MENCARELLI, ANNALISA
 Distribuzione geografica
Continente #
NA - Nord America 150
AS - Asia 114
EU - Europa 97
SA - Sud America 15
AF - Africa 1
Totale 377
Nazione #
US - Stati Uniti d'America 147
SG - Singapore 64
IE - Irlanda 29
DE - Germania 20
CN - Cina 19
HK - Hong Kong 17
BR - Brasile 13
RU - Federazione Russa 11
IT - Italia 8
GB - Regno Unito 7
FI - Finlandia 6
VN - Vietnam 5
CA - Canada 3
FR - Francia 3
PL - Polonia 3
SE - Svezia 3
UA - Ucraina 3
BD - Bangladesh 2
TR - Turchia 2
AT - Austria 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
ES - Italia 1
IQ - Iraq 1
JP - Giappone 1
KG - Kirghizistan 1
KR - Corea 1
MA - Marocco 1
NL - Olanda 1
PY - Paraguay 1
UZ - Uzbekistan 1
Totale 377
Città #
Singapore 46
Dublin 29
Chandler 28
Hong Kong 17
Munich 13
San Mateo 13
Altamura 6
Andover 6
Wilmington 6
Beijing 5
Boardman 5
Brooklyn 5
Falls Church 5
Lawrence 5
Los Angeles 5
Medford 5
Princeton 5
Santa Clara 5
Ashburn 4
Ann Arbor 3
Frankfurt am Main 3
Hanoi 3
Helsinki 3
Turku 3
Columbus 2
New York 2
Nuremberg 2
Orem 2
San Paolo di Civitate 2
Agadir 1
Amsterdam 1
Ankara 1
Annapolis 1
Asunción 1
Baghdad 1
Bexley 1
Bishkek 1
Campinas 1
Cosmópolis 1
Da Nang 1
Falkenstein 1
Foz do Iguaçu 1
Guayaquil 1
Houston 1
Hwang Chow 1
Igarassu 1
Indaiatuba 1
Izmir 1
Jiaozuo 1
Jundiaí 1
London 1
Manchester 1
Maracás 1
Montreal 1
Mossoró 1
Norwalk 1
Olomouc 1
Perth Amboy 1
Redwood City 1
Rio de Janeiro 1
Saint Petersburg 1
Salvador 1
San Francisco 1
Santo Antônio do Sudoeste 1
Seattle 1
Secaucus 1
Senhora dos Remédios 1
Seoul 1
Stockholm 1
São Paulo 1
Tashkent 1
Tokyo 1
Toronto 1
Warsaw 1
Zhengzhou 1
Totale 284
Nome #
Imerslund-Gräsbeck syndrome in an infant with a novel intronic variant in the AMN gene: A case report 85
Pediatric sleep disturbances and treatment with melatonin 83
Report of a novel SHOX missense variant in a boy with short stature and his mother with Leri-Weill dyschondrosteosis 83
Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T > A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma 71
Epileptogenic brain malformations and mutations in tubulin genes: A case report and review of the literature 66
Totale 388
Categoria #
all - tutte 2.040
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 2.040


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202247 0 10 0 1 4 1 1 15 4 1 5 5
2022/202387 5 19 3 1 9 7 0 5 35 0 2 1
2023/202425 3 2 1 0 0 0 6 0 0 1 5 7
2024/202599 2 5 3 7 7 6 9 6 17 7 20 10
2025/2026101 13 12 9 20 31 16 0 0 0 0 0 0
Totale 388