C Anthony Rupar - Department of Biochemistry, University of Western Ontario

基本信息

浏览量：9

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 124 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report

Montaha Almudhry,Chitra Prasad,C. Anthony Rupar,Keng Yeow Tay,Asuri N. Prasad

FRONTIERS IN NEUROLOGY (2024): 1204848-1204848

引用0浏览0WOS引用

Inherited Pediatric Neurotransmitter Disorders: Case Studies and Long-Term Outcomes

Shyann Hang,Chitra Prasad,C. Anthony Rupar, Richa Agnihotri,Asuri N. Prasad

JOURNAL OF PEDIATRIC NEUROLOGYno. 04 (2024): 261-276

引用0浏览0引用

Longitudinal Biomarker Evaluation in Fabry Disease Patients Receiving Lentivirus-Mediated Gene Therapy

Christiane Auray‐Blais,Paméla Lavoie,Tristan Martineau,C. Anthony Rupar,Dwayne L. Barber,Armand Keating, Ronan Foley,Aneal Khan,Michael West, Jeffrey A. Medin

Rare disease and orphan drugs journalno. 3 (2024)

引用0浏览0引用

Methylmalonic Aciduria As a Biochemical Marker for Mitochondrial DNA Depletion Syndrome in Patients with Developmental Delay and Movement Disorders: a Case Series

Montaha Almudhry,Arushi Gahlot Saini,Mohammed A. Al-Omari, Yashu Sharma,Maryam Nabavi Nouri,C. Anthony Rupar,Chitra Prasad,Andrea C. Yu,Savita Verma Attri,Asuri Narayan Prasad

Frontiers in neurology (2023)

引用0浏览0WOS引用

Dual Diagnosis of Trisomy 21 and Lethal Perinatal Gaucher Disease As a Cause of Non-Immune Hydrops Fetalis in a Twin Pregnancy for a Consanguineous Couple

Talib Al Harthy,Samantha Colaiacovo,Robert J. Gratton,Kevin Coughlin,Victoria Mok Siu,Chitra Prasad,Charles Rupar,Maha Saleh

Clinical case reportsno. 8 (2023): e7827-e7827

引用0浏览0WOS引用

A Milder Form of Molybdenum Cofactor Deficiency Type A Presenting As Leigh's Syndrome-Like Phenotype Highlighting the Secondary Mitochondrial Dysfunction: a Case Report

Montaha Almudhry,Asuri N. Prasad,C. Anthony Rupar,Keng Yeow Tay,Suzanne Ratko,Mary E. Jenkins,Chitra Prasad

Frontiers in neurology (2023)

引用0浏览0WOS引用

Pitfalls in Genetic Testing for Consanguineous Pediatric Populations

Maha Saleh,Samantha Colaiacovo,Melanie P Napier,Asuri N Prasad,C Anthony Rupar,Chitra Prasad

Case reports in genetics（2022）

引用0浏览0WOS引用

Clinical Conundrum: Polyhydramnios As a Marker for a Fetal Genetic Syndrome in the Canadian Old Order Mennonite Population

Janine Hutson,Victoria Mok Siu,C. Anthony Rupar

Journal of Obstetrics and Gynaecology Canada（2022）

引用2浏览0WOS引用

Autologous, Lentivirus‐modified, T‐rapa Cell “micropharmacies” for Lysosomal Storage Disorders

Murtaza S. Nagree,Tania C. Felizardo,Mary L. Faber,Jitka Rybova,C. Anthony Rupar,S. Ronan Foley,Maria Fuller,Daniel H. Fowler,Jeffrey A. Medin

EMBO molecular medicine（2022）

引用5浏览0WOS引用

672 Carbonic Anhydrase (CA-VA) Deficiency: an under Recognized Cause of Neonatal Hyperammonemia with Excellent Outcome on Proactive Management

Judy Ibrahim,Suzanne Ratko,Melanie Napier,Natalya Karp,C Anthony Rupar,Chitra Prasad

British Inherited Metabolic Disease Group (2022)

引用0浏览0引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn