Overview
Neelam Makhijani is a Medical Genetics provider in Little Rock, Arkansas. Her top areas of expertise are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, GM1 Gangliosidosis, Pompe Disease, and Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome).
Her clinical research consists of co-authoring 3 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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Locations
1 Childrens Way, Little Rock, AR 72202
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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Uams Sats Program
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Frequently Asked Questions about Dr. Neelam Makhijani
How do I make an appointment with Dr. Neelam Makhijani?
You can book an appointment with Dr. Neelam Makhijani by calling their office at 501-364-1874. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Neelam Makhijani a top-rated expert for 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Neelam Makhijani is classified as an Experienced expert for 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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.
What conditions does Dr. Neelam Makhijani specialize in?
While Dr. Neelam Makhijani is a Medical Genetics, they have specific expertise in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, GM1 Gangliosidosis, and Pompe Disease. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Neelam Makhijani participate in research or clinical trials?
Yes. Dr. Neelam Makhijani has published 3 articles and abstracts on conditions like 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. You can view a list of Dr. Neelam Makhijani'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
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Brachydactyly Mononen TypeDr. Makhijani isExperienced. Learn about Brachydactyly Mononen Type.
- GangliosidosisDr. Makhijani isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisDr. Makhijani isExperienced. Learn about GM1 Gangliosidosis.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Newborn Low Blood SugarDr. Makhijani isExperienced. Learn about Newborn Low Blood Sugar.