Search Results - "Oligny, L L"
-
1
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis
Published in Genetics in medicine (01-07-2018)“…Fetal anomalies represent a poorly studied group of developmental disorders. Our objective was to assess the impact of whole-exome sequencing (WES) on the…”
Get full text
Journal Article -
2
OP17.07: Significance of fetal enteroliths
Published in Ultrasound in obstetrics & gynecology (01-09-2015)Get full text
Journal Article -
3
Exaggerated vasomotor response to ANG II in rats with fetal programming of hypertension associated with exposure to a low-protein diet during gestation
Published in American journal of physiology. Regulatory, integrative and comparative physiology (01-10-2006)“…The renin-angiotensin system plays a key role in the initiation and maintenance of elevated blood pressure associated with altered intrauterine milieu. The…”
Get more information
Journal Article -
4
Intrauterine growth restriction in rats is associated with hypertension and renal dysfunction in adulthood
Published in American journal of physiology: endocrinology and metabolism (01-07-2002)“…Epidemiological studies have produced evidence that unfavorable intrauterine environments during fetal life may lead to adverse outcomes in adulthood. We have…”
Get more information
Journal Article -
5
Sudden death in growth hormone–treated children with Prader-Willi syndrome
Published in The Journal of pediatrics (01-01-2004)“…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…”
Get full text
Journal Article -
6
High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastoma
Published in Histopathology (01-04-2010)“…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 &…”
Get full text
Journal Article -
7
Cardiac pathology in sudden unexpected infant death
Published in The Journal of pediatrics (01-09-2002)“…Objectives: To determine the spectrum of cardiac pathology and circumstances of death in infants with sudden unexpected death and to define the impact of…”
Get full text
Journal Article -
8
Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies
Published in The Journal of pediatrics (01-10-2000)“…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…”
Get full text
Journal Article -
9
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype
Published in Human genetics (01-12-2019)“…Haploinsufficiency of FOXF1 causes alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV), a lethal neonatal lung developmental disorder…”
Get full text
Journal Article -
10
Workload Measurement in Subspecialty Placental Pathology in Canada
Published in Pediatric and developmental pathology (01-11-2022)“…Background Workload measurement is important to help determine optimal staffing and workload distribution for pathology laboratories. The Level 4 Equivalent…”
Get full text
Journal Article -
11
Human papillomavirus (HPV) study of 691 pathological specimens from Quebec by PCR-direct sequencing approach
Published in Journal of medical virology (01-04-2001)“…Human papillomaviruses (HPV) are etiological agents of cervical cancer. In order to address clinical demand for HPV detection and sequence typing, mostly in…”
Get full text
Journal Article -
12
Unilobar congenital pulmonary lymphangiectasis mimicking congenital lobar emphysema: an underestimated presentation?
Published in Journal of pediatric surgery (01-05-2004)“…Congenital lobar emphysema (CLE) is characterized by unilobar alveolar distension secondary to bronchomalacia or absent cartilage. In contrast, congenital…”
Get full text
Journal Article -
13
Childhood adrenocortical tumors: Case series and reevaluation of prognosis—A 24-year experience
Published in Journal of pediatric surgery (01-06-1997)“…Adrenocortical neoplasms are rare in childhood and adolescence. The prognostic significance of tumor size, weight, and histological grade are still very much…”
Get full text
Journal Article Conference Proceeding -
14
Intrahepatic Biliary Cysts Presenting before Hepatic Portoenterostomy in Biliary Atresia
Published in Journal of pediatric gastroenterology and nutrition (01-04-2006)Get full text
Journal Article -
15
Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study
Published in American journal of clinical pathology (01-07-2014)“…To study and compare the effectiveness of p16(INK4a) staining and specific human papillomavirus (HPV) subtypes as a prognostic marker in cervical…”
Get full text
Journal Article -
16
Pediatric adrenocortical tumors: molecular events leading to insulin-like growth factor II gene overexpression
Published in The journal of clinical endocrinology and metabolism (01-05-2000)“…It has been previously shown that adrenocortical tumors (ACT) in adults exhibit structural abnormalities in tumor DNA in approximately 30% of cases. These…”
Get full text
Journal Article -
17
Basal cells of second trimester fetal breasts: immunohistochemical study of myoepithelial precursors
Published in Pediatric and developmental pathology (01-09-2003)“…The molecular characterization of human mammary myoepithelial cells is incomplete, hindering our understanding of its importance in breast physiology and…”
Get full text
Journal Article -
18
Human papillomavirus PCR direct sequencing study of cervical precancerous lesions in Quebec children
Published in Sexually transmitted infections (01-10-2001)“…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…”
Get full text
Journal Article -
19
Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with a de Novo Heterozygous Mutation in the TITF1/NKX2.1 Gene
Published in The journal of clinical endocrinology and metabolism (01-01-2009)“…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…”
Get full text
Journal Article -
20
Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis
Published in Obstetrical & gynecological survey (01-12-2018)“…(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…”
Get full text
Journal Article