IRIS UniCatt

Servidei, Serenella
 Distribuzione geografica
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Continente #
NA - Nord America 4.701
AS - Asia 3.937
EU - Europa 3.794
SA - Sud America 1.134
AF - Africa 136
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 10
AN - Antartide 1
Totale 13.733
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Nazione #
US - Stati Uniti d'America 4.554
SG - Singapore 1.914
DE - Germania 1.080
CN - Cina 987
BR - Brasile 953
SE - Svezia 673
IT - Italia 568
UA - Ucraina 290
VN - Vietnam 274
IE - Irlanda 243
FR - Francia 227
GB - Regno Unito 175
ID - Indonesia 154
IN - India 141
FI - Finlandia 139
RU - Federazione Russa 113
HK - Hong Kong 73
AR - Argentina 65
JP - Giappone 61
NL - Olanda 60
MX - Messico 58
TR - Turchia 58
CA - Canada 55
BD - Bangladesh 47
ZA - Sudafrica 44
PL - Polonia 40
IQ - Iraq 36
AT - Austria 34
ES - Italia 33
BE - Belgio 31
KR - Corea 28
EC - Ecuador 24
IR - Iran 23
CO - Colombia 22
VE - Venezuela 19
PK - Pakistan 17
CL - Cile 16
KE - Kenya 16
AU - Australia 15
EG - Egitto 15
UZ - Uzbekistan 15
CI - Costa d'Avorio 14
MA - Marocco 14
JO - Giordania 13
LT - Lituania 13
AE - Emirati Arabi Uniti 11
IL - Israele 11
CZ - Repubblica Ceca 10
PY - Paraguay 10
SA - Arabia Saudita 10
CH - Svizzera 9
PE - Perù 9
UY - Uruguay 9
DZ - Algeria 8
TH - Thailandia 8
TN - Tunisia 8
KZ - Kazakistan 7
RO - Romania 7
AZ - Azerbaigian 6
BO - Bolivia 6
DK - Danimarca 6
KG - Kirghizistan 6
MD - Moldavia 6
PH - Filippine 6
NP - Nepal 5
NZ - Nuova Zelanda 5
PA - Panama 5
CR - Costa Rica 4
EU - Europa 4
GR - Grecia 4
HN - Honduras 4
JM - Giamaica 4
LB - Libano 4
LV - Lettonia 4
MY - Malesia 4
OM - Oman 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
HU - Ungheria 3
LK - Sri Lanka 3
NG - Nigeria 3
NI - Nicaragua 3
PT - Portogallo 3
RS - Serbia 3
TW - Taiwan 3
A1 - Anonimo 2
AL - Albania 2
BG - Bulgaria 2
EE - Estonia 2
ET - Etiopia 2
GT - Guatemala 2
LU - Lussemburgo 2
MK - Macedonia 2
MU - Mauritius 2
SN - Senegal 2
SV - El Salvador 2
Totale 13.711
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Città #
Singapore 776
Chandler 705
Ashburn 582
Dublin 241
Beijing 235
San Mateo 206
Munich 173
Jacksonville 165
Jakarta 143
New York 142
Los Angeles 131
Rome 115
Boston 112
Nanjing 109
Houston 103
Ho Chi Minh City 96
Hefei 91
Wilmington 91
Princeton 88
São Paulo 72
Dallas 71
Hanoi 71
Ann Arbor 70
Hong Kong 67
Woodbridge 65
Moscow 63
Milan 61
Redmond 61
Redwood City 60
Nürnberg 54
Frankfurt am Main 49
Chicago 48
Helsinki 48
Dearborn 45
Seattle 42
Nanchang 40
Bremen 38
Marseille 38
Rio de Janeiro 37
Lawrence 34
Kent 33
Buffalo 32
Norwalk 32
Fairfield 31
Izmir 30
Cattolica 29
Guangzhou 27
Hebei 27
Santa Clara 26
Seoul 26
Boardman 25
Kunming 25
Tokyo 25
Warsaw 25
London 24
Brooklyn 23
Nuremberg 23
Zhengzhou 23
Belo Horizonte 22
Brussels 22
Johannesburg 22
The Dalles 22
Vienna 22
Mountain View 21
Hangzhou 20
Pune 20
Curitiba 19
Jiaxing 19
Stockholm 19
Tianjin 19
Changsha 18
Lappeenranta 18
Mexico City 18
Shanghai 18
University Park 17
Brasília 16
Atlanta 15
Bari 15
Haiphong 15
Lancaster 15
Abidjan 14
Montreal 14
North Bergen 14
Phoenix 14
Shenyang 14
Tashkent 14
Turku 14
Amman 13
Chennai 13
Denver 13
Detroit 13
Düsseldorf 13
Nairobi 13
Orem 13
Toronto 13
Baghdad 12
Bogotá 12
Dhaka 12
Lauterbourg 12
Salvador 12
Totale 6.598
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Nome #
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 313
Hospital admissions from the emergency department of adult patients affected by myopathies 220
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene 195
Hypoglossal palsy and coeliac disease: an uncommon presentation for a common disease? 182
A rare case of life-threatening giant plexiform schwannoma 178
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation 167
Neurological involvement during legionellosis, look beyond the lung 162
A Case of Hemiabdominal Myoclonus 157
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 157
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 153
Mitochondrial neuropathy: considerations on pathogenesis 152
Sleep Disordered Breathing in a cohort of patients with sporadic Inclusion Body Myositis. 150
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 148
Copper deficiency myelopathy: A report of two cases 146
Muscle MRI in female carriers of dystrophinopathy 140
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene 140
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 138
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 137
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 135
Nerve growth factor eye drop administration improves visual function in a patient with optic glioma 134
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 133
Response to therapy in myasthenia gravis with anti-MuSK antibody 132
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 128
Acute refractory intestinal pseudo-obstruction in MELAS: efficacy of prucalopride 126
Neurological involvement during Legionellosis, look beyond the lung 125
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication 122
Resolution of muscle inflammation after tumor removal in a woman with paraneoplastic dermatomyositis 121
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 121
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: A case report 121
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 116
Acute auditory agnosia as the presenting hearing disorder in MELAS. 116
A Case of Hemiabdominal Myoclonus 115
Redefining phenotypes associated with mitochondrial DNA single deletion 114
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 114
Intestinal pseudo-obstruction in mitochondrial diseases 111
Clinical heterogeneity of seronegative myasthenia gravis 110
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation 110
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 109
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 107
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 106
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 106
Recurrent miller fisher: a new case report and a literature review 106
Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck 106
Midbrain panda sign in a patient with Wilson's disease 105
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 105
Nutritional support in mitochondrial diseases: the state of the art 104
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 104
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 103
Acute necrotizing encephalopathy: a relapsing case in a European adult 100
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity 100
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly 99
Spontaneous recovery from anti-NMDAR encephalitis 98
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience 97
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 97
Subacute combined degeneration 96
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 96
Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome 95
Muscle MRI as a useful biomarker in hereditary transthyretin amyloidosis: A pilot study 95
Incidence and Long-term Functional Outcome of Neurologic Disorders in Hospitalized Patients With COVID-19 Infected With Pre-Omicron Variants 94
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 92
Osteoma of the internal auditory canal 92
Small fibre neuropathy in mitochondrial diseases explored with sudoscan 92
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 92
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma 91
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage disease. 90
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation 89
Hearing Impairment and Neuroimaging Results in Mitochondrial Diseases 87
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population 87
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy 86
Spinal cord involvement in adult mitochondrial diseases: A cohort study 86
Myasthenia gravis during interferon alfa therapy 85
Myoclonus in mitochondrial disorders 85
Resolving Phenotypic Variability in Mitochondrial Diseases: Preliminary Findings of a Proteomic Approach 84
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy 84
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases 83
Acute refractory intestinal pseudo-obstruction in melas: Efficacy of prucalopride 83
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy 81
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. 80
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 80
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 79
Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study 79
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 78
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases 78
Fourier-transform infrared spectroscopy of skeletal muscle tissue: Expanding biomarkers in primary mitochondrial myopathies 78
Mitochondrial encephalomyopathies:gene mutation 77
Instrumental Evaluation of COVID-19 Related Dysautonomia in Non-Critically-Ill Patients: An Observational, Cross-Sectional Study 76
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2 76
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 76
Migraine in mitochondrial disorders: Prevalence and characteristics 76
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 75
Correction to: Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature review 75
Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort study 74
Microvascular involvement in migraine: an optical coherence tomography angiography study 72
Do rare genetic conditions exhibit a specific phonotype? A comprehensive description of the vocal traits associated with Crisponi/Cold-Induced Sweating Syndrome type 1. 70
Microvascular involvement in migraine: an optical coherence tomography angiography study 70
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies 70
Genotype-phenotype correlation in Pompe disease, a step forward 69
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey 69
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study 67
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients 66
Totale 10.846
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Categoria #
all - tutte 64.435
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 64.435
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021407 0 0 0 0 0 31 104 17 70 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
2025/20263.993 1.082 237 442 931 1.036 265 0 0 0 0 0 0
Totale 13.957