Publicacions científiques

Morimoto Y, Yoshida S, Kinoshita A, Satoh C, Mishima H, Yamaguchi N, Matsuda K, Sakaguchi M, Tanaka T, Komohara Y, Imamura A, Ozawa H, Nakashima M, Kurotaki N, Kishino T, Yoshiura KI, Ono S.

Any publicació:

2019

Número de revista:

Neurology vol. 92 n. 20

http://n.neurology.org/content/92/20/e2364.abstract

Resum de comunicació congrés

Nonverbal hand movement durations indicate post-concussion symptoms of athletes. Helmich I, Hedda L

Autor/s:

Helmich I, Hedda L

Any publicació:

2019

Número de revista:

Neurology vol. 93 n. 14 Suppl.1

https://n.neurology.org/content/93/14_Supplement_1/S3.2

Article

Normal gut microbiome in NMDA receptor encephalitis

Autor/s:

Herken J, Bang C, Rühlemann MC, Finke C, Klag J, Franke A, Prüss H.

Any publicació:

2019

Número de revista:

Neurology Neuroimmunology & Neuroinflammation vol. 6 n. 6

http://nn.neurology.org/content/6/6/e632.abstract

Article

Notice of Correction

Correction for: Nowicki M, Pearlman L, Campbell C, Hicks R, Fraser DD, Hutchison J. Agitated behavior scale in pediatric traumatic brain injury. Brain Inj. 2019;33 (7): 916-921 doi:10.1080/02699052.2019.1565893. PMID: 30696278

Any publicació:

2019

https://www.tandfonline.com/doi/full/10.1080/02699052.2019.1599202

Resum de comunicació congrés

Novel Assessment for Interpreting and Documenting an Absence of Suspicion of Injury Including Protocols based on Recognizable Clinically-Relevant Neurophysiological Methods.

Autor/s:

Vincent J, Clark J, Mangine R, Keuhn-Himmler A, Hasselfeld K, Divine J, Colosimo A, Selmanovic E, Giordano N, Jacobs B

Any publicació:

2019

Número de revista:

Neurology vol. 93 n. 14 Suppl.1

https://n.neurology.org/content/93/14_Supplement_1/S31.1

Article

Novel clinical features of glycine receptor antibody syndrome: A series of 17 cases

Autor/s:

Piquet AL, Khan M, Warner JEA, Wicklund MP, Bennett JL, Leehey MA, Seeberger L, Schreiner TL, Paz Soldan MM, Clardy SL.

Any publicació:

2019

Número de revista:

Neurology Neuroimmunology & Neuroinflammation vol. 6 n. 5

http://nn.neurology.org/content/6/5/e592.abstract

Article

Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features

Autor/s:

Ziaei A, Xu X, Dehghani L, Bonnard C, Zellner A, Jin Ng AY, Tohari S, Venkatesh B, Haffner C, Reversade B, Shaygannejad V, Pouladi MA.

Any publicació:

2019

Número de revista:

Neurology® Genetics. vol. 5 n. 4

http://ng.neurology.org/content/5/4/e345.abstract

Article

Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression

Autor/s:

Vihola A, Palmio J, Danielsson O, Penttilä S, Louiselle D, Pittman S, Weihl C, Udd B.

Any publicació:

2019

Número de revista:

Neurology® Genetics. vol. 5 n. 3

http://ng.neurology.org/content/5/3/e337.abstract

Una iniciativa de:

Cercador

NONINVASIVE SPINAL NEUROMODULATION TO MAP AND AUGMENT LOWER URINARY TRACT FUNCTION IN RHESUS MACAQUES

Nonlinguistic Cognitive Factors Predict Treatment-Induced Recovery in Chronic Poststroke Aphasia.

Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities

Nonverbal hand movement durations indicate post-concussion symptoms of athletes. Helmich I, Hedda L

Normal gut microbiome in NMDA receptor encephalitis

Notice of Correction

Novel Assessment for Interpreting and Documenting an Absence of Suspicion of Injury Including Protocols based on Recognizable Clinically-Relevant Neurophysiological Methods.

Novel clinical features of glycine receptor antibody syndrome: A series of 17 cases

Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features

Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression

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