Philip D. Acott
5850/5980 University Ave, PO Box 9700
Halifax, NS B3K6R8, Canada
Halifax, NS B3K6R8, Canada
Last Updated: 09/26/2026
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Found 13 publications
Systemic hypertension in very preterm infants: a population-based study.
Journal: European journal of pediatrics
Published: March 09, 2026
Vomiting, hypotonia and failure to thrive in a 12-month-old female.
Journal: Paediatrics & child health
Published: January 29, 2025
Increased intracranial pressure in a patient with Congenital Heart Defect and Ectodermal Dysplasia (CHDED): Extension of phenotype and review of literature.
Journal: American journal of medical genetics. Part A
Published: May 02, 2022
Oral Losartan After Limited Mandibulectomy for Treatment of Desmoid-Type Fibromatosis.
Journal: Ear, nose, & throat journal
Published: January 25, 2021
Management of Pediatric Kidney Transplant Patients During the COVID-19 Pandemic: Guidance From the Canadian Society of Transplantation Pediatric Group.
Journal: Canadian journal of kidney health and disease
Published: September 24, 2020
Canadian Society of Nephrology Commentary on the Kidney Disease Improving Global Outcomes 2017 Clinical Practice Guideline Update for the Diagnosis, Evaluation, Prevention, and Treatment of Chronic Kidney Disease-Mineral and Bone Disorder.
Journal: Canadian journal of kidney health and disease
Published: May 25, 2020
Pkd1-targeted mutation reveals a role for the Wolffian duct in autosomal dominant polycystic kidney disease.
Journal: Journal of developmental origins of health and disease
Published: August 16, 2019
Radiology and Pathology in a Child With Calcification and Simplified Gyration.
Journal: Pediatric neurology
Published: July 27, 2017
Hypogonadotropic Hypogonadism in Males with Glycogen Storage Disease Type 1.
Journal: JIMD reports
Published: August 30, 2016
Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6.
Journal: Human molecular genetics
Published: May 19, 2016
A novel rearrangement of occludin causes brain calcification and renal dysfunction.
Journal: Human genetics
Published: April 09, 2013
Last Updated: 09/26/2026