Overview
Tina Cowan is a Medical Genetics provider practicing medicine in Palo Alto, California.
Dr. Cowan is highly rated in 5 conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Biotinidase Deficiency, Urea Cycle Disorders (UCD), and Homocystinuria.
She is actively involved in clinical research, co-authoring 51 peer reviewed articles.
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Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.
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Frequently Asked Questions about Dr. Tina M. Cowan
How do I make an appointment with Dr. Tina M. Cowan?
You can book an appointment with Dr. Tina M. Cowan by calling their office at 650-724-7858. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Tina M. Cowan a top-rated expert for Methylmalonic Acidemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Tina M. Cowan is classified as an Distinguished expert for Methylmalonic Acidemia, 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.
What conditions does Dr. Tina M. Cowan specialize in?
While Dr. Tina M. Cowan is a Medical Genetics, they have specific expertise in Methylmalonic Acidemia, Biotinidase Deficiency, and Urea Cycle Disorders (UCD). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Tina M. Cowan participate in research or clinical trials?
Yes. Dr. Tina M. Cowan has published 50 articles and abstracts on conditions like Methylmalonic Acidemia. You can view a list of Dr. Tina M. Cowan'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
- Distinguished
- Methylmalonic AcidemiaDr. Cowan isDistinguished. Learn about Methylmalonic Acidemia.
- Advanced
- Biotinidase DeficiencyDr. Cowan isAdvanced. Learn about Biotinidase Deficiency.
- HomocystinuriaDr. Cowan isAdvanced. Learn about Homocystinuria.
- Urea Cycle Disorders (UCD)Dr. Cowan isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Adrenoleukodystrophy (ALD)Dr. Cowan isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Isovaleric AcidemiaDr. Cowan isExperienced. Learn about Isovaleric Acidemia.
- Maple Syrup Urine DiseaseDr. Cowan isExperienced. Learn about Maple Syrup Urine Disease.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Ornithine Transcarbamylase DeficiencyDr. Cowan isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Zellweger SyndromeDr. Cowan isExperienced. Learn about Zellweger Syndrome.