Connection

ANDREW LEE to Mutation

This is a "connection" page, showing publications ANDREW LEE has written about Mutation.
Connection Strength

0.396
  1. Prothrombin 20210A mutation in acute posterior cerebral artery infarction and branch retinal vein occlusion. Can J Ophthalmol. 2023 12; 58(6):e259-e262.
    View in: PubMed
    Score: 0.076
  2. BRAF and MEK inhibitor-associated optic neuropathy in stage IIIC BRAF+ melanoma. Can J Ophthalmol. 2023 12; 58(6):e251-e253.
    View in: PubMed
    Score: 0.076
  3. Hydroxychloroquine toxicity unmasking an occult retinitis pigmentosa carrier. Can J Ophthalmol. 2023 08; 58(4):e179-e181.
    View in: PubMed
    Score: 0.074
  4. Gene Therapy for Leber's Hereditary Optic Neuropathy: Time to Include a True Placebo Arm? Am J Ophthalmol. 2022 09; 241:A11-A12.
    View in: PubMed
    Score: 0.070
  5. Delayed diagnosis of autosomal dominant optic atrophy until seventh decade of life. Can J Ophthalmol. 2022 06; 57(3):e96-e100.
    View in: PubMed
    Score: 0.066
  6. Leber hereditary optic neuropathy associated with use of ephedra alkaloids. Am J Ophthalmol. 2002 Dec; 134(6):918-20.
    View in: PubMed
    Score: 0.018
  7. Dominant Optic Atrophy: How to Determine the Pathogenicity of Novel Variants? J Neuroophthalmol. 2022 06 01; 42(2):149-153.
    View in: PubMed
    Score: 0.017
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.