Carapella E - Search Results

1

Role of genetic variability in neonatal jaundice. A prospective study on full-term, blood group-compatible infants.

Lucarini N, Gloria-Bottini F, Tucciarone L, Carapella E, Maggioni G, Bottini E. Lucarini N, et al. Among authors: carapella e. Experientia. 1991 Dec 1;47(11-12):1218-21. doi: 10.1007/BF01918389. Experientia. 1991. PMID: 1765134

2

ABO system incompatibility: evaluation of risk of hyperbilirubinaemia at birth by multivariate discriminant analysis.

Orzalesi M, Gloria-Bottini F, Lucarelli P, Lucarini N, Carapella E, Bottini E. Orzalesi M, et al. Among authors: carapella e. Experientia. 1983 Jan 15;39(1):89-91. doi: 10.1007/BF01960645. Experientia. 1983. PMID: 6825785

3

Serum haptoglobin appearance during neonatal period is associated with acid phosphatase (ACP1) phenotype.

Bottini E, Carapella E, Scacchi R, Lucarini N, Gloria-Bottini F, Pascone R, Bonci E, Maggioni G. Bottini E, et al. Among authors: carapella e. Early Hum Dev. 1985 Jan;10(3-4):237-43. doi: 10.1016/0378-3782(85)90054-4. Early Hum Dev. 1985. PMID: 3987576

4

Annotations on the hyperbilirubinaemia of ABO incompatible infants.

Carapella E, Gloria-Bottini F, Tucciarone L, Orzalesi M, Bottini E. Carapella E, et al. Haematologia (Budap). 1982;15(1):127-33. Haematologia (Budap). 1982. PMID: 7117940

5

Adenosine deaminase polymorphism. Associations at clinical level suggest a role in cell functions and immune reactions.

Bottini E, Carapella E, Cataldi L, Nicotra M, Lucarelli P, Lucarini N, Pascone R, Gloria-Bottini F. Bottini E, et al. Among authors: carapella e. J Med Genet. 1981 Oct;18(5):331-4. doi: 10.1136/jmg.18.5.331. J Med Genet. 1981. PMID: 7199090 Free PMC article.

6

Sex ratio in man: an analysis of the relationship with ABO blood groups and placental alkaline phosphatase phenotype.

Gloria-Bottini F, Polzonetti A, Lucarini N, Palmarino R, Orzalesi M, Carapella E, Maggioni G, Bottini E. Gloria-Bottini F, et al. Among authors: carapella e. Hum Hered. 1979;29(3):143-6. doi: 10.1159/000153031. Hum Hered. 1979. PMID: 468272

7

Intrauterine death: an approach to the analysis of genetic heterogeneity.

Bottini E, Coromaldi L, Carapella E, Pascone R, Nicotra M, Coghi I, Lucarini N, Gloria-Bottini F. Bottini E, et al. Among authors: carapella e. J Med Genet. 1983 Jun;20(3):196-98. doi: 10.1136/jmg.20.3.196. J Med Genet. 1983. PMID: 6683759 Free PMC article.

8

Is there a role of erythrocyte acid phosphatase polymorphism in intrauterine development?

Bottini E, Carapella E, Orzalezi M, Lucarelli P, Pascone R, Gloria-Bottini F, Coccia M. Bottini E, et al. Among authors: carapella e. Am J Hum Genet. 1980 Sep;32(5):764-7. Am J Hum Genet. 1980. PMID: 7424917 Free PMC article. No abstract available.

9

MNSs genetic polymorphism and intrauterine selection through habitual abortion.

Bottini E, Bonci E, Gloria-Bottini F, Nicotra M, Carapella E, Coghi I, Lucarini N, Martini PA, Paris D, Bonci M, et al. Bottini E, et al. Among authors: carapella e. Hum Biol. 1987 Feb;59(1):103-20. Hum Biol. 1987. PMID: 3570249 No abstract available.

10

A genetic basis for heterogeneity of asthma syndrome in pediatric ages: adenosine deaminase phenotypes.

Ronchetti R, Lucarini N, Lucarelli P, Martinez F, Macrì F, Carapella E, Bottini E. Ronchetti R, et al. Among authors: carapella e. J Allergy Clin Immunol. 1984 Jul;74(1):81-4. doi: 10.1016/0091-6749(84)90092-7. J Allergy Clin Immunol. 1984. PMID: 6736486

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