MONGINI, Tiziana Enrica
 Distribuzione geografica
Continente #
NA - Nord America 1551
EU - Europa 689
AS - Asia 315
OC - Oceania 25
AF - Africa 18
SA - Sud America 15
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2614
Nazione #
US - Stati Uniti d'America 1507
IT - Italia 240
DE - Germania 230
CN - Cina 115
GB - Regno Unito 53
CA - Canada 40
IN - India 38
JP - Giappone 35
VN - Vietnam 35
HK - Hong Kong 27
PL - Polonia 25
AU - Australia 22
FR - Francia 22
UA - Ucraina 21
TR - Turchia 17
KR - Corea 16
SE - Svezia 14
ZA - Sudafrica 11
AT - Austria 10
BR - Brasile 9
RU - Federazione Russa 9
SG - Singapore 9
CH - Svizzera 8
CZ - Repubblica Ceca 8
NL - Olanda 8
EG - Egitto 7
ES - Italia 7
TW - Taiwan 7
GR - Grecia 6
IE - Irlanda 6
IL - Israele 6
BE - Belgio 5
MX - Messico 4
PT - Portogallo 4
FI - Finlandia 3
AR - Argentina 2
LT - Lituania 2
MY - Malesia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PK - Pakistan 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
SY - Repubblica araba siriana 2
AE - Emirati Arabi Uniti 1
CL - Cile 1
CO - Colombia 1
EC - Ecuador 1
EU - Europa 1
HU - Ungheria 1
ID - Indonesia 1
LV - Lettonia 1
PE - Perù 1
PG - Papua Nuova Guinea 1
Totale 2614
Città #
Fairfield 184
Houston 116
Buffalo 96
Santa Cruz 90
Torino 86
Woodbridge 80
Seattle 77
Ashburn 69
Cambridge 68
Wilmington 59
Ann Arbor 58
Mountain View 38
Fleming Island 35
Beijing 33
University Park 28
Dong Ket 27
Nürnberg 24
Warsaw 23
Guangzhou 22
Pisa 20
Chicago 16
Kharkov 16
Las Vegas 15
Shanghai 15
Turin 15
Central District 13
Clearwater 12
Leawood 12
Rome 12
Melbourne 11
Milan 11
San Diego 10
Henderson 9
Muizenberg 9
Ottawa 9
Phoenix 9
Stockholm 9
Atlanta 8
Encino 8
Los Angeles 8
Wuhan 8
Istanbul 7
Taipei 7
Toronto 7
Boston 6
Brooklyn 6
Duncan 6
Lake Forest 6
New York 6
Provo 6
San Jose 6
Basaksehir 5
Dallas 5
Dearborn 5
Genova 5
New Haven 5
San Francisco 5
St Louis 5
Arlington 4
Bengaluru 4
Dublin 4
Durham 4
Easton 4
Gainesville 4
Hangzhou 4
Hanoi 4
Hobart 4
Jinan 4
Munich 4
Paris 4
Singapore 4
Somerville 4
Tokyo 4
Basel 3
Berlin 3
Brasília 3
Bridgewater 3
Büdelsdorf 3
Changchun 3
Cheadle Hulme 3
Chengdu 3
Columbus 3
Des Moines 3
Ferrara 3
Gurgaon 3
Leeds 3
Livorno 3
Madison 3
North Bergen 3
Padova 3
Suzhou 3
Utrecht 3
Valdagno 3
Vienna 3
Acton 2
Allahabad 2
Ankara 2
Athis-Mons 2
Barcelona 2
Boulder 2
Totale 1701
Nome #
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy, file e27ce427-b401-2581-e053-d805fe0acbaa 306
Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy, file e27ce42c-9136-2581-e053-d805fe0acbaa 280
Intrathecal administration of nusinersen in adult and adolescent patients with spinal muscular atrophy and scoliosis: Transforaminal versus conventional approach, file e27ce42f-47f6-2581-e053-d805fe0acbaa 279
Prevalence of congenital muscular dystrophy in Italy: A population study, file e27ce42a-5a32-2581-e053-d805fe0acbaa 199
Genotype-phenotype correlation in Pompe disease, a step forward, file e27ce427-0447-2581-e053-d805fe0acbaa 195
The empowerment of translational research: lessons from laminopathies, file e27ce427-cfc8-2581-e053-d805fe0acbaa 181
Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy, file e27ce42a-8191-2581-e053-d805fe0acbaa 180
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy, file e27ce42a-229e-2581-e053-d805fe0acbaa 175
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients, file e27ce42a-229c-2581-e053-d805fe0acbaa 168
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes., file e27ce426-f370-2581-e053-d805fe0acbaa 164
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes., file e27ce427-0445-2581-e053-d805fe0acbaa 144
Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation., file e27ce42a-8f95-2581-e053-d805fe0acbaa 92
Assessing cognitive function in neuromuscular diseases: A pilot study in a sample of children and adolescents, file e27ce433-db29-2581-e053-d805fe0acbaa 66
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry, file e27ce432-5b01-2581-e053-d805fe0acbaa 57
Movement disorders in children with a mitochondrial disease: A cross-sectional survey from the nationwide italian collaborative network of mitochondrial diseases, file e27ce435-19df-2581-e053-d805fe0acbaa 32
A man with fever and bilateral limb weakness, file e27ce42e-db00-2581-e053-d805fe0acbaa 28
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements, file e27ce435-50be-2581-e053-d805fe0acbaa 14
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea, file e27ce432-5ecf-2581-e053-d805fe0acbaa 13
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53, file e27ce432-c7b0-2581-e053-d805fe0acbaa 12
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up, file e27ce432-c942-2581-e053-d805fe0acbaa 12
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data, file e27ce432-f365-2581-e053-d805fe0acbaa 9
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing, file e27ce434-8b91-2581-e053-d805fe0acbaa 9
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network, file e27ce435-19dd-2581-e053-d805fe0acbaa 9
Frailties and critical issues in neuromuscular diseases highlighted by SARS-CoV-2 pandemic: how many patients are still "invisible"?, file e27ce435-43ee-2581-e053-d805fe0acbaa 9
Longitudinal effect of eteplirsen vs. historical control on ambulation in DMD, file e27ce432-5ece-2581-e053-d805fe0acbaa 6
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study, file e27ce435-43f0-2581-e053-d805fe0acbaa 6
A Schematic Approach to Defining the Prevalence of COL VI Variants in Five Years of Next-Generation Sequencing, file 8d5d53b1-b2c0-46a6-88bc-b94920e33e8a 4
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey, file d2c54c37-7810-4af7-8aa4-46a46670f6cb 4
Intrathecal administration of nusinersen in adult and adolescent patients with spinal muscular atrophy and scoliosis: Transforaminal versus conventional approach, file e27ce432-5770-2581-e053-d805fe0acbaa 4
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase, file e27ce432-f9b6-2581-e053-d805fe0acbaa 4
Motor Outcome Measures in Pediatric Patients with Congenital Muscular Dystrophies: A Scoping Review, file 162ebb3f-0cae-4e2c-ab74-fbf56f7b8380 3
Improving Recognition of Treatable Rare Neuromuscular Disorders in Primary Care: A Pilot Feasibility Study, file 5437494f-317e-4327-9ce1-2af1a68edf6b 3
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy., file e27ce427-b407-2581-e053-d805fe0acbaa 3
Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures, file e27ce427-d02e-2581-e053-d805fe0acbaa 3
Enzyme Replacement Therapy Improves Respiratory Outcomes in Patients with Late-Onset Type II Glycogenosis and High Ventilator Dependency., file e27ce427-d8d8-2581-e053-d805fe0acbaa 3
Recommendations for anesthesia and perioperative management of patients with neuromuscular disorders., file e27ce427-d9cf-2581-e053-d805fe0acbaa 3
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD), file e27ce432-5ed1-2581-e053-d805fe0acbaa 3
Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review, file e27ce435-412b-2581-e053-d805fe0acbaa 3
Myoclonus in mitochondrial disorders., file e27ce426-f36e-2581-e053-d805fe0acbaa 2
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype, file e27ce427-d201-2581-e053-d805fe0acbaa 2
EFNS review on the role of muscle biopsy in the investigation of myalgia., file e27ce427-de9d-2581-e053-d805fe0acbaa 2
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?, file e27ce427-dea0-2581-e053-d805fe0acbaa 2
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study., file e27ce427-dfe9-2581-e053-d805fe0acbaa 2
Undiagnosed myopathy before surgery and safe anaesthesia table., file e27ce427-e1bd-2581-e053-d805fe0acbaa 2
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency., file e27ce428-09a2-2581-e053-d805fe0acbaa 2
Response to a letter to the editor, file e27ce42f-394f-2581-e053-d805fe0acbaa 2
Functional assessment tools in children with Pompe disease: A pilot comparative study to identify suitable outcome measures for the standard of care, file e27ce432-9c66-2581-e053-d805fe0acbaa 2
The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophy, file e27ce432-a36d-2581-e053-d805fe0acbaa 2
Registries versus tertiary care centers: How do we measure standards of care in Duchenne muscular dystrophy?, file e27ce432-ce84-2581-e053-d805fe0acbaa 2
Early higher dosage of alglucosidase alpha in classic Pompe disease, file e27ce432-dcff-2581-e053-d805fe0acbaa 2
Wearable Inertial Devices in Duchenne Muscular Dystrophy: A Scoping Review, file 49e8fa69-5d18-46cb-a995-bd6dce416a42 1
Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophy., file e27ce426-f36f-2581-e053-d805fe0acbaa 1
Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation., file e27ce426-f765-2581-e053-d805fe0acbaa 1
Vaccination recommendations for patients with neuromuscular disease., file e27ce427-0446-2581-e053-d805fe0acbaa 1
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation., file e27ce427-b5c4-2581-e053-d805fe0acbaa 1
New motor outcome function measures in evaluation of late-onset Pompe disease before and after enzyme replacement therapy., file e27ce427-cd2f-2581-e053-d805fe0acbaa 1
Brain metabolism changes after therapy with chenodeoxycholic acid in a case of cerebrotendinous xanthomatosis., file e27ce427-dd5c-2581-e053-d805fe0acbaa 1
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases., file e27ce427-ef54-2581-e053-d805fe0acbaa 1
Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII), file e27ce428-0f53-2581-e053-d805fe0acbaa 1
New pharmacotherapies for genetic neuromuscular disorders: opportunities and challenges, file e27ce42e-c397-2581-e053-d805fe0acbaa 1
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population, file e27ce432-5ed0-2581-e053-d805fe0acbaa 1
Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry, file e27ce432-bbb9-2581-e053-d805fe0acbaa 1
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements, file e27ce432-bbbb-2581-e053-d805fe0acbaa 1
Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy, file e27ce432-c944-2581-e053-d805fe0acbaa 1
Totale 2723
Categoria #
all - tutte 3620
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 3620


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201812 0000 00 00 00012
2018/2019349 7639 1112 1938 33449770
2019/2020550 45493278 4853 3651 61332638
2020/2021467 29392350 3842 4132 41494439
2021/2022607 70394372 5527 3331 343711848
2022/2023476 182910860 4428 5335 3440234
Totale 2723