Search Results - "Cereda C"

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Effect of nitric oxide on lymphocytes from sporadic amyotrophic lateral sclerosis patients: toxic or protective role?

Authors: Cereda, C. Cova, E. Di Poto, C. et al.

Source: Neurological Sciences. Nov2006, Vol. 27 Issue 5, p312-316. 5p.

Subjects: Amyotrophic lateral sclerosis, Lymphocytes, Nitric oxide, Neurodegeneration, Medical care, Motor neuron diseases

Etiology of first-ever ischaemic stroke in European young adults: the 15 cities young stroke study.

Authors: Yesilot Barlas, N. Putaala, J. Waje‐Andreassen, U. et al.

Source: European Journal of Neurology. Nov2013, Vol. 20 Issue 11, p1431-1439. 9p. 2 Charts, 2 Graphs.

Subjects: Stroke risk factors, Diseases in young adults, Etiology of diseases, Atherosclerosis, Heterogeneity, Transient ischemic attack

Preliminary insights into RNA in CSF of pediatric SMA patients after 6 months of nusinersen.

Authors: Garofalo, M. Bonanno, S. Marcuzzo, S. et al.

Source: Biology Direct. 9/13/2023, Vol. 18 Issue 1, p1-13. 13p.

Neurological picture. Recurrent asystolia in right middle cerebral artery infarct with predominant insular involvement.

Authors: Rey V Cereda C Michel P et al.

Source: Journal of Neurology, Neurosurgery & Psychiatry. Jun2008, Vol. 79 Issue 6, p618-618. 1p.

A novel compound heterozygous mutation of C20orf54 gene associated with Brown- Vialetto- Van Laere syndrome in an Italian family.

Authors: Bandettini di Poggio, M. Gagliardi, S. Pardini, M. et al.

Source: European Journal of Neurology. Jul2013, Vol. 20 Issue 7, pe94-e95. 2p. 1 Graph.

Subjects: Motor neuron diseases, Familial diseases, Families

Geographic Terms: Italy

VPS54 genetic analysis in ALS Italian cohort.

Authors: Corrado, L. Gagliardi, S. Carlomagno, Y. et al.

Source: European Journal of Neurology. Apr2011, Vol. 18 Issue 4, pe41-e42. 2p. 1 Chart.

Subjects: Letters to the editor, Amyotrophic lateral sclerosis

Recovery from Nondominant Thalamopolar Artery Stroke.

Authors: Carota, A. Cereda, C. Calabrese, P. et al.

Source: European Neurology. 2011, Vol. 65 Issue 2, p68-69. 2p. 1 Black and White Photograph, 1 Chart.

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Bi-occipital decompressive craniectomy in refractory post traumatic intracranial hypertension: first report of one case.

Authors: Stefini, R. Bergomi, R. Catenacci, E. et al.

Source: British Journal of Neurosurgery. Oct2007, Vol. 21 Issue 5, p527-531. 5p. 2 Black and White Photographs, 1 Diagram.

P.47 Association between cobalamin deficiency detected through newborn screening and creatine levels in mothers and their offspring in the neonatal period.

Authors: Tosi, M Fiori, L Montanari, C et al.

Source: Molecular Genetics & Metabolism. 2024 Supplement 1, Vol. 141, pN.PAG-N.PAG. 1p.

Inhibition of the de-myelinating properties of Aicardi-Goutières Syndrome lymphocytes by cathepsin D silencing

Authors: Pulliero, A. Marengo, B. Longobardi, M. et al.

Source: Biochemical & Biophysical Research Communications. Jan2013, Vol. 430 Issue 3, p957-962. 6p.

Effect of the 50bp deletion polymorphism in the SOD1 promoter on SOD1 mRNA levels in Italian ALS patients

Authors: Milani, P. Gagliardi, S. Bongioanni, P. et al.

Source: Journal of the Neurological Sciences. Feb2012, Vol. 313 Issue 1/2, p75-78. 4p.

Peripheral expression of key regulatory kinases in Alzheimer's disease and Parkinson's disease

Authors: Armentero, M.T. Sinforiani, E. Ghezzi, C. et al.

Source: Neurobiology of Aging. Dec2011, Vol. 32 Issue 12, p2142-2151. 10p.

Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis.

Authors: Bo, R. Del Tiloca, C. Pensato, V. et al.

Source: Journal of Neurology, Neurosurgery & Psychiatry. Nov2011, Vol. 82 Issue 11, p1239-1243. 5p.

Palmoplantar keratoderma and Charcot–Marie– Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole-exome sequenc.

Authors: Gagliardi, S. Ricca, I. Ferrarini, A. et al.

Source: British Journal of Dermatology. Jul2017, Vol. 177 Issue 1, p284-286. 3p. 1 Color Photograph, 1 Diagram.

Cumulus cells secrete micro-vesicles carrying miRNAs: their role in the acquisition of mouse and human oocyte's developmental competence.

Authors: Cimadomo, D. Fiorentino, G. Innocenti, F. et al.

Source: Reproductive BioMedicine Online (Elsevier Science). 2022 Supplement 1, Vol. 45, pe20-e20. 1p.

New CACNA1A deletions are associated to migraine phenotypes.

Authors: Grieco, G. S. Gagliardi, S. Ricca, I. et al.

Source: Journal of Headache & Pain. 8/30/2018, Vol. 19 Issue 1, p1-1. 1p.

Small cortical stroke in the "hand knob" mimics anterior interosseous syndrome.

Authors: Granziera, C. Kuntzer, T. Vingerhoets, F. et al.

Source: Journal of Neurology. Sep2008, Vol. 255 Issue 9, p1423-1424. 2p. 2 Black and White Photographs.

Development and characterization of 3D spinal cord organoids to advance the study of amyotrophic lateral sclerosis.

Authors: Bordoni M Scarian E Messa L et al.

Source: Molecular biomedicine [Mol Biomed] 2026 Apr 24; Vol. 7 (1). Date of Electronic Publication: 2026 Apr 24.

Publication Type: Letter

Journal Info: Publisher: Springer Singapore Country of Publication: Singapore NLM ID: 9918283581406676 Publication Model: Electronic Cited Medium: Internet ISSN: 2662-8651 (Electronic) Linking ISSN: 26628651 NLM ISO Abbreviation: Mol Biomed Subsets: MEDLINE; In Process