CATALOGO DEI PRODOTTI DELLA RICERCA

VATTEMI, Gaetano Nicola
 Distribuzione geografica
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Continente #
NA - Nord America 6.394
EU - Europa 4.834
AS - Asia 3.720
SA - Sud America 560
Continente sconosciuto - Info sul continente non disponibili 149
AF - Africa 119
OC - Oceania 7
AN - Antartide 1
Totale 15.784
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Nazione #
US - Stati Uniti d'America 6.268
RU - Federazione Russa 1.868
SG - Singapore 1.472
CN - Cina 1.089
GB - Regno Unito 906
BR - Brasile 471
IT - Italia 411
DE - Germania 346
VN - Vietnam 345
HK - Hong Kong 304
FR - Francia 268
SE - Svezia 262
FI - Finlandia 250
IE - Irlanda 204
KR - Corea 128
UA - Ucraina 88
CA - Canada 69
BD - Bangladesh 68
IN - India 61
TR - Turchia 59
NL - Olanda 50
JP - Giappone 38
MX - Messico 36
AR - Argentina 35
ID - Indonesia 35
PL - Polonia 31
BE - Belgio 29
NG - Nigeria 28
ZA - Sudafrica 27
ES - Italia 25
IQ - Iraq 22
PK - Pakistan 21
AT - Austria 19
RO - Romania 15
CH - Svizzera 11
CL - Cile 11
EC - Ecuador 11
KE - Kenya 10
MA - Marocco 10
UZ - Uzbekistan 10
BJ - Benin 9
LT - Lituania 8
MY - Malesia 8
TG - Togo 8
IL - Israele 7
VE - Venezuela 7
AE - Emirati Arabi Uniti 6
CO - Colombia 6
EG - Egitto 6
PY - Paraguay 6
UY - Uruguay 6
AU - Australia 5
DO - Repubblica Dominicana 5
GR - Grecia 5
JO - Giordania 5
NP - Nepal 5
PE - Perù 5
PH - Filippine 5
SA - Arabia Saudita 5
AL - Albania 4
AZ - Azerbaigian 4
BG - Bulgaria 4
KZ - Kazakistan 4
AM - Armenia 3
CG - Congo 3
DZ - Algeria 3
GT - Guatemala 3
HR - Croazia 3
LB - Libano 3
NO - Norvegia 3
PT - Portogallo 3
RS - Serbia 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BO - Bolivia 2
CI - Costa d'Avorio 2
CR - Costa Rica 2
CZ - Repubblica Ceca 2
JM - Giamaica 2
KG - Kirghizistan 2
LV - Lettonia 2
MT - Malta 2
MU - Mauritius 2
OM - Oman 2
PS - Palestinian Territory 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
AQ - Antartide 1
BS - Bahamas 1
BZ - Belize 1
CD - Congo 1
DM - Dominica 1
EE - Estonia 1
ET - Etiopia 1
GN - Guinea 1
Totale 15.621
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Città #
Dallas 968
Singapore 776
Southend 740
Moscow 683
Ashburn 636
San Jose 583
Chandler 552
Jacksonville 498
Woodbridge 380
Hong Kong 300
Verona 229
Beijing 222
Dublin 203
Ann Arbor 202
Council Bluffs 201
Houston 182
The Dalles 156
Munich 141
New York 138
Los Angeles 116
Ho Chi Minh City 111
Wilmington 83
Helsinki 82
Lawrence 82
Princeton 82
Hanoi 78
Jinan 78
Shenyang 66
Nanjing 61
São Paulo 51
Santa Clara 47
Columbus 41
Tianjin 39
Buffalo 36
Hebei 36
Orem 35
London 31
Redondo Beach 31
Tokyo 30
Brussels 28
Seattle 28
Warsaw 28
Haikou 27
Turku 27
Amsterdam 26
Seoul 26
Sindelfingen 26
Abuja 25
Boardman 25
Milan 25
Denver 23
Montreal 23
Toronto 23
Chennai 22
Chicago 22
Hangzhou 22
Jakarta 22
Johannesburg 22
Nanchang 21
Ningbo 21
Changsha 20
Guangzhou 20
Taizhou 20
Haiphong 19
Phoenix 19
Poplar 19
Taiyuan 19
Dearborn 18
Frankfurt am Main 18
Jiaxing 18
Nuremberg 18
Zhengzhou 18
Lappeenranta 15
San Francisco 15
Atlanta 14
Brooklyn 14
Da Nang 14
Rio de Janeiro 14
Fuzhou 13
Mexico City 13
Stockholm 13
Washington 13
Bologna 12
Norwalk 12
Kent 11
Manchester 11
Redwood City 11
Nairobi 10
Redmond 10
Vienna 10
Belo Horizonte 9
Boston 9
Cotonou 9
Falkenstein 9
Lancaster 9
Rome 9
Tashkent 9
Zurich 9
Ankara 8
Lomé 8
Totale 10.057
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Nome #
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 327
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 273
Acute inflammatory demyelinating polyneuropathy as a manifestation of chronic lymphoproliferative disorder of NK cells. 256
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 252
Benign acute viral myositis in African migrants: a clinical, serological and pathological study. 243
Differential regulation of TNF receptors in maternal leukocytes is associated with severe preterm preeclampsia. 233
Bortezomib-induced muscle toxicity in multiple myeloma 232
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 226
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 221
Autophagy, inflammation and innate immunity in inflammatory myopathies. 220
8C.05: EPOXYEICOSATRIENOIC ACIDS ARE INCREASED IN PLACENTAS OF PREECLAMPTIC PREGNANCIES 220
Levofloxacin-induced hemichorea-hemiballism in a patient with previous thalamic infarction 219
Anti-Ma-associated encephalomyeloradiculopathy in a patient with pleural mesothelioma. 213
BACE1 and BACE2 in pathologic and normal human muscle 211
A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae rupture 204
A novel de novo GFAP variant causes a juvenile-onset Alexander disease with bilateral vocal cord paralysis 200
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 200
Pisa syndrome in Parkinson's disease: an electrophysiological and imaging study. 200
Chronic graft-versus-host-disease-related polymyositis: a 17-months-old child with a rare and late complication of haematopoietic stem cell transplantation 196
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 194
McArdle disease and sporadic inclusion-body myositis. 193
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 193
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 191
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 188
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 188
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 187
Amyloid myopathy: an intriguing diagnosis 187
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 184
A novel in-frame deletion in MYOT causes an early adult onset distal myopathy 183
Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis. 182
Autoantibody testing in patients with myositis: clinical accuracy of a multi parametric line immunoassay 182
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 181
Brody syndrome: A clinically heterogeneous entity distinct from Brody disease: A review of literature and a cross-sectional clinical study in 17 patients. 181
Calpain 3 deficiency presenting as fiber type disproportion. 178
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 175
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 173
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 172
Increased epoxyeicosatrienoic acids and reduced soluble epoxide hydrolase expression in the preeclamptic placenta 172
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 172
Polymyositis in solid organ transplant recipients receiving tacrolimus. 171
Muscular dystrophy with reduced beta-sarcoglycan in a cat. 169
T-cell anti-apoptotic mechanisms in inflammatory myopathies 167
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 166
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 165
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 165
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 165
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 164
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 162
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients 162
The role of muscle biopsy in investigating isolated muscle pain 162
Human skeletal muscle as a target organ of trichloroethylene toxicity. 161
Multiple acyl-COA dehydrogenase deficiency in elderly carriers 157
Expanding the clinical and genetic spectrum of pathogenic variants in STIM1 157
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 153
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 152
Transthyretin Val122Ile, accumulated Aβ, and inclusion-body myositis aspects in cultured muscle 151
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 150
Pearls & Oy-sters: An unusual case of varicella-zoster virus cerebellitis and vasculopathy. 150
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 149
Sarcoidosis and inclusion body myositis. 149
Acetylcholine receptor-antibody-positive myasthenia gravis presenting with early atrophy and nonfluctuating weakness of proximal limb muscles 148
Cystatin C colocalizes with amyloid-beta and coimmunoprecipitates with amyloid-beta precursor protein in sporadic inclusion-body myositis muscles 145
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 141
Relapsing-remitting painful masses of the skeletal muscle 141
Upper camptocormia in Parkinson's disease: Neurophysiological and imaging findings of both central and peripheral pathophysiological mechanisms 140
Protein expression of canine and feline muscular dystrophies 140
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx mice. 138
Neuropathology of mitochondrial diseases 138
Reversible upper limb muscle weakness with selective loss of thick filaments 138
Human mutated MYOT and CRYAB genes cause a myopathic phenotype in Zebrafish 137
Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle. 133
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 130
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 124
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 124
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis 123
Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers 120
Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts 119
Neurogenic disease with high CK: think muscle 118
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 118
Neuronal intermediate filament paraneoplastic autoimmunity complicating avelumab therapy of Merkel cell carcinoma 115
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa 114
Diagnostic performance and validation of autoantibody testing in myositis by a commercial line blot assay. 114
Uptake and intracellular distribution of different types of nanoparticles in primary human myoblasts and myotubes 114
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 113
Dermatomyositis and retroperitoneal germ cell cancer 112
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexes. 112
Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy 112
Transcriptional behavior of DMD gene duplications in DMD/BMD males. 110
Physical training promotes remodeling of the skeletal muscle extracellular matrix: An ultrastructural study in a murine model of Down syndrome 99
Novel mitochondrial tRNA(Leu(CUN)) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype 95
Premature skeletal muscle aging in VPS13A deficiency relates to impaired autophagy 88
Sporadic inclusion body myositis at the crossroads between muscle degeneration, inflammation, and aging 85
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network 76
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy 74
Toll-like receptors and IL-7 as potential biomarkers for immune-mediated necrotizing myopathies 72
Evaluation of aggrephagy markers in myofibrillar myopathies 68
The FSHD jigsaw: are we placing the tiles in the right position? 66
Nucleolar FRG2 lncRNAs inhibit rRNA transcription and cytoplasmic translation, linking FSHD to dysregulation of muscle-specific protein synthesis 59
Case Report: Simultaneous presentation of end-stage heart failure with cardiogenic shock requiring emergency transplantation in monozygotic twins with myofibrillar myopathy: a previously unknown genetic disease? 49
Assessment of IBM-FRS total score and specific functional domains in a large cohort of inclusion body myositis patients 36
Totale 15.747
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Categoria #
all - tutte 52.094
article - articoli 51.003
book - libri 0
conference - conferenze 1.091
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 104.188
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022629 0 275 2 47 18 13 8 38 17 12 48 151
2022/20231.474 113 166 143 233 154 329 14 89 177 11 23 22
2023/2024724 29 74 54 73 77 134 27 70 10 44 83 49
2024/20252.324 104 108 80 340 129 112 197 146 366 133 183 426
2025/20267.182 418 692 587 1.103 1.714 427 661 321 570 384 109 196
2026/2027207 65 142 0 0 0 0 0 0 0 0 0 0
Totale 15.784