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Michael V Johnston, M.D.
Professor of Neurology
Expertise: Brain Injury, Neurology
Research Interests: Neurotransmitter glutamates; Neuroprotection; Brain development; Brain plasticity
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The Johns Hopkins Hospital (Main Entrance)
APPOINTMENT PHONE: 443-923-9315
1800 Orleans St. Sheikh Zayed Tower Baltimore, MD 21287
Dr. Michael Johnston is a research scientist, senior vice president and chief medical officer at Kennedy Krieger Institute. He is also a professor of neurology and pediatrics at the Johns Hopkins University School of Medicine.
Dr. Johnston attended Franklin and Marshall College before going on to medical school at the University of Pittsburgh, from which he graduated cum laude in 1971. His post-doctoral training at the Johns Hopkins Hospital included work in pediatrics, neurology, pharmacology and pediatric neurology. After teaching positions and research work at the University of Michigan Medical School and University of Michigan Hospitals, Dr. Johnston returned to Baltimore in 1988.
Today he is the senior vice president and chief medical officer at Kennedy Krieger Institute, as well as director of both Kennedy Krieger Institute's Division of Neurology and Developmental Medicine and the institute's neuroscience laboratory. Dr. Johnston is an attending physician at both Johns Hopkins Hospital and Kennedy Krieger Children's Hospital.
- Professor of Neurology
- Professor of Pediatrics
- Professor of Physical Medicine and Rehabilitation
Departments / Divisions
Centers & Institutes
- MD, University of Pittsburgh School of Medicine (1971)
- Johns Hopkins University School of Medicine / Pediatrics (1974)
- American Board of Pediatrics / Pediatrics (1976)
- American Board of Psychiatry and Neurology / Neurodevelopmental Disabilities (2001)
- American Board of Psychiatry and Neurology / Neurology/Special Child Neurology (1982)
Research & Publications
Dr. Johnston and his group, including Drs. Mary Blue, Mary Ann Wilson and Alec Hoon, perform clinical and basic laboratory research focused on developing therapies to reduce brain injury in infants and children, as well as to promote recovery by enhancing brain plasticity. His laboratory was one of the first to describe the mechanisms through which the neurotransmitter glutamate triggers brain injury from lack of oxygen, trauma and other insults. If administered early enough, drugs that block the effects of glutamate on one of its receptors called the NMDA receptor can totally prevent brain injury in infants. His group also recognized that the major role that glutamate plays in injury during development is related to the important role it plays in normal development. During development, glutamate released from nerve terminals helps to refine the synaptic connections that link neurons into circuits. These mechanisms are enhanced during development to shape circuits in response to environmental stimuli and formation of memories, a process called neuronal plasticity. When the brain is injured, these circuits can be damaged by too much glutamate, much like a computer's chips can be damaged by a power surge during a thunderstorm. Because injury and plasticity are two sides of the same processes in brain development, Dr. Johnston's research has grown beyond mechanisms of injury into processes that control brain plasticity. For example, he studies how the cerebral cortex is reassigned in response to injury, which is the major mechanism for recovery of function from stroke and other disorders. Even learning and long-term memory are based on these same mechanisms since it depends on neurons exciting each other with glutamate and changes in synaptic connections. Numerous disorders associated with intellectual disabilities are caused by genetic flaws in these systems, and Dr. Johnston recently completed a project focused on a defect in a neuronal signaling process involved in a form of X-linked intellectual disability. Dr. Johnston's initial pursuit of ways to reduce brain injury in infants and children with medications has led to a broader understanding of processes involved in plasticity and recovery from injury. The immature brain's glutamate signaling system, with its complex neuronal circuitry, proves to be especially vulnerable to injury. Accordingly, Dr. Johnston's research has proved to be relevant to a broad range of neurodevelopmental disabilities including cerebral palsy, intellectual disabilities, genetic metabolic disorders, and epilepsy, as well as brain injury from trauma and lack of oxygen.
A Diagnostic Approach for Cerebral Palsy in the Genomic Era. Lee RW, Poretti A, Cohen JS, Levey E, Gwynn H, Johnston MV, Hoon AH, Fatemi A. Neuromolecular Med. 2014 Oct 4. [Epub ahead of print] PMID: 25280894
Potential for treatment of severe autism in tuberous sclerosis complex. Gipson TT, Gerner G, Wilson MA, Blue ME, Johnston MV. World J Clin Pediatr. 2013 Aug 8;2(3):16-25. doi: 10.5409/wjcp.v2.i3.16. eCollection 2013 Aug 8. Review. PMID: 25254170
Cognitive and functional impairment associated with care in the PICU*. Johnston MV. Pediatr Crit Care Med. 2014 Sep;15(7):676-7. doi: 10.1097/PCC.0000000000000231. No abstract available. PMID: 25186325
Early neurodevelopmental screening in tuberous sclerosis complex: a potential window of opportunity. Gipson TT, Gerner G, Srivastava S, Poretti A, Vaurio R, Hartman A, Johnston MV. Pediatr Neurol. 2014 Sep;51(3):398-402. doi: 10.1016/j.pediatrneurol.2014.04.028. Epub 2014 May 4. PMID: 25160545
Systemic Injection of CD34+-Enriched Human Cord Blood Cells Modulates Poststroke Neural and Glial Response in a Sex-Dependent Manner in CD1 Mice. Kadam SD, Chen H, Markowitz GJ, Raja S, George S, Shotwell E, Loechelt B, Johnston MV, Kamani N, Fatemi A, Comi AM. Stem Cells Dev. 2014 Sep 23. [Epub ahead of print] PMID:25121827