IRIS UniCatt

Servidei, Serenella
 Distribuzione geografica
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Continente #
NA - Nord America 6.276
AS - Asia 4.975
EU - Europa 4.243
SA - Sud America 1.174
AF - Africa 162
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 10
AN - Antartide 1
Totale 16.865
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Nazione #
US - Stati Uniti d'America 6.083
SG - Singapore 2.289
DE - Germania 1.108
CN - Cina 1.096
BR - Brasile 979
IT - Italia 756
SE - Svezia 675
VN - Vietnam 499
FR - Francia 390
UA - Ucraina 291
IE - Irlanda 249
GB - Regno Unito 194
JP - Giappone 159
ID - Indonesia 158
BD - Bangladesh 150
IN - India 150
FI - Finlandia 146
HK - Hong Kong 124
RU - Federazione Russa 116
CA - Canada 82
NL - Olanda 74
AR - Argentina 67
MX - Messico 64
TR - Turchia 64
IQ - Iraq 50
ZA - Sudafrica 50
PL - Polonia 43
ES - Italia 39
AT - Austria 34
BE - Belgio 31
KR - Corea 31
EC - Ecuador 29
CO - Colombia 25
PK - Pakistan 24
IR - Iran 23
VE - Venezuela 20
UZ - Uzbekistan 19
AU - Australia 18
KE - Kenya 18
CL - Cile 17
JO - Giordania 17
EG - Egitto 16
MA - Marocco 16
SA - Arabia Saudita 16
CI - Costa d'Avorio 14
LT - Lituania 14
AE - Emirati Arabi Uniti 12
DZ - Algeria 12
PH - Filippine 12
TN - Tunisia 12
IL - Israele 11
PY - Paraguay 11
CH - Svizzera 10
CZ - Repubblica Ceca 10
KZ - Kazakistan 10
PE - Perù 10
TH - Thailandia 10
UY - Uruguay 9
CR - Costa Rica 8
MY - Malesia 7
RO - Romania 7
TT - Trinidad e Tobago 7
AZ - Azerbaigian 6
BO - Bolivia 6
DK - Danimarca 6
KG - Kirghizistan 6
MD - Moldavia 6
NP - Nepal 6
NZ - Nuova Zelanda 6
RS - Serbia 6
ET - Etiopia 5
GR - Grecia 5
LB - Libano 5
NG - Nigeria 5
PA - Panama 5
EU - Europa 4
GT - Guatemala 4
HN - Honduras 4
JM - Giamaica 4
LV - Lettonia 4
OM - Oman 4
PT - Portogallo 4
SK - Slovacchia (Repubblica Slovacca) 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AO - Angola 3
CY - Cipro 3
DO - Repubblica Dominicana 3
HU - Ungheria 3
LK - Sri Lanka 3
NI - Nicaragua 3
SI - Slovenia 3
SV - El Salvador 3
TW - Taiwan 3
A1 - Anonimo 2
AL - Albania 2
BG - Bulgaria 2
EE - Estonia 2
KW - Kuwait 2
LU - Lussemburgo 2
MK - Macedonia 2
Totale 16.834
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Città #
Singapore 1.123
Ashburn 754
Chandler 705
San Jose 695
Beijing 249
Dublin 246
San Mateo 206
Munich 173
New York 169
Ho Chi Minh City 168
Jacksonville 165
Rome 152
Lauterbourg 149
Los Angeles 148
Jakarta 145
Hanoi 125
Tokyo 122
Boston 112
Hong Kong 111
Nanjing 109
Houston 106
St Louis 105
Wilmington 92
Hefei 91
Princeton 88
Dallas 77
Milan 76
São Paulo 74
Ann Arbor 71
Frankfurt am Main 70
Woodbridge 65
Moscow 63
Redmond 61
Chicago 60
Redwood City 60
Helsinki 54
Nürnberg 54
Cambridge 48
Dearborn 45
Buffalo 44
Council Bluffs 42
Seattle 42
Santa Clara 41
Nanchang 40
Marseille 39
Bremen 38
Rio de Janeiro 38
Boardman 37
Guangzhou 34
Lawrence 34
Kent 33
Norwalk 33
The Dalles 32
Fairfield 31
Haiphong 31
Izmir 30
Orem 30
Cattolica 29
London 29
Hebei 27
Seoul 26
Warsaw 26
Brooklyn 25
Kunming 25
Nuremberg 25
Toronto 25
Atlanta 24
Johannesburg 24
Paris 24
Shanghai 24
Zhengzhou 24
Belo Horizonte 22
Brussels 22
Vienna 22
Hangzhou 21
Mountain View 21
Stockholm 21
Pune 20
Tianjin 20
Baghdad 19
Curitiba 19
Jiaxing 19
Naples 19
Changsha 18
Da Nang 18
Lappeenranta 18
Mexico City 18
Montreal 18
Phoenix 18
Amsterdam 17
Tashkent 17
University Park 17
Amman 16
Bari 16
Brasília 16
Biên Hòa 15
Denver 15
Lancaster 15
Abidjan 14
Bogotá 14
Totale 8.717
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Nome #
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 334
Hospital admissions from the emergency department of adult patients affected by myopathies 259
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene 255
Hypoglossal palsy and coeliac disease: an uncommon presentation for a common disease? 215
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 206
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 192
A rare case of life-threatening giant plexiform schwannoma 190
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 189
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation 185
Neurological involvement during legionellosis, look beyond the lung 175
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 174
Sleep Disordered Breathing in a cohort of patients with sporadic Inclusion Body Myositis. 168
A Case of Hemiabdominal Myoclonus 166
Copper deficiency myelopathy: A report of two cases 166
Mitochondrial neuropathy: considerations on pathogenesis 165
Muscle MRI in female carriers of dystrophinopathy 164
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 161
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene 159
Response to therapy in myasthenia gravis with anti-MuSK antibody 158
Nerve growth factor eye drop administration improves visual function in a patient with optic glioma 154
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 154
Neurological involvement during Legionellosis, look beyond the lung 152
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 152
Recurrent miller fisher: a new case report and a literature review 151
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 147
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: A case report 146
Resolving Phenotypic Variability in Mitochondrial Diseases: Preliminary Findings of a Proteomic Approach 143
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 142
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 142
Hearing Impairment and Neuroimaging Results in Mitochondrial Diseases 141
Incidence and Long-term Functional Outcome of Neurologic Disorders in Hospitalized Patients With COVID-19 Infected With Pre-Omicron Variants 138
Resolution of muscle inflammation after tumor removal in a woman with paraneoplastic dermatomyositis 137
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication 133
A Case of Hemiabdominal Myoclonus 133
Acute refractory intestinal pseudo-obstruction in MELAS: efficacy of prucalopride 132
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 132
Acute auditory agnosia as the presenting hearing disorder in MELAS. 131
Clinical heterogeneity of seronegative myasthenia gravis 131
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 130
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 130
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group 129
Intestinal pseudo-obstruction in mitochondrial diseases 129
Redefining phenotypes associated with mitochondrial DNA single deletion 127
Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck 126
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 125
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy 124
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 124
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity 122
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 120
Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome 120
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation 119
Early cardiac mechanics abnormalities in patients with mitochondrial diseases 117
Spontaneous recovery from anti-NMDAR encephalitis 116
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 116
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 116
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience 116
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 116
Nutritional support in mitochondrial diseases: the state of the art 115
Midbrain panda sign in a patient with Wilson's disease 113
Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group 113
Muscle MRI as a useful biomarker in hereditary transthyretin amyloidosis: A pilot study 113
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 111
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 111
Small fibre neuropathy in mitochondrial diseases explored with sudoscan 109
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 109
Subacute combined degeneration 108
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly 108
Acute necrotizing encephalopathy: a relapsing case in a European adult 106
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma 106
Myasthenia gravis during interferon alfa therapy 105
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy 104
Osteoma of the internal auditory canal 103
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases 102
Myoclonus in mitochondrial disorders 102
Fourier-transform infrared spectroscopy of skeletal muscle tissue: Expanding biomarkers in primary mitochondrial myopathies 102
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage disease. 101
Spinal cord involvement in adult mitochondrial diseases: A cohort study 101
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study 100
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation 100
Instrumental Evaluation of COVID-19 Related Dysautonomia in Non-Critically-Ill Patients: An Observational, Cross-Sectional Study 99
Do rare genetic conditions exhibit a specific phonotype? A comprehensive description of the vocal traits associated with Crisponi/Cold-Induced Sweating Syndrome type 1. 99
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. 97
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population 97
Correction to: Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature review 97
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2 96
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases 96
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy 95
Acute refractory intestinal pseudo-obstruction in melas: Efficacy of prucalopride 95
Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort study 94
Inflammatory profile in mitochondrial diseases: A cohort study 94
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 93
Migraine in mitochondrial disorders: Prevalence and characteristics 93
Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study 93
Microvascular involvement in migraine: an optical coherence tomography angiography study 91
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report 91
Mitochondrial encephalomyopathies:gene mutation 87
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies 86
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 86
Impact of COVID-19 vaccine on epilepsy in adult subjects: an Italian multicentric experience 85
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 84
Totale 12.984
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Categoria #
all - tutte 74.803
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 74.803
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202116 0 0 0 0 0 0 0 0 0 0 0 16
2021/2022981 80 48 9 62 52 32 8 198 38 53 183 218
2022/20231.949 259 260 150 296 115 280 65 138 266 33 63 24
2023/20241.316 58 347 33 180 34 185 65 48 15 52 157 142
2024/20252.624 58 68 214 114 139 90 134 145 400 228 570 464
2025/20267.184 1.082 237 442 931 1.036 375 1.096 366 442 624 303 250
Totale 17.148