Search Results - "Rypens, F."

VP16.10: Prenatal diagnosis of Coffin‐Siris syndrome: when to think about? by Rypens, F., Wavrant, S., Fallet‐Bianco, C., Delrue, M.

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EP17.10: Early diagnosis of Nager syndrome in dichorionic twins by Zerounian, S., Delrue, M., Rypens, F., Codsi, E., Wavrant, S.

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EP04.29: Antenatal diagnosis of congenital lymphoedema by Zerounian, S., Codsi, E., Delrue, M., Rypens, F., Wavrant, S.

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VP16.17: Pericardiocentesis in severe isolated pericardial effusion: a case report by Carmant, L., Boucoiran, I., Zerounian, S., Karalis, A., Bigras, J., Rypens, F., Wavrant, S.

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EP24.14: A curious uterine tumour in pregnancy by Mathe, M., Rypens, F., Wavrant, S., Boucoiran, I.

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EP06.11: Recurrence of L1CAM syndrome by Dorey, M., Rypens, F., Laberge, A., Perreault, S., Spenard, E., Codsi, E., Wavrant, S.

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EP15.19: A case of prenatally diagnosed Pfeiffer syndrome by Dorey, M., Wavrant, S., Delrue, M., Rypens, F., Lapierre, C., Karalis, A., Audibert, F.

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EP07.03: A case of chondrodyplasia punctata in a lupic mother by Mathe, M., Delrue, M., Moramarco, V., Rypens, F., Wavrant, S.

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EP01.11: A case of large prenatally diagnosed arachnoid cyst by Moramarco, V., Rypens, F., Labrecque, A., Wavrant, S., Audibert, F.

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Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures by Mahmud, A.A., Nahid, N.A., Nassif, C., Sayeed, M.S.B., Ahmed, M.U., Parveen, M., Khalil, M.I., Islam, M.M., Nahar, Z., Rypens, F., Hamdan, F.F., Rouleau, G.A., Hasnat, A., Michaud, J.L.

“…Dominant mutations in PIEZO2, which codes for the principal mechanotransduction channel for proprioception and touch sensation, have been found to cause…”
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OC05.04: Phenotypical spectrum of 4 antenatal diagnosed cases of MOPD type 1 by Moramarco, V., Delrue, M., Labrecque, A., Rypens, F., Wavrant, S., Fallet‐Bianco, C.

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OP12.02: Absent nasal bone without other features of Trisomy 21 in pregnant Caucasian women: check the clavicles for cleidocranial dysplasia by Waelti, S., Delrue, M., Grignon, A., Mathe, M., Dubois, J., Rypens, F.

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EP14.39: Should we consider prenatal diagnosis of Silver–Russell syndrome? by Minsart, A., Wavrant, S., Mathe, M., Morin, L., Rypens, F., Delrue, M.

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Immediate closure of uterine wall following spontaneous rupture at 23 weeks' gestation, allowing prolongation of pregnancy by Leduc, L., Monet, B., Sansregret, A, Gauthier, R., Bourque, J., Rypens, F.

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Prenatal prognosis of congenital diaphragmatic hernia using magnetic resonance imaging measurement of fetal lung volume by Gorincour, G., Bouvenot, J., Mourot, M.G., Sonigo, P., Chaumoitre, K., Garel, C., Guibaud, L., Rypens, F., Avni, F., Cassart, M., Maugey‐Laulom, B., Bourlière‐Najean, B., Brunelle, F., Durand, C., Eurin, D.

“…Objectives To investigate the correlation between fetal lung volume (FLV), measured with magnetic resonance imaging (MRI), and postnatal mortality in newborns…”
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P19.08: Prenatally diagnosed cardiac mass: a case report by Theriault, K., Vobecky, S., Rypens, F., Raboisson, M., Abadir, S., Wavrant, S.

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P14.05: Early prenatal diagnosis of Beckwith‐Wiedemann syndrome by Zaki, D., Dal Soglio, D., Rypens, F., Audibert, F., Delrue, M., Wavrant, S.

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EP09.33: Early prenatal diagnosis of Golabi syndrome by Labrecque, A., Theriault, K., Delrue, M., Lemyre, E., Rypens, F., Wavrant, S.

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P14.07: Like mother, like daughter: maternal diagnosis of COL4A1 mutation after prenatal presentation in offspring by Theriault, K., Hudon, L., Delrue, M., Fallet‐Bianco, C., Lortie, A., Rypens, F.

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P07.11: Spontaneous uterine rupture at 23 weeks' gestation with immediate closure of the uterine wall allowed prolongation of pregnancy by Leduc, L., Monet, B., Sansregret, A., Gauthier, R., Bourque, J., Rypens, F.

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