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Peripheral nerve disease
Citations 1-10 of 10 total displayed.
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Most recent content
(1 Jun 2009):
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Generating hand dysaesthesiae: the "GHD phenomenon" – straight to the diagnosis
- Roisin Lonergan, Grainne Gorman, Michael D Alexander, Ronan Killeen, Catherine de Blacam, and Niall Tubridy
BMJ Case Reports doi: 10.1136/bcr.02.2009.1544
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Past content
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Postural orthostatic tachycardia syndrome
- Una Graham and Kate M Ritchie
BMJ Case Reports doi: 10.1136/bcr.10.2008.1132
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Papilloedema and hypertrichosis: the varied and harried manifestations of POEMS syndrome
- Richard Alan Rison
BMJ Case Reports doi: 10.1136/bcr.09.2008.1000
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Diagnostic value of anti-GQ1b antibodies in a patient with relapsing dysarthria and ataxia
- Mark Kuijf, Liselotte Ruts, Pieter A van Doorn, Peter J Koudstaal, and Bart C Jacobs
BMJ Case Reports doi: 10.1136/bcr.08.2008.0783
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Painful neuropathy with skin denervation after prolonged use of linezolid
- Chi-Chao Chao, Hsin-Yun Sun, Yang-Chyuan Chang, and Sung-Tsang Hsieh
BMJ Case Reports doi: 10.1136/bcr.08.2008.0702
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Hypophosphataemic neuropathy during total parenteral nutrition
- Yohei Iguchi, Keiko Mori, Haruki Koike, Kazuo Mano, Yoji Goto, Takashi Kato, Tomonobu Nakano, and Gen Sobue
BMJ Case Reports doi: 10.1136/bcr.08.2008.0718
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Possible case of peripheral osmotic demyelination syndrome
- P J Serrano-Castro, G Alonso-Verdegay, G López-Martínez, A Arjona-Padillo, J R Callejón, V M Olmedo, P Guardado-Santervás, A Huete-Hurtado, J Olivares-Romero, and C Naranjo Fernández
BMJ Case Reports doi: 10.1136/bcr.08.2008.0710
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Successful repeated treatment with high dose cyclophosphamide and autologous blood stem cell transplantation in CIDP
- Hans W Axelson, Gunnar Öberg, and Håkan Askmark
BMJ Case Reports doi: 10.1136/bcr.09.2008.0927
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Relapse of chronic inflammatory demyelinating polyneuropathy 5 years after autologous stem cell transplantation
- M Vermeulen and M H J van Oers
BMJ Case Reports doi: 10.1136/bcr.08.2008.0646
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A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy
- Maria Muglia, Giovanni Vazza, Alessandra Patitucci, Micaela Milani, Davide Pareyson, Franco Taroni, Aldo Quattrone, and Maria Luisa Mostacciuolo
BMJ Case Reports doi: 10.1136/bcr.08.2008.0652
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