Dr. Douglas Michael Sproule M.D.
Neurologist | Neurology with Special Qualifications in Child Neurology
180 Fort Washington Ave Fl 5 New York NY, 10032About
Dr. Douglas Sproule is a distinguished Neurologist in New York, NY. Dr. Sproule specializes in diagnosing, treating, and managing disorders of the brain and nervous system. With expertise in handling complex conditions like epilepsy, multiple sclerosis, and migraines, Dr. Sproule employs advanced techniques and personalized treatment plans to improve patient outcomes. As a neurologist, Dr. Sproule is committed to staying abreast of the latest developments in neurological research and therapies.
Education and Training
Columbia University College of Physicians and Surgeons 2003
Board Certification
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN- Neuromuscular Medicine
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Wolff-Parkinson-White syndrome in Patients With MELAS.
- Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic
- Increased fat mass and high incidence of overweight despite low body mass index in patients with spinal muscular atrophy.
- Scoliosis surgery in children with neuromuscular disease: findings from the US National Inpatient Sample, 1997 to 2003.
- Bioelectrical impedance analysis can be a useful screen for excess adiposity in spinal muscular atrophy.
- Adiposity is increased among high-functioning, non-ambulatory patients with spinal muscular atrophy.
- Muscle volume estimation by magnetic resonance imaging in spinal muscular atrophy.
- Therapeutic developments in spinal muscular atrophy.
- Observational study of spinal muscular atrophy type 2 and 3: functional outcomes over 1 year.
- Thigh muscle volume measured by magnetic resonance imaging is stable over a 6-month interval in spinal muscular atrophy.
- Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype.
- Spinal muscular atrophy type III: trying to understand subtle functional change
- Age at disease onset predicts likelihood and rapidity of growth failure among infants and young children with spinal muscular atrophy types 1 and 2.
- Independent mobility after early introduction of a power wheelchair in spinal muscular atrophy.
- Diabetic Ketoacidosis in an Adult Patient With Spinal Muscular Atrophy Type II: Further Evidence of Extraneural Pathology Due to Survival Motor Neuron 1 Mutation?
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