CATALOGO DEI PRODOTTI DELLA RICERCA

SCARPELLI, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 1.160
EU - Europa 768
AS - Asia 303
SA - Sud America 3
OC - Oceania 2
AF - Africa 1
Totale 2.237
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Nazione #
US - Stati Uniti d'America 1.157
GB - Regno Unito 285
CN - Cina 269
SE - Svezia 88
FR - Francia 76
IT - Italia 75
IE - Irlanda 71
FI - Finlandia 63
DE - Germania 52
UA - Ucraina 27
KR - Corea 21
BE - Belgio 15
NL - Olanda 6
VN - Vietnam 5
CA - Canada 3
HK - Hong Kong 3
AU - Australia 2
PL - Polonia 2
AR - Argentina 1
AT - Austria 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BO - Bolivia 1
BR - Brasile 1
CH - Svizzera 1
EG - Egitto 1
HR - Croazia 1
HU - Ungheria 1
IN - India 1
IR - Iran 1
LU - Lussemburgo 1
PT - Portogallo 1
RU - Federazione Russa 1
TH - Thailandia 1
TR - Turchia 1
Totale 2.237
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Città #
Southend 233
Chandler 195
Woodbridge 186
Jacksonville 164
Ann Arbor 129
Beijing 76
Dublin 71
Houston 70
Ashburn 53
Wilmington 42
Verona 38
Lawrence 33
Princeton 33
Jinan 31
Shenyang 24
Seoul 21
Brussels 13
Nanchang 13
Nanjing 12
Tianjin 11
Falls Church 10
Jiaxing 10
Auburn Hills 9
Hebei 9
Boardman 8
Cagliari 8
Haikou 8
Hangzhou 8
Changsha 7
Milan 7
Norwalk 7
Guangzhou 6
Helsinki 6
Lancaster 6
Los Angeles 6
New York 6
Redwood City 6
Taiyuan 6
Taizhou 6
Zhengzhou 6
Düsseldorf 5
Sindelfingen 5
Fairfield 4
Mestre 4
Detroit 3
Hong Kong 3
Lanzhou 3
Ningbo 3
Salt Lake City 3
San Francisco 3
Seattle 3
Bonndorf 2
Canberra 2
Cimavilla 2
Dearborn 2
Dong Ket 2
Fuzhou 2
Saint Paul 2
Shanghai 2
Toronto 2
Waanrode 2
Warsaw 2
Washington 2
Almere Stad 1
Baku 1
Bangkok 1
Bologna 1
Buenos Aires 1
Cairo 1
Camden 1
Changle 1
Clearwater 1
Codigoro 1
Durham 1
Fano 1
Florence 1
Hackney 1
Hanoi 1
Kemerovo 1
La Jolla 1
Las Vegas 1
Lisbon 1
London 1
Luxembourg 1
Mariano Comense 1
Mastic Beach 1
Montréal 1
Paris 1
Phoenix 1
Pomezia 1
Riva 1
Sabz 1
Sioux Falls 1
Sofia 1
Spilimbergo 1
Stockholm 1
Sucre 1
Trento 1
Trieste 1
Utrecht 1
Totale 1.693
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Nome #
Course and management of allogeneic stem cell transplantation in patients with mitochondrial neurogastrointestinal encephalomyopathy. 112
The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy. 108
Poor outcome in a mitochondrial neurogastrointestinal encephalomyopathy patient with a novel TYMP mutation: the need for early diagnosis. 103
Mitochondrial sensorineural hearing loss: a retrospective study and a description of cochlear implantation in a MELAS patient. 100
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases. 99
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. 87
Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy. 79
McArdle disease and sporadic inclusion-body myositis. 77
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era 77
FROM PATHOGENESIS TO TREATMENT OF MNGIE AND OTHER MITOCHONDRIAL DEPLETION SYNDROMES 73
Administration of deoxyribonucleosides or inhibition of their catabolism as a pharmacological approach for mitochondrial DNA depletion syndrome 71
Current options in the treatment of mitochondrial diseases. 70
Late-onset glycogen storage disease type 2. 69
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation. 65
Prevalence of asymptomatic vertebral fractures in late-onset Pompe disease. 64
Short stature and high serum transaminase levels: growth hormone deficiency in a child with Becker muscular dystrophy 64
The Frequencies of Different Inborn Errors of Metabolism in Adult Metabolic Centres: Report from the SSIEM Adult Metabolic Physicians Group 63
Redefining phenotypes associated with mitochondrial DNA single deletion 62
The role of mitochondria in neurodegenerative diseases. 61
Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases. 60
Clinical and biochemical improvements in a patient with MNGIE following enzyme replacement. 59
Feeding the deoxyribonucleoside salvage pathway to rescue mitochondrial DNA 59
Neuropathology of mitochondrial diseases 59
Novel mitochondrial tRNA(Leu(CUN)) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype 56
Un caso di insufficienza renale acuta secondaria a malattia di MC-Ardle ad esordio tardivo. [A case of acute renal failure secondary to late-onset McArdle's disease]. 56
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 55
Myoclonus in mitochondrial disorders 54
Mitochondrial DNA haplogroups may influence Fabry Disease phenotypei. 52
Identification and characterization of the novel m.8305C>T MTTK and m.4440G>A MTTM gene mutations causing mitochondrial myopathies 50
Non-muscle involvement in late-onset Glycogenosis II 49
Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients 44
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 42
Strategies for treating mitochondrial disorders: an update. 42
Endoscopic trans-Magendie foramen biopsy of the superior medullary velum: Technical note 15
Totale 2.256
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Categoria #
all - tutte 6.796
article - articoli 6.604
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 192
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13.592
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20199 0 0 0 0 0 0 0 0 0 0 1 8
2019/2020319 40 0 5 21 24 31 32 10 12 35 43 66
2020/2021253 16 61 12 27 34 34 3 11 7 3 32 13
2021/2022226 21 64 2 8 7 8 6 18 12 4 14 62
2022/2023536 44 62 56 83 45 114 6 29 73 2 16 6
2023/2024209 9 31 11 27 35 31 6 26 2 27 4 0
Totale 2.256