Sjö O - Search Results

1

Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.

Jensen H, Warburg M, Sjö O, Schwartz M. Jensen H, et al. Among authors: sjo o. J Med Genet. 1995 May;32(5):348-51. doi: 10.1136/jmg.32.5.348. J Med Genet. 1995. PMID: 7616540 Free PMC article.

2

Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211.

Warburg M, Sjö O, Tranebjaerg L, Fledelius HC. Warburg M, et al. Among authors: sjo o. Am J Med Genet. 1991 Jun 1;39(3):288-93. doi: 10.1002/ajmg.1320390309. Am J Med Genet. 1991. PMID: 1867279

3

Chromosome 6q deletion and retinal cone dystrophy.

Warburg M, Sjö O, Tranebjaerg L. Warburg M, et al. Among authors: sjo o. Am J Med Genet. 1991 Jan;38(1):134. doi: 10.1002/ajmg.1320380127. Am J Med Genet. 1991. PMID: 2012125 No abstract available.

4

Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder.

Nørby S, Lestienne P, Nelson I, Nielsen IM, Schmalbruch H, Sjö O, Warburg M. Nørby S, et al. Among authors: sjo o. J Med Genet. 1994 Jan;31(1):45-50. doi: 10.1136/jmg.31.1.45. J Med Genet. 1994. PMID: 8151637 Free PMC article.

5

Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism. Micro syndrome.

Warburg M, Sjö O, Fledelius HC, Pedersen SA. Warburg M, et al. Among authors: sjo o. Am J Dis Child. 1993 Dec;147(12):1309-12. doi: 10.1001/archpedi.1993.02160360051017. Am J Dis Child. 1993. PMID: 8249951

6

Retinal cone dysfunction and mental retardation associated with a de novo balanced translocation 1;6(q44;q27).

Tranebjaerg L, Sjø O, Warburg M. Tranebjaerg L, et al. Among authors: sjo o. Ophthalmic Paediatr Genet. 1986 Dec;7(3):167-73. doi: 10.3109/13816818609004134. Ophthalmic Paediatr Genet. 1986. PMID: 3561951

7

Acuity card testing of patients with cerebral visual impairment.

Hertz BG, Rosenberg J, Sjö O, Warburg M. Hertz BG, et al. Among authors: sjo o. Dev Med Child Neurol. 1988 Oct;30(5):632-7. doi: 10.1111/j.1469-8749.1988.tb04801.x. Dev Med Child Neurol. 1988. PMID: 3229561

8

Vigabatrin and retinal changes.

Jensen H, Sjö O, Uldall P, Gram L. Jensen H, et al. Among authors: sjo o. Doc Ophthalmol. 2002 Mar;104(2):171-80. doi: 10.1023/a:1014679804792. Doc Ophthalmol. 2002. PMID: 11999624

9

Retinal cone dystrophy and chromosome 6(q26) deletions.

Warburg M, Tranebjaerg L, Sjö O. Warburg M, et al. Among authors: sjo o. Ann Genet. 1990;33(2):124. Ann Genet. 1990. PMID: 2241088 No abstract available.

10

Ocular myopathy and mitochondrial DNA deletion. A presentation of seven identified Danish patients.

Magalhães PJ, Sjö O, Nørby S. Magalhães PJ, et al. Among authors: sjo o. Acta Ophthalmol Scand Suppl. 1996;(219):29-32. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741113

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