Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Kalpana Prasad"'
Autor:
Zhiyong Chen, Monica Saini, Jasmine Shimin Koh, Gareth Zigui Lim, Nancy Jiaojiao Dang, Kalpana Prasad, Swee Hoon Koh, Karine Su Shan Tay, Ming Lee, Helen Lisa Ong, Yi Zhao, Ankit Tandon, Josiah Yui Huei Chai
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background We report a patient with a novel c.737 C > T variant (p.Ser246Leu) of the TPM3 gene presenting with adult-onset distal myopathy. Case presentation A 35-year-old Chinese male patient presented with a history of progressive finger w
Externí odkaz:
https://doaj.org/article/7ca7f92fbd3944b0bcbf8f0ad5df08b7
Autor:
Zhiyong Chen, Monica Saini, Shermyn X. M. Neo, Peng-Soon Ng, Jasmine S. Koh, Kalpana Prasad, Kamal Verma, Sonia Davila, Weng Khong Lim, Ziqun Phua, Michelle M. Li, Corrine Kang, Karine S. S. Tay, Josiah Y. H. Chai
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Charcot-Marie-Tooth type 1A (CMT1A) is typically characterised as a childhood-onset, symmetrical, length-dependent polyneuropathy with a gradual progressive clinical course. Acute to subacute neurological deterioration in CMT1A is rare, and has been
Externí odkaz:
https://doaj.org/article/122ed859f02f48209083cb190856b4b9
Publikováno v:
Journal of Movement Disorders, Vol 10, Iss 2, Pp 99-101 (2017)
We present a case of 32-year-old male with profound mental retardation and autism spectrum disorder who had presented with seizures, rigidity and elevated creatine kinase and was initially diagnosed as neuroleptic malignant syndrome (NMS). The patien
Externí odkaz:
https://doaj.org/article/0e4108ee9c044caf8e10dd01ea36d44a
Autor:
Zhiyong, Chen, Monica, Saini, Jasmine S, Koh, Kalpana, Prasad, Swee Hoon, Koh, Karine S S, Tay, Ming, Lee, Yi Jayne, Tan, Adeline S L, Ng, Stacey Kiat Hong, Tay, Kong Bing, Tan, Ankit, Tandon, Jeane M M, Tan, Josiah Y H, Chai
Publikováno v:
Journal of Neuromuscular Diseases. 10:91-106
Aim: We describe a cohort of five patients with limb-girdle muscular dystrophy (LGMD) 2G/LGMD-R7 in a South-east Asian cohort. Background: LGMD2G/LGMD-R7-telethonin-related is caused by mutations in the TCAP gene that encodes for telethonin. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d40ff6ceedd6b09b9014b46e52ceb028
https://doi.org/10.3233/jnd-221517
https://doi.org/10.3233/jnd-221517
Publikováno v:
GLOBAL JOURNAL FOR RESEARCH ANALYSIS. :1-3
Introduction: Ectopic pregnancy occurs at a rate of about 1-2% of pregnancies and can occur in any sexually active woman of reproductive age. The incidence has been increasing for years and currently it is two to three times higher than it was 20 or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5305908964d76a5bcf9f95408777e2f9
https://doi.org/10.36106/gjra/4305198
https://doi.org/10.36106/gjra/4305198
Autor:
Chen Yu, Karine S S Tay, Chai Beng Tan, Peck Kee Lim, A R Juraidah, Kalpana Prasad, Adeline S.L. Ng, Ming Hui Yong, Thirugnanam Umapathi, Jasmine Shimin Koh, Zhiyong Chen, Su Rong Fam, Monica Saini, Yi Jayne Tan, Josiah Y H Chai, Peng Soon Ng, Kamal Verma
Publikováno v:
Journal of neuromuscular diseases. 8(4)
Background and aims: Studies of hereditary transthyretin amyloidosis (ATTRv amyloidosis) in South-East Asia are underrepresented in the literature. We report the unique phenotypic and genetic characteristics of this disorder in a multiracial South-Ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bfe85b135fb3a9deef8af1b55e4e988
https://pubmed.ncbi.nlm.nih.gov/34024775
https://pubmed.ncbi.nlm.nih.gov/34024775
Publikováno v:
Journal of Movement Disorders
Journal of Movement Disorders, Vol 10, Iss 2, Pp 99-101 (2017)
Journal of Movement Disorders, Vol 10, Iss 2, Pp 99-101 (2017)
We present a case of 32-year-old male with profound mental retardation and autism spectrum disorder who had presented with seizures, rigidity and elevated creatine kinase and was initially diagnosed as neuroleptic malignant syndrome (NMS). The patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::148109049116a7da3e72517a20956ccf
http://europepmc.org/articles/PMC5435832
http://europepmc.org/articles/PMC5435832
Publikováno v:
Neuroimaging Clinics of North America. 24:49-65
This article is a primer on the pathophysiology and clinical evaluation of peripheral neuropathy for the radiologist. Magnetic resonance neurography has utility in the diagnosis of many focal peripheral nerve lesions. When combined with history, exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7f757b3622f9ce124ebcfa4ee3e3a11
https://doi.org/10.1016/j.nic.2013.03.023
https://doi.org/10.1016/j.nic.2013.03.023
Autor:
Christoph S. Burkhart, Chan-Seung Chung, Lena Kilander, Hee Young Kang, D. Cheng, Dorene M. Rentz, P. Wolkow, Andreas J. Fallgatter, Lauren E. Olson, Druck Reinhardt Druck Basel, Reisa A. Sperling, Keith A. Johnson, Young Chul Youn, Maria Lage Barca, J.A. Luchsinger, Kyung Ryeol Cha, Kee Hyung Park, A. Szczudlik, Jun-Young Lee, Luzius A. Steiner, Barbara McKenzie, Geir Selbæk, Duk L. Na, Yong S. Shim, Meghan T. Frey, Bon D. Ku, M. Barcikowska, Alexa Gagneux, A. Klimkowicz-Mrowiec, Daniela Berg, Lars Lannfelt, A. Slowik, So Young Moon, Lynn Wiryasaputra, Meredeth A. Rowe, M.X. Tang, Kalpana Prasad, Alzheimer’s Disease Neuroimaging Initiative, Seong Yoon Kim, R. Mayeux, Sang Yun Kim, Kyung Won Park, Sang Won Seo, Manfred Berres, Katja Hagen, Seol-Heui Han, Andreas U. Monsch, Elke Stransky, Gad A. Marshall, Walter Maetzler, A. Maruszak, Melinda R. Steis, Hae-Kwan Cheong, Jerson Laks, Christoph Laske, J. Alex Becker, Stephan P. Strebel, Mary Elizabeth Bowen, Dagmar Birkner-Binder, Jacqueline E. Maye, M. Styczynska, A. Witkowski, Seong Hye Choi, Satz Mengensatzproduktion, J. Noble, Jung Eun Kim, Amanda Ng, N. Schupf, Björn Zethelius, Elina Rönnemaa, M. Marona, Knut Engedal, Nagaendran Kandiah
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 31:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::353fc86631e0053e01607a4ce7966236
https://doi.org/10.1159/000330829
https://doi.org/10.1159/000330829
Publikováno v:
Brain and Behavior
The Brighton Collaboration criteria have standardized the clinical and laboratory-supported diagnosis of Guillain-Barré syndrome (GBS) and Miller Fisher syndrome (MFS) in a way that is applicable in many parts of the world with variable resources. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8eb6789e00e38683060db5b4fec59e7
https://doi.org/10.1002/brb3.960
https://doi.org/10.1002/brb3.960