Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

26 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy.
Kjer P, Jensen OA, Klinken L. Kjer P, et al. Acta Ophthalmol (Copenh). 1983 Apr;61(2):300-12. doi: 10.1111/j.1755-3768.1983.tb01424.x. Acta Ophthalmol (Copenh). 1983. PMID: 6880639
Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects.
Kjer B, Eiberg H, Kjer P, Rosenberg T. Kjer B, et al. Among authors: kjer p. Acta Ophthalmol Scand. 1996 Feb;74(1):3-7. doi: 10.1111/j.1600-0420.1996.tb00672.x. Acta Ophthalmol Scand. 1996. PMID: 8689476
Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families.
KJER P. KJER P. Acta Ophthalmol Suppl. 1959;164(Supp 54):1-147. Acta Ophthalmol Suppl. 1959. PMID: 13660776 No abstract available.
Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.
Eiberg H, Kjer B, Kjer P, Rosenberg T. Eiberg H, et al. Among authors: kjer p. Hum Mol Genet. 1994 Jun;3(6):977-80. doi: 10.1093/hmg/3.6.977. Hum Mol Genet. 1994. PMID: 7951248
Hereditary infantile optic atrophy with dominant transmission.
KJER P. KJER P. Acta Genet Stat Med. 1957;7(2):290-1. doi: 10.1159/000150988. Acta Genet Stat Med. 1957. PMID: 13469166 No abstract available.
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect.
Thiselton DL, Alexander C, Morris A, Brooks S, Rosenberg T, Eiberg H, Kjer B, Kjer P, Bhattacharya SS, Votruba M. Thiselton DL, et al. Among authors: kjer p. Hum Genet. 2001 Nov;109(5):498-502. doi: 10.1007/s004390100600. Epub 2001 Oct 3. Hum Genet. 2001. PMID: 11735024
Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig.
Jonasdottir A, Eiberg H, Kjer B, Kjer P, Rosenberg T. Jonasdottir A, et al. Among authors: kjer p. Hum Genet. 1997 Jan;99(1):115-20. doi: 10.1007/s004390050323. Hum Genet. 1997. PMID: 9003507
Hereditary infantile optic atrophy with dominant transmission; preliminary report.
KJER P. KJER P. Dan Med Bull. 1956 Aug;3(5):135-41. Dan Med Bull. 1956. PMID: 13356616 No abstract available.
Diagnosis of carotid artery disease. A preliminary report.
von Wowern F, Eiken M, Hansen OE, Jorgensen OE, Kjer P, Kristensen JK, Mortensen T. von Wowern F, et al. Among authors: kjer p. Dan Med Bull. 1968 Sep;15(7):218-21. Dan Med Bull. 1968. PMID: 5708587 No abstract available.
Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies.
La Morgia C, Ross-Cisneros FN, Sadun AA, Hannibal J, Munarini A, Mantovani V, Barboni P, Cantalupo G, Tozer KR, Sancisi E, Salomao SR, Moraes MN, Moraes-Filho MN, Heegaard S, Milea D, Kjer P, Montagna P, Carelli V. La Morgia C, et al. Among authors: kjer p. Brain. 2010 Aug;133(Pt 8):2426-38. doi: 10.1093/brain/awq155. Epub 2010 Jul 21. Brain. 2010. PMID: 20659957 Free PMC article.
26 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback