Overview
Brian Kirmse is a Medical Genetics specialist and a Pediatrics provider in Birmingham, Alabama. Dr. Kirmse is rated as an Experienced provider by MediFind in the treatment of Gaucher Disease Type 1. His top areas of expertise are Pyruvate Carboxylase Deficiency, PEPCK 1 Deficiency, Pyruvate Decarboxylase Deficiency, and Pyruvate Dehydrogenase Deficiency. Dr. Kirmse is currently accepting new patients.
His clinical research consists of co-authoring 43 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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
2000 6th Ave S, Birmingham, AL 35233
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.
Ali Al-Beshri is a Medical Genetics provider in Birmingham, Alabama. Dr. Al-Beshri is rated as an Experienced provider by MediFind in the treatment of Gaucher Disease Type 1. His top areas of expertise are Trisomy 12 Mosaicism, Mosaic Trisomy 8, Chromosome 8p Deletion, and Gaucher Disease. Dr. Al-Beshri is currently accepting new patients.
Sarah Dean is a Medical Genetics provider in Birmingham, Alabama. Dr. Dean is rated as an Experienced provider by MediFind in the treatment of Gaucher Disease Type 1. Her top areas of expertise are Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Maple Syrup Urine Disease, Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Dean is currently accepting new patients.
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.
- 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.