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Acute pontine infarction in a patient with persistent left superior vena cava

  • Jeong, Da-Eun;Lee, Jun;Hwang, Woosub
    • Annals of Clinical Neurophysiology
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    • v.20 no.2
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    • pp.105-108
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    • 2018
  • Persistent left superior vena cava (PLSVC) is a common venous anomaly of the thorax and usually drains into the right atrium. Less often it drains into the left atrium and has previously been related to ischemic stroke. We report a case of PLSCV that founded during ischemic stroke evaluation in a 77-year-old woman which was detected on transesophageal echocardiography (TEE) and transcranial Doppler ultrasonography (TCD) with saline agitated test and computed tomography.

Application of near-infrared spectroscopy in clinical neurology

  • Kim, Yoo Hwan;Kim, Byung-Jo;Bae, Jong Seok
    • Annals of Clinical Neurophysiology
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    • v.20 no.2
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    • pp.57-65
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    • 2018
  • Near-infrared spectroscopy (NIRS) monitoring has been used mainly to detect reduced perfusion of the brain during orthostatic stress in order to assess orthostatic intolerance (OI). Many studies have investigated the use of NIRS to reveal the pathophysiology of patients with OI. Research using NIRS in other neurological diseases (e.g., stroke, epilepsy, and migraine) is continuing. NIRS may play an important role in monitoring the regional distribution of the hemodynamic flow in real time and thereby reveal the underlying pathophysiology and facilitate the management of not only patients with OI symptoms but also those with various neurological diseases.

Determination of dextromethorphan and its metabolite dextrorphan in human urine by High-performance liquid chromatography

  • Son, Haeng-Ja;Park, Mee-Jung;Choi, Sang-Kil;Lim, Mi-Ae;Chung, Hee-Sun
    • Proceedings of the PSK Conference
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    • 2003.04a
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    • pp.279.2-280
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    • 2003
  • A simple and accurate reverse-phase high performance liquid chromatography (HPLC) coupled with photodiode array was developed for the determination of dextromethorphan(DM) and its metabolite dextrorphan(DX) in human urine. Chromatographic separation was accomplished on a cyano analytical column at 220 nm using a mobile phase containing 25 mM triethylammonium phosphate buffer(PH 3.0) in a 0-70% ACN gradient and triazolam(TZ) was used as internal standard(I.S). (omitted)

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Carotidynia presenting with acute ischemic stroke after carotid sinus massage

  • Kwak, Hyo Sung;Chung, Gyung Ho;Lee, Chan-Hyuk;Jeong, Seul-Ki;Ryu, Han Uk
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.46-49
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    • 2017
  • Carotidynia is characterized by unilateral neck pain around the carotid artery. We describe a 50-year-old woman who presented with transient left-side weakness and right-side neck pain. She frequently massaged the uncomfortable neck area during the symptomatic course of the condition. Magnetic resonance imaging revealed multifocal cerebral infarctions and a carotid intramural thrombus ipsilateral to the carotidynia.Long-term carotidynia might result in the involvement of an intramural thrombus and intimal disruption, and ischemic stroke after carotidynia may be provoked by carotid sinus massage.

Acute-onset chronic inflammatory demyelinating polyneuropathy following hepatitis A virus infection

  • Jung, Eui Sung;Kim, Ye Sel;Min, Ju-Hong;Kang, Kyusik;Lee, Jung Ju;Park, Jong-Moo;Kim, Byung-Kun;Kwon, Ohyun
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.50-53
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    • 2017
  • An infection is less likely to elicit chronic inflammatory demyelinating polyneuropathy (CIDP) than Guillain-$Barr{\acute{e}}$ syndrome. We here report a case of acute-onset CIDP following hepatitis A virus infection and briefly comment on the potential mechanisms regarding the induction and chronicity of autoimmunity after a viral infection.

Distal acquired demyelinating symmetric neuropathy associated with anti-GM1 and anti-GD1b antibodies

  • Ko, Keun Hyuk;Jwa, Seung-Joo;Park, Sung Joo;Kang, Sa-Yoon
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.54-57
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    • 2017
  • Distal acquired demyelinating symmetric (DADS) neuropathy is a variant form of chronic inflammatory demyelinating polyradiculoneuropathy. A 54-year-old man presented with gait disturbance owing to weakness in both legs. Nerve conduction studies showed demyelinating sensorimotor polyneuropathy, and laboratory studies demonstrated anti-GM1 and anti-GD1b IgG antibodies, but no anti-myelin associated glycoprotein activity. We suggest that an antiganglioside antibodies assay needs to be applied when DADS neuropathy is suspected in order to improve the classification of dysimmune neuropathies.

EEG spikes resembling cardiac M-shaped waves in the EKG: the cerebral M pattern

  • Janati, A.Bruce;ALGhasab, Naif S.;Aziz, Tariq;Haq, Fazal;ALGhassab, Fahad Saad;Iqhbal, Tariq;Alenazy, Rehab Khaleel
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.58-63
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    • 2017
  • Studies of interictal epileptiform discharges are essential for improving the diagnosis, classification, and management of epilepsy. In this case series we sought to identify the clinical and neurophysiological significance of bifid spikes, whose pattern bears a strong resemblance to the cardiac M pattern. We hypothesize that, analogous to the cardiac M pattern, the cerebral M pattern is generated by a conduction defect associated with asynchronous spatiotemporal averaging of electrical signals in the cortex, resulting in the signals reaching the scalp with different latencies. Unlike the cardiac M pattern, the pathology underlying the cerebral M pattern is unknown, although congenital CNS anomalies may be a culprit.

Flail arm syndrome with several issues related to the diagnostic process

  • Kim, Jae-Youn;Park, Yun Kyung;Yoon, Bora;Lee, Kee Ook;Kim, Yong-Duk;Na, Sang-Jun
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.68-70
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    • 2017
  • Flail arm syndrome (FAS), known as one of the atypical amyotrophic lateral sclerosis (ALS) variants, has a similar clinical course and pathologic findings as ALS. Therefore it is difficult to differentiate between ALS and FAS at a glance. There are few reports involving individual analysis of FAS patients to date. The findings of polysomnography (PSG) in patient with FAS are not well known. We report a male FAS patient with review of literatures and several issues related to the diagnostic process.

Spinal segmental myoclonus improved with epidural blockade in a patient with herpes zoster radiculitis

  • Han, Su-Hyun;Jeong, Hae-Bong;Yoo, Il-Han;Ahn, Suk-Won
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.71-73
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    • 2017
  • The spinal segmental myoclonus by viral radiculitis has been rarely reported and the pathophysiology remains to be elucidated. However, the hyperactivity of contiguous anterior horn neurons induced by viral irritation has been suggested to be a possible patho-mechanism. In general, spinal segmental myoclonus is not well-controlled by medication and the patient suffers from continuous involuntary movement. We recently experienced a case of spinal segmental myoclonus induced by herpes zoster radiculitis, and which was successfully relieved by epidural injections.

Sensory and motor axons are different: implications for neurological disease

  • Burke, David;Howells, James;Kiernan, Matthew C.
    • Annals of Clinical Neurophysiology
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    • v.19 no.1
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    • pp.3-12
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    • 2017
  • Using threshold tracking, differences have been established between large myelinated sensory and ${\alpha}$ motor axons in humans. Major differences are that sensory axons are relatively depolarised at rest such that they have a greater persistent $Na^+$ current, and have greater activity of hyperpolarisation-activated cyclic nucleotide-gated (HCN) channels. Sensory axons may thereby be protected from hyperpolarising stresses, and are less likely to develop conduction block. However, the corollary is that sensory axons are more excitable and more likely to become ectopically active.