Search Results - "Oligny, L."

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis by Boissel, Sarah, Fallet-Bianco, Catherine, Chitayat, David, Kremer, Valérie, Nassif, Christina, Rypens, Françoise, Delrue, Marie-Ange, Dal Soglio, Dorothée, Oligny, Luc L., Patey, Natalie, Flori, Elisabeth, Cloutier, Mireille, Dyment, David, Campeau, Philippe, Karalis, Aspasia, Nizard, Sonia, Fraser, William D., Audibert, François, Lemyre, Emmanuelle, Rouleau, Guy A., Hamdan, Fadi F., Kibar, Zoha, Michaud, Jacques L.

“…Fetal anomalies represent a poorly studied group of developmental disorders. Our objective was to assess the impact of whole-exome sequencing (WES) on the…”
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OP17.07: Significance of fetal enteroliths by Rypens, F., Lapierre, C., Grignon, A., Wavrant, S., Delrue, M., Aspirot, A., Oligny, L., Garel, L.

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Exaggerated vasomotor response to ANG II in rats with fetal programming of hypertension associated with exposure to a low-protein diet during gestation by Yzydorczyk, C, Gobeil, Jr, F, Cambonie, G, Lahaie, I, Lê, N L O, Samarani, S, Ahmad, A, Lavoie, J C, Oligny, L L, Pladys, P, Hardy, P, Nuyt, A M

“…The renin-angiotensin system plays a key role in the initiation and maintenance of elevated blood pressure associated with altered intrauterine milieu. The…”
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Intrauterine growth restriction in rats is associated with hypertension and renal dysfunction in adulthood by Battista, Marie-Claude, Oligny, Luc L, St-Louis, Jean, Brochu, Michèle

“…Epidemiological studies have produced evidence that unfavorable intrauterine environments during fetal life may lead to adverse outcomes in adulthood. We have…”
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Sudden death in growth hormone–treated children with Prader-Willi syndrome by Vliet, Guy Van, Deal, Cheri L., Crock, Patricia A., Robitaille, Yves, Oligny, Luc L.

“…A 4-year-old boy with Prader-Willi syndrome died suddenly while asleep on day 67 of growth hormone treatment. During treatment, snoring had worsened. Autopsy…”
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High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastoma by Sartelet, Hervé, Ohta, Shigeru, Barrette, Stephane, Rougemont, Anne-Laure, Brevet, Marie, Regairaz, Marie, Harvey, Isabelle, Bernard, Chantal, Fabre, Monique, Gaboury, Louis, Oligny, Luc L, Bosq, Jacques, Valteau-Couanet, Dominique, Vassal, Gilles

“…Sartelet H, Ohta S, Barrette S, Rougemont A‐Laure, Brevet M, Regairaz M, Harvey I, Bernard C, Fabre M, Gaboury L, Oligny L L, Bosq J, Valteau‐Couanet D &…”
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Cardiac pathology in sudden unexpected infant death by Dancea, Adrian, Côté, Aurore, Rohlicek, Charles, Bernard, Chantal, Oligny, Luc L.

“…Objectives: To determine the spectrum of cardiac pathology and circumstances of death in infants with sudden unexpected death and to define the impact of…”
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Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies by Mircescu, Hortensia, Parma, Jasmine, Huot, Céline, Deal, Cheri, Oligny, Luc L., Vassart, Gilbert, Van Vliet, Guy

“…We identified a papillary carcinoma in an 11-year-old girl with a hyperfunctioning thyroid nodule. A met453thr mutation in TSHR was found in the nodule but not…”
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Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype by Szafranski, Przemyslaw, Liu, Qian, Karolak, Justyna A., Song, Xiaofei, de Leeuw, Nicole, Faas, Brigitte, Gerychova, Romana, Janku, Petr, Jezova, Marta, Valaskova, Iveta, Gibbs, Kathleen A., Surrey, Lea F., Poisson, Virginie, Bérubé, Denis, Oligny, Luc L., Michaud, Jacques L., Popek, Edwina, Stankiewicz, Paweł

“…Haploinsufficiency of FOXF1 causes alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV), a lethal neonatal lung developmental disorder…”
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Workload Measurement in Subspecialty Placental Pathology in Canada by Wright, James R., Chan, Suzanne, Morgen, Eric K., Maung, Raymond T. A., Brundler, Marie-Anne, El Demellawy, Dina, Fraser, Robert B., Kurek, Kyle C., Magee, Fergall, Nizalik, Elizabeth, Oligny, Luc L., Somers, Gino R., Stefanovici, Camelia, Terry, Jefferson

“…Background Workload measurement is important to help determine optimal staffing and workload distribution for pathology laboratories. The Level 4 Equivalent…”
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Human papillomavirus (HPV) study of 691 pathological specimens from Quebec by PCR-direct sequencing approach by Feoli-Fonseca, Juan Carlos, Oligny, Luc L., Brochu, Pierre, Simard, Pierre, Falconi, Sarah, Yotov, Wagner V.

“…Human papillomaviruses (HPV) are etiological agents of cervical cancer. In order to address clinical demand for HPV detection and sequence typing, mostly in…”
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Unilobar congenital pulmonary lymphangiectasis mimicking congenital lobar emphysema: an underestimated presentation? by Chapdelaine, Joyaube, Beaunoyer, Mona, St-Vil, Dickens, Oligny, Luc L., Garel, Laurent, Bütter, Andreana, Di Lorenzo, Maria

“…Congenital lobar emphysema (CLE) is characterized by unilobar alveolar distension secondary to bronchomalacia or absent cartilage. In contrast, congenital…”
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Childhood adrenocortical tumors: Case series and reevaluation of prognosis—A 24-year experience by Mayer, S.K, Oligny, L.L, Deal, C, Yazbeck, S, Gagné, N, Blanchard, H

“…Adrenocortical neoplasms are rare in childhood and adolescence. The prognostic significance of tumor size, weight, and histological grade are still very much…”
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Intrahepatic Biliary Cysts Presenting before Hepatic Portoenterostomy in Biliary Atresia by Mas, Emmanuel, Alvarez, Fernando, Oligny, Luc L., Martin, Steven

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Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study by Razmpoosh, Maryam, Sansregret, Andrée, Oligny, Luc L, Patey, Natalie, Dormoy-Raclet, Virginie, Ducruet, Thierry, Bouron-Dal Soglio, Dorothée

“…To study and compare the effectiveness of p16(INK4a) staining and specific human papillomavirus (HPV) subtypes as a prognostic marker in cervical…”
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Pediatric adrenocortical tumors: molecular events leading to insulin-like growth factor II gene overexpression by Wilkin, F, Gagné, N, Paquette, J, Oligny, L L, Deal, C

“…It has been previously shown that adrenocortical tumors (ACT) in adults exhibit structural abnormalities in tumor DNA in approximately 30% of cases. These…”
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Basal cells of second trimester fetal breasts: immunohistochemical study of myoepithelial precursors by Jolicoeur, Francine, Gaboury, Louis A, Oligny, Luc L

“…The molecular characterization of human mammary myoepithelial cells is incomplete, hindering our understanding of its importance in breast physiology and…”
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Human papillomavirus PCR direct sequencing study of cervical precancerous lesions in Quebec children by Oligny, Luc L, Feoli-Fonseca, Juan Carlos, Brochu, Pierre, Simard, Pierre, Falconi, Sarah, Yotov, Wagner V

“…In the group of cervical biopsies from adolescent girls with CIN (n = 36, age 14-17), as well as in the larger control group of adult women (n = 487, age…”
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Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with a de Novo Heterozygous Mutation in the TITF1/NKX2.1 Gene by Maquet, Emilie, Costagliola, Sabine, Parma, Jasmine, Christophe-Hobertus, Christiane, Oligny, Luc L., Fournet, Jean-Christophe, Robitaille, Yves, Vuissoz, Jean-Marc, Payot, Antoine, Laberge, Sophie, Vassart, Gilbert, Van Vliet, Guy, Deladoëy, Johnny

“…Context: Thyroid transcription factor 1 (TITF1/NKX2.1) is expressed in the thyroid, lung, ventral forebrain, and pituitary. In the lung, TITF1/NKX2.1 activates…”
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Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis by Boissel, Sarah, Fallet-Bianco, Catherine, Chitayat, David, Kremer, Valérie, Nassif, Christina, Rypens, Françoise, Delrue, Marie-Ange, Soglio, Dorothée Dal, Oligny, Luc L, Patey, Natalie, Flori, Elisabeth, Cloutier, Mireille, Dyment, David, Campeau, Philippe, Karalis, Aspasia, Nizard, Sonia, Fraser, William D, Audibert, François, Lemyre, Emmanuelle, Rouleau, Guy A, Hamdan, Fadi F, Kibar, Zoha, Michaud, Jacques L

“…(Abstracted from Genet Med 2018;20(7):745–753)Birth defects are a leading cause of mortality and mortality in infants and children. The etiology of birth…”
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