MENCARELLI, Amedea
 Distribuzione geografica
Continente #
NA - Nord America 582
EU - Europa 344
AS - Asia 266
OC - Oceania 1
SA - Sud America 1
Totale 1.194
Nazione #
US - Stati Uniti d'America 577
IE - Irlanda 107
SG - Singapore 89
VN - Vietnam 74
UA - Ucraina 65
HK - Hong Kong 48
IT - Italia 39
CN - Cina 36
SE - Svezia 27
DE - Germania 26
FI - Finlandia 26
GB - Regno Unito 12
RU - Federazione Russa 12
BE - Belgio 11
KR - Corea 10
CH - Svizzera 5
RO - Romania 3
TR - Turchia 3
CA - Canada 2
CZ - Repubblica Ceca 2
FR - Francia 2
GR - Grecia 2
LB - Libano 2
MX - Messico 2
AD - Andorra 1
AE - Emirati Arabi Uniti 1
AT - Austria 1
AU - Australia 1
EC - Ecuador 1
IM - Isola di Man 1
JM - Giamaica 1
JP - Giappone 1
LK - Sri Lanka 1
NL - Olanda 1
PL - Polonia 1
UZ - Uzbekistan 1
Totale 1.194
Città #
Chandler 129
Dublin 107
Singapore 76
Dong Ket 74
Ann Arbor 52
San Mateo 50
Hong Kong 48
Boardman 33
Jacksonville 32
Santa Clara 28
Medford 23
Princeton 23
Wilmington 21
Altamura 17
Beijing 17
Lawrence 17
Des Moines 15
Andover 12
Brussels 11
Helsinki 11
Seoul 10
Munich 6
Ashburn 5
Falls Church 5
Los Angeles 5
Redwood City 5
Woodbridge 5
New York 4
Perugia 4
Saint Petersburg 4
Izmir 3
San Diego 3
Brno 2
Lausanne 2
Mountain View 2
Norwalk 2
Shijiazhuang 2
Andorra la Vella 1
Beauharnois 1
Benevento 1
Cattolica 1
Colombo 1
Dallas 1
Den Haag 1
Douglas 1
Dubai 1
Frankfurt am Main 1
Grefrath 1
Guayaquil 1
Hwang Chow 1
Landshut 1
Lappeenranta 1
Milan 1
Nuremberg 1
Ottawa 1
Redmond 1
Rovato 1
San Paolo di Civitate 1
Shanghai 1
Stockholm 1
Sydney 1
Terni 1
Tokyo 1
Totale 891
Nome #
Effect of the acute promyelocytic leukemia PML/RAR alpha protein on differentiation and survival of myeloid precursors. 96
Anti-HIV Protease Inhibitors Interact With NSAIDs and Exacerbate Small Intestine Enteropathy Induced by NSAIDs 90
Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. 72
Cooperation between RING+B1-B2 and coiled-coil domains of PML is necesary for its effects on cell growth 70
The acute promyelocytic leukaemia specific PML/RARa fusion protein inhibits differentiation and promotes survival of myeloid precursor cells. 70
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism 68
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 58
Pathogenetic Relevance Of The Acute Promyelocytic Leukemia-Specific PML/RARa Fusion Protein 56
Efficient infection and selection of hematopoietic progenitors by a novel GFP based retroviral vector 54
Natural killer cell-mediated lysis of autologous cells modified by gene therapy 54
A Clinical and Molecular Survey of 62 Cystic Fibrosis Patients from Umbria (Central Italy) Disclosing a High Frequency (2.4%) of the 2184insA Allele: Implications for Screening 53
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 49
Lethal and non-lethal GLIS1 related malformation syndromes 47
Report of a novel SHOX missense variant in a boy with short stature and his mother with Leri-Weill dyschondrosteosis 46
Molecular Genetics Of The T(15;17) Of Acute Promyelocytic Leukemia 44
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. 41
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 41
Identification of a dna methylation episignature in the 22q11.2 deletion syndrome 39
Bile-acid-activated receptors: targeting TGR5 and farnesoid-X-receptor in lipid and glucose disorders. 37
A patient with novel MBOAT7 variant: The cerebellar atrophy is progressive and displays a peculiar neurometabolic profile 36
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene 35
A rare case of brachyolmia with amelogenesis imperfecta caused by a new pathogenic splicing variant in ltbp3 31
The acute promyelocytic leukemia PML/RARa protein affects differentiation and survival of myeloid precursor cells 29
NFIA haploinsufficiency: case series and literature review 14
A New De Novo Missense Variant of the TET3 Gene in a Patient with Epilepsy and Macrocephaly 9
Totale 1.239
Categoria #
all - tutte 5.965
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 5.965


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202053 0 0 0 0 0 0 13 1 12 19 3 5
2020/2021208 6 12 2 12 48 12 12 0 10 8 10 76
2021/2022182 4 36 10 10 9 2 5 50 4 5 21 26
2022/2023374 26 69 10 30 30 52 0 10 131 0 15 1
2023/2024165 12 20 11 2 0 4 49 0 4 5 25 33
2024/2025162 13 28 23 26 38 34 0 0 0 0 0 0
Totale 1.239