CATALOGO DEI PRODOTTI DELLA RICERCA

VATTEMI, Gaetano Nicola
 Distribuzione geografica
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Continente #
NA - Nord America 2.894
EU - Europa 2.137
AS - Asia 916
SA - Sud America 5
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
Totale 5.959
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Nazione #
US - Stati Uniti d'America 2.879
GB - Regno Unito 812
CN - Cina 737
SE - Svezia 248
FR - Francia 226
IE - Irlanda 195
IT - Italia 193
FI - Finlandia 153
DE - Germania 150
UA - Ucraina 74
SG - Singapore 73
KR - Corea 32
TR - Turchia 32
RU - Federazione Russa 25
BE - Belgio 23
CA - Canada 15
RO - Romania 13
IN - India 10
JP - Giappone 9
ES - Italia 6
NL - Olanda 6
VN - Vietnam 6
HK - Hong Kong 5
IL - Israele 5
AU - Australia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BG - Bulgaria 2
BR - Brasile 2
CH - Svizzera 2
CL - Cile 2
IQ - Iraq 2
LV - Lettonia 2
PK - Pakistan 2
SK - Slovacchia (Repubblica Slovacca) 2
AL - Albania 1
AT - Austria 1
CO - Colombia 1
EE - Estonia 1
IR - Iran 1
IS - Islanda 1
KZ - Kazakistan 1
MA - Marocco 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
SA - Arabia Saudita 1
Totale 5.959
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Città #
Southend 740
Chandler 552
Jacksonville 496
Woodbridge 378
Ann Arbor 202
Dublin 195
Houston 172
Beijing 166
Ashburn 118
Verona 104
Wilmington 83
Lawrence 82
Princeton 82
Jinan 78
New York 75
Shenyang 66
Nanjing 61
Singapore 50
Hebei 36
Tianjin 32
Helsinki 31
Haikou 27
Sindelfingen 26
Boardman 25
Brussels 23
Seattle 23
Seoul 23
Hangzhou 21
Nanchang 21
Ningbo 21
Taizhou 20
Taiyuan 18
Dearborn 17
Jiaxing 17
Changsha 16
Milan 15
Chicago 13
Fuzhou 13
Los Angeles 13
Zhengzhou 13
Norwalk 12
Guangzhou 11
Kent 11
Redwood City 11
Toronto 11
Redmond 10
Lancaster 9
Washington 9
Bologna 8
Clearwater 7
Falls Church 7
Riva 7
San Francisco 7
Tappahannock 7
Moscow 6
Orastie 6
Fairfield 5
Gangdong-gu 5
Lanzhou 5
San Diego 5
Auburn Hills 4
Buk-gu 4
Catania 4
Hong Kong 4
Kemerovo 4
Mehlingen 4
Renton 4
Saint Louis 4
Tokyo 4
Barcelona 3
Detroit 3
Dongguan 3
Lappeenranta 3
Montréal 3
Novokuznetsk 3
Qingdao 3
Amsterdam 2
Augusta 2
Bratislava 2
Brescia 2
Chillicothe 2
Dalian 2
Des Moines 2
Dong Ket 2
Evanston 2
Furuichiba 2
Legnago 2
Melbourne 2
Montemarano 2
Noida 2
Pergine Valsugana 2
Phoenix 2
Schio 2
Sofia 2
Stockport 2
Valladolid 2
Yalta 2
Yicheng 2
Zurich 2
Almaty 1
Totale 4.427
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Nome #
Differential regulation of TNF receptors in maternal leukocytes is associated with severe preterm preeclampsia. 116
Levofloxacin-induced hemichorea-hemiballism in a patient with previous thalamic infarction 115
Acute inflammatory demyelinating polyneuropathy as a manifestation of chronic lymphoproliferative disorder of NK cells. 113
Abnormal expression of RNA polymerase II associated proteins in muscle of patients with myofibrillar myopathies. 110
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria. 110
Pisa syndrome in Parkinson's disease: an electrophysiological and imaging study. 109
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 106
Human skeletal muscle as a target organ of trichloroethylene toxicity. 99
T-cell anti-apoptotic mechanisms in inflammatory myopathies 94
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency. 93
The role of muscle biopsy in investigating isolated muscle pain 92
Transthyretin Val122Ile, accumulated Aβ, and inclusion-body myositis aspects in cultured muscle 91
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 91
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 90
Autoantibody testing in patients with myositis: clinical accuracy of a multi parametric line immunoassay 90
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders 90
Endothelial dysfunction and increased oxidative stress in mitochondrial diseases. 89
8C.05: EPOXYEICOSATRIENOIC ACIDS ARE INCREASED IN PLACENTAS OF PREECLAMPTIC PREGNANCIES 89
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 89
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 88
BACE1 and BACE2 in pathologic and normal human muscle 87
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 86
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 86
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 86
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. 86
Increased epoxyeicosatrienoic acids and reduced soluble epoxide hydrolase expression in the preeclamptic placenta 86
Brody Disease: insights into biochemical features of SERCA1 and identification of a novel mutation. 85
Benign acute viral myositis in African migrants: a clinical, serological and pathological study. 84
Autophagy, inflammation and innate immunity in inflammatory myopathies. 83
Calpain 3 deficiency presenting as fiber type disproportion. 81
Reversible upper limb muscle weakness with selective loss of thick filaments 81
Brody syndrome: A clinically heterogeneous entity distinct from Brody disease: A review of literature and a cross-sectional clinical study in 17 patients. 80
Anti-Ma-associated encephalomyeloradiculopathy in a patient with pleural mesothelioma. 80
McArdle disease and sporadic inclusion-body myositis. 79
Expression of Protein Kinase C isoforms and interleukin-1beta in myofibrillar myopathy 78
Cystatin C colocalizes with amyloid-beta and coimmunoprecipitates with amyloid-beta precursor protein in sporadic inclusion-body myositis muscles 77
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 77
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. 76
Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis. 76
Bortezomib-induced muscle toxicity in multiple myeloma 76
Chronic graft-versus-host-disease-related polymyositis: a 17-months-old child with a rare and late complication of haematopoietic stem cell transplantation 75
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy 73
Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3. 73
Polymyositis in solid organ transplant recipients receiving tacrolimus. 73
Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers 71
Immunoblot as a potential diagnostic tool for myofibrillar myopathies 71
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 71
Dermatomyositis and retroperitoneal germ cell cancer 70
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx mice. 70
Amyloid myopathy: an intriguing diagnosis 70
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 68
Muscular dystrophy with reduced beta-sarcoglycan in a cat. 68
Sarcoidosis and inclusion body myositis. 68
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. 66
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis 65
Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle. 64
A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae rupture 64
Pearls & Oy-sters: An unusual case of varicella-zoster virus cerebellitis and vasculopathy. 62
Multiple acyl-COA dehydrogenase deficiency in elderly carriers 62
Neuropathology of mitochondrial diseases 61
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. 60
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation 60
Acute sarcomeric M-Line Disease associated with ATP synthase subunit α autoantibodies in ankylosing spondylitis 59
Novel mitochondrial tRNA(Leu(CUN)) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype 58
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 58
Uptake and intracellular distribution of different types of nanoparticles in primary human myoblasts and myotubes 56
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome 52
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexes. 50
Diagnostic performance and validation of autoantibody testing in myositis by a commercial line blot assay. 48
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis 48
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 48
Relapsing-remitting painful masses of the skeletal muscle 47
Non-hematologic toxicity of bortezomib in multiple myeloma: the neuromuscular and cardiovascular adverse effects 47
Acetylcholine receptor-antibody-positive myasthenia gravis presenting with early atrophy and nonfluctuating weakness of proximal limb muscles 47
Transcriptional behavior of DMD gene duplications in DMD/BMD males. 46
Expanding the clinical and genetic spectrum of pathogenic variants in STIM1 46
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition 45
Upper camptocormia in Parkinson's disease: Neurophysiological and imaging findings of both central and peripheral pathophysiological mechanisms 42
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients 40
Protein expression of canine and feline muscular dystrophies 37
Neuronal intermediate filament paraneoplastic autoimmunity complicating avelumab therapy of Merkel cell carcinoma 30
Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy 22
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 16
A novel in-frame deletion in MYOT causes an early adult onset distal myopathy 14
Physical training promotes remodeling of the skeletal muscle extracellular matrix: An ultrastructural study in a murine model of Down syndrome 12
The FSHD jigsaw: are we placing the tiles in the right position? 12
Human mutated MYOT and CRYAB genes cause a myopathic phenotype in Zebrafish 11
Toll-like receptors and IL-7 as potential biomarkers for immune-mediated necrotizing myopathies 6
Sporadic inclusion body myositis at the crossroads between muscle degeneration, inflammation, and aging 4
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy 4
Totale 6.084
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Categoria #
all - tutte 20.021
article - articoli 19.490
book - libri 0
conference - conferenze 531
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 40.042
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020777 82 24 3 59 58 111 97 64 35 83 49 112
2020/2021710 78 97 39 109 92 83 11 49 43 12 83 14
2021/2022715 86 275 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
2024/202513 13 0 0 0 0 0 0 0 0 0 0 0
Totale 6.084