• Issue

    Journal of the Peripheral Nervous System: Volume 24, Issue 2

    165-229
    June 2019
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ISSUE INFORMATION

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Issue Information

  • Pages: 165-167
  • First Published: 20 June 2019

RESEARCH REPORTS

The utility of Guillain-Barré syndrome prognostic models in Malaysian patients

Cheng-Yin Tan,  Siti N. O. Razali,  Khean-Jin Goh,  Nortina Shahrizaila, 
  • Pages: 168-173
  • First Published: 19 April 2019

Diagnosis and treatment response in the asymmetric variant of chronic inflammatory demyelinating polyneuropathy

Ilse M. Lucke,  Luuk Wieske,  Anneke J. van der Kooi,  Ivo N. van Schaik,  Filip Eftimov,  Camiel Verhamme, 
  • Pages: 174-179
  • First Published: 15 May 2019

One-year follow-up study of neuropathic pain in chronic inflammatory demyelinating polyradiculoneuropathy

Bogdan Bjelica,  Stojan Peric,  Ivo Bozovic,  Aleksandra Kacar,  Mina Cobeljic,  Ivana Dejanovic,  Zorica Stevic,  Ivana Basta, 
  • Pages: 180-186
  • First Published: 11 April 2019

Serum neurofilament light chain in chronic inflammatory demyelinating polyneuropathy

Gwen G. A. van Lieverloo,  Luuk Wieske,  Camiel Verhamme,  Alexander F. J. Vrancken,  Pieter A. van Doorn,  Zuzanna Michalak,  Christian Barro,  Ivo N. van Schaik,  Jens Kuhle,  Filip Eftimov, 
  • Pages: 187-194
  • First Published: 11 April 2019

In situ molecular characterization of endoneurial microvessels that form the blood-nerve barrier in normal human adult peripheral nerves

Xuan Ouyang,  Chaoling Dong,  Eroboghene E. Ubogu, 
  • Pages: 195-206
  • First Published: 23 May 2019

New novel mutations in Brazilian families with X-linked Charcot-Marie-Tooth disease

Silmara P. Gouvea,  Pedro J. Tomaselli,  Luiza S. Barretto,  Keity C. B. Perina,  Fulviana S. Nyshyama,  Nilson Nicolau Jr,  Charles M. Lourenço,  Wilson Marques Jr, 
  • Pages: 207-212
  • First Published: 23 May 2019

CASE REPORTS

POLG mutations presenting as Charcot-Marie-Tooth disease

Jade Phillips,  Steve Courel,  Adriana P. Rebelo,  Dana M. Bis-Brewer,  Tanya Bardakjian,  Lois Dankwa,  Ali G. Hamedani,  Stephan Züchner,  Steven S. Scherer, 
  • Pages: 213-218
  • First Published: 06 March 2019

A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene

Stefano Tozza,  Stefania Magri,  Elena Maria Pennisi,  Erika Schirinzi,  Chiara Pisciotta,  Francesca Balistreri,  Daniele Severi,  Giulia Ricci,  Gabriele Siciliano,  Franco Taroni,  Lucio Santoro,  Fiore Manganelli, 
  • Pages: 219-223
  • First Published: 06 March 2019

Hereditary sensory and autonomic neuropathy type IC accompanied by upper motor neuron abnormalities and type II juxtafoveal retinal telangiectasias

James Triplett,  Garth Nicholson,  Carolyn Sue,  Thorsten Hornemann,  Con Yiannikas, 
  • Pages: 224-229
  • First Published: 13 March 2019