IRIS UniCatt

Servidei, Serenella
 Distribuzione geografica
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Continente #
NA - Nord America 5.797
AS - Asia 4.863
EU - Europa 4.117
SA - Sud America 1.170
AF - Africa 162
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 10
AN - Antartide 1
Totale 16.144
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Nazione #
US - Stati Uniti d'America 5.630
SG - Singapore 2.284
DE - Germania 1.108
CN - Cina 1.081
BR - Brasile 977
SE - Svezia 675
IT - Italia 646
VN - Vietnam 499
FR - Francia 388
UA - Ucraina 291
IE - Irlanda 249
GB - Regno Unito 188
JP - Giappone 159
ID - Indonesia 158
IN - India 150
FI - Finlandia 145
HK - Hong Kong 122
RU - Federazione Russa 116
NL - Olanda 70
AR - Argentina 67
CA - Canada 67
MX - Messico 64
TR - Turchia 64
BD - Bangladesh 62
IQ - Iraq 50
ZA - Sudafrica 50
PL - Polonia 43
ES - Italia 38
AT - Austria 34
BE - Belgio 31
KR - Corea 31
EC - Ecuador 29
PK - Pakistan 24
CO - Colombia 23
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
CZ - Repubblica Ceca 10
KZ - Kazakistan 10
PE - Perù 10
TH - Thailandia 10
CH - Svizzera 9
UY - Uruguay 9
RO - Romania 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
CR - Costa Rica 5
ET - Etiopia 5
GR - Grecia 5
LB - Libano 5
MY - Malesia 5
NG - Nigeria 5
PA - Panama 5
EU - Europa 4
HN - Honduras 4
JM - Giamaica 4
LV - Lettonia 4
OM - Oman 4
PT - Portogallo 4
SK - Slovacchia (Repubblica Slovacca) 4
TT - Trinidad e Tobago 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AO - Angola 3
CY - Cipro 3
DO - Repubblica Dominicana 3
GT - Guatemala 3
HU - Ungheria 3
LK - Sri Lanka 3
NI - Nicaragua 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
MU - Mauritius 2
PS - Palestinian Territory 2
Totale 16.116
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Città #
Singapore 1.121
Ashburn 723
Chandler 705
San Jose 575
Beijing 246
Dublin 246
San Mateo 206
Munich 173
Ho Chi Minh City 168
Jacksonville 165
New York 150
Lauterbourg 149
Jakarta 145
Los Angeles 139
Rome 130
Hanoi 125
Tokyo 122
Boston 112
Hong Kong 109
Nanjing 109
Houston 105
Wilmington 92
Hefei 91
Princeton 88
São Paulo 74
Dallas 72
Milan 71
Ann Arbor 70
Frankfurt am Main 70
St Louis 68
Woodbridge 65
Moscow 63
Redmond 61
Redwood City 60
Chicago 55
Helsinki 54
Nürnberg 54
Cambridge 48
Dearborn 45
Seattle 42
Council Bluffs 40
Nanchang 40
Santa Clara 40
Marseille 39
Bremen 38
Rio de Janeiro 37
Buffalo 34
Guangzhou 34
Lawrence 34
Kent 33
Norwalk 32
The Dalles 32
Fairfield 31
Haiphong 31
Izmir 30
Orem 30
Cattolica 29
Hebei 27
London 27
Seoul 26
Warsaw 26
Boardman 25
Kunming 25
Nuremberg 25
Brooklyn 24
Johannesburg 24
Paris 24
Shanghai 24
Zhengzhou 24
Belo Horizonte 22
Brussels 22
Vienna 22
Atlanta 21
Hangzhou 21
Mountain View 21
Stockholm 21
Pune 20
Baghdad 19
Curitiba 19
Jiaxing 19
Tianjin 19
Changsha 18
Da Nang 18
Lappeenranta 18
Mexico City 18
Amsterdam 17
Montreal 17
Tashkent 17
University Park 17
Amman 16
Bari 16
Brasília 16
Toronto 16
Biên Hòa 15
Denver 15
Lancaster 15
Phoenix 15
Abidjan 14
Chennai 14
Nairobi 14
Totale 8.403
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Nome #
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 329
Hospital admissions from the emergency department of adult patients affected by myopathies 254
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene 254
Hypoglossal palsy and coeliac disease: an uncommon presentation for a common disease? 209
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 189
A rare case of life-threatening giant plexiform schwannoma 185
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation 183
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 182
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 179
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 172
Neurological involvement during legionellosis, look beyond the lung 171
Sleep Disordered Breathing in a cohort of patients with sporadic Inclusion Body Myositis. 166
Copper deficiency myelopathy: A report of two cases 164
A Case of Hemiabdominal Myoclonus 163
Mitochondrial neuropathy: considerations on pathogenesis 163
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 161
Muscle MRI in female carriers of dystrophinopathy 161
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene 159
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 152
Response to therapy in myasthenia gravis with anti-MuSK antibody 151
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 150
Neurological involvement during Legionellosis, look beyond the lung 146
Nerve growth factor eye drop administration improves visual function in a patient with optic glioma 145
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 144
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 142
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: A case report 142
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 136
Resolution of muscle inflammation after tumor removal in a woman with paraneoplastic dermatomyositis 135
Recurrent miller fisher: a new case report and a literature review 133
Acute refractory intestinal pseudo-obstruction in MELAS: efficacy of prucalopride 132
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication 130
A Case of Hemiabdominal Myoclonus 130
Intestinal pseudo-obstruction in mitochondrial diseases 129
Acute auditory agnosia as the presenting hearing disorder in MELAS. 128
Clinical heterogeneity of seronegative myasthenia gravis 128
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 128
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 127
Incidence and Long-term Functional Outcome of Neurologic Disorders in Hospitalized Patients With COVID-19 Infected With Pre-Omicron Variants 127
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 125
Redefining phenotypes associated with mitochondrial DNA single deletion 125
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 125
Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck 125
Hearing Impairment and Neuroimaging Results in Mitochondrial Diseases 122
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity 121
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 120
Resolving Phenotypic Variability in Mitochondrial Diseases: Preliminary Findings of a Proteomic Approach 119
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation 118
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 116
Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome 115
Spontaneous recovery from anti-NMDAR encephalitis 114
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 114
Nutritional support in mitochondrial diseases: the state of the art 113
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 112
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 112
Muscle MRI as a useful biomarker in hereditary transthyretin amyloidosis: A pilot study 112
Midbrain panda sign in a patient with Wilson's disease 110
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 109
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience 109
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 109
Subacute combined degeneration 107
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly 107
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma 106
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 106
Acute necrotizing encephalopathy: a relapsing case in a European adult 105
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 104
Small fibre neuropathy in mitochondrial diseases explored with sudoscan 103
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy 102
Osteoma of the internal auditory canal 102
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation 100
Spinal cord involvement in adult mitochondrial diseases: A cohort study 100
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases 99
Fourier-transform infrared spectroscopy of skeletal muscle tissue: Expanding biomarkers in primary mitochondrial myopathies 99
Myasthenia gravis during interferon alfa therapy 97
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage disease. 97
Myoclonus in mitochondrial disorders 97
Instrumental Evaluation of COVID-19 Related Dysautonomia in Non-Critically-Ill Patients: An Observational, Cross-Sectional Study 96
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population 96
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy 95
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2 94
Acute refractory intestinal pseudo-obstruction in melas: Efficacy of prucalopride 94
Do rare genetic conditions exhibit a specific phonotype? A comprehensive description of the vocal traits associated with Crisponi/Cold-Induced Sweating Syndrome type 1. 93
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. 93
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy 93
Correction to: Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature review 93
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases 92
Migraine in mitochondrial disorders: Prevalence and characteristics 91
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 89
Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study 89
Microvascular involvement in migraine: an optical coherence tomography angiography study 87
Inflammatory profile in mitochondrial diseases: A cohort study 87
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report 87
Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort study 86
Early cardiac mechanics abnormalities in patients with mitochondrial diseases 86
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study 86
Mitochondrial encephalomyopathies:gene mutation 85
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 84
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies 83
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 83
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy 82
Microvascular involvement in migraine: an optical coherence tomography angiography study 82
Totale 12.481
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Categoria #
all - tutte 69.432
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 69.432
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021185 0 0 0 0 0 0 0 0 0 34 135 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
2025/20266.462 1.082 237 442 931 1.036 375 1.096 366 442 455 0 0
Totale 16.426