Zobrazeno 1 - 10
of 196
pro vyhledávání: '"M, Campogrande"'
Publikováno v:
Donald School Journal of Ultrasound in Obstetrics and Gynecology. 1:37-44
There are few 3D well-documented studies about thoraco- abdominal malformations, except for the evaluation of fetal lung volume. Three-dimensional ultrasound provides additional diagnostic information for the evaluation of fetal thorax both for the d
Autor:
Augusto Ferrari, Laura Cremonesi, Elsa Viora, Gabriella Restagno, S. Bastonero, Marco Pagliano, Maddalena Smid, Dania Gambini, Maurizio Ferrari, Silvia Galbiati, M. Campogrande, Stefano Calza
Publikováno v:
Human Genetics. 117:243-248
The presence of fetal DNA in maternal plasma may represent a source of genetic material which can be obtained noninvasively. We wanted to assess whether fetal DNA is detectable in all pregnant women, to define the range and distribution of fetal DNA
Publikováno v:
Prenatal Diagnosis. 25:511-515
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 Down syndrome. Methods Fetal nasal bone assessment was performed in 439
Autor:
Terrence W. Hallahan, C. M. Bilardo, M. Campogrande, E. Viora, Cinzia Rossi, David A. Krantz, Francesco Orlandi
Publikováno v:
Ultrasound in obstetrics & gynecology, 22(1), 36-39. John Wiley and Sons Ltd
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. Methods Fetal nasal bone assessment was attempted in 1089 consecutive
Publikováno v:
Prenatal Diagnosis. 23:784-787
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 obstetric population referred to our Centre. Methods A total of 1906 consecutive fetus
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 19:88-91
Prenatal diagnosis of short-rib polydactyly syndrome is possible and has been reported in literature, but a precise ultrasound diagnosis is not easy. We report a case in which three-dimensional ultrasound was used in the evaluation of the disorder. T
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 15:431-434
A case of an isolated cranio-facial vascular anomaly, extending from the left parietal bone to the lateral margin of the omolateral orbit is presented. Detection and differential diagnosis of fetal hemangioma is important for a variety of reasons. Fi
Autor:
Dario Bruzzese, Pasquale Martinelli, Mariangela Rustico, M. Campogrande, Elsa Viora, Dario Paladini, Umberto Giani
Publikováno v:
Prenatal diagnosis. 25(6)
Objective To describe size charts developed from fetuses of Italian couples. Method Prospective cross-sectional investigation conducted in three referral centers for prenatal diagnosis. The population of the study included fetuses between the 16th an
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 12:132-135
Arteriovenous fistulas of the placenta rarely occur in singleton pregnancies. This report describes the fetal and neonatal hemodynamic pattern in a singleton gestation in which multiple placental artery-to-vein anastomoses were associated with a larg
Publikováno v:
The Breast. 13:239-241
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 breast tumor caused by a PTEN gene mutation, which was detected within a National