Bicocca Open Archive

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CARECCHIO, MIRYAM
 Distribuzione geografica
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Continente #
AS - Asia 241
NA - Nord America 155
EU - Europa 134
SA - Sud America 10
AF - Africa 2
OC - Oceania 1
Totale 543
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Nazione #
US - Stati Uniti d'America 150
HK - Hong Kong 140
SG - Singapore 63
IT - Italia 50
CN - Cina 26
RU - Federazione Russa 18
NL - Olanda 14
BR - Brasile 10
DE - Germania 10
GB - Regno Unito 9
IE - Irlanda 8
DK - Danimarca 6
UA - Ucraina 6
CA - Canada 5
SE - Svezia 5
IN - India 4
ID - Indonesia 3
SI - Slovenia 3
AT - Austria 2
FR - Francia 2
AU - Australia 1
EG - Egitto 1
FI - Finlandia 1
IR - Iran 1
JP - Giappone 1
KR - Corea 1
PK - Pakistan 1
SC - Seychelles 1
TR - Turchia 1
Totale 543
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Città #
Hong Kong 140
Singapore 26
Wilmington 21
Ann Arbor 14
Ashburn 14
Fairfield 13
Dearborn 11
Santa Clara 11
Dublin 8
Milan 8
Nanjing 7
Woodbridge 6
Cambridge 5
Cagliari 4
Dongguan 4
Houston 4
New York 4
Princeton 4
Seattle 4
Shanghai 4
Altamura 3
Jakarta 3
Ljubljana 3
Rimini 3
Rome 3
San Diego 3
Absecon 2
Council Bluffs 2
Desio 2
Edmonton 2
Guangzhou 2
Jacksonville 2
Los Angeles 2
Ningbo 2
Nuremberg 2
Villafranca Padovana 2
Würzburg 2
Amsterdam 1
Ananindeua 1
Andover 1
Atlanta 1
Belo Horizonte 1
Bengaluru 1
Boardman 1
Böblingen 1
Campina Grande 1
Chandler 1
Contagem 1
Cornaredo 1
Darmstadt 1
Dehradun 1
Evanston 1
Giza 1
Görwihl 1
Haikou 1
Hebei 1
Helsinki 1
Hortolândia 1
Istanbul 1
Kiev 1
Kingston 1
Kunming 1
Köln 1
Lawrence 1
London 1
Mainz 1
Melbourne 1
Modena 1
Moscow 1
Mountain View 1
Nanchang 1
Naples 1
Norwalk 1
Orange 1
Ottawa 1
Padova 1
Penápolis 1
Pune 1
Recife 1
Reggio Calabria 1
Ribeirão Preto 1
Riese Pio X 1
Seodaemun-gu 1
Serra 1
Shenyang 1
Taizhou 1
Tomsk 1
Toronto 1
Vienna 1
Villeurbanne 1
Vitória 1
Totale 406
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Nome #
SPG5 siblings with different phenotypes showing reduction of 27-hydroxycholesterol after simvastatin-ezetimibe treatment 179
The impact of Next Generation Sequencing in rare movement disorders diagnosis: results from a tertiary referral center. 118
EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia 35
A novel MRPS34 gene mutation with combined OXPHOS deficiency in an adult patient with Leigh syndrome 32
Molecular genetics of niemann–pick type c disease in italy: An update on 105 patients and description of 18 NPC1 novel variants 21
Clinical, cognitive, and morphometric profiles of progressive supranuclear palsy phenotypes 17
Illustration of the long-term efficacy of pallidal deep brain stimulation in a patient with PKAN dystonia 13
NKX2.1 run-on mutation associated to familial brain–lung–thyroid syndrome 12
Olfactory and rhinological evaluations in SARS-CoV-2 patients complaining of olfactory loss 11
Correction to: Long-term safety, discontinuation and mortality in an Italian cohort with advanced Parkinson’s disease on levodopa/carbidopa intestinal gel infusion (Journal of Neurology, (2022), 10.1007/s00415-022-11269-7) 11
Correction to: Cerebellar and cortical hypometabolism in progressive stimulus-sensitive limb myoclonus in celiac disease (Neurological Sciences, (2021), 42, 8, (3453-3455), 10.1007/s10072-021-05264-5) 9
Family History in Parkinson's Disease: A National Cross-Sectional Study 9
MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism 9
Adult-onset KMT2B-related dystonia 9
ANO3 as a Cause of Early-Onset Chorea Combined with Dystonia: Illustration of Phenotypic Evolution 9
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants 8
Immune landscape of the enteric nervous system differentiates Parkinson's disease patients from controls: The PADUA-CESNE cohort 8
Impact of social and mobility restrictions in Parkinson’s disease during COVID-19 lockdown 8
Adult diagnosis of Cockayne syndrome 8
Duodenal alpha-Synuclein Pathology and Enteric Gliosis in Advanced Parkinson's Disease 8
Increased glucosylsphingosine levels and Gaucher disease in GBA1-associated Parkinson's disease 7
Rapidly progressive multiple system atrophy in a patient carrying LRRK2 G2019S mutation 7
Correction to: A case of childhood‑onset dystonia‑parkinsonism due to homozygous parkin mutations and effect of globus pallidus deep brain stimulation (Neurological Sciences, (2023), 44, 9, (3323-3326), 10.1007/s10072-023-06832-7) 7
Scoping Review on ADCY5-Related Movement Disorders 7
Functional and idiopathic cervical dystonia in two family members: A challenging diagnosis 7
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 7
Reply to: “Heterogeneous Phenotypic Evolution in ANO3-Related Dystonia Due to the Recurrent p.Glu510Lys Variant” 7
Genetic mutations in Parkinson’s disease: screening of a selected population from North-Eastern Italy 7
The clinical and genetic spectrum of primary familial brain calcification 7
Dominant VPS16 Pathogenic Variants: Not Only Isolated Dystonia 7
Neurotransmitter and receptor systems in the subthalamic nucleus 7
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum 7
A case of childhood-onset dystonia-parkinsonism due to homozygous parkin mutations and effect of globus pallidus deep brain stimulation 7
Primary brain calcification: an international study reporting novel variants and associated phenotypes 7
Long-term effect of subthalamic and pallidal deep brain stimulation for status dystonicus in children with methylmalonic acidemia and GNAO1 mutation 6
Caspr1 antibodies autoimmune paranodopathy with severe tetraparesis: Potential relevance of antibody titers in monitoring treatment response 6
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study 6
Parkinsonism in neurometabolic diseases 6
Non-Motor Symptoms in Primary Familial Brain Calcification 6
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome 6
Inborn errors of coenzyme a metabolism and neurodegeneration 5
Harmful iron-calcium relationship in pantothenate kinase associated neurodegeneration 5
Antiphospholipid-Related Chorea: Two Case Reports and Role of Metabolic Imaging 5
GPi-DBS for KMT2B-Associated Dystonia: Systematic Review and Meta-Analysis 5
Long-term safety, discontinuation and mortality in an Italian cohort with advanced Parkinson’s disease on levodopa/carbidopa intestinal gel infusion 5
An adult patient with 3-methylglutaconic aciduria type 1 and movement disorders 5
Variants in ATP5F1B are associated with dominantly inherited dystonia 5
Pallidal deep brain stimulation in DYT6 dystonia: Clinical outcome and predictive factors for motor improvement 5
Effect of Intensive Rehabilitation Program in Thermal Water on a Group of People with Parkinson’s Disease: A Retrospective Longitudinal Study 5
High prolactin levels in dihydropteridine reductase deficiency: A sign of therapy failure or additional pathology? 5
Cerebellar and cortical hypometabolism in progressive stimulus-sensitive limb myoclonus in celiac disease 5
Diagnostic and therapeutic recommendations in adult dystonia: a joint document by the Italian Society of Neurology, the Italian Academy for the Study of Parkinson’s Disease and Movement Disorders, and the Italian Network on Botulinum Toxin 5
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 4
Totale 732
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Categoria #
all - tutte 3.594
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 3.594
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202030 0 0 0 0 0 0 0 8 7 7 6 2
2020/202139 4 2 9 9 1 1 1 1 2 2 3 4
2021/202215 2 3 3 0 0 0 1 0 2 1 1 2
2022/202326 3 6 4 0 2 4 0 1 5 1 0 0
2023/202453 0 1 1 0 4 5 2 5 3 0 0 32
2024/2025442 9 24 12 6 185 14 148 44 0 0 0 0
Totale 732