IRIS
RODOLICO, Carmelo
 Distribuzione geografica
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Continente #
NA - Nord America 8.897
EU - Europa 8.355
AS - Asia 5.445
SA - Sud America 2.229
AF - Africa 147
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 8
AN - Antartide 1
Totale 25.090
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Nazione #
US - Stati Uniti d'America 8.737
RU - Federazione Russa 2.767
SG - Singapore 2.346
BR - Brasile 1.948
CN - Cina 1.505
IE - Irlanda 1.503
SE - Svezia 1.168
HK - Hong Kong 745
DE - Germania 660
IT - Italia 558
UA - Ucraina 451
FI - Finlandia 320
PL - Polonia 310
VN - Vietnam 299
GB - Regno Unito 223
FR - Francia 134
IN - India 127
AR - Argentina 105
CA - Canada 83
NL - Olanda 60
TR - Turchia 59
BE - Belgio 58
EC - Ecuador 49
BD - Bangladesh 45
ZA - Sudafrica 45
MX - Messico 43
ID - Indonesia 42
AT - Austria 40
VE - Venezuela 35
IQ - Iraq 33
UZ - Uzbekistan 31
JP - Giappone 29
CO - Colombia 28
PK - Pakistan 27
PY - Paraguay 25
ES - Italia 23
CZ - Repubblica Ceca 19
MA - Marocco 19
CI - Costa d'Avorio 18
TN - Tunisia 18
IL - Israele 16
LT - Lituania 16
JO - Giordania 15
KE - Kenya 15
AZ - Azerbaigian 14
IR - Iran 14
PE - Perù 14
UY - Uruguay 11
NP - Nepal 10
CL - Cile 9
DO - Repubblica Dominicana 9
EG - Egitto 9
KZ - Kazakistan 9
AE - Emirati Arabi Uniti 8
KG - Kirghizistan 8
LB - Libano 8
AM - Armenia 6
DZ - Algeria 6
EU - Europa 6
JM - Giamaica 6
KR - Corea 6
OM - Oman 6
SA - Arabia Saudita 6
AU - Australia 5
BO - Bolivia 5
PS - Palestinian Territory 5
AL - Albania 4
BY - Bielorussia 4
CH - Svizzera 4
KW - Kuwait 4
NI - Nicaragua 4
PA - Panama 4
AO - Angola 3
BG - Bulgaria 3
BH - Bahrain 3
GT - Guatemala 3
HU - Ungheria 3
LV - Lettonia 3
NG - Nigeria 3
NZ - Nuova Zelanda 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
BN - Brunei Darussalam 2
CR - Costa Rica 2
DK - Danimarca 2
EE - Estonia 2
GA - Gabon 2
GE - Georgia 2
GR - Grecia 2
LA - Repubblica Popolare Democratica del Laos 2
LK - Sri Lanka 2
LU - Lussemburgo 2
MD - Moldavia 2
MN - Mongolia 2
MY - Malesia 2
PR - Porto Rico 2
RO - Romania 2
SN - Senegal 2
A1 - Anonimo 1
AF - Afghanistan, Repubblica islamica di 1
Totale 25.065
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Città #
Dublin 1.494
Moscow 1.378
Dallas 1.173
Chandler 1.081
Singapore 1.079
Jacksonville 936
Ashburn 934
Hong Kong 743
Nyköping 713
Beijing 652
Warsaw 298
Princeton 276
Los Angeles 243
Medford 230
Cambridge 226
The Dalles 226
Ann Arbor 203
Des Moines 191
Dearborn 174
São Paulo 140
New York 131
Munich 129
Messina 126
Buffalo 125
Boardman 110
Ho Chi Minh City 109
Wilmington 86
Shenyang 73
Jinan 72
Tianjin 72
San Mateo 70
Nanjing 63
Belo Horizonte 62
Turku 60
Hanoi 59
Redondo Beach 57
Rio de Janeiro 54
Bremen 51
Woodbridge 48
Brooklyn 45
Lancaster 45
Rome 41
Brussels 40
Hyderabad 40
Ningbo 40
Frankfurt am Main 37
Council Bluffs 35
Hebei 34
Pune 33
Brasília 32
Hangzhou 30
Houston 30
Seattle 30
Zhengzhou 30
Helsinki 29
Haikou 28
Santa Clara 27
Tashkent 27
Dong Ket 26
Falls Church 26
Montreal 26
Stockholm 26
Tokyo 26
Porto Alegre 25
Guangzhou 24
San Francisco 24
Boston 23
Campinas 23
Curitiba 23
Johannesburg 23
Milan 23
Vienna 22
Denver 21
Orem 21
Atlanta 20
Guayaquil 20
Taizhou 20
Nürnberg 19
Salvador 19
Abidjan 18
Ottawa 18
Amsterdam 17
Catania 17
Chennai 17
Jakarta 17
Norwalk 17
Nuremberg 17
Toronto 17
Biên Hòa 16
Düsseldorf 16
Fortaleza 16
Manaus 16
São José dos Campos 16
Waanrode 16
Fuzhou 15
Juiz de Fora 15
London 15
Nairobi 15
Phoenix 15
Poplar 15
Totale 15.421
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Nome #
Severe rhabdomyolysis in a patient with “Heat Stroke” 249
Clinical and pathological features of focal myositis 233
A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy 193
Le sindromi miasteniche congenite 169
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies 168
A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci 168
Circulating microRNAs Profile in Patients With Transthyretin Variant Amyloidosis 166
A life threatening case of β-enolase deficiency 159
Acute motor axonal polyneuropathy after a cisatracurium infusion and concomitant corticosteroid therapy 157
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study 155
Five years experience on 3,4-diaminopyridine phosphate in Lambert-Eaton syndrome: Case reports 155
"Dropped- head" syndrome due to isolated myositis of neck extensor muscles: MRI findings 153
Hippo signaling pathway is altered in Duchenne muscular dystrophy 153
Acute motor axonal polyneuropathy after a cisatracurium infusion and concomitant corticosteroid therapy. 149
Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatment 145
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD) 144
Advances in assessing myotonia: Can sensor-engineered glove have a role? 144
Vacuolated PAS-positive lymphocytes on blood smear: An easy screening tool and a possible biomarker for monitoring therapeutic responses in Late Onset Pompe Disease (LOPD) 143
Onset of hypothyroidism with polymyositis-like clinical features in elderly patients 141
ANT1 expression and RAGE-NF-kB pathway activation in sporadic inclusion-body myositis 136
ANT1 expression and RAGE-NF-kB pathway in sporadic inclusion body myositis. 136
Bone mass and metabolism in patients with myastenia gravis: a possible anabolic role for pyridostigmine on bone tissue 136
A standardized clinical evaluation of patients affected by facioscapulohumeralmuscular dystrophy: The FSHD clinical score. 135
Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls 132
ANT1 is reduced in sporadic inclusion body myositis. 132
Cardiovascular autonomic control in Becker muscular dystrophy 131
Toward a more personalized motor function rehabilitation in myotonic dystrophy type 1: The role of neuroplasticity 131
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies 130
Italian recommendations for the diagnosis and treatment of myasthenia gravis 130
Autoimmune juvenile limb-girdle myasthenia 130
Central and peripheral autonomic failure in cold induced sweating syndrome type 1 129
A new phenotype of muscle glycogen synthase deficiency (GSD0B) characterized by an adult onset myopathy without cardiomyopathy 128
Miotonia congenita, epilessia, schizofrenia: un'insolita associazione 128
Clinical and genetic characterization in two families with muscle phosphofructokinase deficiency 125
AUDITORY SYSTEM INVOLVEMENT IN LATE ONSET POMPE DISEASE: A STUDY OF 20 ITALIAN PATIENTS 125
Amyloid myopathy presenting with rhabdomyolysis: Evidence of complement activation 124
NfL as a biomarker in ATTRv amyloidosis: potential and limitations 123
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci 122
Apoptosis and apoptosis-related proteins in thyroid myopathies 122
Myopathy as the persistently isolated symptomatology of primary autoimmune hypothyroidism 121
A 5-year clinical follow-up study from the Italian National Registry for FSHD 121
Asymptomatic hyperCKemia in a case of Danon disease due to a missense mutation in Lamp-2 gene 120
MicroRNA signatures predict dysregulated Vitamin D receptor and calcium pathways status in Limb Girdle muscle dystrophies (LGMD) 2A/2B. 120
Neuropsychological patter in centronuclear myopathy due to DNM2 gene mutations. 120
Aging-associated genes and let-7 microRNAs: a contribution to myogenic program dysregulation in oculopharyngeal muscular dystrophy 119
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 119
Juvenile limb-girdle myasthenia gravis 118
Clinical and genetic charactherization in two families with muscle phosphofructokinase deficiency 118
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes 118
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita 118
Hypothyroid myopathy: A peculiar clinical presentation of thyroid failure. Review of the literature. 118
A robust tool to quantify disability in patients affected by facio-scapulo-humeral muscular dystrophy. 117
Risk of Myopathy in Patients in Therapy with Statins: Identification of Biological Markers in a Pilot Study 117
Involvement of miR-126 in autoimmune disorders 117
Clinical, biochemical and genetic features in muscle phosphofructokinase deficiency 116
First report of a family with a DMD out of frame exon 2 deletion associated with asymptomatic phenotypes. 116
Deficit multiplo di AcilCoA deidrogenasi ad esordio tardivo. Descrizione di un caso clinico. 116
Telomere shortening and telomere-associated proteins in Duchenne muscular dystrophy. 115
Progressiva comparsa di miopatia, neuropatia e miastenia in un paziente con ipotiroidismo primario autoimmune. 115
Amyloid myopathy presenting with rhabdomyolysis 113
About the physiopathological mechanism of statin myopathy: evidence of a diffuse reduction of CoQ10 levels in skeletal muscle. 113
Activation of NF-kappaB pathway in Duchenne muscular dystrophy: relation to age 113
Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy 113
Amino acid sequence homology between thyroid autoantigens and central nervous system proteins: Implications for the steroid-responsive encephalopathy associated with autoimmune thyroiditis 113
Severe rhabdomyolysis in a patient with “Heat Stroke” 111
LOCALIZATION OF VINCULIN AND TALIN AT PERINEURIAL CELLS OF HUMAN SURAL NERVE 110
Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene 110
Facioscapulohumeral Muscular Dystrophy and Poliomyelitis followed by Multiple Sclerosis: A “triple trouble” case report and review of the literature on the association of MS and muscle disorders 110
Amyloid myopathy presenting with rhabdomyolysis: evidence of complement activation. 109
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 109
An unusual association of dominant optic atrophy with OPA1 mutations and parkinsonian syndrome. 108
Endocrine myopathies: Clinical and histopathological features of the major forms 108
Fatal R631C mutation is also present in the adult form of CPTII deficiency 107
ANT1 expression and RAGE-NF-kB pathway in sporadic inclusion body myositis 107
Multifocal motor neuropathy and asymptomatic Hashimoto's thyroiditis: first report of an association 106
Studio dell'espressione genica del muscolo scheletrico in pazienti affetti da glicogenosi II 106
Predictors of adaptation to non-invasive ventilation in neuromuscular disorders. 106
Chanarin-Dorfman disease (CDD): clinical, genetic and neuroradiological aspects in an adult case followed over 25 years 105
Amyloid myopathy presenting with rhabdomyolisis: evidence of complement activation. 105
First report of a family with a DMD out of frame exon 2 deletion associated with asymptomatic phenotypes. 105
Clinical heterogeneity and molecular basis of myoadenilate deaminase deficiency 104
Espressione di ANT1 e attivazione della via RAGE-NF-kB nella miosite a corpi inclusi. 104
Calpain 3 deficiency in Quail Eater's disease 104
Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII). 104
Rituximab in AChR subtype of myasthenia gravis: systematic review 103
Recurrent rhabdomyolysis due to muscle β-enolase deficiency: very rare or underestimated? 103
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 103
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 102
Tetraplegia flaccida dopo prolungata infusione di cisatracurio 102
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 102
Ischemic stroke due to hypoperfusion in a patient with a previously unrecognized Danon disease 101
Dp116, talin, vinculin and vimentin immunoreactivities following nerve transection 100
Clinical, morphological and genetic features of a large cohort of late onset GSDII patients: typical and atypical presentation 100
Malattia di Chanarin-Dorfman: aspetti clinici, gemetici e neuroradiologici di un caso adulto seguito per 25 anni 99
Late-onset mitochondrial neuromyopathy: an age-related phenomenon ? 99
Amyloid myopathy presenting with rhabdomyolysis. 99
Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data. 98
Selective short-term verbal memory involvement in two siblings carrying centronuclear myopathy due to DNM2 gene mutations 98
TRPV4 related scapuloperoneal spinal muscular atrophy: Report of an Italian family and review of the literature 98
Molecular analysis of LGMD-2B and MM patients: Identification of novel DYSF mutations and possible founder effect in the Italian population 97
Totale 12.395
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Categoria #
all - tutte 94.362
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 94.362
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021796 0 0 0 0 0 144 73 131 35 228 119 66
2021/20221.664 13 215 20 71 82 23 170 77 35 177 207 574
2022/20234.280 344 364 182 300 345 434 42 263 1.829 19 120 38
2023/20241.035 97 176 70 87 81 210 36 46 2 82 31 117
2024/20255.403 88 41 77 314 219 148 139 1.118 1.335 348 561 1.015
2025/20268.398 813 1.130 1.254 1.081 1.252 2.868 0 0 0 0 0 0
Totale 25.633