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N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Fallet-Bianco C, De Bie I, Désilets V, Oligny LL.
PMID: 30390950
J Obstet Gynaecol Can. 2018 Oct;40(10):1367-1377.e6. doi: 10.1016/j.jogc.2018.08.006.

OBJECTIF: Examiner les données sur les autopsies fœtales et périnatales, le processus de consentement et les options de collecte de renseignements à la suite d'un diagnostic prénatal d'anomalies non chromosomiques afin d'aider les fournisseurs de soins à offrir du...

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Fallet-Bianco C, De Bie I, Désilets V, et al. N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale. J Obstet Gynaecol Can. 2018;40(10):1367-1377.e6doi: 10.1016/j.jogc.2018.08.006.
Fallet-Bianco, C., De Bie, I., Désilets, V., & Oligny, L. L. (2018). N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC, 40(10), 1367-1377.e6. https://doi.org/10.1016/j.jogc.2018.08.006
Fallet-Bianco, Catherine, et al. "N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale." Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC vol. 40,10 (2018): 1367-1377.e6. doi: https://doi.org/10.1016/j.jogc.2018.08.006
Fallet-Bianco C, De Bie I, Désilets V, Oligny LL. N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale. J Obstet Gynaecol Can. 2018 Oct;40(10):1367-1377.e6. doi: 10.1016/j.jogc.2018.08.006. PMID: 30390950.
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Impact of PAC Fines in Fouling of Polymeric and Ceramic Low-Pressure Membranes for Drinking Water Treatment.

Membranes

Oligny L, Bérubé PR, Barbeau B.
PMID: 27399788
Membranes (Basel). 2016 Jul 07;6(3). doi: 10.3390/membranes6030038.

This study assessed the issue of membrane fouling in a Hybrid Membrane Process (HMP) due to the export of powdered activated carbon (PAC) fines from a pretreatment contactor. Two parallel pilot-scale ceramic and polymeric membranes were studied. Reversible and...

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Oligny L, Bérubé PR, Barbeau B. Impact of PAC Fines in Fouling of Polymeric and Ceramic Low-Pressure Membranes for Drinking Water Treatment. Membranes (Basel). 2016;6(3)doi: 10.3390/membranes6030038.
Oligny, L., Bérubé, P. R., & Barbeau, B. (2016). Impact of PAC Fines in Fouling of Polymeric and Ceramic Low-Pressure Membranes for Drinking Water Treatment. Membranes, 6(3), . https://doi.org/10.3390/membranes6030038
Oligny, Laurent, et al. "Impact of PAC Fines in Fouling of Polymeric and Ceramic Low-Pressure Membranes for Drinking Water Treatment." Membranes vol. 6,3 (2016). doi: https://doi.org/10.3390/membranes6030038
Oligny L, Bérubé PR, Barbeau B. Impact of PAC Fines in Fouling of Polymeric and Ceramic Low-Pressure Membranes for Drinking Water Treatment. Membranes (Basel). 2016 Jul 07;6(3). doi: 10.3390/membranes6030038. PMID: 27399788; PMCID: PMC5041029.
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Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping.

Clinical case reports

Carmant L, Karalis A, Rypens F, Oligny L, Wavrant S, Lapeyraque AL, Codsi E.
PMID: 33768790
Clin Case Rep. 2021 Jan 12;9(3):1101-1103. doi: 10.1002/ccr3.3663. eCollection 2021 Mar.

We know that glutaric aciduria type II is an inborn metabolism. This case report highlights that polycystic kidneys with hepatomegaly in prenatal ultrasound are suggestive of glutaric aciduria type II and it identifies a new variant as pathogenic.

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Carmant L, Karalis A, Rypens F, et al. Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping. Clin Case Rep. 2021;9(3):1101-1103doi: 10.1002/ccr3.3663.
Carmant, L., Karalis, A., Rypens, F., Oligny, L., Wavrant, S., Lapeyraque, A. L., & Codsi, E. (2021). Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping. Clinical case reports, 9(3), 1101-1103. https://doi.org/10.1002/ccr3.3663
Carmant, Laurence, et al. "Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping." Clinical case reports vol. 9,3 (2021): 1101-1103. doi: https://doi.org/10.1002/ccr3.3663
Carmant L, Karalis A, Rypens F, Oligny L, Wavrant S, Lapeyraque AL, Codsi E. Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping. Clin Case Rep. 2021 Jan 12;9(3):1101-1103. doi: 10.1002/ccr3.3663. eCollection 2021 Mar. PMID: 33768790; PMCID: PMC7981664.
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Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13.

Journal of pediatric intensive care

Nardi N, Proulx F, Brunel-Guiton C, Oligny LL, Piché N, Mitchell GA, Joyal JS.
PMID: 31984159
J Pediatr Intensive Care. 2020 Mar;9(1):54-59. doi: 10.1055/s-0039-1697620. Epub 2019 Oct 10.

Necrotizing enterocolitis (NEC) is exceptional after the neonatal period. A toddler with encephalopathy, mitochondrial myopathy, and hypertrophic cardiomyopathy developed fatal NEC and multiple organ dysfunction within 48 hours of the introduction of enteral feeding. She was subsequently found to...

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Nardi N, Proulx F, Brunel-Guiton C, et al. Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13. J Pediatr Intensive Care. 2019;9(1):54-59doi: 10.1055/s-0039-1697620.
Nardi, N., Proulx, F., Brunel-Guiton, C., Oligny, L. L., Piché, N., Mitchell, G. A., & Joyal, J. S. (2020). Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13. Journal of pediatric intensive care, 9(1), 54-59. https://doi.org/10.1055/s-0039-1697620
Nardi, Nicolas, et al. "Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13." Journal of pediatric intensive care vol. 9,1 (2020): 54-59. doi: https://doi.org/10.1055/s-0039-1697620
Nardi N, Proulx F, Brunel-Guiton C, Oligny LL, Piché N, Mitchell GA, Joyal JS. Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13. J Pediatr Intensive Care. 2020 Mar;9(1):54-59. doi: 10.1055/s-0039-1697620. Epub 2019 Oct 10. PMID: 31984159; PMCID: PMC6978174.
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Showing 1 to 4 of 4 entries