singapore 445
SE - Svezia 352
FR - Francia 315
FI - Finlandia 272
RU - Federazione Russa 262
DE - Germania 252
IT - Italia 246
IE - Irlanda 234
UA - Ucraina 116
BR - Brasile 40
TR - Turchia 35
BE - Belgio 32
KR - Corea 25
NL - Olanda 16
CA - Canada 10
ES - Italia 8
IN - India 8
IL - Israele 6
JP - Giappone 6
CL - Cile 5
AU - Australia 4
MX - Messico 4
AL - Albania 3
AZ - Azerbaigian 3
EG - Egitto 3
IR - Iran 3
PT - Portogallo 3
VN - Vietnam 3
CH - Svizzera 2
CZ - Repubblica Ceca 2
EU - Europa 2
HU - Ungheria 2
ID - Indonesia 2
IQ - Iraq 2
JO - Giordania 2
KG - Kirghizistan 2
LU - Lussemburgo 2
LV - Lettonia 2
MY - Malesia 2
SK - Slovacchia (Repubblica Slovacca) 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
CM - Camerun 1
CO - Colombia 1
DK - Danimarca 1
EC - Ecuador 1
EE - Estonia 1
HK - Hong Kong 1
IS - Islanda 1
KE - Kenya 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
MA - Marocco 1
MK - Macedonia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PH - Filippine 1
PK - Pakistan 1
PS - Palestinian Territory 1
RO - Romania 1
SA - Arabia Saudita 1
SC - Seychelles 1
UZ - Uzbekistan 1
Totale 9.270
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Città #
Southend 1.290
Jacksonville 838
Chandler 605
Woodbridge 558
Singapore 353
Ann Arbor 318
Dublin 234
Houston 227
Ashburn 170
Beijing 154
Lawrence 111
Princeton 111
Wilmington 111
Jinan 105
Nanjing 96
Verona 95
New York 93
Shenyang 87
Helsinki 67
Hebei 54
Munich 46
Sindelfingen 44
Dearborn 40
Tianjin 40
Changsha 36
Taiyuan 36
Taizhou 35
Nanchang 34
Haikou 32
Ningbo 32
Hangzhou 30
Lancaster 30
Milan 28
Brussels 27
Guangzhou 27
Los Angeles 27
Boardman 25
Jiaxing 23
Zhengzhou 23
Norwalk 18
Seattle 18
Fuzhou 17
Santa Clara 17
Seoul 16
Auburn Hills 15
Dallas 13
Lanzhou 13
Moscow 13
Riva 13
Chicago 12
Falls Church 11
Fairfield 10
Kent 10
Clearwater 9
Redmond 8
San Francisco 8
Washington 8
Detroit 6
Redwood City 6
Rome 6
San Mateo 6
Chiusdino 5
Düsseldorf 5
Gangdong-gu 5
Madrid 5
Novokuznetsk 5
Toronto 5
Amsterdam 4
Buk-gu 4
Catania 4
Dongguan 4
Kemerovo 4
Montréal 4
Qingdao 4
Renton 4
Shanghai 4
Torino 4
Venice 4
Waanrode 4
Augusta 3
Baku 3
Cairo 3
Chongqing 3
Dalian 3
Foggia 3
Lisbon 3
London 3
Melbourne 3
Monmouth Junction 3
Morelos 3
Mumbai 3
Philadelphia 3
Puxian 3
Saint Louis 3
Schio 3
Tokyo 3
Valladolid 3
Andover 2
Ardabil 2
Austin 2
Totale 6.683
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Nome #
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 155
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 150
Oral zinc sulphate treatment in Wilson's disease 144
Hypokalemic periodic paralysis: a single fiber electromyographic study 139
Il granuloma polmonare lipoideo nel morbo di Parkinson [Lipoid pulmonary granuloma in Parkinson's disease. Presentation of clinical case] 135
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 133
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 127
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 124
Polimiosite infantile: descrizione di un caso [Infantile polymyositis: a case description] 123
Acute reversible paralysis in critically ill patients 121
AZT-induced mitochondrial myopathy 116
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 115
Two and half years of oral zinc sulphate therapy in an adult patient with Wilson's disease. 112
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 112
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 110
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 107
Human skeletal muscle as a target organ of trichloroethylene toxicity. 106
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] 105
[Myopathy with lipid accumulation and type-II glutaric aciduria] 104
Involvement of the peripheral nervous system in spino-cerebellar ataxia (neurophysiological and histopathological findings) 103
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 103
T-cell anti-apoptotic mechanisms in inflammatory myopathies 101
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 100
The role of muscle biopsy in investigating isolated muscle pain 100
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 100
Aspetti elettromiografici e istologici in corso di Malattia di Friedreich[Electromyographic and histological aspects during a course of Friedreich's disease] 99
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 99
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 98
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 98
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 97
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 97
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 97
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 97
Malattia del motoneurone 96
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 96
Neuropatie familiari con tendenza alla paralisi da compressione. Correlazioni cliniche, neurofisiologiche ed istopatologiche 95
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 95
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers 94
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 94
Autophagy, inflammation and innate immunity in inflammatory myopathies. 94
Miotoniche, sindromi 93
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 93
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] 91
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 91
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 91
Critical illness myopathy and neuropathy 89
Calpain 3 deficiency presenting as fiber type disproportion. 89
Anti-acetylcoline receptor antibodies, thymic histology and clinical parameters in myastenia gravis. 88
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 88
McArdle disease and sporadic inclusion-body myositis. 87
Reversible upper limb muscle weakness with selective loss of thick filaments 86
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 85
Bortezomib-induced muscle toxicity in multiple myeloma 84
Polymyositis in solid organ transplant recipients receiving tacrolimus. 82
Increased serum levels of ICAM-1 ELAM-1 and TNF-a in inflammatory disorders of peripheral nervous system 81
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 81
Phenytoin-phenobarbiatl interaction: importance of free plasma phenytoin monitoring 80
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality? 80
Current options in the treatment of mitochondrial diseases. 80
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 79
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 79
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 78
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 78
Chronic alcoholic and corticosteroid myopathy 75
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 75
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 75
Motor neuron disease and HIV-infection in 30-years-old HIV positive heroin abuser: a causal relationship? 74
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 74
A case of persistent thyrotoxic myopathy 74
Sarcoidosis and inclusion body myositis. 74
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 74
Sporadic adult onset distal myopathy 73
Critically ill patients: immunological evidence of inflammation in muscle biopsy 72
Transitory L-carnitine depletion in rat skeletal muscle by D-carnitine 72
Dermatomyositis and retroperitoneal germ cell cancer 72
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. 72
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 71
The role of mitochondria in neurodegenerative diseases. 71
Progression of carotid atheromatous involvement in cerebrovascular patients. 70
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. 70
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 70
Paraplegia spastica familiare 69
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 69
Neuropathology of mitochondrial diseases 69
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 68
Polyglucosan body myopathy: a new case 68
Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. 66
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction 66
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene. 65
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 64
Novel mitochondrial tRNA(Leu(CUN)) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype 62
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 62
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients 59
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 59
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 57
Relapsing-remitting painful masses of the skeletal muscle 56
Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects 55
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 55
Critical illness myopathy. 55
Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutation 54
Totale 8.830
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Categoria #
all - tutte 31.893
article - articoli 29.618
book - libri 0
conference - conferenze 1.234
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.041
Totale 63.786
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020680 0 0 0 0 0 0 152 108 47 130 52 191
2020/2021975 103 146 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
2024/2025949 126 135 59 344 133 100 52 0 0 0 0 0
Totale 9.363