SAPUPPO, ANNAMARIA
 Distribuzione geografica
Continente #
NA - Nord America 233
EU - Europa 192
AS - Asia 99
AF - Africa 44
SA - Sud America 21
Totale 589
Nazione #
US - Stati Uniti d'America 230
IT - Italia 127
SG - Singapore 70
CI - Costa d'Avorio 35
IE - Irlanda 21
BR - Brasile 19
CN - Cina 15
DE - Germania 9
IN - India 8
RU - Federazione Russa 7
SN - Senegal 7
FI - Finlandia 6
NL - Olanda 6
FR - Francia 4
CH - Svizzera 3
IQ - Iraq 3
SE - Svezia 3
CA - Canada 2
NG - Nigeria 2
SI - Slovenia 2
UA - Ucraina 2
CL - Cile 1
EC - Ecuador 1
GB - Regno Unito 1
GE - Georgia 1
JP - Giappone 1
KZ - Kazakistan 1
MX - Messico 1
NO - Norvegia 1
Totale 589
Città #
Santa Clara 69
Singapore 40
Abidjan 35
Chandler 31
Chicago 28
Catania 23
Dublin 21
Ashburn 16
Civitanova Marche 13
Boardman 12
Dakar 7
Andover 6
Bremen 6
Cambridge 6
Kochi 6
Lawrence 6
Bologna 5
Hefei 5
Milan 5
Des Moines 4
Lappeenranta 4
Rome 4
Brescia 3
Jacksonville 3
Lago 3
Torino 3
Turin 3
Abuja 2
Amsterdam 2
Boston 2
Helsinki 2
Ljubljana 2
Mosul 2
Munich 2
Palermo 2
Parma 2
Porza 2
Saint Petersburg 2
Salerno 2
Scordia 2
Trecastagni 2
Troina 2
Altamira 1
Anápolis 1
Baghdad 1
Belpasso 1
Betim 1
Bismarque 1
Cachoeira do Sul 1
Caçapava 1
Cerro Azul 1
Civitavecchia 1
Colima 1
Comercinho 1
Itaguaí 1
Limeira 1
Los Angeles 1
Maceió 1
Mainz 1
Mascali 1
Monteiro 1
Montreal 1
Moscow 1
New Delhi 1
New York 1
Norwalk 1
Piedimonte Etneo 1
Pontecagnano 1
Pozzo Di Gotto 1
Pune 1
Reggio Emilia 1
Rondonópolis 1
San Francisco 1
San Mateo 1
Sant'Agata di Militello 1
Santiago 1
Semey 1
Serafina Corrêa 1
Siena 1
Stockholm 1
Sumaré 1
São Gonçalo 1
Tbilisi 1
Teixeira de Freitas 1
Tokyo 1
Toronto 1
Vitória da Conquista 1
Wilmington 1
Xambioá 1
Totale 444
Nome #
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 109
GRIN2A and GRIN2B and Their Related Phenotypes 83
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype 66
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 58
Deciphering the invdupdel(8p) genotype–phenotype correlation: Our opinion 58
PRRT2 Related Epilepsies: A Gene Review 50
PANS/PANDAS: Clinical Experience in IVIG Treatment and State of the Art in Rehabilitation Approaches 44
Higher frequency of TMEM199-CDG in the southern mediterranean area is associated with c.92G>C (p.Arg31Pro) mutation 41
Obesity as a Confounding Factor in the Diagnosis of Wilson’s Disease: Case Report of Two Siblings with the Same Genotype but Different Clinical Courses 31
Positive Impact of Home ERT for Mucopolysaccharidoses and Pompe Disease: The Lesson Learnt from the COVID-19 Pandemic 29
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 27
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 17
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 4
Totale 617
Categoria #
all - tutte 2.911
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 2.911


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206 0 0 0 0 0 0 0 0 0 0 0 6
2020/202133 3 2 3 6 6 0 2 1 0 3 6 1
2021/202273 1 7 12 1 8 4 22 1 4 3 0 10
2022/2023103 8 9 2 13 7 14 0 17 21 0 8 4
2023/202498 3 15 3 2 6 35 0 8 0 3 12 11
2024/2025302 8 41 14 30 51 34 9 14 48 25 28 0
Totale 617