ACNP - Italian Periodicals Catalogue

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Results: 1-20 |

Results: 20

Fetal lung volume measurement by magnetic resonance imaging in congenital diaphragmatic hernia

Authors: Mahieu-Caputo, D Sonigo, P Dommergues, M Fournet, JC Thalabard, JC Abarca, C Benachi, A Brunelle, F Dumez, Y

Citation: D. Mahieu-caputo et al., Fetal lung volume measurement by magnetic resonance imaging in congenital diaphragmatic hernia, BR J OBST G, 108(8), 2001, pp. 863-868

Congenital erythropoietic porphyria: Prenatal diagnosis and autopsy findings in two sibling fetuses

Authors: Daikha-Dahmane, F Dommergues, M Narcy, F Gubler, MC Dumez, Y Gauthier, E Nordmann, Y Nessmann, C Terrasse, G Muller, F

Citation: F. Daikha-dahmane et al., Congenital erythropoietic porphyria: Prenatal diagnosis and autopsy findings in two sibling fetuses, PEDIATR D P, 4(2), 2001, pp. 180-184

Pathogenesis of twin-twin transfusion syndrome: The renin-angiotensin system hypothesis

Authors: Mahieu-Caputo, D Muller, F Joly, D Gubler, MC Lebidois, J Fermont, L Dumez, Y Dommergues, M

Citation: D. Mahieu-caputo et al., Pathogenesis of twin-twin transfusion syndrome: The renin-angiotensin system hypothesis, FETAL DIAGN, 16(4), 2001, pp. 241-244

Prenatal diagnosis of sporadic Apert syndrome: A sequential diagnostic approach combining three-dimensional computed tomography and molecular biology

Authors: Mahieu-Caputo, D Sonigo, P Amiel, J Simon, I Aubry, MC Lemerrer, M Delezoide, AL Gigarel, N Dommergues, M Dumez, Y

Citation: D. Mahieu-caputo et al., Prenatal diagnosis of sporadic Apert syndrome: A sequential diagnostic approach combining three-dimensional computed tomography and molecular biology, FETAL DIAGN, 16(1), 2001, pp. 10-12

Determination of the anatomical location of an antenatal intestinal occlusion by magnetic resonance imaging

Authors: Benachi, A Sonigo, P Jouannic, JM Simon, I Revillon, Y Brunelle, F Dumez, Y

Citation: A. Benachi et al., Determination of the anatomical location of an antenatal intestinal occlusion by magnetic resonance imaging, ULTRASOUN O, 18(2), 2001, pp. 163-165

Prenatal diagnosis of respiratory chain deficiency by direct mutation screening

Authors: Amiel, J Gigarel, N Benacki, A Benit, P Valnot, I Parfait, W Von Kleist-Retzow, JC Raclin, V Hadj-Rabia, S Dumez, Y Rustin, P Bonnefont, JP Munnich, A Rotig, A

Citation: J. Amiel et al., Prenatal diagnosis of respiratory chain deficiency by direct mutation screening, PRENAT DIAG, 21(7), 2001, pp. 602-604

Successful intrauterine shunting of a sacrococcygeal teratoma (SCT) causing fetal bladder obstruction

Authors: Jouannic, JM Dommergues, M Auber, F Bessis, R Nihoul-Fekete, C Dumez, Y

Citation: Jm. Jouannic et al., Successful intrauterine shunting of a sacrococcygeal teratoma (SCT) causing fetal bladder obstruction, PRENAT DIAG, 21(10), 2001, pp. 824-826

Pain in the fetus

Authors: Mahieu-Caputo, D Dommergues, M Muller, F Dumez, Y

Citation: D. Mahieu-caputo et al., Pain in the fetus, PRESSE MED, 29(12), 2000, pp. 663-669

Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency

Authors: Faivre, L Cormier-Daire, V Chretien, D von Kleist-Retzow, JC Amiel, J Dommergues, M Saudubray, JM Dumez, Y Rotig, A Rustin, P Munnich, A

Citation: L. Faivre et al., Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency, PRENAT DIAG, 20(9), 2000, pp. 732-737

Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at risk

Authors: Lepinard, C Descamps, P Meneguzzi, G Blanchet-Bardon, C Germain, DP Larget-Piet, L Beringue, F Berchel, C Muller, F Dumez, Y

Citation: C. Lepinard et al., Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at risk, PRENAT DIAG, 20(1), 2000, pp. 70-75

Fetal serum beta(2)-microglobulin predicts postnatal renal function in bilateral uropathies

Authors: Dommergues, M Muller, F Ngo, S Hohlfeld, P Oury, JF Bidat, L Mahieu-Caputo, D Sagot, P Body, G Favre, R Dumez, Y

Citation: M. Dommergues et al., Fetal serum beta(2)-microglobulin predicts postnatal renal function in bilateral uropathies, KIDNEY INT, 58(1), 2000, pp. 312-316

Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up

Authors: Sanlaville, D Aubry, MC Dumez, Y Nolen, MC Amiel, J Pinson, MP Lyonnet, S Munnich, A Vekemans, M Morichon-Delvallez, N

Citation: D. Sanlaville et al., Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up, J MED GENET, 37(7), 2000, pp. 525-528

Twin-to-twin transfusion syndrome - Role of the fetal renin-angiotensin system

Authors: Mahieu-Caputo, D Dommergues, M Delezoide, AL Lacoste, M Cai, Y Narcy, F Jolly, D Gonzales, M Dumez, Y Gubler, MC

Citation: D. Mahieu-caputo et al., Twin-to-twin transfusion syndrome - Role of the fetal renin-angiotensin system, AM J PATH, 156(2), 2000, pp. 629-636

The reasons for termination of pregnancy in the third trimester

Authors: Dommergues, M Benachi, A Benifla, JL des Noettes, R Dumez, Y

Citation: M. Dommergues et al., The reasons for termination of pregnancy in the third trimester, BR J OBST G, 106(4), 1999, pp. 297-303

Prenatal diagnosis of fetal anomalies: importance of prognostic evaluations

Authors: Dommergues, M Mahieu-Caputo, D Jouanic, JM Dumez, Y

Citation: M. Dommergues et al., Prenatal diagnosis of fetal anomalies: importance of prognostic evaluations, ARCH PED, 6, 1999, pp. 243S-245S

Role of genetics

Authors: Lyonnet, S Morichon, N Dommergues, M Dumez, Y Briard, ML Vekemans, M Munnich, A

Citation: S. Lyonnet et al., Role of genetics, ARCH PED, 6, 1999, pp. 246S-248S

Prenatal diagnosis of a satellited non-acrocentric chromosome derived froma maternal translocation (10;13)(p13;p12) and review of literature

Authors: Faivre, L Morichon-Delvallez, N Viot, G Larget-Piet, A Narcy, F Turleau, C Pinson, MP Dumez, Y Munnich, A Vekemans, M

Citation: L. Faivre et al., Prenatal diagnosis of a satellited non-acrocentric chromosome derived froma maternal translocation (10;13)(p13;p12) and review of literature, PRENAT DIAG, 19(3), 1999, pp. 282-286

First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X,an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex

Authors: Rouillac, C Aral, B Fouque, F Marchant, D Saudubray, JM Dumez, Y Lindsay, G Abitbol, M Dufier, JL Marsac, C Benelli, C

Citation: C. Rouillac et al., First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X,an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex, PRENAT DIAG, 19(12), 1999, pp. 1160-1164

Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature

Authors: Favire, L Morichon-Delvallez, N Viot, G Martinovic, J Pinson, MP Aubry, JP Raclin, V Edery, P Dumez, Y Munnich, A Vekemans, M

Citation: L. Favire et al., Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature, PRENAT DIAG, 19(1), 1999, pp. 49-53

Pregnancy reduction in multifetal pregnancies

Authors: Dommergues, M Dumez, Y Evans, MI

Citation: M. Dommergues et al., Pregnancy reduction in multifetal pregnancies, INTERVENTIONAL ULTRASOUND IN OBSTETRICS, GYNAECOLOGY AND THE BREAST, 1998, pp. 151-154

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