Search Results - "Shahrizaila, N"

Bickerstaff brainstem encephalitis and Fisher syndrome: anti-GQ1b antibody syndrome by Shahrizaila, Nortina, Yuki, Nobuhiro

“…In the 1950s, Bickerstaff and Fisher independently described cases with a unique presentation of ophthalmoplegia and ataxia. The neurological features were…”
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S6: Motor and sensory conduction in inflammatory and hereditary neuropathies by Shahrizaila, N

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Amyotrophic lateral sclerosis and motor neuron syndromes in Asia by Shahrizaila, N, Sobue, G, Kuwabara, S, Kim, S H, Birks, Carol, Fan, D S, Bae, J S, Hu, C J, Gourie-Devi, M, Noto, Y, Shibuya, K, Goh, K J, Kaji, R, Tsai, CP, Cui, L, Talman, P, Henderson, R D, Vucic, S, Kiernan, M C

“…While the past 2 decades have witnessed an increasing understanding of amyotrophic lateral sclerosis (ALS) arising from East Asia, particularly Japan, South…”
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Anti-GQ1b antibody syndrome: anti-ganglioside complex reactivity determines clinical spectrum by Fukami, Y., Wong, A. H. Y., Funakoshi, K., Safri, A.Y., Shahrizaila, N., Yuki, N.

“…Background and purpose Anti‐GQ1b antibodies have been found in patients with Miller Fisher syndrome as well as its related conditions. Our aim was to identify…”
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Relationship between ultrasonographic nerve morphology and severity of diabetic sensorimotor polyneuropathy by Arumugam, T., Razali, S. N. O., Vethakkan, S. R., Rozalli, F. I., Shahrizaila, N.

“…Background and purpose In the current study, the aim was to characterize the nerve ultrasound cross‐sectional areas (CSAs) of type 2 diabetic patients with…”
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Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathy by Shahrizaila, N, Noto, Y, Simon, NG, Huynh, W, Shibuya, K, Matamala, JM, Dharmadasa, T, Devenney, E, Kennerson, ML, Nicholson, GA, Kiernan, MC

“…Highlights • Charcot-Marie-Tooth (CMT) patients have increased muscle echogenicity of hand and lower leg muscles. • In CMT, the volume and thickness of the…”
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43. The quest for optimal electrodiagnosis of Guillain–Barre’ syndrome subtypes: criteria sets versus a linear discriminant analysis model by Uncini, A, Ippoliti, L, Shahrizaila, N, Sekiguchi, Y, Kuwabara, S

“…Up to 38% of Guillain-Barré syndrome (GBS) patients change electrophysiological classification after serial recordings. Aim of this study is to compare at the…”
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The value of comparing mortality of Guillain–Barré syndrome across different regions by Wong, A.H.Y, Umapathi, T, Shahrizaila, N, Chan, Y.C, Kokubun, N, Fong, M.K, Chu, Y.P, Lau, P.K, Yuki, N

“…Abstract Objective To study the clinical profile of Guillain–Barré syndrome (GBS) patients who died in 4 Asian countries in order to understand factors…”
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Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies by Tey, S., Ahmad-Annuar, A., Drew, A.P., Shahrizaila, N., Nicholson, G.A., Kennerson, M.L.

“…The cytoplasmic dynein–dynactin genes are attractive candidates for neurodegenerative disorders given their functional role in retrograde transport along…”
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Respiratory involvement in inherited primary muscle conditions by Shahrizaila, N, Kinnear, W J M, Wills, A J

“…Patients with inherited muscle disorders can develop respiratory muscle weakness leading to ventilatory failure. Predicting the extent of respiratory…”
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Successful treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) in systemic lupus erythematosus (SLE) with oral cyclophosphamide by Jasmin, R, Sockalingam, S, Shahrizaila, N, Cheah, T-E, Zain, AA, Goh, K-J

“…Peripheral neuropathy is a known manifestation of systemic lupus erythematosus. However, the association of primary autoimmune inflammatory neuropathies such…”
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G.P.74 by Ambang, T, Tan, J.S, Cheah, T.E, Shahrizaila, N, Wong, K.T, Goh, K.J

“…Anti-Signal Recognition Particle (SRP) myopathy is a complement dependent antibody-mediated necrotising myopathy which is often clinically more severe and…”
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Myopathy with anti-signal recognition particle antibodies: Clinical and HLA associations in Malaysian patients by Ambang, T, Shanmugam, H, Tan, J, Tan, C, Cheah, T, Sargunan, S, Shahrizaila, N, Wong, K, Goh, K

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Significance of Beevor’s sign in facioscapulohumeral dystrophy and other neuromuscular diseases by Shahrizaila, N, Wills, A J

“…An atypical presentation of facioscapulohumeral dystrophy (FSH) is described, where the presence of a positive Beevor’s sign led to genetic testing and…”
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P34-17 The clinical features of myasthenia gravis in a Malaysian population by Shahrizaila, N, Lee, S.C, Goh, K.J

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PO26-TH-07 Respiratory and cardiac complications in familial tubular aggregate myopathy with pupillary miosis by Shahrizaila, N, Nicholl, D, Wills, A.J

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P21-14 Acquired neuromyotonia presenting with cold allodynia: a case report by Goh, K.-J, Yeap, S.-S, Shahrizaila, N, Tan, C.-T

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P1.21 Genetic mutations in dysferlinopathy in a Malaysian population by Looi, R.Y, Goh, K.J, Shahrizaila, N, Thong, M.K, Ahmad-Annuar, A, Wong, K.T

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P1.31 Genetic mutations in sarcoglycanopathies in a Malaysian population by Looi, R.Y, Thong, M.K, Goh, K.J, Ahmad-Annuar, A, Shahrizaila, N, Thomas, T, Khoo, T.B, Wong, K.T

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FP51-TH-05 Good clinical practice points on the use of acetylcholinesterase inhibitors in myasthenia gravis: recommendations from a South-East Asian regional special interest group on myasthenia gravis by Goh, K.J, Umapathi, T, Puvanarajah, S.D, Lo, Y.K, Goh, K.Y, Witoonpanich, R, Chankrachang, S, Misbach, J, Wibowo, B.S, Rosales, R.L, Damian, H.L.F, Chan, K.H, Chiu, H.C, Shahrizaila, N

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