Search Results - "Liew, Wendy K.M"

Longitudinal Patterns of Thalidomide Neuropathy in Children and Adolescents by Liew, Wendy K.M., MBChB, MRCPCH, Pacak, Christina A., PhD, Visyak, Nicole, MA, MS, Darras, Basil T., MD, Bousvaros, Athos, MD, MPH, Kang, Peter B., MD

“…Objective To characterize the longitudinal clinical and electrophysiological patterns of thalidomide neuropathy in children and adolescents. Study design…”
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Teaching NeuroImages: Characteristic phenotype of Ullrich congenital muscular dystrophy by Liew, Wendy K.M, Darras, Basil T

“…A 21-year-old woman presented with clinically classic signs of Ullrich congenital muscular dystrophy (figure). Genetic testing of collagen VI genes revealed a…”
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Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD) Syndrome May Have a Hypothalamus–Periaqueductal Gray Localization by Chow, Cristelle, MBBS, MRCPCH, MMed (Paeds), Fortier, Marielle Valerie, MD, FRCPC, Das, Lena, MD, FAAP, Menon, Anuradha P., MBBS, MRCPCH, MMed (Paeds), Vasanwala, Rashida, MBBS, MRCPCH, MD (Paeds), Lam, Joyce C.M., MBBS, MRCPCH, MMed (Paeds), Ng, Zhi Min, MBBS, MRCPCH, MMed (Paeds), Ling, Simon Robert, MBBS, FRACP, Chan, Derrick W.S., BMBS, MRCPCH, Choong, Chew Thye, MBBS, MMed (Paeds), Liew, Wendy K.M., MBChB, MRCPCH, Thomas, Terrence, MD, MRCPCH

“…Abstract Background Anatomical localization of the rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD)…”
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Teaching Neuro Images : Characteristic phenotype of Ullrich congenital muscular dystrophy by Liew, Wendy K.M., Darras, Basil T.

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Comparison of plasmapheresis and intravenous immunoglobulin as maintenance therapies for juvenile myasthenia gravis by Liew, Wendy K M, Powell, Christine A, Sloan, Steven R, Shamberger, Robert C, Weldon, Christopher B, Darras, Basil T, Kang, Peter B

“…Juvenile myasthenia gravis (MG) is a relatively rare autoimmune disorder. The comparative efficacy of plasmapheresis (PLEX) vs immunoglobulin as maintenance…”
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Update on juvenile myasthenia gravis by Liew, Wendy K M, Kang, Peter B

“…Juvenile myasthenia gravis is a relatively rare autoimmune neuromuscular disorder. The pathophysiology of juvenile myasthenia gravis is similar to that of…”
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Current advances in drug development in spinal muscular atrophy by Singh, Priyamvada, Liew, Wendy K M, Darras, Basil T

“…Spinal muscular atrophy (SMA) is a pediatric neuromuscular condition characterized by progressive proximal muscle weakness. It is one of the most common…”
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Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxia by Liew, Wendy K M, Ben-Omran, Tawfeg, Darras, Basil T, Prabhu, Sanjay P, De Vivo, Darryl C, Vatta, Matteo, Yang, Yaping, Eng, Christine M, Chung, Wendy K

“…Ataxia in children is a diagnostic challenge. Besides the more common acquired causes of ataxia, there are more than 50 inherited disorders associated with…”
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Recent developments in the treatment of Duchenne muscular dystrophy and spinal muscular atrophy by Liew, Wendy K. M., Kang, Peter B.

“…Pediatric neuromuscular disorders comprise a large variety of disorders that can be classified based on their neuroanatomical localization, patterns of…”
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