Associate Professor of Neurology, University Tex Houston
Neurology
Dr. Pedro Mancias, MD
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Pedro Mancias, MD works in the field of Neurology. He researched medicine at University of Arkansas for Medical Sciences. University of Arkansas for Medical Sciences has a rank of 83 in research and a 35 in primary care He over the years received 2 awards: "Top Doctors:SE Texas" and "Top MD". Pedro Mancias is also a published doctor. He has 26 paper published. The most recent paper is: Does short-term antiepileptic drug treatment in children result in cognitive or behavioral changes?
Publications
- Dysferlinopathy presenting as rhabdomyolysis and acute renal failure.
- Functional, histopathologic and natural history study of Neuropathy associated with EGR2 mutations.
- Living-donor nerve transplantation for global obstetric brachial plexus Palsy.
- MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
- SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.
- Poliomyelitis-like Syndrome in a child with West Nile virus infection.
- Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations.
- Trigeminal myokymia in a young girl.
- CMT4A: identification of a Hispanic GDAP1 founder mutation.
- Schwann cell expression of PLP1 but not DM20 is necessary to prevent Neuropathy.
- Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease.
- Lumbar Spinal stenosis causing congenital clubfoot.
- Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation.
- Brain plasticity for sensory and linguistic functions: a functional imaging study using magnetoencephalography with children and young adults.
- Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathies.
- Does short-term antiepileptic drug treatment in children result in cognitive or behavioral changes?
- Laminin alpha2 Muscular dystrophy: genotype/phenotype studies of 22 patients.
- Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies.
- Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as Inflammatory myopathy.
- Behavioral descriptors that differentiate between seizure and nonseizure events in a pediatric population.
- Polymyositis associated with chronic myelogenous leukemia.
- Combined Brachial plexus injury and root avulsion after complicated delivery.
- Treatment-resistant eosinophilic polymyositis in a child.
- Amoxapine overdose in a young man: a transient mitochondrial Abnormality?
- CT and ultrasound imaging of retropharyngeal abscesses in children.
Procedures Preformed
- EEG (Electroencephalogram)
- EMG (Electromyography)
Conditions Treated
- Ataxia
- Bell's Palsy
- Brachial Plexus Palsy
- Brain Injury
- View All
Doctors Specialties
- Clinical Neurophysiology
- Neurology
Accepted Insurances
Awards
- Top Doctors:SE Texas
- Top MD
Education
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University of Texas Health Science Center -
University of Arkansas for Medical Sciences -
University of Texas Medical School
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