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Showing 25 to 28 of 28 entries
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European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force-Second revision.

Journal of the peripheral nervous system : JPNS

Van den Bergh PYK, van Doorn PA, Hadden RDM, Avau B, Vankrunkelsven P, Allen JA, Attarian S, Blomkwist-Markens PH, Cornblath DR, Eftimov F, Goedee HS, Harbo T, Kuwabara S, Lewis RA, Lunn MP, Nobile-Orazio E, Querol L, Rajabally YA, Sommer C, Topaloglu HA.
PMID: 34085743
J Peripher Nerv Syst. 2021 Sep;26(3):242-268. doi: 10.1111/jns.12455. Epub 2021 Jul 30.

To revise the 2010 consensus guideline on chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Seventeen disease experts, a patient representative, and two Cochrane methodologists constructed 12 Population/Intervention/Comparison/Outcome (PICO) questions regarding diagnosis and treatment to guide the literature search. Data were extracted...

Fatigue in chronic inflammatory demyelinating polyradiculoneuropathy.

Muscle & nerve

Peric SZ, Cornblath DR.
PMID: 33002222
Muscle Nerve. 2020 Dec;62(6):649-651. doi: 10.1002/mus.27076. Epub 2020 Oct 07.

No abstract available.

Preliminary Findings of a Dedicated Ocular Myasthenia Gravis Rating Scale: The OMGRate.

Neuro-ophthalmology (Aeolus Press)

Wong SH, Eggenberger E, Cornblath W, Xhepa A, Miranda E, Lee H, Burke A, Barnett C.
PMID: 32395166
Neuroophthalmology. 2019 Oct 09;44(3):148-156. doi: 10.1080/01658107.2019.1660686. eCollection 2020 Jun.

There is a pressing need for a robust rating scale for ocular myasthenia gravis (OMG). Rating scales for myasthenia gravis (MG) research have a predominant focus on generalised disease. We present results of the first dedicated rating scale for...

A recurrent MORC2 mutation causes Charcot-Marie-Tooth disease type 2Z.

Journal of the peripheral nervous system : JPNS

Vujovic D, Cornblath DR, Scherer SS.
PMID: 33844363
J Peripher Nerv Syst. 2021 Jun;26(2):184-186. doi: 10.1111/jns.12443. Epub 2021 Apr 19.

We found a p.Ala406Val (c.1217C > T) mutation in MORC2 in three individuals, from two families. All three individuals were evaluated and clinical electrophysiology was completed. The neuropathy began in childhood to early adulthood, with distal weakness progressing to...

Showing 25 to 28 of 28 entries