Shin Joong Oh

Last updated
Shin Joong Oh
Dr. Shin J. Oh.jpg
Born
Korea
NationalitySouth Korea, United States
Alma mater Seoul National University
Occupation Distinguished Professor Emeritus
Known forContributions to neurology and electrodiagnostic medicine

Shin Joong Oh is a Korean physician who is Distinguished Professor of Neurology Emeritus at The University of Alabama at Birmingham in the United States. Oh is a clinician, researcher, and educator known for his contributions to the fields of neurology and electrodiagnostic medicine, particularly electromyography. He retired in 2014.

Contents

Early life and education

Oh was born in Haeju, Korea in 1936 and moved to South Korea in 1947. He received his M.D. degree at the Seoul National University (SNU) College of Medicine in 1960. [1] He completed residencies in neurology at the SNU National Medical Center in Korea and at Georgetown University in Washington, D.C. in the United States in 1970. [2] [3] [4]

Career

Oh joined the faculty of the University of Alabama at Birmingham (UAB) School of Medicine in 1970. He was given the title of Distinguished Professor of Neurology and Professor of Pathology in 2007. [3] During his tenure, Oh served as chief of Neurology at the Veterans Affairs Medical Center, as director of the Electromyography and Evoked potential Laboratory, and as director of the Muscle and Nerve Histopathology Laboratory [2] By serving in these positions for 43 years, he held one of the longest neurology tenures in American medicine. [2] He also served as director of the UAB Muscular Dystrophy Association Clinic and the Myasthenia Gravis Clinic and is a fellow member of the American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM), American Academy of Neurology, and American Neurological Association. [5]

In 2009, to recognize his accomplishments, the UAB Muscle and Nerve Histpathology Laboratory was renamed to "The Dr. Shin J. Oh Muscle and Nerve Histopathology Laboratory at UAB" by the board of the University of Alabama. [6]

In 1994, Oh and his wife, M. Kim Oh, established an endowed lectureship through the UAB Department of Neurology entitled "The Oh Lecture on Neuromuscular Diseases." The couple established this lectureship in memory of their late daughter, Julie Oh. [7]

Research and contributions

As of 2015, Oh had published 230 articles, 28 books and book chapters, and 237 abstracts, some of which have become classics of the field. [2] Notable contributions to the fields of neurology and electrodiagnostic medicine include:

  1. Subacute inflammatory demyelinating neuropathy (SIDP) [9]
  2. Chronic demyelinating sensory neuropathy as a form of chronic inflammatory demyelinating neuropathy (CIDP) [10]
  3. Chronic inflammatory axonal polyneuropathy (CIAP) [11]
  4. Uniform type I fiber congenital neuromuscular disease as a new disease entity [12]
  5. A second case of Danon disease [13]

Textbook publications

Awards and recognitions

Related Research Articles

In neuroscience, an F wave is one of several motor responses which may follow the direct motor response (M) evoked by electrical stimulation of peripheral motor or mixed nerves. F-waves are the second of two late voltage changes observed after stimulation is applied to the skin surface above the distal region of a nerve, in addition to the H-reflex which is a muscle reaction in response to electrical stimulation of innervating sensory fibers. Traversal of F-waves along the entire length of peripheral nerves between the spinal cord and muscle, allows for assessment of motor nerve conduction between distal stimulation sites in the arm and leg, and related motoneurons (MN's) in the cervical and lumbosacral cord. F-waves are able to assess both afferent and efferent loops of the alpha motor neuron in its entirety. As such, various properties of F-wave motor nerve conduction are analyzed in nerve conduction studies (NCS), and often used to assess polyneuropathies, resulting from states of neuronal demyelination and loss of peripheral axonal integrity.

<span class="mw-page-title-main">Lambert–Eaton myasthenic syndrome</span> Medical condition

Lambert–Eaton myasthenic syndrome (LEMS) is a rare autoimmune disorder characterized by muscle weakness of the limbs.

Neuromyotonia (NMT) is a form of peripheral nerve hyperexcitability that causes spontaneous muscular activity resulting from repetitive motor unit action potentials of peripheral origin. NMT along with Morvan's syndrome are the most severe types in the Peripheral Nerve Hyperexciteability spectrum. Example of two more common and less severe syndromes in the spectrum are Cramp Fasciculation Syndrome and Benign Fasciculation Syndrome. NMT can have both hereditary and acquired forms. The prevalence of NMT is unknown.

<span class="mw-page-title-main">Polyneuropathy</span> Medical condition

Polyneuropathy is damage or disease affecting peripheral nerves in roughly the same areas on both sides of the body, featuring weakness, numbness, and burning pain. It usually begins in the hands and feet and may progress to the arms and legs and sometimes to other parts of the body where it may affect the autonomic nervous system. It may be acute or chronic. A number of different disorders may cause polyneuropathy, including diabetes and some types of Guillain–Barré syndrome.

<span class="mw-page-title-main">Nerve conduction study</span> Diagnostic test for nerve function

A nerve conduction study (NCS) is a medical diagnostic test commonly used to evaluate the function, especially the ability of electrical conduction, of the motor and sensory nerves of the human body. These tests may be performed by medical specialists such as clinical neurophysiologists, physical therapists, physiatrists, and neurologists who subspecialize in electrodiagnostic medicine. In the United States, neurologists and physiatrists receive training in electrodiagnostic medicine as part of residency training and in some cases acquire additional expertise during a fellowship in clinical neurophysiology, electrodiagnostic medicine, or neuromuscular medicine. Outside the US, clinical neurophysiologists learn needle EMG and NCS testing.

<span class="mw-page-title-main">Neuritis</span> Inflammation of a nerve or generally any part of the nervous system

Neuritis is inflammation of a nerve or the general inflammation of the peripheral nervous system. Inflammation, and frequently concomitant demyelination, cause impaired transmission of neural signals and leads to aberrant nerve function. Neuritis is often conflated with neuropathy, a broad term describing any disease process which affects the peripheral nervous system. However, neuropathies may be due to either inflammatory or non-inflammatory causes, and the term encompasses any form of damage, degeneration, or dysfunction, while neuritis refers specifically to the inflammatory process.

<span class="mw-page-title-main">Nerve conduction velocity</span> Speed at which an electrochemical impulse propagates down a neural pathway

In neuroscience, nerve conduction velocity (CV) is the speed at which an electrochemical impulse propagates down a neural pathway. Conduction velocities are affected by a wide array of factors, which include age, sex, and various medical conditions. Studies allow for better diagnoses of various neuropathies, especially demyelinating diseases as these conditions result in reduced or non-existent conduction velocities. CV is an important aspect of nerve conduction studies.

<span class="mw-page-title-main">Neuromuscular disease</span> Medical condition

A neuromuscular disease is any disease affecting the peripheral nervous system (PNS), the neuromuscular junctions, or skeletal muscles, all of which are components of the motor unit. Damage to any of these structures can cause muscle atrophy and weakness. Issues with sensation can also occur.

<span class="mw-page-title-main">Chronic inflammatory demyelinating polyneuropathy</span> Medical condition

Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired autoimmune disease of the peripheral nervous system characterized by progressive weakness and impaired sensory function in the legs and arms. The disorder is sometimes called chronic relapsing polyneuropathy (CRP) or chronic inflammatory demyelinating polyradiculoneuropathy. CIDP is closely related to Guillain–Barré syndrome and it is considered the chronic counterpart of that acute disease. Its symptoms are also similar to progressive inflammatory neuropathy. It is one of several types of neuropathy.

<span class="mw-page-title-main">Hereditary motor and sensory neuropathy</span> Medical condition

Hereditary motor and sensory neuropathies (HMSN) is a name sometimes given to a group of different neuropathies which are all characterized by their impact upon both afferent and efferent neural communication. HMSN are characterised by atypical neural development and degradation of neural tissue. The two common forms of HMSN are either hypertrophic demyelinated nerves or complete atrophy of neural tissue. Hypertrophic condition causes neural stiffness and a demyelination of nerves in the peripheral nervous system, and atrophy causes the breakdown of axons and neural cell bodies. In these disorders, a patient experiences progressive muscle atrophy and sensory neuropathy of the extremities.

Neuromuscular junction disease is a medical condition where the normal conduction through the neuromuscular junction fails to function correctly.

<span class="mw-page-title-main">Pronator teres syndrome</span> Medical condition

Pronator teres syndrome is a compression neuropathy of the median nerve at the elbow. It is rare compared to compression at the wrist or isolated injury of the anterior interosseous branch of the median nerve.

Repetitive nerve stimulation is a variant of the nerve conduction study where electrical stimulation is delivered to a motor nerve repeatedly several times per second. By observing the change in the muscle electrical response (CMAP) after several stimulations, a physician can assess for the presence of a neuromuscular junction disease, and differentiate between presynaptic and postsynaptic conditions. The test was first described by German neurologist Friedrich Jolly in 1895, and is also known as Jolly's test.

Multifocal motor neuropathy (MMN) is a progressively worsening condition where muscles in the extremities gradually weaken. The disorder, a pure motor neuropathy syndrome, is sometimes mistaken for amyotrophic lateral sclerosis (ALS) because of the similarity in the clinical picture, especially if muscle fasciculations are present. MMN is thought to be autoimmune. It was first described in the mid-1980s.

Electromyoneurography (EMNG) is the combined use of electromyography and electroneurography This technique allows for the measurement of a peripheral nerve's conduction velocity upon stimulation (electroneurography) alongside electrical recording of muscular activity (electromyography). Their combined use proves to be clinically relevant by allowing for both the source and location of a particular neuromuscular disease to be known, and for more accurate diagnoses.

Charles Francis Bolton, MD, CM, MS, FRCP(C), is a Canadian professor of neurology at Queen's University in Ontario, Canada. He was first to describe critical illness polyneuropathy in a series of patients.

Electrodiagnosis (EDX) is a method of medical diagnosis that obtains information about diseases by passively recording the electrical activity of body parts or by measuring their response to external electrical stimuli. The most widely used methods of recording spontaneous electrical activity are various forms of electrodiagnostic testing (electrography) such as electrocardiography (ECG), electroencephalography (EEG), and electromyography (EMG). Electrodiagnostic medicine is a medical subspecialty of neurology, clinical neurophysiology, cardiology, and physical medicine and rehabilitation. Electrodiagnostic physicians apply electrophysiologic techniques, including needle electromyography and nerve conduction studies to diagnose, evaluate, and treat people with impairments of the neurologic, neuromuscular, and/or muscular systems. The provision of a quality electrodiagnostic medical evaluation requires extensive scientific knowledge that includes anatomy and physiology of the peripheral nerves and muscles, the physics and biology of the electrical signals generated by muscle and nerve, the instrumentation used to process these signals, and techniques for clinical evaluation of diseases of the peripheral nerves and sensory pathways.

The American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM) is a medical society for the medical subspecialty of neuromuscular and electrodiagnostic medicine based in the United States. Members are primarily neurologists and physiatrists—as well as allied health professionals and PhD researchers.

Edward Lambert was an American neurophysiologist, best known for his description of the Lambert–Eaton myasthenic syndrome and regarded as one of the founders of electromyography.

References

  1. Judy Michaels (August 22, 2018). "Shin J Oh MD, a Neurologist practicing in Birmingham, AL". Health News Today.
  2. 1 2 3 4 5 "UAB's Oh receives prestigious lifetime award from AANEM". UAB News.
  3. 1 2 3 4 "Dr. Shin Oh Named Distinguished Professor". Birmingham Medical News.
  4. 1 2 "UAB's Oh Garners Distinguished Researcher Award". News Archive, The University of Alabama at Birmingham.
  5. "Member Directory – AANEM". American Association of Neuromuscular & Electrodiagnostic Medicine.
  6. 1 2 "Shin J. Oh Muscle and Nerve Histopathology Laboratory – About". UAB Department of Neurology.
  7. "Twelfth Annual Oh Lecture Looks at Neuromuscular Diseases". News Archive, The University of Alabama at Birmingham.
  8. Shin J Oh (2016). "Myasthenia gravis Lambert-Eaton overlap syndrome". Muscle & Nerve. 53 (1): 20–26. doi:10.1002/mus.24921.
  9. Shin J Oh (2016). "Subacute inflammatory demyelinating polyneuropathy". Neurology. 61 (11): 1507–1512. doi:10.1212/01.wnl.0000096166.28131.4c.
  10. Shin J Oh (1992). ""Chronic sensory demyelinating neuropathy": chronic inflammatory demyelinating polyneuropathy presenting as a pure sensory neuropathy". Journal of Neurology, Neurosurgery & Psychiatry. 55 (8): 677–680. doi: 10.1136/jnnp.55.8.677 .
  11. Shin J Oh (2005). "Electrophysiological diagnostic criteria of Lambert–Eaton myasthenic syndrome". Muscle & Nerve. 32 (4): 515–520. doi:10.1002/mus.20389.
  12. Shin J Oh (1983). "Nonprogressive Congenital Neuromuscular Disease With Uniform Type 1 Fiber". Archives of Neurology. 40 (3): 147–150. doi:10.1001/archneur.1983.04050030041007.
  13. Moris J. Danon (1981). "Lysosomal glycogen storage disease with normal acid maltase". Neurology. 31 (1). doi:10.1212/WNL.31.1.51.
  14. Shin J Oh (2007). "Neuropathies of the foot". Clinical neurophysiology. 118 (5): 954–980. doi:10.1016/j.clinph.2006.12.016.
  15. Shin J Oh (1985). "The near-nerve sensory nerve conduction in tarsal tunnel syndrome". Journal of Neurology, Neurosurgery & Psychiatry. 48 (10): 999–1003. doi: 10.1136/jnnp.48.10.999 .
  16. Shin J Oh (2015). "On-nerve needle nerve conduction study in the sural nerve: A new technique for evaluation of peripheral neuropathy". Clinical Neurophysiology. 126 (9): 1811–1816. doi:10.1016/j.clinph.2014.12.008.
  17. Shin J Oh (2010). "Intraoperative on-nerve conduction study and conversion factor in the sural nerve". Muscle & Nerve. 42 (3): 373–378. doi:10.1002/mus.21696.
  18. Shin J Oh (2005). "Electrophysiological diagnostic criteria of Lambert–Eaton myasthenic syndrome". Muscle & Nerve. 32 (4): 515–520. doi:10.1002/mus.20389.
  19. "UAB professor named Distinguished Researcher by neurophysiology group". Birmingham Business Journal. July 25, 2006.