Overview
Ian Alexander practices practicing medicine in Westmead, Australia.
Mr. Alexander is highly rated in 4 conditions, according to our data. His clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), X-Linked Severe Combined Immunodeficiency, Orotic Aciduria Type 1, and Liver Transplant.
He is actively involved in clinical research, co-authoring 105 peer reviewed articles.
Gender
Locations
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.
Frequently Asked Questions about Ian E. Alexander
Is Ian E. Alexander a top-rated expert for Ornithine Transcarbamylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Ian E. Alexander is classified as an Elite expert for Ornithine Transcarbamylase Deficiency, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Ian E. Alexander participate in research or clinical trials?
Yes. Ian E. Alexander has published 105 articles and abstracts on conditions like Ornithine Transcarbamylase Deficiency. You can view a list of Ian E. Alexander's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Elite
- Ornithine Transcarbamylase Deficiency
- Distinguished
- Urea Cycle Disorders (UCD)Mr. Alexander isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Orotic Aciduria Type 1Mr. Alexander isAdvanced. Learn about Orotic Aciduria Type 1.
- X-Linked Severe Combined Immunodeficiency
- Experienced
- Addison's DiseaseMr. Alexander isExperienced. Learn about Addison's Disease.
- Adrenal Insufficiency PediatricMr. Alexander isExperienced. Learn about Adrenal Insufficiency Pediatric.
- Argininosuccinic AciduriaMr. Alexander isExperienced. Learn about Argininosuccinic Aciduria.
- Blood ClotsMr. Alexander isExperienced. Learn about Blood Clots.
- CholestasisMr. Alexander isExperienced. Learn about Cholestasis.
- Congenital Adrenal Hyperplasia (CAH)Mr. Alexander isExperienced. Learn about Congenital Adrenal Hyperplasia (CAH).
- GlomerulonephritisMr. Alexander isExperienced. Learn about Glomerulonephritis.
- Glycogen Storage Disease Type 5Mr. Alexander isExperienced. Learn about Glycogen Storage Disease Type 5.
- Heart BlockMr. Alexander isExperienced. Learn about Heart Block.
- Hemophilia AMr. Alexander isExperienced. Learn about Hemophilia A.
- Hemophilia BMr. Alexander isExperienced. Learn about Hemophilia B.
- Homozygous Familial Hypercholesterolemia (HoFH)
- IntersexMr. Alexander isExperienced. Learn about Intersex.
- Liver CancerMr. Alexander isExperienced. Learn about Liver Cancer.
- Liver TransplantMr. Alexander isExperienced. Learn about Liver Transplant.
- Muscle AtrophyMr. Alexander isExperienced. Learn about Muscle Atrophy.
- Myoglobinuria RecurrentMr. Alexander isExperienced. Learn about Myoglobinuria Recurrent.
- NeurofibromatosisMr. Alexander isExperienced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)Mr. Alexander isExperienced. Learn about Neurofibromatosis Type 1 (NF1).
- Phenylketonuria (PKU)Mr. Alexander isExperienced. Learn about Phenylketonuria (PKU).
- Primary Lateral SclerosisMr. Alexander isExperienced. Learn about Primary Lateral Sclerosis.
- Progressive Familial Intrahepatic Cholestasis Type 1
- Progressive Familial Intrahepatic Cholestasis Type 2
- Progressive Familial Intrahepatic Cholestasis Type 3
- Properdin DeficiencyMr. Alexander isExperienced. Learn about Properdin Deficiency.
- Severe Combined Immunodeficiency (SCID)Mr. Alexander isExperienced. Learn about Severe Combined Immunodeficiency (SCID).
- Spinal Muscular Atrophy (SMA)Mr. Alexander isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinal Muscular Atrophy Type 2Mr. Alexander isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Mr. Alexander isExperienced. Learn about Spinal Muscular Atrophy Type 3.