IRIS
DE MICHELE, GIOVANNA
 Distribuzione geografica
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Continente #
NA - Nord America 401
EU - Europa 233
AS - Asia 118
AF - Africa 12
Totale 764
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Nazione #
US - Stati Uniti d'America 398
IT - Italia 129
SG - Singapore 84
UA - Ucraina 34
NL - Olanda 23
DE - Germania 19
CN - Cina 13
BG - Bulgaria 11
CI - Costa d'Avorio 11
IE - Irlanda 7
IN - India 6
PH - Filippine 5
TR - Turchia 5
MK - Macedonia 4
VN - Vietnam 4
CA - Canada 3
GB - Regno Unito 3
FI - Finlandia 1
IR - Iran 1
PL - Polonia 1
RS - Serbia 1
ZA - Sudafrica 1
Totale 764
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Città #
Chandler 94
Singapore 68
Ashburn 34
Amsterdam 22
Santa Clara 22
Millbury 21
Naples 21
Lawrence 17
Des Moines 11
Sofia 11
Wilmington 11
Munich 10
Gricignano di Aversa 8
Boston 7
Fairfield 7
Napoli 7
Monteforte Irpino 5
Dong Ket 4
Izmir 4
Los Angeles 4
Nanjing 4
Pune 4
Telese 4
Aversa 3
Bitola 3
General Mariano Alvarez 3
Guangzhou 3
Messina 3
Montecorvino Pugliano 3
Rome 3
San Mateo 3
Washington 3
Woodbridge 3
Battipaglia 2
Beijing 2
Dublin 2
Florence 2
Jinan 2
Milan 2
Parma 2
Phoenix 2
Pompei 2
Princeton 2
Redwood City 2
Sassari 2
Torre Del Greco 2
Turin 2
Aleksandrów Kujawski 1
Andover 1
Ardabil 1
Augusta 1
Bacoli 1
Belgrade 1
Böblingen 1
Caloocan City 1
Clifton 1
Dallas 1
Hebei 1
Houston 1
Istanbul 1
Jiaxing 1
Lappeenranta 1
Latina 1
London 1
Lviv 1
Monmouth Junction 1
Muizenberg 1
Mumbai 1
New Delhi 1
Norwalk 1
Ottawa 1
Padova 1
San Giuseppe Vesuviano 1
Sant'Antimo 1
Sant'angelo D'alife 1
Sant'arpino 1
Scafati 1
Tavagnacco 1
Terracina 1
Toronto 1
Trescore Balneario 1
Vertova 1
Totale 493
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Nome #
Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation 75
Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction 52
Screening for Fabry disease in a series of Parkinson’s disease patients and literature review 48
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family. 46
Prevalence and features of non-motor symptoms in Wilson's disease 46
Cutaneous sensory and autonomic denervation in Progressive Supranuclear Palsy 44
Magnetic resonance parkinsonism indices and interpeduncular angle in idiopathic normal pressure hydrocephalus and progressive supranuclear palsy 37
The “crab sign”: an imaging feature of spinocerebellar ataxia type 48 36
Anti-CRMP5 paraneoplastic chorea: selective external capsule MRI involvement resolving after tumour resection 34
Reversible valproate-induced subacute encephalopathy associated with a MT-ATP8 variant in the mitochondrial genome 30
New AARS2 Mutations in Two Siblings With Tremor, Downbeat Nystagmus, and Primary Amenorrhea: A Benign Phenotype Without Leukoencephalopathy 29
Degenerative and acquired sporadic adult onset ataxia 28
Motor and non-motor features in Parkinson's Disease patients carrying GBA gene mutations 27
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families 27
Conventional MRI findings in hereditary degenerative ataxias: a pictorial review 27
Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosis. 26
Assessment of non-motor and autonomic symptoms in Wilson's disease patients 26
Spinocerebellar ataxia type 48: last but not least 25
Othello syndrome in Parkinson's disease: a systematic review and report of a case series 25
Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families 24
Safety and feasibility of upper limb cardiopulmonary exercise test in Friedreich ataxia 23
Of cognition and cerebellum in SCA48 19
Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes. 18
A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A 12
A Review of Brain and Pituitary Gland MRI Findings in Patients with Ataxia and Hypogonadism 8
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations 8
CHARON: An Imaging-Based Diagnostic Algorithm to Navigate Through the Sea of Hereditary Degenerative Ataxias 6
Totale 806
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Categoria #
all - tutte 4.130
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 4.130
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203 0 0 0 0 2 0 0 0 0 0 1 0
2020/202198 12 3 2 6 9 3 13 19 12 1 11 7
2021/2022149 3 6 3 1 4 2 3 5 18 11 40 53
2022/2023231 23 18 9 11 25 30 10 16 35 33 18 3
2023/2024168 6 20 12 21 12 10 21 22 4 5 26 9
2024/2025132 31 38 6 17 40 0 0 0 0 0 0 0
Totale 806