Overview
Robert Conway is a Medical Genetics specialist and a Pediatrics provider practicing medicine in West Fargo, North Dakota.
Dr. Conway is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Hypermethioninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
He is actively involved in clinical research, co-authoring 19 peer reviewed articles and participating in 2 clinical trials. Dr. Conway is currently accepting new patients.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MEDICARE MAPD
Locations
1220 Sheyenne St, West Fargo, ND 58078
801 Broadway N, Fargo, ND 58102
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.
2 Clinical Trials
Sanford Veterans Square Clinic
Kari Casas, MD, is a specialist in pediatric and metabolic genetics. She offers consultations for patients with inherited metabolic conditions, chromosomal changes and other genetic syndromes. Dr. Casas provides a three-generation review of family history, genetic physical examination and ordering and interpretation of genetic and genomic testing results. She also serves as a clinical associate professor of pediatrics at the University of North Dakota School of Medicine and Health Sciences and is a metabolic consultant for the North Dakota Department of Health newborn screening program. Speaks: English. Dr. Casas is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, Pyruvate Decarboxylase Deficiency, and Phenylketonuria (PKU). Dr. Casas is board certified in American Board Of Medical Genetics: Clinical Genetics Br> American Board Of Medical Genetics: Clinical Biochemical Genetics. Dr. Casas is currently accepting new patients.
Sanford South University Eye Center &Amp; Optical
Dr. Ahmed Kassem diagnoses and treats eye disorders in children and adults. Visit Dr. Kassem to get treatment for common eye disorders, including strabismus (eyes that don’t look in the same direction), double vision and blocked tear ducts. He performs eye muscle surgery for adult patients. He treats these conditions in children: Speaks: English. Dr. Kassem is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Strabismus, Meibomianitis, Eyelid Bump, and Esotropia. Dr. Kassem is currently accepting new patients.
Office
Jessica Kuhn is a Pediatrics provider practicing medicine in Fargo, North Dakota. Dr. Kuhn is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Otitis Media with Effusion. Dr. Kuhn is currently accepting new patients.
Frequently Asked Questions about Dr. Robert L. Conway
How do I make an appointment with Dr. Robert L. Conway?
You can book an appointment with Dr. Robert L. Conway by calling their office at 701-234-4445. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Robert L. Conway a top-rated expert for Hypermethioninemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Robert L. Conway is classified as an Distinguished expert for Hypermethioninemia, 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. Robert L. Conway specialize in?
While Dr. Robert L. Conway is a Medical Genetics, they have specific expertise in Hypermethioninemia, Phenylketonuria (PKU), and Biotinidase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Robert L. Conway participate in research or clinical trials?
Yes. Dr. Robert L. Conway has published 19 articles and abstracts on conditions like Hypermethioninemia. You can view a list of Dr. Robert L. Conway's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Robert L. Conway accept my insurance?
Dr. Robert L. Conway accepts most major insurance plans, including Blue Cross Blue Shield and Humana. We recommend calling the office directly at 701-234-4445 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
- Distinguished
- HypermethioninemiaDr. Conway isDistinguished. Learn about Hypermethioninemia.
- Advanced
- Biotinidase DeficiencyDr. Conway isAdvanced. Learn about Biotinidase Deficiency.
- Dihydropteridine Reductase Deficiency
- Isovaleric AcidemiaDr. Conway isAdvanced. Learn about Isovaleric Acidemia.
- Maternal HyperphenylalaninemiaDr. Conway isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Phenylketonuria (PKU)Dr. Conway isAdvanced. Learn about Phenylketonuria (PKU).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Conway isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- CitrullinemiaDr. Conway isExperienced. Learn about Citrullinemia.
- Classic GalactosemiaDr. Conway isExperienced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Conway isExperienced. Learn about Danon Disease.
- Gastroesophageal Reflux in InfantsDr. Conway isExperienced. Learn about Gastroesophageal Reflux in Infants.
- HomocystinuriaDr. Conway isExperienced. Learn about Homocystinuria.
- HypotoniaDr. Conway isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Conway isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Leigh SyndromeDr. Conway isExperienced. Learn about Leigh Syndrome.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Pompe DiseaseDr. Conway isExperienced. Learn about Pompe Disease.
- Pyridoxine DeficiencyDr. Conway isExperienced. Learn about Pyridoxine Deficiency.
- Pyruvate Decarboxylase DeficiencyDr. Conway isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Conway isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Urea Cycle Disorders (UCD)Dr. Conway isExperienced. Learn about Urea Cycle Disorders (UCD).

