IRIS PubliCatt

Servidei, Serenella
 Distribuzione geografica
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Continente #
NA - Nord America 3.398
EU - Europa 2.867
AS - Asia 946
AF - Africa 27
OC - Oceania 17
SA - Sud America 12
Continente sconosciuto - Info sul continente non disponibili 9
Totale 7.276
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Nazione #
US - Stati Uniti d'America 3.377
DE - Germania 842
SE - Svezia 626
CN - Cina 502
IT - Italia 379
UA - Ucraina 277
IE - Irlanda 236
SG - Singapore 209
FR - Francia 149
GB - Regno Unito 86
RU - Federazione Russa 79
IN - India 77
FI - Finlandia 64
JP - Giappone 40
TR - Turchia 32
NL - Olanda 31
BE - Belgio 30
IR - Iran 19
HK - Hong Kong 18
AU - Australia 14
ES - Italia 14
VN - Vietnam 14
AT - Austria 12
CI - Costa d'Avorio 11
CA - Canada 10
ZA - Sudafrica 10
CZ - Repubblica Ceca 8
KR - Corea 7
MX - Messico 7
PL - Polonia 6
BR - Brasile 4
EU - Europa 4
GR - Grecia 4
IL - Israele 4
PK - Pakistan 4
RO - Romania 4
TH - Thailandia 4
A2 - ???statistics.table.value.countryCode.A2??? 3
CO - Colombia 3
DK - Danimarca 3
HU - Ungheria 3
MD - Moldavia 3
NZ - Nuova Zelanda 3
SK - Slovacchia (Repubblica Slovacca) 3
A1 - Anonimo 2
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
CH - Svizzera 2
LB - Libano 2
MY - Malesia 2
NG - Nigeria 2
OM - Oman 2
PA - Panama 2
PE - Perù 2
PH - Filippine 2
TW - Taiwan 2
BD - Bangladesh 1
BO - Bolivia 1
CL - Cile 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
HN - Honduras 1
ID - Indonesia 1
KE - Kenya 1
LU - Lussemburgo 1
MK - Macedonia 1
MM - Myanmar 1
MT - Malta 1
PY - Paraguay 1
SA - Arabia Saudita 1
SC - Seychelles 1
SI - Slovenia 1
Totale 7.276
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Città #
Chandler 705
Ashburn 397
Dublin 235
San Mateo 206
Jacksonville 163
Singapore 111
Nanjing 109
Boston 101
New York 95
Houston 94
Wilmington 90
Princeton 88
Ann Arbor 70
Rome 65
Woodbridge 65
Beijing 61
Redmond 61
Redwood City 60
Moscow 57
Nürnberg 54
Dearborn 45
Milan 45
Nanchang 39
Marseille 38
Bremen 37
Seattle 35
Lawrence 34
Norwalk 32
Fairfield 31
Cattolica 29
Izmir 29
Munich 29
Hebei 27
Guangzhou 26
Boardman 25
Kunming 24
Zhengzhou 22
Brussels 21
Mountain View 21
Chicago 20
Pune 19
Hangzhou 18
Jiaxing 18
Changsha 17
Los Angeles 17
Shanghai 17
University Park 17
Tianjin 15
Hanoi 14
Hong Kong 14
Shenyang 14
Lancaster 12
Abidjan 11
Detroit 10
Monza 10
Vienna 10
Andover 9
Waanrode 9
Augusta 8
Bari 8
Leawood 8
Washington 8
Auburn Hills 7
Helsinki 7
Jinan 7
Berlin 6
Brno 6
Cambridge 6
Fremont 6
Mola di Bari 6
Sydney 6
Amsterdam 5
Brugherio 5
Changchun 5
Falls Church 5
Lanzhou 5
London 5
Naples 5
Seoul 5
Shahid 5
Tokyo 5
Athens 4
Busto Arsizio 4
Hadamar 4
Hefei 4
Las Vegas 4
Lodi 4
Ningbo 4
Santa Barbara 4
Tsukuba 4
Baltimore 3
Bangkok 3
Bogotá 3
Cape Town 3
Catania 3
Chisinau 3
Clearwater 3
Encinitas 3
Fondi 3
Göttingen 3
Totale 3.952
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Nome #
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 276
A rare case of life-threatening giant plexiform schwannoma 134
Hypoglossal palsy and coeliac disease: an uncommon presentation for a common disease? 127
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation 121
Neurological involvement during legionellosis, look beyond the lung 120
A Case of Hemiabdominal Myoclonus 120
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene 117
Sleep Disordered Breathing in a cohort of patients with sporadic Inclusion Body Myositis. 112
Copper deficiency myelopathy: A report of two cases 110
Mitochondrial neuropathy: considerations on pathogenesis 110
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 109
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 104
Neurological involvement during Legionellosis, look beyond the lung 100
Muscle MRI in female carriers of dystrophinopathy 99
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 95
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 94
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene 92
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication 91
Acute refractory intestinal pseudo-obstruction in MELAS: efficacy of prucalopride 91
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 91
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 89
Nerve growth factor eye drop administration improves visual function in a patient with optic glioma 88
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 86
Redefining phenotypes associated with mitochondrial DNA single deletion 83
Intestinal pseudo-obstruction in mitochondrial diseases 83
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 83
Response to therapy in myasthenia gravis with anti-MuSK antibody 82
Resolution of muscle inflammation after tumor removal in a woman with paraneoplastic dermatomyositis 81
A Case of Hemiabdominal Myoclonus 75
Clinical heterogeneity of seronegative myasthenia gravis 74
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 73
Nutritional support in mitochondrial diseases: the state of the art 73
Acute auditory agnosia as the presenting hearing disorder in MELAS. 72
Acute necrotizing encephalopathy: a relapsing case in a European adult 71
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation 71
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 71
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 69
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 67
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 67
Spontaneous recovery from anti-NMDAR encephalitis 66
Subacute combined degeneration 65
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 64
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation 64
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population 63
Midbrain panda sign in a patient with Wilson's disease 62
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 62
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma 61
Myasthenia gravis during interferon alfa therapy 59
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage disease. 59
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 59
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 59
Osteoma of the internal auditory canal 58
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly 58
Acute refractory intestinal pseudo-obstruction in melas: Efficacy of prucalopride 58
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 58
Small fibre neuropathy in mitochondrial diseases explored with sudoscan 57
Recurrent miller fisher: a new case report and a literature review 57
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 56
Myoclonus in mitochondrial disorders 54
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 54
Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome 54
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity 54
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience 52
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: A case report 52
Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck 51
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy 47
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 47
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. 47
Focal status epilepticus as unique clinical feature of COVID-19: A case report 47
Migraine in mitochondrial disorders: Prevalence and characteristics 46
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 46
Teaching Video NeuroImages: Palatal tremor associated with SPG7 variants 46
Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study 46
Muscle MRI as a useful biomarker in hereditary transthyretin amyloidosis: A pilot study 45
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 45
Epilepsy management in mitochondrial diseases 44
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2 43
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases 42
Genotype-phenotype correlation in Pompe disease, a step forward 42
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 42
Patisiran in hereditary transthyretin-mediated amyloidosis 42
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 41
Mitochondrial encephalomyopathies:gene mutation 41
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia 41
Awareness of rare and genetic neurological diseases among italian neurologist. A national survey 41
Muscle pain in mitochondrial diseases: a picture from the Italian network 38
Patisiran in hereditary transthyretin-mediated amyloidosis 38
Spinal cord involvement in adult mitochondrial diseases: A cohort study 38
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy 36
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies 36
Enzyme replacement therapy improves respiratory outcomes in patients with late-onset type II glycogenosis and high ventilator dependency 36
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy 36
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report 36
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey 35
Enhanced dystrophic progression in mdx mice by exercise and beneficial effects of taurine and insulin-like growth factor-1 34
Cerebellar ataxia and coenzyme Q10 deficiency 33
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases 33
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine 33
Constitutive activation of MAPK cascade in Acute Quadriplegic Myopathy 31
Incomplete penetrance in a SPG3A-linked family with a new mutation in the atlastin gene 31
Totale 6.692
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Categoria #
all - tutte 35.028
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 35.028
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020550 0 0 29 38 51 48 56 30 68 63 96 71
2020/2021643 25 59 8 67 77 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
2024/2025126 58 68 0 0 0 0 0 0 0 0 0 0
Totale 7.466