IRIS UniCatt

Servidei, Serenella
 Distribuzione geografica
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Continente #
NA - Nord America 6.865
AS - Asia 5.008
EU - Europa 4.371
SA - Sud America 1.185
Continente sconosciuto - Info sul continente non disponibili 298
AF - Africa 162
OC - Oceania 25
AN - Antartide 1
Totale 17.915
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Nazione #
US - Stati Uniti d'America 6.629
SG - Singapore 2.296
DE - Germania 1.108
CN - Cina 1.106
BR - Brasile 986
IT - Italia 862
SE - Svezia 675
VN - Vietnam 499
FR - Francia 393
UA - Ucraina 293
IE - Irlanda 249
GB - Regno Unito 196
BD - Bangladesh 161
ID - Indonesia 160
JP - Giappone 159
IN - India 151
FI - Finlandia 146
HK - Hong Kong 124
RU - Federazione Russa 116
CA - Canada 103
NL - Olanda 77
AR - Argentina 67
MX - Messico 67
TR - Turchia 66
IQ - Iraq 50
ZA - Sudafrica 50
ES - Italia 43
PL - Polonia 43
AT - Austria 34
BE - Belgio 31
KR - Corea 31
EC - Ecuador 30
CO - Colombia 26
PK - Pakistan 24
IR - Iran 23
VE - Venezuela 21
AU - Australia 19
UZ - Uzbekistan 19
CL - Cile 18
KE - Kenya 18
JO - Giordania 17
EG - Egitto 16
MA - Marocco 16
SA - Arabia Saudita 16
CI - Costa d'Avorio 14
LT - Lituania 14
CH - Svizzera 13
AE - Emirati Arabi Uniti 12
DZ - Algeria 12
PH - Filippine 12
TN - Tunisia 12
IL - Israele 11
JM - Giamaica 11
PY - Paraguay 11
CR - Costa Rica 10
CZ - Repubblica Ceca 10
KZ - Kazakistan 10
PE - Perù 10
TH - Thailandia 10
UY - Uruguay 9
GT - Guatemala 8
RO - Romania 8
TT - Trinidad e Tobago 8
MY - Malesia 7
AZ - Azerbaigian 6
BO - Bolivia 6
DK - Danimarca 6
GR - Grecia 6
HN - Honduras 6
KG - Kirghizistan 6
MD - Moldavia 6
NP - Nepal 6
NZ - Nuova Zelanda 6
RS - Serbia 6
ET - Etiopia 5
LB - Libano 5
NG - Nigeria 5
PA - Panama 5
PT - Portogallo 5
EU - Europa 4
LV - Lettonia 4
NI - Nicaragua 4
OM - Oman 4
SK - Slovacchia (Repubblica Slovacca) 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AG - Antigua e Barbuda 3
AO - Angola 3
CY - Cipro 3
DO - Repubblica Dominicana 3
HU - Ungheria 3
LK - Sri Lanka 3
SI - Slovenia 3
SV - El Salvador 3
TW - Taiwan 3
A1 - Anonimo 2
AL - Albania 2
BA - Bosnia-Erzegovina 2
BG - Bulgaria 2
EE - Estonia 2
KW - Kuwait 2
Totale 17.593
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Città #
Singapore 1.127
Ashburn 853
San Jose 726
Chandler 706
Beijing 253
Dublin 246
San Mateo 206
New York 190
Munich 173
Ho Chi Minh City 168
Jacksonville 166
Rome 166
Los Angeles 159
Lauterbourg 149
Jakarta 145
Hanoi 125
Tokyo 122
Boston 112
Hong Kong 111
Houston 110
Nanjing 109
St Louis 107
Wilmington 95
Milan 92
Hefei 91
Princeton 88
Dallas 87
São Paulo 75
Ann Arbor 71
Chicago 70
Frankfurt am Main 70
Woodbridge 66
Moscow 63
Redmond 61
Redwood City 60
Buffalo 54
Helsinki 54
Nürnberg 54
Santa Clara 54
Cambridge 48
Dearborn 46
Seattle 45
Council Bluffs 42
Nanchang 40
Marseille 39
Bremen 38
Rio de Janeiro 38
Boardman 37
Guangzhou 34
Lawrence 34
Norwalk 34
Kent 33
The Dalles 32
Fairfield 31
Haiphong 31
Orem 31
Atlanta 30
Izmir 30
London 30
Cattolica 29
Brooklyn 28
Hebei 27
Phoenix 27
Seoul 26
Toronto 26
Warsaw 26
Kunming 25
Nuremberg 25
Shanghai 25
Johannesburg 24
Paris 24
Zhengzhou 24
Belo Horizonte 22
Brussels 22
Vienna 22
Hangzhou 21
Mountain View 21
Naples 21
Stockholm 21
Montreal 20
Pune 20
Tianjin 20
Baghdad 19
Curitiba 19
Denver 19
Jiaxing 19
Changsha 18
Da Nang 18
Lappeenranta 18
Mexico City 18
Amsterdam 17
Bari 17
Tashkent 17
University Park 17
Amman 16
Brasília 16
Biên Hòa 15
Bogotá 15
Detroit 15
Lancaster 15
Totale 9.011
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Nome #
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 335
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 291
Hospital admissions from the emergency department of adult patients affected by myopathies 261
Copper deficiency myelopathy: A report of two cases 257
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? 217
Hearing Impairment and Neuroimaging Results in Mitochondrial Diseases 205
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 196
A rare case of life-threatening giant plexiform schwannoma 193
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 193
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation 186
Neurological involvement during legionellosis, look beyond the lung 181
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 181
Sleep Disordered Breathing in a cohort of patients with sporadic Inclusion Body Myositis. 174
Recurrent miller fisher: a new case report and a literature review 172
Muscle MRI in female carriers of dystrophinopathy 168
A Case of Hemiabdominal Myoclonus 168
Mitochondrial neuropathy: considerations on pathogenesis 167
Nerve growth factor eye drop administration improves visual function in a patient with optic glioma 164
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 163
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene 163
Response to therapy in myasthenia gravis with anti-MuSK antibody 159
Neurological involvement during Legionellosis, look beyond the lung 157
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 156
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 154
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 151
Resolving Phenotypic Variability in Mitochondrial Diseases: Preliminary Findings of a Proteomic Approach 148
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 147
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: A case report 146
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 145
Incidence and Long-term Functional Outcome of Neurologic Disorders in Hospitalized Patients With COVID-19 Infected With Pre-Omicron Variants 143
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group 139
Resolution of muscle inflammation after tumor removal in a woman with paraneoplastic dermatomyositis 138
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 135
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication 134
Acute refractory intestinal pseudo-obstruction in MELAS: efficacy of prucalopride 134
A Case of Hemiabdominal Myoclonus 134
Acute auditory agnosia as the presenting hearing disorder in MELAS. 133
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 133
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy 132
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 132
Clinical heterogeneity of seronegative myasthenia gravis 131
Intestinal pseudo-obstruction in mitochondrial diseases 131
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 131
Redefining phenotypes associated with mitochondrial DNA single deletion 129
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
Early cardiac mechanics abnormalities in patients with mitochondrial diseases 124
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity 124
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 123
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation 122
Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome 122
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 120
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 119
Nutritional support in mitochondrial diseases: the state of the art 119
Spontaneous recovery from anti-NMDAR encephalitis 117
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience 117
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 117
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 116
Midbrain panda sign in a patient with Wilson's disease 115
Muscle MRI as a useful biomarker in hereditary transthyretin amyloidosis: A pilot study 115
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies 114
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 113
Small fibre neuropathy in mitochondrial diseases explored with sudoscan 111
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma 111
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly 110
Acute necrotizing encephalopathy: a relapsing case in a European adult 109
Subacute combined degeneration 109
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 109
Myasthenia gravis during interferon alfa therapy 108
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy 106
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage disease. 105
Osteoma of the internal auditory canal 105
Do rare genetic conditions exhibit a specific phonotype? A comprehensive description of the vocal traits associated with Crisponi/Cold-Induced Sweating Syndrome type 1. 103
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study 103
Myoclonus in mitochondrial disorders 103
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation 103
Spinal cord involvement in adult mitochondrial diseases: A cohort study 103
Instrumental Evaluation of COVID-19 Related Dysautonomia in Non-Critically-Ill Patients: An Observational, Cross-Sectional Study 102
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases 102
Fourier-transform infrared spectroscopy of skeletal muscle tissue: Expanding biomarkers in primary mitochondrial myopathies 102
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. 100
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2 100
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population 100
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy 98
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases 98
Correction to: Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature review 98
Inflammatory profile in mitochondrial diseases: A cohort study 97
Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort study 96
Acute refractory intestinal pseudo-obstruction in melas: Efficacy of prucalopride 96
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 95
Migraine in mitochondrial disorders: Prevalence and characteristics 95
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia 95
Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study 95
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 94
Impact of COVID-19 vaccine on epilepsy in adult subjects: an Italian multicentric experience 93
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report 93
Microvascular involvement in migraine: an optical coherence tomography angiography study 92
Efficacy of galcanezumab in proline-rich transmembrane protein 2 (PRRT2)-associated familial hemiplegic migraine: A case series 90
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies 88
Totale 13.527
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Categoria #
all - tutte 79.236
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 79.236
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022901 0 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
2025/20267.210 1.082 237 442 931 1.036 375 1.096 366 442 624 303 276
2026/2027741 477 264 0 0 0 0 0 0 0 0 0 0
Totale 17.915