Overview
Brian Kirmse is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Birmingham, Alabama.
Dr. Kirmse is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Pyruvate Carboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, PEPCK 1 Deficiency, and Autosomal Recessive Congenital Methemoglobinemia.
He is actively involved in clinical research, co-authoring 43 peer reviewed articles. Dr. Kirmse is currently accepting new patients.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- INSURANCE PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
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. 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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UAB Women And Infants Center
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Frequently Asked Questions about Dr. Brian M. Kirmse
How do I make an appointment with Dr. Brian M. Kirmse?
You can book an appointment with Dr. Brian M. Kirmse by calling their office at 205-934-9999. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Brian M. Kirmse a top-rated expert for Pyruvate Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Brian M. Kirmse is classified as an Advanced expert for Pyruvate Carboxylase 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. Brian M. Kirmse specialize in?
While Dr. Brian M. Kirmse is a Medical Genetics, they have specific expertise in Pyruvate Carboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, and PEPCK 1 Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Brian M. Kirmse participate in research or clinical trials?
Yes. Dr. Brian M. Kirmse has published 43 articles and abstracts on conditions like Pyruvate Carboxylase Deficiency. You can view a list of Dr. Brian M. Kirmse's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Brian M. Kirmse accept my insurance?
Dr. Brian M. Kirmse accepts most major insurance plans, including Blue Cross Blue Shield and Cigna. We recommend calling the office directly at 205-934-9999 to verify that your specific plan is currently accepted before your visit.
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
- Advanced
- Autosomal Recessive Congenital Methemoglobinemia
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- PEPCK 1 DeficiencyDr. Kirmse isAdvanced. Learn about PEPCK 1 Deficiency.
- Pyruvate Carboxylase DeficiencyDr. Kirmse isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Pyruvate Decarboxylase DeficiencyDr. Kirmse isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Kirmse isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Experienced
- Alpha MannosidosisDr. Kirmse isExperienced. Learn about Alpha Mannosidosis.
- Argininosuccinic AciduriaDr. Kirmse isExperienced. Learn about Argininosuccinic Aciduria.
- AspartylglucosaminuriaDr. Kirmse isExperienced. Learn about Aspartylglucosaminuria.
- Beta-MannosidosisDr. Kirmse isExperienced. Learn about Beta-Mannosidosis.
- Biotinidase DeficiencyDr. Kirmse isExperienced. Learn about Biotinidase Deficiency.
- FucosidosisDr. Kirmse isExperienced. Learn about Fucosidosis.
- Gaucher Disease Type 1Dr. Kirmse isExperienced. Learn about Gaucher Disease Type 1.
- Giardia InfectionDr. Kirmse isExperienced. Learn about Giardia Infection.
- HIV/AIDSDr. Kirmse isExperienced. Learn about HIV/AIDS.
- HypotoniaDr. Kirmse isExperienced. Learn about Hypotonia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaDr. Kirmse isExperienced. Learn about Methylmalonic Acidemia.
- Multiple Sulfatase DeficiencyDr. Kirmse isExperienced. Learn about Multiple Sulfatase Deficiency.
- Schindler DiseaseDr. Kirmse isExperienced. Learn about Schindler Disease.
- SialidosisDr. Kirmse isExperienced. Learn about Sialidosis.
- ToxocariasisDr. Kirmse isExperienced. Learn about Toxocariasis.
- Von Gierke DiseaseDr. Kirmse isExperienced. Learn about Von Gierke Disease.