M Campogrande
Overview
Explore the profile of M Campogrande including associated specialties, affiliations and a list of published articles.
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Articles
57
Citations
81
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Recent Articles
1.
Viora E, Zamboni C, Mortara G, Stillavato S, Bastonero S, Errante G, et al.
Am J Med Genet A
. 2007 Feb;
143A(6):553-7.
PMID: 17318852
The aim of this article is evaluate the sonograhic findings in fetuses with trisomy 18 at different gestational ages. The cases were recruited from pregnant women, who underwent to prenatal...
2.
Sciarrone A, Masturzo B, Botta G, Bastonero S, Campogrande M, Viora E
Prenat Diagn
. 2005 Oct;
25(12):1129-32.
PMID: 16231299
Prevalence of congenital heart disease increases with nuchal translucency (NT) thickness. First-trimester fetal bradycardia may result from heart block associated with complex congenital heart disease. We report two cases detected...
3.
Viora E, Errante G, Sciarrone A, Bastonero S, Masturzo B, Martiny G, et al.
Prenat Diagn
. 2005 Jun;
25(6):511-5.
PMID: 15968623
Objectives: To assess the feasibility of measuring nasal bone length in the second trimester of pregnancy and to confirm if fetal nasal bone absence or hypoplasia is a marker for...
4.
Cirigliano V, Voglino G, Canadas M, Marongiu A, Ejarque M, Ordonez E, et al.
Mol Hum Reprod
. 2004 Sep;
10(11):839-46.
PMID: 15361554
The quantitative fluorescent PCR (QF-PCR) assay, introduced during the last few years, allows prenatal diagnoses of common chromosome aneuploidies in a few hours after sampling. We report the first assessment...
5.
Viora E, Sciarrone A, Bastonero S, Errante G, Mortara G, Chiappa E, et al.
Fetal Diagn Ther
. 2004 Aug;
19(5):440-7.
PMID: 15305101
Objective: To evaluate sonographic appearance, natural history, and neonatal outcome of fetal venous anomalies. Methods: We performed an observational study, including all fetuses affected by abnormalities of the venous system...
6.
Cremonesi L, Galbiati S, Foglieni B, Smid M, Gambini D, Ferrari A, et al.
Ann N Y Acad Sci
. 2004 Jul;
1022:105-12.
PMID: 15251947
Fetal DNA in maternal plasma may represent a source of genetic material for prenatal noninvasive diagnosis of genetic diseases. We evaluated a cohort of physiological pregnancies to determine if fetal...
7.
Bau M, Arisio R, CRISTINI G, Bertone E, Campogrande M
Breast
. 2004 Jun;
13(3):239-41.
PMID: 15177429
Cowden syndrome is a hereditary genetic disease whose incidence is still not precisely defined; it is due to a germline mutation in the PTEN gene. We reported a case of...
8.
Viora E, Masturzo B, Errante G, Sciarrone A, Bastonero S, Campogrande M
Prenat Diagn
. 2003 Oct;
23(10):784-7.
PMID: 14558019
Objective: The aim of this study is to evaluate the significance of nasal bone ossification as a marker for trisomy 21 at 11 to 14 weeks' gestation in an unselected...
9.
Orlandi F, Bilardo C, Campogrande M, Krantz D, Hallahan T, Rossi C, et al.
Ultrasound Obstet Gynecol
. 2003 Jul;
22(1):36-9.
PMID: 12858300
Objectives: To assess the feasibility of measuring nasal bone length in first-trimester pregnancy and to confirm if the absence of a fetal nasal bone is a marker for Down syndrome....
10.
Viora E, Sciarrone A, Bastonero S, Errante G, Botta G, Franceschini P, et al.
Ultrasound Obstet Gynecol
. 2003 Feb;
21(2):200-2.
PMID: 12601849
No abstract available.