Zobrazeno 1 - 10
of 16
pro vyhledávání: '"M. C. Padilla"'
Autor:
F. A., Douriet-Marín1, M. C., Padilla-Desgarennes2 mcpadillad@prodigy.net.mx
Publikováno v:
Dermatología Revista Mexicana. May/Jun2016, Vol. 60 Issue 3, p219-228. 10p.
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 44:116-118
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 32:515-519
Objective To evaluate parameters of fetal breathing movements—displacement of the fetal abdominal wall during inspiration and expiration, time of inspiration and expiration and speed of inspiration and expiration—between 30 and 36 weeks' gestatio
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 39(6)
Objectives To assess a new method for numerical quantification of cervical elastography during pregnancy and to evaluate the repeatability of the measurements. Methods Cervical elastography was carried out twice by a single operator in 112 singleton
Autor:
Alberto Salamanca, R. M. Sabatel, M. C. Padilla, Francisco González-Gómez, M. Camara, J. L. Cuadros
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 2:95-100
A better understanding of the ultrasound findings in each of the different types of fetal anencephaly can help to reduce the number of false-negative diagnoses of this condition during the prenatal period. Errors in the estimation of the remaining ce
Publikováno v:
Acta clinica Croatica
Volume 46
Issue 2
Volume 46
Issue 2
Autor:
Alberto Salamanca, M. C. Padilla, Miguel Angel Motos, K. Stemper, R. M. Sabatel, Francisco González-Gómez
Publikováno v:
Geburtshilfe und Frauenheilkunde. 52:783-785
Holoprosencephaly is a malformation complex, in which the foetal forebrain (prosencephalon) fails to cleave. The aetiology of holoprosencephaly is heterogeneous. In the last years, a new malformation syndrome has been described, including holoprosenc
Autor:
M. C. Padilla, Miguel Angel Motos, R. M. Sabatel, Francisco Zorrilla, Alberto Salamanca, Francisco González-Gómez
Publikováno v:
Prenatal diagnosis. 14(8)
Foramina parietalia permagna (FPP) is an extremely uncommon congenital defect, inherited as an autosomal dominant condition. Its characteristics are two symmetrical orifices in the parietal bones (not of fixed size) on both sides of the midline. This
Publikováno v:
Anales espanoles de pediatria. 38(4)
With the final aim of preventing neonatal respiratory distress syndrome (RDS), the present study was carried out on premature rabbits (28 days of gestation) that showed a moderate level of RDS. These animals were treated intratracheally with 25 micro
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 47(3)
The incorporation of high-frequency transvaginal probes in commercial ultrasonic equipment allows now for the earlier detection of fetal malformations and the possibility of interrupting pregnancy when such an anomaly is incompatible with postnatal l