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Check Dr. Daniel K. Arrington's experience treating your condition:
About Dr. Daniel K. Arrington

Daniel Arrington is a Neurologist and a Child Neurologist in Boise, Idaho. His top areas of expertise are Brain Abscess, Epilepsy in Children, Status Epilepticus, and Craniopharyngioma. He is licensed to treat patients in Arizona. Arrington is currently accepting new patients.

His clinical research consists of co-authoring 5 peer reviewed articles in the past 15 years.

Areas of Expertise

Many experts have expertise treating multiple conditions. MediFind uses a variety of data sources to determine what conditions aexpert treats and their level of experience.

Insurance

MediFind strives to display the most accurate insurance information for every doctor. If you do not see your insurance listed for Dr. Daniel K. Arrington it is best to call his office and ask if your insurance is accepted.

Accepts Medicare

Dr. Daniel K. Arrington accepts the following insurance:

  •  Ambetter
  •  Montana Health Cooperative
  •  Moda Health

Call to see if your plan is accepted.
Locations
305 E Jefferson St, Boise, ID 83712
Other Locations
305 E Jefferson St, Boise, ID 83712
2550 Addison Ave E, Suites A, B, And F, Twin Falls, ID 83301
Background & Education
Graduate Institution
George Washington University School Of Medicine, 2006.0
Specialties
Neurology
Child Neurology
Licenses
Neurology with Special Qualifications in Neurology in AZ
Hospital Affiliations
St Lukes Nampa Medical Center
St Lukes Boise Medical Center
Languages Spoken
English
Gender
Male
Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Doctors 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.


5 Total Publications

Autism and developmental disability caused by KCNQ3 gain-of-function variants.
Summary: Autism and developmental disability caused by KCNQ3 gain-of-function variants.


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