Experienced in Multiple Carboxylase Deficiency

Roula Ghaoui

SA Pathology
Adelaide, SA, AU 
Experienced in Multiple Carboxylase Deficiency
SA Pathology
Adelaide, SA, AU 
OverviewLocationsClinical Research

Overview

Roula Ghaoui practices in Adelaide, Australia. Ms. Ghaoui is rated as an Experienced expert by MediFind in the treatment of Multiple Carboxylase Deficiency. Her top areas of expertise are CHARGE Syndrome, Limb-Girdle Muscular Dystrophy, Tubular Aggregate Myopathy, and Horizontal Gaze Palsy with Progressive Scoliosis.

Her clinical research consists of co-authoring 28 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Multiple Carboxylase Deficiency.

Gender
Female

Locations

SA Pathology
Adelaide, SA, Australia
Other Locations
Sydney, NSW 2145, Australia
Westmead, NSW, Australia

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

2 Clinical Trials

A Phase 1, Open-Label, Single and Multiple Ascending Dose Study of ABC008 in Adult Patients With Inclusion Body Myositis (IBM)
A Phase 1, Open-Label, Single and Multiple Ascending Dose Study of ABC008 in Adult Patients With Inclusion Body Myositis (IBM)
Enrollment Status: Completed
Publish Date: February 20, 2025
Intervention Type: Drug
Study Drug: ABC008
Study Phase: Phase 1
A Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of 24 Weeks Treatment With REN001 in Patients With Primary Mitochondrial Myopathy
A Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of 24 Weeks Treatment With REN001 in Patients With Primary Mitochondrial Myopathy
Enrollment Status: Completed
Publish Date: May 08, 2024
Intervention Type: Drug
Study Drug: REN001
Study Phase: Phase 2
View 1 Less Clinical Trial

28 Total Publications

Long-read sequencing for diagnosis of genetic myopathies.
Long-read sequencing for diagnosis of genetic myopathies.
Journal: BMJ neurology open
Published: November 25, 2024

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

Learn more about MediFind’s expert tiers

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