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Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

Autor: Li, Rong, Johnson, Anne B., Salomons, Gajja, Goldman, James E., Naidu, Sakkubai, Quinlan, Roy, Cree, Bruce, Ruyle, Stephanie Z., Banwell, Brenda, D'Hooghe, Marc, Siebert, Joseph R., Rolf, Cristin M., Cox, Helen, Reddy, Alyssa, Gutiérrez-Solana, Luis González, Collins, Amanda, Weller, Roy O., Messing, Albee, Van Der Knaap, Marjo S., Brenner, Michael

Publikováno v: Annals of neurology, 57(3), 310-326. John Wiley and Sons Inc.
Annals of Neurology, 57(3), 310-326. John Wiley and Sons Inc.
Li, R, Johnson, A B, Salomons, G, Goldman, J E, Naidu, S, Quinlan, R, Cree, B, Ruyle, S Z, Banwell, B, D'Hooghe, M, Siebert, J R, Rolf, C M, Cox, H, Reddy, A, Gutiérrez-Solana, L G, Collins, A, Weller, R O, Messing, A, Van Der Knaap, M S & Brenner, M 2005, ' Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease ', Annals of Neurology, vol. 57, no. 3, pp. 310-326 . https://doi.org/10.1002/ana.20406

Alexander disease is a progressive, usually fatal neurological disorder defined by the widespread and abundant presence in astrocytes of protein aggregates called Rosenthal fibers. The disease most often occurs in infants younger than 2 years and has

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https://pure.amc.nl/en/publications/glial-fibrillary-acidic-protein-mutations-in-infantile-juvenile-and-adult-forms-of-alexander-disease(ad90b0a8-7e80-459e-a35c-902e73b7d3ee).html

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Plasma cell granulomas of the brain: pediatric case presentation and review of the literature.

Autor: Tresser, Nancy, Rolf, Cristin, Cohen, Mark

Publikováno v: Child's Nervous System; Jan1996, Vol. 12 Issue 1, p52-57, 6p

Authors' Response.

Autor: Pepin, Melanie, Byers, Peter H., Shields, Lisa B.E., Rolf, Cristin M., Davis, Gregory J., Hunsaker, John C.

Publikováno v: Journal of Forensic Sciences; Sep2011, Vol. 56 Issue 5, p1397-1397, 1p