Professor, Physical Medicine and Rehabilitation, UC, Davis School of Medicine
Physical Medicine/Rehab
Dr. Craig M. McDonald, MD
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Craig McDonald works in the field of Physical Medicine/Rehab. He went to University of Washington School of Medicine. Dr. Craig M. McDonald is a published MD as well. He has 98 publications published. The latest was: Spinal deformity in progressive neuromuscular disease. Natural history and management.
Publications
- Baseline results of the NeuroNEXT spinal Muscular atrophy infant biomarker study.
- Genetic modifiers of ambulation in the cooperative international NeuroMuscular research group Duchenne natural history study.
- Outcome reliability in non-Ambulatory Boys/Men with duchenne Muscular dystrophy.
- Evaluation of Phrenic Nerve and Diaphragm Function with Peripheral Nerve Stimulation and M-Mode Ultrasonography in Potential Pediatric Phrenic Nerve or Diaphragm Pacin...
- Discovery of Serum Protein Biomarkers in the mdx mouse model and cross-species comparison to Duchenne Muscular Dystrophy patients.
- One Year Outcome of Boys With Duchenne Muscular Dystrophy Using the Bayley-III Scales of Infant and Toddler Development.
- Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network.
- The 6-minute walk test and other endpoints in Duchenne Muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study.
- The 6-minute walk test and other clinical endpoints in Duchenne Muscular dystrophy: Reliability, concurrent validity, and minimal clinically important differences from...
- The cooperative international neuroMuscular research group duchenne natural history study-a longitudinal investigation in the era of glucocorticoid therapy: Design of ...
- The cooperative international neuroMuscular research group Duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional mileston...
- Why short stature is beneficial in duchenne Muscular dystrophy.
- Treatment of spine Deformity in neuromuscular diseases.
- Mobility-assistive technology in progressive neuromuscular Disease.
- Neuromuscular Disease Management and Rehabilitation, Part II: Specialty Care and Therapeutics.
- LTBP4 genotype predicts age of ambulatory loss in duchenne Muscular dystrophy.
- The role of the neuromuscular medicine and physiatry specialists in the multiDisciplinary management of neuromuscular disease.
- Clinical approach to the diagnostic evaluation of hereditary and acquired neuromuscular Diseases.
- Exercise in neuromuscular Diseases.
- Prevention and management of limb contractures in neuromuscular Diseases.
- Neuromuscular Disease management and rehabilitation, part I: diagnostic and therapy issues.
- Dedication.
- Regional and whole-body dual-energy x-ray absorptiometry to guide treatment and monitor Disease progression in neuromuscular Disease.
- Quality-of-Life Measures in Children With Neurological Conditions: Pediatric Neuro-QOL.
- The 6-minute walk test in Duchenne/Becker Muscular dystrophy: longitudinal observations.
- Classification of the Gait patterns of boys with Duchenne muscular dystrophy and their relationship to function.
- Relationship between clinical outcome measures and parent proxy reports of health-related quality of life in ambulatory children with Duchenne Muscular dystrophy.
- The 6-minute walk test as a new outcome measure in Duchenne Muscular dystrophy.
- Impact of biopsychosocial factors on chronic Pain in persons with myotonic and facioscapulohumeral muscular dystrophy.
- Assessment of regional body composition with dual-energy X-ray absorptiometry in Duchenne Muscular dystrophy: correlation of regional lean mass and quantitative strength.
- Pain in myotonic muscular dystrophy, type 1.
- Change in life satisfaction of adults with pediatric-onset spinal cord Injury.
- Pain in persons with postpolio syndrome: frequency, intensity, and impact.
- Convexity of scoliosis related to handedness in identical twin boys with Duchenne's Muscular dystrophy: a case report.
- Diagnosis and clinical management of spinal Muscular atrophy.
- The validity of compliance monitors to assess wearing time of thoracic-lumbar-sacral orthoses in children with spinal cord Injury.
- Chronic Pain in persons with myotonic dystrophy and facioscapulohumeral dystrophy.
- Reliability of radiographic parameters in neuroMuscular scoliosis.
- Metabolic Syndrome in adolescents with spinal cord dysfunction.
- Behavioral intervention, exercise, and nutrition education to improve health and fitness (BENEfit) in adolescents with mobility impairment due to spinal cord dysfunction.
- Body composition and resting energy expenditure in patients aged 11 to 21 years with spinal cord dysfunction compared to controls: comparisons and relationships among ...
- Body mass index and body composition measures by dual x-ray absorptiometry in patients aged 10 to 21 years with spinal cord Injury.
- Aerobic fitness and upper extremity strength in patients aged 11 to 21 years with spinal cord dysfunction as compared to ideal weight and overweight controls.
- Depression in adults who sustained spinal cord injuries as children or adolescents.
- Challenges in drug development for muscle Disease: a stakeholders' meeting.
- Effect of thoracolumbosacral orthoses on reachable workspace volumes in children with spinal cord Injury.
- Impact of prophylactic thoracolumbosacral orthosis bracing on functional activities and activities of daily living in the pediatric spinal cord Injury population.
- Development and pilot test of the shriners pediatric instrument for neuroMuscular scoliosis (SPNS): a quality of life questionnaire for children with spinal cord injur...
- Effectiveness of an upper extremity exercise device integrated with computer gaming for aerobic training in adolescents with spinal cord dysfunction.
- Body composition and water compartment measurements in boys with Duchenne Muscular dystrophy.
- Chronic Pain in persons with neuromuscular disease.
- Use of step activity monitoring for continuous physical activity assessment in boys with Duchenne Muscular dystrophy.
- Utility of a step activity monitor for the measurement of daily ambulatory activity in children.
- Altered body composition affects resting energy expenditure and interpretation of body mass index in children with spinal cord Injury.
- Physical activity, health impairments, and disability in neuromuscular Disease.
- New clinical end points in rehabilitation medicine: tools for measuring quality of life.
- Development of items designed to evaluate activity performance and participation in children and adolescents with spinal cord Injury.
- Recognition and management of autonomic dysreflexia in pediatric spinal cord Injury.
- The relationship between regional body composition and quantitative strength in facioscapulohumeral Muscular dystrophy (FSHD).
- A randomized, double-blind trial of lisinopril and losartan for the treatment of cardiomyopathy in duchenne Muscular dystrophy.
- The natural history of cardiac and pulmonary function decline in patients with duchenne Muscular dystrophy.
- Profiles of neuromuscular Diseases. Becker's muscular dystrophy.
- Profiles of neuromuscular Diseases. Duchenne muscular dystrophy.
- Profiles of neuromuscular Diseases. Spinal muscular atrophy.
- Profiles of neuromuscular Diseases. Facioscapulohumeral muscular dystrophy.
- Preserving function in Duchenne Dystrophy with long-term pulse prednisone therapy.
- Effect of bracing on paralytic scoliosis secondary to spinal cord Injury.
- Profiles of neuromuscular Diseases. Hereditary motor and sensory neuropathy, types I and II.
- Timed motor test for wheelchair users: initial development and application in children with spinal cord Injury.
- Profiles of neuromuscular diseases. Limb-girdle Syndromes.
- Leisure characteristics of the pediatric spinal cord Injury population.
- Symptoms of upper gastrointestinal dysfunction in Duchenne Muscular dystrophy: case-control study.
- Randomized, blinded trial of weekend vs daily prednisone in Duchenne Muscular dystrophy.
- Magnetic resonance imaging of denervated muscle: comparison to electromyography.
- A prospective evaluation of the WeeFIM in patients with cerebral Palsy undergoing orthopaedic surgery.
- Profiles of functional recovery in fifty traumatically brain-injured patients after acute rehabilitation.
- Focal posterior interosseous Neuropathy in the presence of hereditary motor and sensory Neuropathy, type I.
- Spinal Deformity in progressive neuromuscular disease. Natural history and management.
- Limb contractures in progressive neuromuscular Disease and the role of stretching, orthotics, and surgery.
- Comparison of indices of traumatic brain Injury severity as predictors of neurobehavioral outcome in children.
- Clinical approach to the diagnostic evaluation of progressive neuromuscular Diseases.
- Nonsense mutation-associated Becker Muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.
- Urodynamic findings in the tethered spinal cord Syndrome: does surgical release improve bladder function?
- Peripheral neuropathies of childhood.
- Rehabilitation of children with spinal dysraphism.
- Ambulatory outcome of children with myelomeningocele: effect of lower-extremity muscle strength.
- Isolated femoral monoNeuropathy to the vastus lateralis: EMG and MRI findings.
- SPP1 genotype is a determinant of Disease severity in Duchenne muscular dystrophy.
- Variable phenotypes associated with mutations in DOK7.
- Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multiDisciplinary care.
- Modifications to the traditional description of neurosegmental innervation in myelomeningocele.
- Assessment of muscle strength in children with meningomyelocele: accuracy and stability of measurements over time.
- The 6-minute walk test and person-reported outcomes in boys with duchenne Muscular dystrophy and typically developing controls: longitudinal comparisons and clinically...
- Rehabilitation following childhood Injury.
- Presynaptic congenital myasthenic Syndrome due to quantal release deficiency.
- Transcranial cortical stimulation in syringomyelia.
- Diagnosis and management of Duchenne Muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
Schools
University Of Washington School Of Medicine
University Of Wa School Of Med
Conditions Treated
- Achilles Tendinitis
- Ankle and Foot Instability or Derangement
- Arthritis
- Ataxia
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Doctors Specialties
- Neuromusculoskeletal Medicine
- Pediatric Rehabilitation
- Physical Medicine/Rehab
Accepted Insurances
Education
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University of Washington -
UCLA Medical Center -
University of Washington School of Medicine
Hospital
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University of California, Davis Medical Center
Drug Facts
| NPI NUMBER | 1144201047 | |
| NPPES Provider LastName | MCDONALD | |
| NPPES Provider FirstName | CRAIG | |
| NPPES Provider ZIPCode | 958172307 | |
| NPPES Provider State | CA | |
| Specialty Description | Physical Medicine and Rehabilitation | |
| Total Claim Count | 16.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1144201047 |
| Last Name Of The Provider | MCDONALD |
| First Name Of The Provider | CRAIG |
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