Overview
Matthew Freeman is a Neurologist in College Station, Texas. Dr. Freeman and is rated as an Advanced provider by MediFind in the treatment of Hyperglycerolemia. His top areas of expertise are Seizures, Memory Loss, Lactate Dehydrogenase Deficiency, and Hyperglycerolemia. Dr. Freeman is currently accepting new patients.
His clinical research consists of co-authoring 49 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- FirstCare
- Scott and White Health
- Humana
Locations
700 Scott And White Dr, College Station, TX 77845
5251 W Hwy 290, Baylor Scott And White Clinic Austin Oak, Austin, TX 78735
1605 S 31st St, Baylor Scott And White Center For Dia, Temple, TX 76508
2401 S 31st St, Temple, TX 76508
425 University Blvd, Round Rock, TX 78665
100 Medical Pkwy, Lakeway, TX 78738
810 W U Ave, Temple, TX 76508
2600 E Pflugerville Pkwy, Pflugerville, TX 78660
1701 E Pflugerville Pkwy, Pflugerville, TX 78660
810 W Hwy 71, Marble Falls, TX 78654
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.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Memory Loss
- Seizures
- Advanced
- Cerebellar Degeneration
- Essential Pentosuria
- Hyperglycerolemia
- Lactate Dehydrogenase Deficiency
- Renal Glycosuria
- Transient Global Amnesia
- Experienced
- Athetosis
- Autosomal Dominant Partial Epilepsy with Auditory Features
- Axillary Nerve Dysfunction
- Benign Rolandic Epilepsy
- CAPOS Syndrome
- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy