Zobrazeno 1 - 10
of 128
pro vyhledávání: '"C, Largillière"'
Publikováno v:
Gynécologie Obstétrique & Fertilité. 31:378-381
Resume Ces dernieres annees ont vu se confirmer la faisabilite et l’interet potentiel du Doppler uterin au troisieme mois de grossesse. L’appreciation du morphogramme uterin par voie abdominale est possible des 12–14 SA. Un tiers des patientes
Publikováno v:
Fetal Diagnosis and Therapy. 16:284-288
We report a case of sirenomelia diagnosed at 13 gestational weeks. This rare malformation sequence is characterized by fusion and rotation of the lower limbs to various degrees and anorectal atresia, usually associated with absence of bladder and age
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 18:272-274
A woman was referred to our unit at 25 weeks' gestation because of fetal ascites. Conventional and three-dimensional ultrasound examinations revealed coarse facies and micromelia which strongly suggested storage disease, despite the absence of an ind
Autor:
J. N. Hugues, S. Kanafani, Brigitte Benzacken, Eva Pipiras, Pierre Gressens, Azzedine Aboura, Anne-Claude Tabet, Michèle Uzan, Martine Bucourt, Jean-Philippe Wolf, E Lachassinne, C Roumegoux, C. Garel, Lionel Carbillon, C. Largillière, I. Cedrin-Durnerin
Publikováno v:
Prenatal diagnosis. 27(3)
We report a semilobar holoprosencephaly (HPE) in a post-intracytoplasmic-sperm-injection pregnancy. It was suggested by ultrasonography (US), documented on karyotype, identified with magnetic resonance imaging (MRI), established after birth and confi
Autor:
A. Batallan, Céline Dupont, Martine Bucourt, Brigitte Benzacken, C. Largillière, Jean-Pierre Siffroi, Sandra Chantot-Bastaraud, Michèle Uzan, Jean-Philippe Wolf, Eva Pipiras
Publikováno v:
Prenatal diagnosis. 24(2)
True structural chromosomal mosaicism are rare events in prenatal cytogenetics practice and may lead to diagnostic and prognostic problems. Here is described the case of a fetus carrying an abnormal chromosome 15 made of a whole chromosome 2p translo
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 73:F103-F105
Very long chain acyl-CoA dehydrogenase is a newly characterised enzyme in mitochondrial fatty acid oxidation. A girl who presented on the second day of life with a sudden and severe illness due to deficiency of this enzyme is reported. There is evide
Autor:
Jacques Pariès, N. Perrot, I. Pharizien, A. Tigaizin, Serge Uzan, Michèle Uzan, Lionel Carbillon, C. Largillière
Publikováno v:
Fetal diagnosis and therapy. 19(4)
Objective: Uterine artery flow velocity was prospectively assessed using Doppler ultrasound at 12–14 and 22–24 weeks of gestation in the prediction of subsequent complications related to uteroplacental insufficiency: preeclampsia, pregnancy-induc
Publikováno v:
Gynecologie, obstetriquefertilite. 31(4)
Last years, feasibility and possible interest of uterine artery Doppler during the third month of gestation were confirmed. Doppler flow velocity waveforms can be obtained and assessed in both uterine arteries using abdominal ultrasonography at 12-14
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 18(3)
A woman was referred to our unit at 25 weeks' gestation because of fetal ascites. Conventional and three-dimensional ultrasound examinations revealed coarse facies and micromelia which strongly suggested storage disease, despite the absence of an ind
Publikováno v:
Fetal diagnosis and therapy. 16(5)
We report a case of sirenomelia diagnosed at 13 gestational weeks. This rare malformation sequence is characterized by fusion and rotation of the lower limbs to various degrees and anorectal atresia, usually associated with absence of bladder and age