Madia, Francesca
 Distribuzione geografica
Continente #
EU - Europa 1.394
NA - Nord America 956
AS - Asia 292
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.649
Nazione #
US - Stati Uniti d'America 951
DE - Germania 763
CN - Cina 200
SE - Svezia 194
UA - Ucraina 112
IT - Italia 80
FR - Francia 75
GB - Regno Unito 48
IE - Irlanda 35
SG - Singapore 33
FI - Finlandia 28
RU - Federazione Russa 24
IN - India 18
TR - Turchia 17
BE - Belgio 15
NL - Olanda 8
PL - Polonia 7
CI - Costa d'Avorio 6
JP - Giappone 6
CA - Canada 5
VN - Vietnam 5
HK - Hong Kong 4
IR - Iran 4
CH - Svizzera 2
IL - Israele 2
A2 - ???statistics.table.value.countryCode.A2??? 1
ES - Italia 1
HR - Croazia 1
KR - Corea 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
RO - Romania 1
Totale 2.649
Città #
Chandler 210
Ashburn 103
Nürnberg 71
San Mateo 61
Nanjing 54
Jacksonville 50
New York 46
Ann Arbor 40
Dublin 35
Nanchang 33
Boston 26
Marseille 26
Singapore 23
Wilmington 21
Dearborn 19
Moscow 18
Woodbridge 17
Lawrence 16
Izmir 15
Redmond 15
Brussels 13
Detroit 12
Hangzhou 12
Houston 12
Seattle 12
Fairfield 11
Milan 11
Redwood City 11
Hebei 10
Norwalk 10
Shenyang 10
Kunming 9
Rome 9
Bremen 8
University Park 8
Munich 7
Zhengzhou 7
Abidjan 6
Beijing 6
Busto Arsizio 6
Helsinki 6
Leawood 6
Mountain View 6
Philadelphia 6
Princeton 6
Cattolica 5
Changsha 5
Hanoi 5
Jiaxing 5
Monza 5
Shanghai 5
Changchun 4
Chicago 4
Guangzhou 4
Hefei 4
Hong Kong 4
Kraków 4
Rotonda 4
Andover 3
Boardman 3
Bologna 3
Indiana 3
Lancaster 3
Ningbo 3
Tianjin 3
Clearwater 2
Corte Franca 2
Fairport 2
Fremont 2
Jinan 2
London 2
Saint Louis 2
San Francisco 2
Simi Valley 2
Stockholm 2
Taizhou 2
Toronto 2
Waanrode 2
Amsterdam 1
Augusta 1
Birmingham 1
Brescia 1
Buffalo 1
Buonabitacolo 1
Calgary 1
Cambridge 1
Casoria 1
Chengdu 1
Città Di Castello 1
Colombo 1
Costa Mesa 1
Cupertino 1
Desio 1
Easton 1
Espoo 1
Falls Church 1
Fuzhou 1
Guidonia 1
Guiyang 1
Kish 1
Totale 1.246
Nome #
Natural History of Young-Adult Amyotrophic Lateral Sclerosis. 299
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy. 177
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutaton causing a double patogenetic effect 131
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy. 129
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation 127
Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS 124
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. 112
Restless Legs Syndrome with Periodic Limb Movements: a possible cause of idiopathic hyperCKemia. 108
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies. 107
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. 100
Neurologic improvement after peripheral blood stem cell transplantation in poems 93
Acute myopathic quadriplegia in COVID-19 patients in the intensive care unit 93
Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy 91
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. 91
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia. 90
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. 85
Teaching NeuroImage: MRI of diabetic lumbar plexopathy treated with local steroid injection. 85
Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer. 83
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients 82
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. 81
Case of postpartum Parsonage-Turner syndrome 79
Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. 75
Economic Consequences of Investing in Anti-HCV Antiviral Treatment from the Italian NHS Perspective: A Real-World-Based Analysis of PITER Data 65
Clinical features and comorbidity pattern of HCV infected migrants compared to native patients in care in Italy: A real-life evaluation of the PITER cohort 61
Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center 58
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 58
Isolated compression of the ulnar motor branch due to carpal joint ganglia: clinical series, surgical technique and postoperative outcomes 13
Totale 2.697
Categoria #
all - tutte 8.483
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 8.483


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020342 71 15 27 19 28 39 27 5 19 31 33 28
2020/2021227 20 20 2 29 26 6 28 6 32 9 45 4
2021/2022299 36 22 9 43 8 11 8 48 9 12 41 52
2022/2023569 57 73 65 88 39 78 38 47 64 2 15 3
2023/2024292 14 69 7 15 6 51 29 16 4 12 27 42
2024/20257 7 0 0 0 0 0 0 0 0 0 0 0
Totale 2.697