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Neurosciences Area

As seen in: Oxford University Press (OUP), Frontiers
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Articles by Neurosciences Area

Immune cell population and cytokine profiling suggest age dependent differences in the response to SARS-CoV-2 infection

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By San Sebastian, Neurosciences Area, UGC Laboratories Gipuzkoa
| Frontiers
Larraitz A.
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Retinoids and Amyotrophic Lateral Sclerosis

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By Neurosciences Area, Javier Riancho
| JAMA (The Journal of the American Medical Association) Verified
To the Editor We read with great interest the article by Rosenbohm and colleagues.1 They conducted a case-control study and reported that retinol-binding protein 4 had an inverse association with both risk for amyotrophic lateral sclerosis (ALS) and disease prognosis. Although we agree with the relevance of the reported results and their interpretation, we would like to comment on 2 issues that might also correlate with these findings.
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Dominant LGMD2A: alternative diagnosis or hidden digenism?

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By Neurosciences Area, López de Munain
| Oxford University Press (OUP)
We read with great interest the work recently published in Brain (Vissing et al., 2016), in which the findings on limb girdle muscular dystrophy families from the UK, Denmark and Sweden are described. The cases showed a segregation pattern compatible with a dominant transmission. All the affected cases except for one share a heterozygous mutation in the CAPN3 gene previously described in recessive forms of limb girdle muscular dystrophy 2A (LGMD2A) (Richard et al., 1997; Groen et al., 2007).
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Dominant LGMD2A: alternative diagnosis or hidden digenism?

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By Neurosciences Area, López de Munain, Walter MC, De Paula F
| Oxford University Press (OUP)
We read with great interest the work recently published in Brain (Vissing et al., 2016), in which the findings on limb girdle muscular dystrophy families from the UK, Denmark and Sweden are described. The cases showed a segregation pattern compatible with a dominant transmission. All the affected cases except for one share a heterozygous mutation in the CAPN3 gene previously described in recessive forms of limb girdle muscular dystrophy 2A (LGMD2A) (Richard et al., 1997; Groen et al., 2007).
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