statistiche ricercatore

statistiche per Modoni, Anna

Distribuzione geografica
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Continente #
EU - Europa 1554
NA - Nord America 767
AS - Asia 364
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 1
OC - Oceania 1
Totale 2691
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Nazione #
DE - Germania 990
US - Stati Uniti d'America 750
CN - Cina 270
PL - Polonia 143
UA - Ucraina 139
IT - Italia 84
GB - Regno Unito 77
FI - Finlandia 45
IN - India 44
FR - Francia 34
TR - Turchia 33
MX - Messico 16
BE - Belgio 11
NL - Olanda 11
JP - Giappone 10
RU - Federazione Russa 6
VN - Vietnam 5
SE - Svezia 4
ES - Italia 3
EU - Europa 3
CH - Svizzera 2
A1 - ???statistics.table.value.countryCode.A1??? 1
AT - Austria 1
AU - Australia 1
CA - Canada 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
HK - Hong Kong 1
IR - Iran 1
PT - Portogallo 1
RO - Romania 1
ZA - Sudafrica 1
Totale 2691
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Città #
Jacksonville 154
Warsaw 138
Nanjing 85
Nürnberg 70
Woodbridge 70
Ann Arbor 68
Houston 57
Dearborn 51
Ashburn 37
Redwood City 34
Izmir 33
Nanchang 32
Wilmington 27
Cattolica 26
Beijing 23
Fairfield 22
Munich 22
Seattle 22
Redmond 20
Hebei 16
Kunming 13
University Park 13
Jiaxing 11
Lancaster 11
Mountain View 11
Zhengzhou 11
Hangzhou 10
Kansas City 10
Milan 10
Shenyang 10
Tianjin 10
Changsha 9
Shanghai 8
Waanrode 8
Renton 7
Cambridge 6
Detroit 6
Guangzhou 6
Hefei 6
Hanoi 5
Kraków 5
Norwalk 5
Simi Valley 5
Cuauhtémoc 4
Fremont 4
Jinan 4
Köln 4
Phoenix 4
Lanzhou 3
Ningbo 3
Rome 3
Anguillara Sabazia 2
Auburn Hills 2
Brussels 2
Chatsworth 2
Clearwater 2
Göteborg 2
Leawood 2
Milwaukee 2
Saint Petersburg 2
San Mauro Pascoli 2
Venezia 2
Andria 1
Apopka 1
Bari 1
Brno 1
Buffalo 1
Burwood 1
Carol Stream 1
Castellana Grotte 1
Changchun 1
Chengdu 1
Chiba 1
Chicago 1
Chongqing 1
Costa Mesa 1
Dallas 1
Düsseldorf 1
Florence 1
Frankfurt 1
Fuzhou 1
Guidonia 1
Irvine 1
Jinhua 1
Lock Haven 1
Los Angeles 1
Mcallen 1
Ottawa 1
Oviedo 1
Padova 1
Reggio Nell'emilia 1
San Jose 1
Sesto Fiorentino 1
Settimo San Pietro 1
Silandro 1
Stuttgart 1
Taizhou 1
Teramo 1
Tivoli 1
Urbana 1
Totale 1292
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Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 286
Abnormal sexual behaviour during sleep. 148
Sleeep quality in Facioscapulohumeral muscular dystrophy. 141
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 138
Alternative splicing alterations of Ca(2+) handling genes are associated with Ca(2+) signal dysregulation in DM1 and DM2 myotubes 111
Persistence of abnormal electrophysiological findings after carpal tunnel release 97
null 87
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 77
Sleep quality in Facioscapulohumeral muscular dystrophy 74
Successful treatment of acute autoimmune limbic encephalitis with negative VGKC and NMDAR antibodies: a case report 71
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 71
Polymorphism of CAG motif of SK3 gene is associated with acute oxaliplatin neurotoxicity 67
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experience 64
Novel SACS mutations in two unrelated Italian patients with spastic ataxia: clinico-diagnostic characterization and results of serial brain MRI studies 62
Cognitive impairment in myotonic dystrophy type 1 (DM1) : A longitudinal follow-up study 61
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 58
Successful treatment of acute autoimmune limbic encephalitis with negative VGKC and NMDAR antibodies: a case report 58
Lambert-Eaton Myasthenic Syndrome associated with gastric schwannoma 58
Central Nervous System involvement in Myotonic Dystrophies 50
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 46
DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7 46
Analysis of ryanodine receptor 1 (RyR1) and voltage-gated Ca2+ channel (VGCC) alpha1S subunit (Cav1.1) pre-mRNA splicing and correlation with intracellular calcium signals in myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2) myotubes. 45
A novel mutation in the SACS gene associated with a complicated form of spastic ataxia. 44
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenita 44
Positive outcome in a patient with Wilson's disease treated with reduced zinc dosage in pregnancy 40
Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors (J Nerol, 10.1007/s00415-015-8006-y) 39
Do not jump to easy conclusions! Lessons from pitfall in the molecular diagnosis of ARSACS 37
An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy. 36
Cognitive impairment in myotonic dystrophy type 1 (DM1): a longitudinal follow-up study 34
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease 32
SIADH in a patient with sensory ataxic neuropathy with anti-disialosyl antibodies (CANOMAD) 31
Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2). 31
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenita 31
Teaching NeuroImages: cochleitis: a rare cause of acute deafness in a patient with HCV 30
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 30
Nerve conduction studies of the sural nerve: Normative data from a single-center experience 29
Effect of mexiletine on transitory depression of compound motor action potential in recessive myotonia congenita 29
Homozygosity for c 6325T>G transition in the ATM gene causes an atypical, late-onset variant form of ataxia-telangiectasia. 26
Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: Peculiar characteristics of decremental pattern from a single-centre experience 26
Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors 26
Dramatic improvement of myotonia permanens with flecainide: a two-case report of a possible bench-to-bedside pharmacogenetics strategy 25
An atypical case of acute disseminated encephalomyelitis associated with cytomegalovirus infection 22
Serial neuroimaging findings in a novel case of sporadic progressive ataxia and palatal tremor (PAPT) 21
Progressive multifocal leukoencephalopathy in patients with follicular lymphoma treated with bendamustine plus rituximab followed by rituximab maintenance 16
Evidence of white matter involvement in SCA 7. 14
Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors 14
Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubes 14
DJ-1 modulates mitochondrial response to oxidative stress: Clues from a novel diagnosis of PARK7 13
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia 12
Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2 12
Secondary hypokalemic periodic paralysis as a rare clinical presentation of Conn syndrome 11
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype" 11
null 10
Cognitive impairment in myotonic dystrophy type 1 (DM1) : A longitudinal follow-up study. 6
Muscle hypertrophy in amyloid myopathy 6
Characterization of the Pattern of Cognitive Impairment in Myotonic Dystrophy Type 1. 5
A man with sarcoidosis and slurred speech 5
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression 4
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. 3
Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population. 3
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 3
High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study 3
Single-fiber PRC in MELAS3243 patients: Correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotype 2
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency 2
Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia 2
Subdural hematoma in a young woman with an "old" brain 2
Totale 2752
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Categoria #
all - tutte 2752
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 2752
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2015/2016147 0000 00 00 0397137
2016/2017495 44336563 4747 2424 36246325
2017/2018429 39225390 3421 1539 56211821
2018/2019566 20251544 9960 7139 30417052
2019/2020786 140495346 6758 6430 55669860
2020/2021329 18521553 5934 980 0000
Totale 2752
 
 
 
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