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Susi Scappaticci

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Carla Olivieri; Fabio Pagella; Lucia Semino; Luca Lanzarini; Cristina Valacca; Andrea Pilotto; Sabrina Corno; Susi Scappaticci; Guido Manfredi; Elisabetta Buscarini; Cesare Danesino
Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies.
A Guala; G Pastore; F Fagioli; Susi Scappaticci; C Danesino
Hemihypertrophy and myelodysplasia.
Tiziano Pramparo; Sabrina Giglio; Giuliana Gregato; Manuela De Gregori; Maria Grazia Patricelli; Roberto Ciccone; Susi Scappaticci; Gaetano Mannino; claudio lombardi; Barbara Pirola; Roberto Giorda; Mariano Rocchi; Orsetta Zuffardi
Inverted duplications: how many of them are mosaic?

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All Publications

2007: Carla Olivieri; Fabio Pagella; Lucia Semino; Luca Lanzarini; Cristina Valacca; Andrea Pilotto; Sabrina Corno; Susi Scappaticci; Guido Manfredi; Elisabetta Buscarini; Cesare Danesino
Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies.
Journal of human genetics 2007;52(10):820-9.
2004: A Guala; G Pastore; F Fagioli; Susi Scappaticci; C Danesino
Hemihypertrophy and myelodysplasia.
Pediatric blood & cancer 2004;43(6):707-8.
2004: Tiziano Pramparo; Sabrina Giglio; Giuliana Gregato; Manuela De Gregori; Maria Grazia Patricelli; Roberto Ciccone; Susi Scappaticci; Gaetano Mannino; claudio lombardi; Barbara Pirola; Roberto Giorda; Mariano Rocchi; Orsetta Zuffardi
Inverted duplications: how many of them are mosaic?
European journal of human genetics : EJHG 2004;12(9):713-7.
2004: Carla Olivieri; Cesare Danesino; Susi Scappaticci; Mauro Bozzola
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children?
Journal of endocrinological investigation 2004;27(4):308-10.
2001: Maurizio Aricò; R Haupt; V S Russotto; G Bossi; Susi Scappaticci; Cesare Danesino
Langerhans cell histiocytosis in two generations: a new family and review of the literature.
Medical and pediatric oncology 2001;36(2):314-6.
2000: Susi Scappaticci; Cesare Danesino; E Rossi; Catherine Klersy; G M Fiori; Rita Clementi; V S Russotto; G Bossi; Maurizio Aricò
Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histocytosis. AIEOP-Istiocitosi Group.
British journal of haematology 2000;111(1):258-62.
2000: Emanuela Maserati; Antonella Minelli; Carla Olivieri; L Bonvini; A Marchi; Mauro Bozzola; Cesare Danesino; Susi Scappaticci; Francesco Pasquali
Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Cancer genetics and cytogenetics 2000;121(2):167-71.
1999: Susi Scappaticci; Francesco Pasquali; E Capra; Carla Olivieri; S Tateo
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer.
Cancer genetics and cytogenetics 1999;110(2):140-2.
1998: Antonella Minelli; E Capra; C Dellavecchia; Cesare Danesino; Carla Olivieri; S Tateo; P Tenti; Susi Scappaticci
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms.
European journal of gynaecological oncology 1998;19(3):234-8.
1997: Mauro Bozzola; K Tettoni; Francesca Severi; E Capra; Cesare Danesino; Susi Scappaticci
Does growth hormone treatment increase chromosomal abnormalities?
Clinical endocrinology 1997;47(3):363-6.
1996: Oshima Junko; Chang-En Yu; C Piussan; G Klein; J Jabkowski; S Balci; T Miki; Jun Nakura; T Ogihara; J Ells; M Smith; M I Melaragno; M Fraccaro; Susi Scappaticci; J Matthews; S Ouais; A Jarzebowicz; Gerard D Schellenberg; George M Martin
Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Human molecular genetics 1996;5(12):1909-13.
1995: E Capra; Susi Scappaticci; M P Spina
Chromosomal abnormalities in tumor and lymphocyte cultures from patients with pituitary adenomas.
Cancer genetics and cytogenetics 1995;84(1):89.
1995: Susi Scappaticci; G S Fossati; L Valenti; M Scabini; S Tateo; G Nastasi; M P Spina; E Capra
A search for double minute chromosomes in cultured lymphocytes from different types of tumors.
Cancer genetics and cytogenetics 1995;82(1):50-3.
1994: Susi Scappaticci; E Capra; M Cortinovis; R Cortinovis; E Arbustini; Marta Diegoli; M Fraccaro
Cytogenetic studies in venous tissue from patients with varicose veins.
Cancer genetics and cytogenetics 1994;75(1):26-30.
1994: Andrea Casasco; Emanuela Maserati; M Giordano; Marco Casasco; M Ciuffreda; S Sander; Marco Danova; Susi Scappaticci; Alberto Calligaro; D R Springall
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp.
Archives of oral biology 1994;39(3):245-9.
1993: Maria Luisa Brandi; Günther Weber; A Svensson; Alberto Falchetti; Francesco Tonelli; Roberto Castello; L Furlani; Susi Scappaticci; M Fraccaro; C Larsson
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1).
American journal of human genetics 1993;53(6):1167-72.
1993: Paola Maraschio; A Pezzolo; M L Brandi; M Cortinovis; E Dainotti; Susi Scappaticci; M Fraccaro
Cytogenetics of multiple endocrine neoplasia syndromes. III. Analysis of an insulinoma from a subject with MEN 1 by chromosome painting.
Cancer genetics and cytogenetics 1993;70(1):68-70.
1993: E Capra; G Rindi; G Santi; M P Spina; Susi Scappaticci
Chromosome abnormalities in a case of pituitary adenoma.
Cancer genetics and cytogenetics 1993;68(2):140-2.
1992: Susi Scappaticci; M L Brandi; E Capra; M Cortinovis; Paola Maraschio; M Fraccaro
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a glucagonoma from two subjects with MEN1.
Cancer genetics and cytogenetics 1992;63(1):17-21.
1992: Susi Scappaticci; G Arrigoni; E Capra; Paola Maraschio; M Fraccaro
Cytogenetics of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia.
Cancer genetics and cytogenetics 1992;59(1):51-3.
1991: Susi Scappaticci; Paola Maraschio; N del Ciotto; G S Fossati; Aris Zonta; M Fraccaro
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1.
Cancer genetics and cytogenetics 1991;52(1):85-92.
1991: G Orecchia; Luca Perfetti; Susi Scappaticci
Porokeratosis and chromosomal abnormalities.
Dermatologica 1991;182(1):65-6.
1990: Susi Scappaticci; A Forabosco; Giovanni Borroni; G Orecchia; M Fraccaro
Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndrome.
Annales de génétique 1990;33(1):5-8.
1989: Susi Scappaticci; M Fraccaro; Decio Cerimele
Chromosome abnormalities in dyskeratosis congenita.
American journal of medical genetics 1989;34(4):609-10.
1989: Susi Scappaticci; S Lambiase; M Fraccaro; G Orecchia
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease.
Cancer genetics and cytogenetics 1989;43(2):249-50.
1989: Susi Scappaticci; S Lambiase; G Orecchia; M Fraccaro
Clonal chromosome abnormalities with preferential involvement of chromosome 3 in patients with porokeratosis of Mibelli.
Cancer genetics and cytogenetics 1989;43(1):89-94.
1989: Susi Scappaticci; M Fraccaro; G Orecchia
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma.
Cancer genetics and cytogenetics 1989;42(2):309-11.
1989: M Stefanini; Susi Scappaticci; P Lagomarsini; Giovanni Borroni; Enzo Berardesca; Fiorella Nuzzo
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defects.
Mutation research 1989;219(3):179-85.
1989: Giovanni Borroni; Gabriele Vignati; C Zaccone; Valeria Brazzelli; Susi Scappaticci; Decio Cerimele; G Rabbiosi
[Werner's syndrome and intracranial meningioma].
Giornale italiano di dermatologia e venereologia : organo ufficiale, Società italiana di dermatologia e sifilografia 1989;124(5):225-9.
1988: M Fraccaro; Susi Scappaticci; M Aricò
Shwachman syndrome and chromosome breakage.
Human genetics 1988;79(2):194.
1988: Susi Scappaticci; Decio Cerimele; M Tondi; R Vivarelli; Alberto Fois; M Fraccaro
Chromosome abnormalities in tuberous sclerosis.
Human genetics 1988;79(2):151-6.
1988: Pier Luigi Fiori; G Monaco; Susi Scappaticci; A Pugliese; N Canu; Piero Cappuccinelli
Establishment of cell cultures from hydatid cysts of Echinococcus granulosus.
International journal for parasitology 1988;18(3):297-305.
1986: Susi Scappaticci; Decio Cerimele; Francesca Cottoni; F Pasquali; M Fraccaro
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma.
Human genetics 1986;72(4):311-7.
1985: M Fraccaro; Susi Scappaticci; Decio Cerimele
A population and cytogenetic study of the Werner syndrome in Sardinia.
Advances in experimental medicine and biology 1985;190():547-52.
1984: Decio Cerimele; Licinio Contu; Susi Scappaticci; Francesca Cottoni
Kaposi's sarcoma in Sardinia: an epidemiologic and genetic investigation.
Annals of the New York Academy of Sciences 1984;437():216-27.
1983: Decio Cerimele; Susi Scappaticci; E Cattaneo; Francesca Cottoni
Failure to demonstrate early and late antigens of cytomegalovirus in tissue cultures from Kaposi's sarcoma patients.
Archives of dermatological research 1983;275(3):197-8.
1982: Decio Cerimele; Francesca Cottoni; Susi Scappaticci; G Rabbiosi; Giovanni Borroni; E Sanna; G Zei; M Fraccaro
High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency.
Human genetics 1982;62(1):25-30.
1982: Susi Scappaticci; Decio Cerimele; M Fraccaro
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome.
Human genetics 1982;62(1):16-24.
1982: S Subino; P L Fiori; G Lubinu; Susi Scappaticci; Decio Cerimele
Immunofluorescence of the tubulin system in human skin fibroblasts in Werner's syndrome, Kaposi sarcoma, and psoriasis.
Archives of dermatological research 1982;272(1-2):143-5.