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Items: 1 to 50 of 61

1.

Value of cytogenetic abnormalities in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a study of the MYSEC project.

Mora B, Giorgino T, Guglielmelli P, Rumi E, Maffioli M, Rambaldi A, Caramella M, Komrokji R, Gotlib J, Kiladjian JJ, Cervantes F, Devos T, Palandri F, De Stefano V, Ruggeri M, Silver RT, Benevolo G, Albano F, Cavalloni C, Barraco D, Merli M, Pietra D, Casalone R, Barbui T, Rotunno G, Cazzola M, Vannucchi AM, Passamonti F.

Haematologica. 2018 Apr 5. pii: haematol.2017.185751. doi: 10.3324/haematol.2017.185751. [Epub ahead of print] No abstract available.

2.

gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML.

Rainero A, Angaroni F, D'Avila F, Conti A, Pirrone C, Micheloni G, Tararà L, Millefanti G, Maserati E, Valli R, Spinelli O, Buklijas K, Michelato A, Casalone R, Barlassina C, Barcella M, Sirchia S, Piscitelli E, Caccia M, Porta G.

Cell Death Dis. 2018 Mar 2;9(3):349. doi: 10.1038/s41419-018-0387-2.

3.

A clinical-molecular prognostic model to predict survival in patients with post polycythemia vera and post essential thrombocythemia myelofibrosis.

Passamonti F, Giorgino T, Mora B, Guglielmelli P, Rumi E, Maffioli M, Rambaldi A, Caramella M, Komrokji R, Gotlib J, Kiladjian JJ, Cervantes F, Devos T, Palandri F, De Stefano V, Ruggeri M, Silver RT, Benevolo G, Albano F, Caramazza D, Merli M, Pietra D, Casalone R, Rotunno G, Barbui T, Cazzola M, Vannucchi AM.

Leukemia. 2017 Dec;31(12):2726-2731. doi: 10.1038/leu.2017.169. Epub 2017 May 31.

PMID:
28561069
4.

A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion.

Pessina C, Basilico C, Genoni A, Meroni E, Elli L, Granata P, Righi R, Pallotti F, Mora B, Ferrario A, Passamonti F, Casalone R.

Leuk Lymphoma. 2017 Aug;58(8):1977-1980. doi: 10.1080/10428194.2016.1262952. Epub 2016 Dec 2. No abstract available.

PMID:
27911132
5.

Driver mutations' effect in secondary myelofibrosis: an international multicenter study based on 781 patients.

Passamonti F, Mora B, Giorgino T, Guglielmelli P, Cazzola M, Maffioli M, Rambaldi A, Caramella M, Komrokji R, Gotlib J, Kiladjian JJ, Cervantes F, Devos T, Palandri F, De Stefano V, Ruggeri M, Silver R, Benevolo G, Albano F, Caramazza D, Rumi E, Merli M, Pietra D, Casalone R, Barbui T, Pieri L, Vannucchi AM.

Leukemia. 2017 Apr;31(4):970-973. doi: 10.1038/leu.2016.351. Epub 2016 Nov 25. No abstract available.

PMID:
27885272
6.

Authors' Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia.

Mattarucchi E, Pallotti F, Casalone R.

Mol Diagn Ther. 2015 Aug;19(4):253-4. doi: 10.1007/s40291-015-0152-5. No abstract available.

PMID:
26224626
7.

Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia.

Mattarucchi E, Pallotti F, Casalone R.

Mol Diagn Ther. 2015 Jun;19(3):139-40. doi: 10.1007/s40291-015-0139-2. No abstract available.

PMID:
25855586
8.

FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy.

Pallotti F, Elli L, Maroni P, Chelazzi P, Agosti M, Casalone R.

Clin Chem Lab Med. 2015 Sep 1;53(10):e275-7. doi: 10.1515/cclm-2014-1045. No abstract available.

PMID:
25720123
9.

Optimizing the molecular diagnosis of GALNS: novel methods to define and characterize Morquio-A syndrome-associated mutations.

Caciotti A, Tonin R, Rigoldi M, Ferri L, Catarzi S, Cavicchi C, Procopio E, Donati MA, Ficcadenti A, Fiumara A, Barone R, Garavelli L, Rocco MD, Filocamo M, Antuzzi D, Scarpa M, Mooney SD, Li B, Skouma A, Bianca S, Concolino D, Casalone R, Monti E, Pantaleo M, Giglio S, Guerrini R, Parini R, Morrone A.

Hum Mutat. 2015 Mar;36(3):357-68. doi: 10.1002/humu.22751.

PMID:
25545067
10.

It is time to change thrombosis risk assessment for PV and ET?

Passamonti F, Caramazza D, Mora B, Casalone R, Maffioli M.

Best Pract Res Clin Haematol. 2014 Jun;27(2):121-7. doi: 10.1016/j.beha.2014.07.005. Epub 2014 Jul 18. Review.

PMID:
25189723
11.

Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history.

Gangat N, Wassie EA, Lasho TL, Finke C, Ketterling RP, Hanson CA, Pardanani A, Wolanskyj AP, Maffioli M, Casalone R, Passamonti F, Tefferi A.

Eur J Haematol. 2015 Jan;94(1):31-6. doi: 10.1111/ejh.12389. Epub 2014 Dec 4.

PMID:
24889737
12.

Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: a collaborative study of 1027 patients.

Tefferi A, Wassie EA, Guglielmelli P, Gangat N, Belachew AA, Lasho TL, Finke C, Ketterling RP, Hanson CA, Pardanani A, Wolanskyj AP, Maffioli M, Casalone R, Pacilli A, Vannucchi AM, Passamonti F.

Am J Hematol. 2014 Aug;89(8):E121-4. doi: 10.1002/ajh.23743. Epub 2014 May 16.

13.

Extraordinary response to omalizumab in a child with severe chronic urticaria.

Asero R, Casalone R, Iemoli E.

Eur Ann Allergy Clin Immunol. 2014 Jan;46(1):41-2.

PMID:
24702874
14.

Looking for CALR mutations in familial myeloproliferative neoplasms.

Maffioli M, Genoni A, Caramazza D, Mora B, Bussini A, Merli M, Giorgino T, Casalone R, Passamonti F.

Leukemia. 2014 Jun;28(6):1357-60. doi: 10.1038/leu.2014.33. Epub 2014 Jan 20. No abstract available.

PMID:
24441291
15.

Isolation and characterization of multipotent cells from human fetal dermis.

Chinnici CM, Amico G, Monti M, Motta S, Casalone R, Petri SL, Spada M, Gridelli B, Conaldi PG.

Cell Transplant. 2014;23(10):1169-85. doi: 10.3727/096368913X668618. Epub 2013 Jun 13.

PMID:
23768775
16.

Partial Trisomy 13 and Partial Monosomy 8 Mosaicism Secondary to an Unbalanced De Novo Translocation: Highlighting an Uncommon Chromosomal Abnormality.

Baranello G, Cesaretti C, Zambonin F, Casalone R, Granata P, Esposito S, Alfei E, Natacci F.

J Child Neurol. 2013 Nov;28(11):1463-1466. Epub 2013 Apr 22.

PMID:
23611886
17.

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.

Novelli A, Grati FR, Ballarati L, Bernardini L, Bizzoco D, Camurri L, Casalone R, Cardarelli L, Cavalli P, Ciccone R, Clementi M, Dalprà L, Gentile M, Gelli G, Grammatico P, Malacarne M, Nardone AM, Pecile V, Simoni G, Zuffardi O, Giardino D.

Ultrasound Obstet Gynecol. 2012 Apr;39(4):384-8. doi: 10.1002/uog.11092. Review.

18.

Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.

Kleefstra T, van Zelst-Stams WA, Nillesen WM, Cormier-Daire V, Houge G, Foulds N, van Dooren M, Willemsen MH, Pfundt R, Turner A, Wilson M, McGaughran J, Rauch A, Zenker M, Adam MP, Innes M, Davies C, López AG, Casalone R, Weber A, Brueton LA, Navarro AD, Bralo MP, Venselaar H, Stegmann SP, Yntema HG, van Bokhoven H, Brunner HG.

J Med Genet. 2009 Sep;46(9):598-606. doi: 10.1136/jmg.2008.062950. Epub 2009 Mar 4.

PMID:
19264732
19.

De novo balanced chromosome rearrangements in prenatal diagnosis.

Giardino D, Corti C, Ballarati L, Colombo D, Sala E, Villa N, Piombo G, Pierluigi M, Faravelli F, Guerneri S, Coviello D, Lalatta F, Cavallari U, Bellotti D, Barlati S, Croci G, Franchi F, Savin E, Nocera G, Amico FP, Granata P, Casalone R, Nutini L, Lisi E, Torricelli F, Giussani U, Facchinetti B, Guanti G, Di Giacomo M, Susca FP, Pecile V, Romitti L, Cardarelli L, Racalbuto E, Police MA, Chiodo F, Rodeschini O, Falcone P, Donti E, Grimoldi MG, Martinoli E, Stioui S, Caufin D, Lauricella SA, Tanzariello SA, Voglino G, Lenzini E, Besozzi M, Larizza L, Dalprà L.

Prenat Diagn. 2009 Mar;29(3):257-65. doi: 10.1002/pd.2215.

PMID:
19248039
20.

Acute myeloid leukemia with associated translocation t(15;17) and 11q23/MLL abnormality.

Campiotti L, Appio L, Casalone R, Righi R, Ageno W, Solbiati F, Grandi AM, Venco A.

Leuk Lymphoma. 2008 Mar;49(3):592-5. doi: 10.1080/10428190701882153. No abstract available.

PMID:
18297541
21.

Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories.

Dalprà L, Giardino D, Finelli P, Corti C, Valtorta C, Guerneri S, Ilardi P, Fortuna R, Coviello D, Nocera G, Amico FP, Martinoli E, Sala E, Villa N, Crosti F, Chiodo F, di Cantogno LV, Savin E, Croci G, Franchi F, Venti G, Donti E, Migliori V, Pettinari A, Bonifacio S, Centrone C, Torricelli F, Rossi S, Simi P, Granata P, Casalone R, Lenzini E, Artifoni L, Pecile V, Barlati S, Bellotti D, Caufin D, Police A, Cavani S, Piombo G, Pierluigi M, Larizza L.

Genet Med. 2005 Nov-Dec;7(9):620-5.

PMID:
16301863
22.

Culture of skeletal myoblasts from human donors aged over 40 years: dynamics of cell growth and expression of differentiation markers.

Baj A, Bettaccini AA, Casalone R, Sala A, Cherubino P, Toniolo AQ.

J Transl Med. 2005 May 12;3(1):21.

23.

Establishment of a non-tumorigenic papillary thyroid cell line (FB-2) carrying the RET/PTC1 rearrangement.

Basolo F, Giannini R, Toniolo A, Casalone R, Nikiforova M, Pacini F, Elisei R, Miccoli P, Berti P, Faviana P, Fiore L, Monaco C, Pierantoni GM, Fedele M, Nikiforov YE, Santoro M, Fusco A.

Int J Cancer. 2002 Feb 10;97(5):608-14.

24.

Nonrandom chromosome changes in Kaposi sarcoma: cytogenetic and FISH results in a new cell line (KS-IMM) and literature review.

Casalone R, Albini A, Righi R, Granata P, Toniolo A.

Cancer Genet Cytogenet. 2001 Jan 1;124(1):16-9. Review.

PMID:
11165317
25.

Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case.

Granata P, Mazzola D, Righi R, Minelli E, Salvatoni A, Baroli P, Maggi F, Casalone R.

Ann Genet. 2000 Jan-Mar;43(1):45-50. Review.

PMID:
10818221
26.

Cytogenetic and interphase FISH analyses of 73 basal cell and three squamous cell carcinomas: different findings in direct preparations and short-term cell cultures.

Casalone R, Mazzola D, Righi R, Granata P, Minelli E, Salvadore M, Lombardo M, Bertani E.

Cancer Genet Cytogenet. 2000 Apr 15;118(2):136-43.

PMID:
10748294
27.

Cytokine production by a new undifferentiated human thyroid carcinoma cell line, FB-1.

Fiore L, Pollina LE, Fontanini G, Casalone R, Berlingieri MT, Giannini R, Pacini F, Miccoli P, Toniolo A, Fusco A, Basolo F.

J Clin Endocrinol Metab. 1997 Dec;82(12):4094-100.

PMID:
9398720
28.

The Hoyeraal-Hreidarsson syndrome: the presentation of the seventh case.

Nespoli L, Lascari C, Maccario R, Nosetti L, Broggi U, Locatelli F, Binda S, Gaudio F, Casalone R, Bosi F.

Eur J Pediatr. 1997 Oct;156(10):818-20. No abstract available.

PMID:
9365078
29.

Cytogenetic and interphase cytogenetic analyses reveal chromosome instability but no clonal trisomy 8 in Dupuytren contracture.

Casalone R, Mazzola D, Meroni E, Righi R, Minelli E, Granata P, Panattoni A, Viotto AM, Modesti M, Pilato G.

Cancer Genet Cytogenet. 1997 Nov;99(1):73-6.

PMID:
9352799
30.

Age-related increase of baseline frequencies of sister chromatid exchanges, chromosome aberrations, and micronuclei in human lymphocytes.

Bolognesi C, Abbondandolo A, Barale R, Casalone R, Dalprà L, De Ferrari M, Degrassi F, Forni A, Lamberti L, Lando C, Migliore L, Padovani P, Pasquini R, Puntoni R, Sbrana I, Stella M, Bonassi S.

Cancer Epidemiol Biomarkers Prev. 1997 Apr;6(4):249-56. Review.

31.

Large T antigen coding sequences of two DNA tumor viruses, BK and SV40, and nonrandom chromosome changes in two glioblastoma cell lines.

Tognon M, Casalone R, Martini F, De Mattei M, Granata P, Minelli E, Arcuri C, Collini P, Bocchini V.

Cancer Genet Cytogenet. 1996 Aug;90(1):17-23.

PMID:
8780741
32.

Clonal chromosome changes in non-neoplastic ureters.

Casalone R, Minelli E, Righi R, Granata P, Meroni E, Caruso V, Mazzola D, Salvadore M, Pozzi E, Bono AV.

Cancer Genet Cytogenet. 1995 Aug;83(1):28-31.

PMID:
7656200
33.

Chromosome changes in lymphocytes of patients with scleroderma.

Casalone R, Granata P, Minelli E, Righi R, Meroni E, Mazzola D, Sammarelli G, Baratelli E, Broggini M.

Ann Genet. 1995;38(3):145-50.

PMID:
8540685
34.

Serum levels of gamma interferon in patients with Down's syndrome.

Torre D, Broggini M, Zeroli C, Agrifoglio L, Bottà V, Casalone R, Ferrario G.

Infection. 1995 Jan-Feb;23(1):66-7. No abstract available.

PMID:
7744499
35.

Cerebral germ cell tumor and XXY karyotype.

Casalone R, Righi R, Granata P, Portentoso P, Minelli E, Meroni, Solero CL, Allegranza A.

Cancer Genet Cytogenet. 1994 May;74(1):25-9. Review.

PMID:
8194043
36.

Chromosome changes in benign prostatic hyperplasia and their significance in the origin of prostatic carcinoma.

Casalone R, Portentoso P, Granata P, Minelli E, Righi R, Meroni E, Pozzi E, Chiaravalli AM.

Cancer Genet Cytogenet. 1993 Jul 15;68(2):126-30.

PMID:
7689034
37.

Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq.

Bardoni B, Floridia G, Guioli S, Peverali G, Anichini C, Cisternino M, Casalone R, Danesino C, Fraccaro M, Zuffardi O, et al.

Hum Genet. 1993 May;91(4):333-8.

PMID:
8099057
38.

Clonal chromosome changes in renal carcinoma do not correlate with clinical stages and histopathologic grades.

Granata P, Portentoso P, Minelli E, Righi R, Meroni E, Bono AV, Pozzi E, Salvadore M, Simi P, Casalone R.

Cancer Genet Cytogenet. 1992 Nov;64(1):30-4.

PMID:
1333879
39.

Significance of the clonal and sporadic chromosome abnormalities in non-neoplastic renal tissue.

Casalone R, Granata Casalone P, Minelli E, Portentoso P, Righi R, Meroni E, Giudici A, Donati D, Riva C, Salvatore S, et al.

Hum Genet. 1992 Sep-Oct;90(1-2):71-8.

PMID:
1427791
40.

Changes in glial fibrillary acidic protein and karyotype during culturing of two cell lines established from human glioblastoma multiforme.

Bocchini V, Casalone R, Collini P, Rebel G, Lo Curto F.

Cell Tissue Res. 1991 Jul;265(1):73-81.

PMID:
1655272
41.

Cytogenetic analysis reveals clonal proliferation of smooth muscle cells in atherosclerotic plaques.

Casalone R, Granata P, Minelli E, Portentoso P, Giudici A, Righi R, Castelli P, Socrate A, Frigerio B.

Hum Genet. 1991 Jun;87(2):139-43.

PMID:
2066101
42.

[Cytogenetic studies in renal carcinoma].

Casalone R, Bono AV, Pozzi C, Granata P.

Arch Ital Urol Nefrol Androl. 1991 Jun;63(2):225-8. Italian.

PMID:
1830669
43.

Pseudodicentric isochromosome(22) in meningiomas.

Casalone R, Minelli E, Granata P, Giudici A.

Cancer Genet Cytogenet. 1990 Apr;45(2):273-5. No abstract available. Erratum in: Cancer Genet Cytogenet 1990 Sep;48(2):following 283.

PMID:
2317777
44.

Clonal duplication of the Y chromosome and fra(X)(q28) in a case of epidermoid carcinoma of the esophagus.

Casalone R, Minelli E, Portensoso P, Giudici A.

Cancer Genet Cytogenet. 1990 Apr;45(2):269-71. No abstract available.

PMID:
2317776
45.

Correlation between cytogenetic and histopathological findings in 65 human meningiomas.

Casalone R, Simi P, Granata P, Minelli E, Giudici A, Butti G, Solero CL.

Cancer Genet Cytogenet. 1990 Apr;45(2):237-43.

PMID:
2317772
46.

Multiple meningiomas: a clinical, surgical, and cytogenetic analysis.

Butti G, Assietti R, Casalone R, Paoletti P.

Surg Neurol. 1989 Apr;31(4):255-60.

PMID:
2928917
47.

Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia.

Maserati E, Campagnoli E, Truglio F, Casalone R, Geniram A, Invernizzi R, Pasquali F.

Hereditas. 1989;111(3):305-8. No abstract available.

48.

A case of chronic myelocytic leukemia with five Philadelphia chromosomes.

Casalone R, Maserati E.

Cancer Genet Cytogenet. 1988 Sep;34(2):257-9. No abstract available.

PMID:
3165698
49.

Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase.

Maserati E, Cavalli P, Casalone R, Morandi S, Pasquali F.

Hum Genet. 1988 Mar;78(3):248-50.

PMID:
3162225
50.

Gene dosage effect in cells with monosomy of chromosome 22 derived from human meningiomas.

Casalone R, Minelli A, Butti G, Gaetani P, Silvani V, Solero CL, Danesino C.

Acta Neurochir Suppl (Wien). 1988;43:114-7.

PMID:
2975141

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