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Expanding the phenotype of <i>TARDBP</i> mutation in a Tunisian family with clinical phenotype heterogeneity.

Kacem I, Sghaier I, Ticozzi N, Mrabet S, Paverelli S, Nasri A, Ratti A, Ben Djebara M, Gargouri-Berrachid A, Silani V, Gouider R.

Amyotroph Lateral Scler Frontotemporal Degener · 2022-07-05

DOI: 10.1080/21678421.2022.2089856PMID: 35793404

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Pre-clinical Studies Identifying Molecular Pathways of Neuroinflammation in Parkinson's Disease: A Systematic Review.

Fathi M, Vakili K, Yaghoobpoor S, Qadirifard MS, Kosari M, Naghsh N, Asgari Taei A, Klegeris A, Dehghani M, Bahrami A, Taheri H, Mohamadkhani A, Hajibeygi R, Rezaei Tavirani M, Sayehmiri F.

Front Aging Neurosci · 2022-07-04

DOI: 10.3389/fnagi.2022.855776PMID: 35912090

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

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