IRIS
SCAPPATICCI, MARIA ASSUNTA
 Distribuzione geografica
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Continente #
NA - Nord America 1.259
EU - Europa 1.027
AS - Asia 699
OC - Oceania 7
AF - Africa 4
SA - Sud America 2
Totale 2.998
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Nazione #
US - Stati Uniti d'America 1.250
CN - Cina 646
IE - Irlanda 297
UA - Ucraina 217
FI - Finlandia 128
DE - Germania 112
SE - Svezia 79
GB - Regno Unito 70
IT - Italia 59
FR - Francia 36
SG - Singapore 30
JP - Giappone 17
BE - Belgio 13
CA - Canada 8
NL - Olanda 5
AU - Australia 4
MU - Mauritius 4
RU - Federazione Russa 4
NZ - Nuova Zelanda 3
GR - Grecia 2
IN - India 2
IR - Iran 2
AR - Argentina 1
BG - Bulgaria 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
ID - Indonesia 1
LT - Lituania 1
LV - Lettonia 1
PE - Perù 1
RO - Romania 1
SA - Arabia Saudita 1
Totale 2.998
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Città #
Dublin 297
Chandler 270
Jacksonville 261
Nanjing 187
Boardman 85
Beijing 74
Nanchang 72
Ashburn 66
Shenyang 62
Ann Arbor 56
Princeton 52
Lawrence 51
Changsha 50
Medford 50
Hebei 49
New York 41
Jiaxing 37
Wilmington 35
Tianjin 31
Shanghai 30
Milan 28
Helsinki 26
Hangzhou 23
Woodbridge 23
Tokyo 17
Singapore 15
Verona 15
Brussels 13
Los Angeles 11
Norwalk 11
Auburn Hills 6
Houston 6
Toronto 6
Seattle 5
Chicago 4
Des Moines 4
Auckland 3
Borås 3
Jinan 3
Melbourne 3
Washington 3
Augusta 2
Fuzhou 2
Nantong 2
Ningbo 2
Taizhou 2
Amsterdam 1
Anchorage 1
Berlin 1
Brackley 1
Buffalo 1
Casier 1
Changchun 1
Codigoro 1
Fairfield 1
Frankfurt am Main 1
Gosport 1
Grenaa 1
Grimsby 1
Guangzhou 1
Gunzenhausen 1
Kunming 1
Lanzhou 1
Leawood 1
Lissone 1
Milazzo 1
Monmouth Junction 1
Moquegua 1
Newark 1
Novokuznetsk 1
Orange 1
Ottawa 1
Pavia 1
Pune 1
Redmond 1
Riyadh 1
Sacramento 1
San Mateo 1
Sarnia 1
Sofia 1
Surabaya 1
Sydney 1
Timisoara 1
Vilnius 1
Zhengzhou 1
Totale 2.133
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Nome #
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease 102
Chromosomal breaks in lymphocytes from respiratory syncytial virus-infected infants. 95
Chromosome abnormalities in a case of pituitary adenoma. 90
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma. 81
Citochimica, autoradiografia e ultrastruttura di cellule della granulosa ovarica umana "in vitro". 78
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children? 76
Isochromosome (7) (q10) in Schwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders. 75
Contributi morfologici alla conoscenza delle mucopolisaccaridosi. 74
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis. 71
Chromosome abnormalities in Dyskeratosis congenita. 70
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langherans cell histiocytosis 69
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms 68
Cytogenetic studies in venous tissues from patients with vericose venis. 66
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders 66
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. 65
A family with Autosomal Dominant leukodystrophy linked to 5q23.2-q23.3. 65
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. 64
Lipoid proteinosis: lipid inclusions in fibroblasts. 64
Chromosome abnormalities in Tuberous Sclerosis. 63
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli. 63
Due anomalie "non-random" nelle leucemie mieloidi acute: t(8:21), t(15;17). 63
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histocytosis. AIEOP-Istiocitosi Group. 60
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease. 60
Erratum: Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster. (vol 17, pg 213, 2007) 59
Hemihypertrophy and myelodysplasia. 58
Non fluorescent Y chromosome in a 45,X/46,XY mosaic. 58
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities. 57
Langerhans cell histiocytosis in two generations: a new family and review of the literature.REVIEW 56
Premature centromere disjunction and other chromosome anomalies in Tuberous Sclerosis. 56
A search for double minute chromosomes in cultured lymphocytes from different types of tumors. 56
Focal dermal hypoplasia: report of a family with 7 affected women in 3 generations. 56
XO and male phenotype 54
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp. 52
Failure to demonstrate early and late antigens of cytomegalovirus in tissue from Kaposi's sarcoma patients. 52
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defect. 50
Shwachman syndrome and chromosome breakage. Letter to the Editor. 50
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosomes 18p11.1-21.1 markers. 49
Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41). 49
homozygosity mapping of the Werner syndrome locus (WRN). 47
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langherans cell histiocytosis. 46
Clonal structural chromosomal rearrangements in primary fibroblastic cultures and in lymphocytes of patients with Werner's syndroe. 46
Risultati di uno studio sull'oocita umano coltivato "in vitro". 45
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125). 45
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile. 44
Epidemiology and clinical aspects of Werner'ssyndrome in North Sardinia: description of a cluster. 42
Identification of a structurally abnormal Y chromosome. 42
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1. 42
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere. 41
Cytogenetic of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia. 41
Langerhans cell histiocytosis in two generations: a new family and review of the lietrature. 40
Endocrine function and diagnostic problems inn a prepubertal case of 48,XXYY. 31
Totale 3.012
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Categoria #
all - tutte 10.368
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 10.368
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020265 0 0 0 41 2 43 14 43 0 68 54 0
2020/2021382 47 37 10 42 1 52 3 56 10 56 57 11
2021/2022236 7 3 4 3 4 9 3 16 15 3 40 129
2022/2023802 94 66 7 44 99 79 0 50 343 2 13 5
2023/2024273 28 42 6 17 27 82 5 27 2 8 9 20
2024/202594 8 59 20 7 0 0 0 0 0 0 0 0
Totale 3.012