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Amber Stocco

Baylor College of Medicine

12

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796

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Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain.

2021 Genetics in Medicine
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Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

2020 medRxiv
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Does a Standardized Multidisciplinary Approach Improve Outcomes for Children with NMDA Receptor Antibody Encephalitis? A Preliminary Assessment of a Single Center Experience (I6-5E)

2015 Neurology
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Dystonia-Spasticity in a Patient with a Novel SLC25A12 Mutation (P2.138)

2015 Neurology
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Earlier treatment of NMDAR antibody encephalitis in children results in a better outcome

2015 Neuroimmunology and Neuroinflammation
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Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease

2014 Neurology
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Pediatric Dystonia: DBS and Diversity in Diencephalic Dysfunction

2014
- Aaron L. Cardon
- Amber Stocco
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Approach to Pediatric Autoimmune Encephalitis

2014
- Amber Stocco
- Eyal Muscal
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Deep brain stimulation for severe secondary stereotypies

2014 Parkinsonism & Related Disorders
- Amber Stocco
- José Fidel Baizabal-Carvallo
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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

2010 Journal of Medical Genetics
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