Carozzi F - Search Results

1

Mutations in the P53 and RAS family genes are associated with tumor progression of BCR/ABL negative chronic myeloproliferative disorders.

Gaidano G, Guerrasio A, Serra A, Carozzi F, Cambrin GR, Petroni D, Saglio G. Gaidano G, et al. Among authors: carozzi f. Leukemia. 1993 Jul;7(7):946-53. Leukemia. 1993. PMID: 8321046

2

Transient cytogenetic relapse in a Ph1-positive chronic myelogenous leukemia patient previously treated with alpha-interferon.

Rege-Cambrin G, Guerrasio A, Scaravaglio P, Rosso C, Carozzi F, Kerim S, Saglio G. Rege-Cambrin G, et al. Among authors: carozzi f. Leukemia. 1992 Jul;6(7):738-41. Leukemia. 1992. PMID: 1625497

3

Extra translocation +der(1q9p) is a prognostic indicator in myeloproliferative disorders.

Rege-Cambrin G, Speleman F, Kerim S, Scaravaglio P, Carozzi F, Dal Cin P, Michaux JL, Offner F, Saglio G, Van den Berghe H. Rege-Cambrin G, et al. Among authors: carozzi f. Leukemia. 1991 Dec;5(12):1059-63. Leukemia. 1991. PMID: 1774954 Review.

4

Karyotypic analysis of gastric carcinoma cell lines carrying an amplified c-met oncogene.

Rege-Cambrin G, Scaravaglio P, Carozzi F, Giordano S, Ponzetto C, Comoglio PM, Saglio G. Rege-Cambrin G, et al. Among authors: carozzi f. Cancer Genet Cytogenet. 1992 Dec;64(2):170-3. doi: 10.1016/0165-4608(92)90350-h. Cancer Genet Cytogenet. 1992. PMID: 1486568

5

Effect of recombinant human IL-3 on the mitotic index and karyotype of hemopoietic cells.

Kerim S, Rege-Cambrin G, Scaravaglio P, Carozzi F, Saglio G, Aglietta M. Kerim S, et al. Among authors: carozzi f. Cancer Genet Cytogenet. 1991 Sep;55(2):235-41. doi: 10.1016/0165-4608(91)90083-7. Cancer Genet Cytogenet. 1991. PMID: 1933826

6

Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative study.

Simoni G, Fraccaro M, Arslanian A, Bacchetta M, Baccichetti C, Bignone FA, Cagiano A, Carbonara AO, Carozzi F, Cuoco C, Bricarelli FD, Dallapiccola B, Dalprà L, Carbone LD, Ferranti G, Filippi G, Frateschi M, Gimelli G, Gualtieri RM, Lenzini E, Micara G, Migone N, Montacuti V, Neri G, Papa R, Pecile V, Rocchi M, Savin E, Serra A, Tenconi R, Terzoli GL, Tibiletti MG. Simoni G, et al. Among authors: carozzi f. Hum Genet. 1982;60(1):63-8. doi: 10.1007/BF00281266. Hum Genet. 1982. PMID: 7076250

7

Cystic hygroma: prenatal diagnosis and genetic counselling.

Marchese C, Savin E, Dragone E, Carozzi F, De Marchi M, Campogrande M, Dolfin GC, Pagliano G, Viora E, Carbonara A. Marchese C, et al. Among authors: carozzi f. Prenat Diagn. 1985 May-Jun;5(3):221-7. doi: 10.1002/pd.1970050310. Prenat Diagn. 1985. PMID: 3895219

8

True hermaphroditism with XX/XY sex chromosome mosaicism: report of a case.

De Marchi M, Carbonara AO, Carozzi F, Massara F, Belforte L, Molinatti GM, Bisbocci D, Passarino MP, Palestro G. De Marchi M, et al. Among authors: carozzi f. Clin Genet. 1976 Nov;10(5):265-72. doi: 10.1111/j.1399-0004.1976.tb00047.x. Clin Genet. 1976. PMID: 991437

9

[Prenatal diagnosis. Indications and risks of early amniocentesis by placental puncture and fetoscopy].

Massobrio M, Coppo F, Carozzi F, De Marchi M, Migone N, Ottone PL, Ansaldi E, Carbonara A. Massobrio M, et al. Among authors: carozzi f. Minerva Ginecol. 1980 Jun;32(6):527-38. Minerva Ginecol. 1980. PMID: 7243054 Italian. No abstract available.

10

Partial trisomy 3q in a newborn female.

De Marchi M, Zuffardi O, Carozzi F, Schmid W, Carbonara AO. De Marchi M, et al. Among authors: carozzi f. Ric Clin Lab. 1977 Jul-Sep;7(3):225-32. doi: 10.1007/BF02881818. Ric Clin Lab. 1977. PMID: 605339

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