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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1977 1
1978 1
1979 2
2006 1
2008 1
2012 1
2013 1
2020 1
2021 0
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9 results
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Page 1
Phenotypic variability in chorea-acanthocytosis associated with novel VPS13A mutations.
Niemelä V, Salih A, Solea D, Lindvall B, Weinberg J, Miltenberger G, Granberg T, Tzovla A, Nordin L, Danfors T, Savitcheva I, Dahl N, Paucar M. Niemelä V, et al. Among authors: miltenberger g. Neurol Genet. 2020 Apr 27;6(3):e426. doi: 10.1212/NXG.0000000000000426. eCollection 2020 Jun. Neurol Genet. 2020. PMID: 32494755 Free PMC article.
Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation.
Chester C, de Carvalho M, Miltenberger G, Pereira S, Dillen L, van der Zee J, van Broeckhoven C, de Mendonça A. Chester C, et al. Among authors: miltenberger g. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Jan;14(1):70-2. doi: 10.3109/17482968.2012.690418. Epub 2012 Jun 29. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 22742426
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome.
Auer-Grumbach M, Fischer C, Papić L, John E, Plecko B, Bittner RE, Bernert G, Pieber TR, Miltenberger G, Schwarz R, Windpassinger C, Grill F, Timmerman V, Speicher MR, Janecke AR. Auer-Grumbach M, et al. Among authors: miltenberger g. Neuropediatrics. 2008 Feb;39(1):33-8. doi: 10.1055/s-2008-1077085. Neuropediatrics. 2008. PMID: 18504680 Free PMC article.
Central auditory testing with peripheral hearing loss.
Miltenberger GE, Dawson GJ, Raica AN. Miltenberger GE, et al. Arch Otolaryngol. 1978 Jan;104(1):11-5. doi: 10.1001/archotol.1978.00790010015004. Arch Otolaryngol. 1978. PMID: 619879