IRIS PubliCatt

Servidei, Serenella
 Distribuzione geografica
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Continente #
NA - Nord America 3.369
EU - Europa 2.741
AS - Asia 681
AF - Africa 25
OC - Oceania 17
SA - Sud America 12
Continente sconosciuto - Info sul continente non disponibili 9
Totale 6.854
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Nazione #
US - Stati Uniti d'America 3.348
DE - Germania 840
SE - Svezia 626
CN - Cina 445
IT - Italia 340
UA - Ucraina 277
IE - Irlanda 236
FR - Francia 148
GB - Regno Unito 84
IN - India 77
FI - Finlandia 62
JP - Giappone 40
NL - Olanda 31
TR - Turchia 31
BE - Belgio 30
IR - Iran 19
HK - Hong Kong 16
AU - Australia 14
ES - Italia 14
VN - Vietnam 14
AT - Austria 12
CI - Costa d'Avorio 11
CA - Canada 10
RU - Federazione Russa 10
SG - Singapore 10
ZA - Sudafrica 10
MX - Messico 7
PL - Polonia 6
KR - Corea 5
BR - Brasile 4
CZ - Repubblica Ceca 4
EU - Europa 4
IL - Israele 4
RO - Romania 4
TH - Thailandia 4
A2 - ???statistics.table.value.countryCode.A2??? 3
CO - Colombia 3
DK - Danimarca 3
HU - Ungheria 3
NZ - Nuova Zelanda 3
SK - Slovacchia (Repubblica Slovacca) 3
A1 - Anonimo 2
BG - Bulgaria 2
CH - Svizzera 2
LB - Libano 2
MY - Malesia 2
OM - Oman 2
PA - Panama 2
PE - Perù 2
PH - Filippine 2
PK - Pakistan 2
TW - Taiwan 2
BD - Bangladesh 1
BO - Bolivia 1
CL - Cile 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
GR - Grecia 1
HN - Honduras 1
ID - Indonesia 1
KE - Kenya 1
MK - Macedonia 1
MM - Myanmar 1
MT - Malta 1
PY - Paraguay 1
SA - Arabia Saudita 1
SC - Seychelles 1
SI - Slovenia 1
Totale 6.854
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Città #
Chandler 705
Ashburn 395
Dublin 235
San Mateo 206
Jacksonville 163
Nanjing 109
Boston 101
New York 95
Houston 94
Wilmington 90
Princeton 88
Ann Arbor 70
Woodbridge 65
Redmond 61
Beijing 60
Redwood City 60
Nürnberg 54
Rome 53
Dearborn 45
Milan 42
Nanchang 39
Marseille 38
Bremen 37
Seattle 35
Lawrence 34
Norwalk 32
Fairfield 31
Cattolica 29
Izmir 29
Munich 28
Hebei 27
Guangzhou 26
Kunming 24
Zhengzhou 22
Brussels 21
Mountain View 21
Chicago 20
Pune 19
Hangzhou 18
Jiaxing 18
Changsha 17
Shanghai 17
University Park 17
Tianjin 15
Hanoi 14
Shenyang 14
Boardman 12
Hong Kong 12
Lancaster 12
Abidjan 11
Detroit 10
Vienna 10
Andover 9
Los Angeles 9
Waanrode 9
Augusta 8
Bari 8
Leawood 8
Washington 8
Auburn Hills 7
Helsinki 7
Jinan 7
Berlin 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
Shahid 5
Tokyo 5
Busto Arsizio 4
Hadamar 4
Hefei 4
Las Vegas 4
Ningbo 4
Nuremberg 4
Santa Barbara 4
Tsukuba 4
Baltimore 3
Bangkok 3
Bogotá 3
Cape Town 3
Catania 3
Clearwater 3
Encinitas 3
Fondi 3
Göttingen 3
Indiana 3
Košice 3
Monmouth Junction 3
Pamplona 3
Philadelphia 3
Phoenix 3
Sacramento 3
Totale 3.735
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Nome #
Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: Pitfalls and tips in the diagnosis 274
A rare case of life-threatening giant plexiform schwannoma 130
Hypoglossal palsy and coeliac disease: an uncommon presentation for a common disease? 123
A Case of Hemiabdominal Myoclonus 118
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation 117
Neurological involvement during legionellosis, look beyond the lung 115
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene 114
Sleep Disordered Breathing in a cohort of patients with sporadic Inclusion Body Myositis. 110
Mitochondrial neuropathy: considerations on pathogenesis 107
Copper deficiency myelopathy: A report of two cases 106
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 103
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 102
Neurological involvement during Legionellosis, look beyond the lung 97
Muscle MRI in female carriers of dystrophinopathy 96
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 90
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication 88
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience 88
Acute refractory intestinal pseudo-obstruction in MELAS: efficacy of prucalopride 87
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 87
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene 86
Nerve growth factor eye drop administration improves visual function in a patient with optic glioma 85
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 83
Intestinal pseudo-obstruction in mitochondrial diseases 80
P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis 79
Redefining phenotypes associated with mitochondrial DNA single deletion 79
Resolution of muscle inflammation after tumor removal in a woman with paraneoplastic dermatomyositis 78
Response to therapy in myasthenia gravis with anti-MuSK antibody 77
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort 77
Acute auditory agnosia as the presenting hearing disorder in MELAS. 71
Clinical heterogeneity of seronegative myasthenia gravis 71
Bilateral thoracic long nerve involvement in motor multifocal neuropathy 71
A Case of Hemiabdominal Myoclonus 71
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features 69
Acute necrotizing encephalopathy: a relapsing case in a European adult 67
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation 67
Nutritional support in mitochondrial diseases: the state of the art 67
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene 66
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 66
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 65
Spontaneous recovery from anti-NMDAR encephalitis 63
Subacute combined degeneration 62
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 62
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population 61
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation 59
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma 59
Midbrain panda sign in a patient with Wilson's disease 58
To the Editor: Fasciculations in Late-Onset Pompe Disease: A Sign of Motor Neuron Involvement? 58
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement 58
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage disease. 57
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 57
Myasthenia gravis during interferon alfa therapy 55
Osteoma of the internal auditory canal 55
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly 55
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction 55
Acute refractory intestinal pseudo-obstruction in melas: Efficacy of prucalopride 54
Small fibre neuropathy in mitochondrial diseases explored with sudoscan 54
Small fibre involvement in multifocal motor neuropathy explored with sudoscan: a single-centre experience 53
Recurrent miller fisher: a new case report and a literature review 53
Myoclonus in mitochondrial disorders 52
Drug-resistant epilepsy in MELAS: safety and potential efficacy of lacosamide 51
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience 51
Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome 51
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity 50
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: A case report 48
Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck 47
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy 45
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years 45
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. 45
Focal status epilepticus as unique clinical feature of COVID-19: A case report 44
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 43
Teaching Video NeuroImages: Palatal tremor associated with SPG7 variants 43
Migraine in mitochondrial disorders: Prevalence and characteristics 42
Epilepsy management in mitochondrial diseases 42
Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study 41
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 41
Genotype-phenotype correlation in Pompe disease, a step forward 40
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia 40
Patisiran in hereditary transthyretin-mediated amyloidosis 40
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2 39
Awareness of rare and genetic neurological diseases among italian neurologist. A national survey 39
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre 39
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 37
Muscle pain in mitochondrial diseases: a picture from the Italian network 37
Muscle MRI as a useful biomarker in hereditary transthyretin amyloidosis: A pilot study 37
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy 35
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report 35
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies 34
Enzyme replacement therapy improves respiratory outcomes in patients with late-onset type II glycogenosis and high ventilator dependency 34
Mitochondrial encephalomyopathies:gene mutation 34
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy 34
Patisiran in hereditary transthyretin-mediated amyloidosis 34
Spinal cord involvement in adult mitochondrial diseases: A cohort study 34
Enhanced dystrophic progression in mdx mice by exercise and beneficial effects of taurine and insulin-like growth factor-1 33
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey 33
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases 32
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine 32
Cerebellar ataxia and coenzyme Q10 deficiency 30
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients 30
Constitutive activation of MAPK cascade in Acute Quadriplegic Myopathy 29
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases 29
Totale 6.366
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Categoria #
all - tutte 29.006
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 29.006
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201978 0 0 0 0 0 0 0 0 0 0 50 28
2019/2020783 190 43 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
2023/20241.019 58 347 33 180 34 185 65 48 15 53 1 0
Totale 7.043