Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Munier Nour"'
Autor:
Yuwen Zheng, Mahdi Rostami Haji Abadi, Jonathan Gough, James J. D. Johnston, Munier Nour, Saija Kontulainen
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
AimsHigher prevalence of overweight and obesity in children and adolescents with type 1 diabetes (T1D) suggests alterations are required in body composition. However, differences in body composition between children with T1D and typically developing
Externí odkaz:
https://doaj.org/article/8571a544f79b4357a69b77e82723d77e
Autor:
Celia Rodd, Arati Mokashi, Glenville Jones, Maury Pinsk, R. Todd Alexander, Caroline Zuijdwijk, Indra R. Gupta, Karlpiet Schlingmann, Munier Nour, Isabelle Rousseau-Nepton, Karine Khatchadourian, Martin Kaufmann, Danièle Pacaud
Publikováno v:
Hormone Research in Paediatrics. 94:124-132
Objectives: Biallelic pathogenic variants in CYPA24A1 and SLC34A1 are causes of idiopathic infantile hypercalcemia. Pathogenic variants in both may also give rise to hypercalciuria with nephrocalcinosis or nephrolithiasis without previous hypercalcem
Autor:
Yuwen Zheng, Mahdi Rostami Haji Abadi, Zahra Ghafouri, Suelen Meira Goes, James (J.D.) Johnston, Munier Nour, Saija Kontulainen
Publikováno v:
Bone. 163
Deficits in bone mineral and weaker bone structure in children with type 1 diabetes (T1D) may contribute to a lifelong risk of fracture. However, there is no meta-analysis comparing bone properties beyond density between children with T1D and typical
Publikováno v:
Canadian Journal of Diabetes. 45:S25-S26
Autor:
Julie Ho, Allison Dart, Brandy Wicklow, B. Dufault, Stasia Hadjiyannakis, Teresa E. Pinto, Constadina Panagiotopoulos, Elizabeth Sellers, Jill Hamilton, Jon Mcgavock, S. Samuel, Mary M. Jetha, Melissa Gabbs, M.C. Samaan, Munier Nour
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp S208-(2021)
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 20, Iss 1, Pp 1-6 (2020)
BMC Pediatrics, Vol 20, Iss 1, Pp 1-6 (2020)
Background Primary hyperparathyroidism may present in a myriad of manners, varying from an incidental asymptomatic biochemical finding to gastrointestinal, psychiatric, renal, and bone manifestations. While hyperparathyroidism remains a rare diagnosi
Autor:
Stasia Hadjiyannakis, Jill Hamilton, Aysha Ayub, Michael A. Irvine, Mélanie Henderson, Shazhan Amed, Elizabeth Sellers, Munier Nour, Teresa E. Pinto, Brandy Wicklow, Trisha J. Patel
Publikováno v:
Diabetes. 69
Objectives: There is limited data on MID in children. This study aimed to compare the demographic and clinical characteristics of 1) a historical MID cohort to a new cohort and 2) children with MID based on overweight/obese BMI (O-BMI) and normal wei
Publikováno v:
Practical Diabetes. 39:12
Autor:
Mark Inman, Munier Nour
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 31:235-238
Background: Insulin-mediated pseudoacromegaly is a rarely described pediatric phenotype. We present two patients displaying excessive growth associated with marked acanthosis nigricans, hyperinsulinemia and metabolic dysregulation. Case presentation:
Autor:
Chantelle L. Baril, Ayisha Kurji, Adam D.G. Baxter-Jones, Munier Nour, Marta C Erlandson, Saija A. Kontulainen
Publikováno v:
Bone Abstracts.