SANTORELLI, Filippo Maria
 Distribuzione geografica
Continente #
NA - Nord America 165
EU - Europa 93
AS - Asia 9
AF - Africa 4
OC - Oceania 3
SA - Sud America 2
Totale 276
Nazione #
US - Stati Uniti d'America 164
IT - Italia 48
FR - Francia 28
GB - Regno Unito 5
DE - Germania 4
IN - India 4
ZA - Sudafrica 4
CN - Cina 3
AU - Australia 2
CZ - Repubblica Ceca 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
BO - Bolivia 1
CA - Canada 1
CL - Cile 1
ES - Italia 1
FI - Finlandia 1
NL - Olanda 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
TW - Taiwan 1
UA - Ucraina 1
Totale 276
Città #
Rome 31
Santa Cruz 26
Ashburn 14
Woodbridge 14
Buffalo 12
Fairfield 12
Houston 6
Seattle 6
Kolkata 4
Cambridge 3
Chicago 3
Des Moines 3
Riva 3
Wilmington 3
Council Bluffs 2
Las Vegas 2
London 2
Manchester 2
Milan 2
Muizenberg 2
Paris 2
Sydney 2
Ancona 1
Andover 1
Ann Arbor 1
Atlanta 1
Auckland 1
Boardman 1
Brandico 1
Busto Arsizio 1
Cape Town 1
Clearwater 1
Columbus 1
Dallas 1
Dordrecht 1
Falkirk 1
Hangzhou 1
La Paz 1
Legnano 1
Lille 1
Lincoln 1
Lisbon 1
Los Angeles 1
Milwaukee 1
Modena 1
New York 1
Oak Lawn 1
Ottawa 1
Phoenix 1
Portland 1
Providence 1
San Diego 1
San Francisco 1
San Giuliano Milanese 1
San Jose 1
Silverton 1
Sofia 1
Strasbourg 1
Taipei 1
Vedra 1
Totale 194
Nome #
Brain imaging in Kufs disease type B. case reports, file e3835313-1cd7-15e8-e053-a505fe0a3de9 88
Maternally inherited cardiomyopathy: clinical and molecula characterization of a large kindred harboring the A4300G point mutation in mtDNA, file e3835328-5bb0-15e8-e053-a505fe0a3de9 58
Genetics influences drug consumption in medication overuse headache, not in migraine. Evidence from Wolframin His611Arg polymorphism analysis, file e383532a-6cf7-15e8-e053-a505fe0a3de9 47
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations, file e383532d-f3cd-15e8-e053-a505fe0a3de9 27
New cellular imaging-based method to distinguish the SPG4 subtype of hereditary spastic paraplegia, file b04948eb-6237-4931-877c-a85f917a8938 21
Next generation molecular diagnosis of hereditary spastic paraplegias: an italian cross-sectional study, file 14b6d477-2cdc-4a79-83a2-36fcbf9f17c1 14
A next generation sequencing-based analysis of a large cohort of ataxic patients refines the clinical spectrum associated with spinocerebellar ataxia 21, file 81c26002-26c2-43f6-b419-18c8713cec57 9
Spinocerebellar ataxia type 3 in Italy. time to change mind, file e3835315-9c4a-15e8-e053-a505fe0a3de9 4
Progressive myoclonus epilepsy and ceroidolipofuscinosis 14. The multifaceted phenotypic spectrum of KCTD7-related disorders, file e383531e-1773-15e8-e053-a505fe0a3de9 2
Genetic basis of the neurophysiological findings, file e383532a-5176-15e8-e053-a505fe0a3de9 2
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias, file 65a00b51-179c-436c-b38f-3331be2b3384 1
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family, file e3835316-1e8b-15e8-e053-a505fe0a3de9 1
Possible Involvement of the CACNA1E gene in migraine. A Search for single nucleotide polymorphism in different clinical phenotypes, file e3835318-b128-15e8-e053-a505fe0a3de9 1
Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review, file e383532a-b3e5-15e8-e053-a505fe0a3de9 1
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ10 deficiency in muscle or skin fibroblasts, file e383532b-dddd-15e8-e053-a505fe0a3de9 1
Monoallelic KIF1A‑related disorders: a multicenter cross sectional study and systematic literature review, file e383532e-b8a9-15e8-e053-a505fe0a3de9 1
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness, file e383532e-c65b-15e8-e053-a505fe0a3de9 1
Totale 279
Categoria #
all - tutte 1.083
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 1.083


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20197 0 0 0 0 0 0 0 0 0 0 5 2
2019/202024 2 2 1 1 2 3 2 3 3 2 2 1
2020/202120 2 0 2 0 0 2 0 1 9 1 1 2
2021/202271 2 2 1 1 2 2 5 9 7 4 24 12
2022/202365 4 1 24 14 1 6 3 1 3 4 4 0
2023/202472 2 2 6 3 9 11 15 8 3 11 2 0
Totale 279