IRIS
SCAPPATICCI, MARIA ASSUNTA
 Distribuzione geografica
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Continente #
NA - Nord America 1.200
EU - Europa 1.024
AS - Asia 640
OC - Oceania 5
AF - Africa 4
SA - Sud America 2
Totale 2.875
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Nazione #
US - Stati Uniti d'America 1.191
CN - Cina 633
IE - Irlanda 297
UA - Ucraina 217
FI - Finlandia 128
DE - Germania 112
SE - Svezia 79
GB - Regno Unito 70
IT - Italia 57
FR - Francia 36
BE - Belgio 12
CA - Canada 8
NL - Olanda 5
MU - Mauritius 4
RU - Federazione Russa 4
NZ - Nuova Zelanda 3
AU - Australia 2
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
JP - Giappone 1
LT - Lituania 1
LV - Lettonia 1
PE - Perù 1
RO - Romania 1
SA - Arabia Saudita 1
Totale 2.875
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Città #
Dublin 297
Chandler 270
Jacksonville 261
Nanjing 187
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
Boardman 34
Tianjin 31
Milan 28
Helsinki 26
Hangzhou 23
Woodbridge 23
Shanghai 22
Verona 15
Brussels 12
Los Angeles 11
Norwalk 11
Auburn Hills 6
Houston 6
Toronto 6
Seattle 5
Des Moines 4
Auckland 3
Borås 3
Jinan 3
Washington 3
Augusta 2
Fuzhou 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
Melbourne 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
Tokyo 1
Vilnius 1
Zhengzhou 1
Totale 2.034
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Nome #
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease 100
Chromosomal breaks in lymphocytes from respiratory syncytial virus-infected infants. 92
Chromosome abnormalities in a case of pituitary adenoma. 86
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma. 79
Isochromosome (7) (q10) in Schwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders. 74
Citochimica, autoradiografia e ultrastruttura di cellule della granulosa ovarica umana "in vitro". 74
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children? 73
Contributi morfologici alla conoscenza delle mucopolisaccaridosi. 72
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langherans cell histiocytosis 68
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms 66
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis. 66
Chromosome abnormalities in Dyskeratosis congenita. 66
Cytogenetic studies in venous tissues from patients with vericose venis. 64
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. 63
A family with Autosomal Dominant leukodystrophy linked to 5q23.2-q23.3. 63
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders 63
Due anomalie "non-random" nelle leucemie mieloidi acute: t(8:21), t(15;17). 62
Chromosome abnormalities in Tuberous Sclerosis. 61
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. 59
Lipoid proteinosis: lipid inclusions in fibroblasts. 59
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli. 59
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histocytosis. AIEOP-Istiocitosi Group. 57
Erratum: Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster. (vol 17, pg 213, 2007) 57
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease. 57
Hemihypertrophy and myelodysplasia. 56
Non fluorescent Y chromosome in a 45,X/46,XY mosaic. 56
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities. 55
Langerhans cell histiocytosis in two generations: a new family and review of the literature.REVIEW 54
Premature centromere disjunction and other chromosome anomalies in Tuberous Sclerosis. 54
A search for double minute chromosomes in cultured lymphocytes from different types of tumors. 53
Focal dermal hypoplasia: report of a family with 7 affected women in 3 generations. 52
XO and male phenotype 52
Failure to demonstrate early and late antigens of cytomegalovirus in tissue from Kaposi's sarcoma patients. 51
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp. 50
Shwachman syndrome and chromosome breakage. Letter to the Editor. 48
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defect. 47
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. 46
Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41). 46
homozygosity mapping of the Werner syndrome locus (WRN). 45
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langherans cell histiocytosis. 45
Risultati di uno studio sull'oocita umano coltivato "in vitro". 44
Clonal structural chromosomal rearrangements in primary fibroblastic cultures and in lymphocytes of patients with Werner's syndroe. 44
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125). 43
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile. 42
Epidemiology and clinical aspects of Werner'ssyndrome in North Sardinia: description of a cluster. 41
Identification of a structurally abnormal Y chromosome. 40
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere. 40
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1. 39
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. 38
Langerhans cell histiocytosis in two generations: a new family and review of the lietrature. 38
Endocrine function and diagnostic problems inn a prepubertal case of 48,XXYY. 30
Totale 2.889
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Categoria #
all - tutte 8.529
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 8.529
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20193 0 0 0 0 0 0 0 0 0 0 1 2
2019/2020778 211 302 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
2023/2024244 28 42 6 17 27 82 5 27 2 8 0 0
Totale 2.889