PORTARO, SIMONA
 Distribuzione geografica
Continente #
EU - Europa 1.007
NA - Nord America 928
AS - Asia 244
Totale 2.179
Nazione #
US - Stati Uniti d'America 926
IE - Irlanda 339
SE - Svezia 258
CN - Cina 202
IT - Italia 148
PL - Polonia 118
DE - Germania 34
FI - Finlandia 31
BE - Belgio 24
IN - India 21
UA - Ucraina 21
GB - Regno Unito 18
VN - Vietnam 14
NL - Olanda 6
FR - Francia 4
IR - Iran 3
TR - Turchia 3
CA - Canada 2
CH - Svizzera 1
CZ - Repubblica Ceca 1
ES - Italia 1
KR - Corea 1
LT - Lituania 1
PT - Portogallo 1
RU - Federazione Russa 1
Totale 2.179
Città #
Dublin 338
Chandler 224
Nyköping 147
Warsaw 112
Beijing 72
Ashburn 71
Jacksonville 68
Messina 57
New York 50
Ann Arbor 45
Dearborn 44
Princeton 44
Medford 37
Cambridge 27
Des Moines 24
Brussels 22
Pune 20
Shenyang 20
Jinan 18
Wilmington 16
Dong Ket 14
Boardman 13
Rome 12
Caltagirone 11
Hangzhou 11
Mascali 11
Nanjing 11
Bremen 10
Haikou 9
Ningbo 9
San Mateo 9
Tianjin 9
Lancaster 8
Taizhou 8
Fuzhou 7
Catania 6
Bydgoszcz 5
Helsinki 5
Washington 5
Falls Church 4
Taiyuan 4
Woodbridge 4
Zhengzhou 4
Hebei 3
Houston 3
Izmir 3
Milan 3
Naples 3
Norwalk 3
Seattle 3
Acireale 2
Ardabil 2
Guangzhou 2
Jiaxing 2
Leno 2
Nanchang 2
Paris 2
Portomaggiore 2
San Giuliano Milanese 2
Sevenoaks 2
Siracusa 2
Torino 2
Waanrode 2
Atlanta 1
Augusta 1
Bitonto 1
Brno 1
Castricum 1
Changsha 1
Chicago 1
Edinburgh 1
Fairfield 1
Genova 1
Gibellina 1
Glasgow 1
Kirkland 1
Lausanne 1
Linda a Velha 1
Montréal 1
Mumbai 1
Nashville 1
Nürnberg 1
Pescara 1
Pisa 1
Putignano 1
Redmond 1
Redwood City 1
Rio Saliceto 1
Rosate 1
Sant'antonino Di Susa 1
Vigo 1
Vilnius 1
Xiangfen 1
Totale 1.722
Nome #
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation. 105
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 91
Five years experience on 3,4-diaminopyridine phosphate in Lambert-Eaton syndrome: Case reports 81
A CMT1A PATIENT WITH PAINFUL AND DISABLING SYMPTOMS: FAST RECOVERY AFTER IVIG TREATMENT. 78
Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls 77
Force and strain during horseback riding: bridging the gap between theory and clinical practice 74
Toward a more personalized motor function rehabilitation in myotonic dystrophy type 1: The role of neuroplasticity 74
La miopatia ipotiroidea 69
Bone mass and metabolism in patients with myastenia gravis: a possible anabolic role for pyridostigmine on bone tissue 67
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 61
Hypothyroid myopathy: A peculiar clinical presentation of thyroid failure. Review of the literature. 59
null 58
Advances in assessing myotonia: Can sensor-engineered glove have a role? 57
ANT1 is reduced in sporadic inclusion body myositis. 54
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita 54
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 53
Chasing the chameleon: Psychogenic paraparesis responding to non-invasive brain stimulation 53
A dental implant dislocated in the ethmoidal sinus: a case report 53
Malattia di Chanarin-Dorfman: aspetti clinici, gemetici e neuroradiologici di un caso adulto seguito per 25 anni 51
Chanarin-Dorfman disease (CDD): clinical, genetic and neuroradiological aspects in an adult case followed over 25 years 50
TRPV4 related scapuloperoneal spinal muscular atrophy: Report of an Italian family and review of the literature 48
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype 47
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype 46
Telerehabilitation in individuals with severe acquired brain injury 46
Tubular aggregates: do they help in diagnosing neuromuscular disorders? 45
A case of necrotizing myopathy with proximal weakness and cardiomyopathy 45
null 45
Paving the way for a better understanding of the pathophysiology of gait impairment in myotonic dystrophy: A pilot study focusing on muscle networks 44
Can muscle vibration be the future in the treatment of cerebral palsy-related drooling? A feasibility study 43
SPINALNERVE ROOT THICKENING AND ANHANCEMENT CAUSING PAINFUL AND DISABLING SYMPTOMS IN CMT 1A: FAST RECOVERY AFTER HIGH DOSAGE IVIG. 42
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 38
Deletion of the Williams Beuren syndrome critical region unmasks facioscapulohumeral muscular dystrophy 36
New versus Old Oral Anticoagulants: How can we set the Scale needle? Considerations on a Case Report 33
null 31
Telemedicine for Facio-Scapulo-Humeral Muscular Dystrophy: A multidisciplinary approach to improve quality of life and reduce hospitalization rate? 30
null 28
null 27
The role of brain oscillations in post-stroke motor recovery: An overview 25
Tubular aggregates: do they help in diagnosing neuromuscular disorders ? 25
Prevalence study of genetically defined skeletal muscle channelopathies in England 24
null 24
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 23
Hemangiomas of the tongue and the oral cavity in a myotonic dystrophy type 1 patient: A case report 21
null 20
Long-Term Follow-Up in Infantile-Onset Lambert-Eaton Myasthenic Syndrome 20
null 18
A new explanation for recessive myotonia congenita Exon deletions and duplications in CLCN1 18
Steroid Management in a Patient with Myasthenia Gravis Undergoing COVID-19 Vaccination 16
Sporadic late-onset nemaline myopathy in a woman with multiple myeloma successfully treated with lenalidomide/dexamethasone. 16
Bone Health Status in Individuals with Amyotrophic Lateral Sclerosis: A Cross-Sectional Study on the Role of the Trabecular Bone Score and Its Implications in Neurorehabilitation 12
Stiffness as a presenting symptom of an odd clinical condition caused by multiple sclerosis and myotonia congenita 12
Haemophilia and Fragility Fractures: From Pathogenesis to Multidisciplinary Approach 12
A case report of recessive myotonia congenita and early onset cognitive impairment 10
Totale 2.289
Categoria #
all - tutte 7.593
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 7.593


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201916 0 0 0 0 0 0 0 0 2 5 5 4
2019/2020268 11 6 0 7 4 43 20 18 4 101 36 18
2020/2021360 25 21 58 15 75 16 21 22 35 41 11 20
2021/2022344 3 37 3 9 15 6 52 17 4 78 22 98
2022/2023894 70 95 34 65 47 88 9 50 391 2 35 8
2023/2024262 22 47 13 36 24 102 8 10 0 0 0 0
Totale 2.289