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Alexander-Krankheit (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alexander-Krankheit" in German language version.

refsWebsite
Global rank German rank
10nih.gov
4th place
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1oxfordjournals.org
1,389th place
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1web.archive.org
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1ajnr.org
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1zdb-katalog.de
123rd place
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1doi.org
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1sciencedirect.com
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1ionistrials.com
low place
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1umassmed.edu
low place
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1hsr.it
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1merckvetmanual.com
9,011th place
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ajnr.org

  • van der Knaap u. a.: Alexander disease: diagnosis with MR imaging. In: AJNR Am J Neuroradiol. 2001; 22(3), S. 541–552, PMID 11237983 (Volltext).

doi.org

  • Ylenia Vaia, Eleonora Mura, Davide Tonduti: Type I Alexander disease: Update and validation of the clinical evolution-based classification. In: Molecular Genetics and Metabolism. Band 138, Nr. 3, 1. März 2023, ISSN 1096-7192, S. 107540, doi:10.1016/j.ymgme.2023.107540 (sciencedirect.com [abgerufen am 1. Juli 2023]).

hsr.it

research.hsr.it

ionistrials.com

merckvetmanual.com

nih.gov

ncbi.nlm.nih.gov

  • Scolding: Regenerating myelin. In: Brain. 2004; 127, S. 2144–2147, PMID 11673315 (Volltext).
  • Alexander: Progressive fibrinoid degeneration of fibrillary astrozytes associated with mental retardation in a hydrozephalic infant. In: Brain. 1949; 72, S. 373–381, PMID 15409268 (Erstbeschreibung).
  • Pareyson u. a.: Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature. In: Brain. 2008; 131(Pt 9), S. 2321–2331, PMID 18684770.
  • van der Knaap u. a.: Alexander disease: diagnosis with MR imaging. In: AJNR Am J Neuroradiol. 2001; 22(3), S. 541–552, PMID 11237983 (Volltext).
  • Farina u. a.: Can MR imaging diagnose adult-onset Alexander disease? In: AJNR Am J Neuroradiol. 2008; 29(6), S. 1190–1196, PMID 18388212.
  • Brenner u. a.: Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander Disease. In: Nature Genetics. 2001; 27, S. 117–120, PMID 11138011.
  • Gorospe: Alexander disease. In: Gene Reviews. (Volltext)
  • Rodriguez u. a.: Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation. In: Am J Hum Genet. 2001; 69(5), S. 1134–1140, PMID 11567214.
  • Wohlwill u. a.: Dysmyelinogenic leukodystrophy; report of a case of a new, presumably familial type of leukodystrophy with megalobarencephaly. In: J Neuropathol Exp Neurol. 1959; 18(3), S. 359–383, PMID 13665382.
  • Li u. a.: Propensity for paternal inheritance of de novo mutations in Alexander disease. In: Hum Genet. 2006; 119, S. 137–144, PMID 16365765.

oxfordjournals.org

brain.oxfordjournals.org

sciencedirect.com

  • Ylenia Vaia, Eleonora Mura, Davide Tonduti: Type I Alexander disease: Update and validation of the clinical evolution-based classification. In: Molecular Genetics and Metabolism. Band 138, Nr. 3, 1. März 2023, ISSN 1096-7192, S. 107540, doi:10.1016/j.ymgme.2023.107540 (sciencedirect.com [abgerufen am 1. Juli 2023]).

umassmed.edu

web.archive.org

zdb-katalog.de

  • Ylenia Vaia, Eleonora Mura, Davide Tonduti: Type I Alexander disease: Update and validation of the clinical evolution-based classification. In: Molecular Genetics and Metabolism. Band 138, Nr. 3, 1. März 2023, ISSN 1096-7192, S. 107540, doi:10.1016/j.ymgme.2023.107540 (sciencedirect.com [abgerufen am 1. Juli 2023]).