MONTALBANO, GIUSEPPE
 Distribuzione geografica
Continente #
NA - Nord America 1068
EU - Europa 423
AS - Asia 208
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 1702
Nazione #
US - Stati Uniti d'America 1067
UA - Ucraina 189
TR - Turchia 78
VN - Vietnam 65
CN - Cina 60
IT - Italia 60
FI - Finlandia 42
SE - Svezia 42
FR - Francia 36
DE - Germania 29
GB - Regno Unito 17
BE - Belgio 3
BG - Bulgaria 2
MY - Malesia 2
AM - Armenia 1
AR - Argentina 1
AU - Australia 1
BD - Bangladesh 1
CA - Canada 1
EU - Europa 1
HU - Ungheria 1
IN - India 1
NL - Olanda 1
RU - Federazione Russa 1
Totale 1702
Città #
Fairfield 163
Jacksonville 144
Ann Arbor 121
Woodbridge 83
Houston 81
Chandler 76
Ashburn 57
Wilmington 57
Dearborn 55
Princeton 54
Cambridge 48
Seattle 44
Izmir 41
Dong Ket 34
Como 27
Nyköping 21
San Diego 14
Beijing 13
San Mateo 11
Kunming 9
Milan 8
Guangzhou 7
Kocaeli 7
Nanjing 7
Hefei 6
Phoenix 5
Redmond 5
Redwood City 5
Jinan 4
Norwalk 4
Brussels 3
Saint Paul 3
Düsseldorf 2
Helsinki 2
Kuala Lumpur 2
Maccagno 2
Sofia 2
Verona 2
Athens 1
Auburn Hills 1
Bangalore 1
Birmingham 1
Budapest 1
Catania 1
Changsha 1
Falls Church 1
Fuzhou 1
Hangzhou 1
Hebei 1
Indiana 1
Lunamatrona 1
Mcallen 1
Nanchang 1
New Orleans 1
New York 1
Ningbo 1
Pavia 1
Pisa 1
Pomezia 1
Quzhou 1
Rotterdam 1
Saint Petersburg 1
San Francisco 1
Shaoxing 1
Shelburne 1
Sydney 1
Yerevan 1
Totale 1258
Nome #
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability 126
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION 122
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms 109
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis 100
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome 98
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes 92
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells 90
null 74
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME 73
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498) 63
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES 61
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH 60
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype 58
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment? 56
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients 54
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients 53
Chromosome anomalies as cause of congenital bone marrow failure syndromes 53
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento dei geni FLI1 e MPL 45
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family 45
L’utilizzo della comparative genomic hybridization su microarray (a-CGH) per rilevare e definire sbilanci cromosomici nel midollo osseo di pazienti affetti dalla sindrome di Shwachman-Diamond 41
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND 40
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1 39
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms 38
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME 38
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND 37
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis 34
Novel evidence of karyotype instability in Shwachman Diamond Syndrome 32
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene 8
Totale 1739
Categoria #
all - tutte 2696
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 2696


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201853 0000 040 102 0001
2018/2019217 39441 44 224 2153970
2019/2020458 18161075 2158 8166 23401832
2020/2021406 746749 2148 932 56293369
2021/2022274 22441111 1338 1216 18282635
2022/2023141 37562721 00 00 0000
Totale 1739