Katz BJ - Search Results

1

Selective loss of the electroretinogram B-wave in a patient with Creutzfeldt-Jakob disease.

Katz BJ, Warner JE, Digre KB, Creel DJ. Katz BJ, et al. J Neuroophthalmol. 2000 Jun;20(2):116-8. doi: 10.1097/00041327-200020020-00011. J Neuroophthalmol. 2000. PMID: 10870926

2

Acquired and progressive retinal nerve fiber layer myelination in an adolescent.

Jean-Louis G, Katz BJ, Digre KB, Warner JE, Creger DD. Jean-Louis G, et al. Among authors: katz bj. Am J Ophthalmol. 2000 Sep;130(3):361-2. doi: 10.1016/s0002-9394(00)00550-x. Am J Ophthalmol. 2000. PMID: 11020421

3

Persistent severe visual and electroretinographic abnormalities after intravenous Cisplatin therapy.

Katz BJ, Ward JH, Digre KB, Creel DJ, Mamalis N. Katz BJ, et al. J Neuroophthalmol. 2003 Jun;23(2):132-5. doi: 10.1097/00041327-200306000-00005. J Neuroophthalmol. 2003. PMID: 12782925

4

Panhypopituitarism as an initial manifestation of primary central nervous system non-Hodgkin's lymphoma.

Katz BJ, Jones RE, Digre KB, Warner JE, Moore KR. Katz BJ, et al. Endocr Pract. 2003 Jul-Aug;9(4):296-300. doi: 10.4158/EP.9.4.296. Endocr Pract. 2003. PMID: 14561574

5

Posner-Schlossman syndrome and nonarteritic anterior ischemic optic neuropathy.

Irak I, Katz BJ, Zabriskie NA, Zimmerman PL. Irak I, et al. Among authors: katz bj. J Neuroophthalmol. 2003 Dec;23(4):264-7. doi: 10.1097/00041327-200312000-00005. J Neuroophthalmol. 2003. PMID: 14663306

6

Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.

Payne M, Yang Z, Katz BJ, Warner JE, Weight CJ, Zhao Y, Pearson ED, Treft RL, Hillman T, Kennedy RJ, Meire FM, Zhang K. Payne M, et al. Among authors: katz bj. Am J Ophthalmol. 2004 Nov;138(5):749-55. doi: 10.1016/j.ajo.2004.06.011. Am J Ophthalmol. 2004. PMID: 15531309

7

Progression from anomalous optic discs to visible optic disc drusen.

Spencer TS, Katz BJ, Weber SW, Digre KB. Spencer TS, et al. Among authors: katz bj. J Neuroophthalmol. 2004 Dec;24(4):297-8. doi: 10.1097/00041327-200412000-00006. J Neuroophthalmol. 2004. PMID: 15662245

8

Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A).

Jiang L, Katz BJ, Yang Z, Zhao Y, Faulkner N, Hu J, Baird J, Baehr W, Creel DJ, Zhang K. Jiang L, et al. Among authors: katz bj. Mol Vis. 2005 Feb 20;11:143-51. Mol Vis. 2005. PMID: 15735604 Free article.

9

Measurement of the scleral canal using optical coherence tomography in patients with optic nerve drusen.

Floyd MS, Katz BJ, Digre KB. Floyd MS, et al. Among authors: katz bj. Am J Ophthalmol. 2005 Apr;139(4):664-9. doi: 10.1016/j.ajo.2004.11.041. Am J Ophthalmol. 2005. PMID: 15808162

10

Metamorphopsia as an initial complaint of idiopathic intracranial hypertension.

Warner JE, Katz BJ. Warner JE, et al. Among authors: katz bj. Arch Ophthalmol. 2005 Jul;123(7):1003-6. doi: 10.1001/archopht.123.7.1003. Arch Ophthalmol. 2005. PMID: 16009846 No abstract available.

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