R01 EY10864/EY/NEI NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1995	2
1996	1
1997	2
1998	1
1999	1
2001	1
2021	0

1

Hereditary optic neuropathies.

Johns DR, Newman NJ. Johns DR, et al. Semin Ophthalmol. 1995 Sep;10(3):203-13. doi: 10.3109/08820539509060974. Semin Ophthalmol. 1995. PMID: 10159745 Review. No abstract available.

2

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease.

Johns DR. Johns DR. N Engl J Med. 1995 Sep 7;333(10):638-44. doi: 10.1056/NEJM199509073331007. N Engl J Med. 1995. PMID: 7637726 Review. No abstract available.

3

The other human genome: mitochondrial DNA and disease.

Johns DR. Johns DR. Nat Med. 1996 Oct;2(10):1065-8. doi: 10.1038/nm1096-1065. Nat Med. 1996. PMID: 8837595 Review. No abstract available.

4

A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic?

Simon DK, Tarnopolsky MA, Greenamyre JT, Johns DR. Simon DK, et al. J Med Genet. 2001 Jan;38(1):58-61. doi: 10.1136/jmg.38.1.58. J Med Genet. 2001. PMID: 11332403 Free PMC article. No abstract available.

5

Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles.

Engle EC, Goumnerov BC, McKeown CA, Schatz M, Johns DR, Porter JD, Beggs AH. Engle EC, et al. Ann Neurol. 1997 Mar;41(3):314-25. doi: 10.1002/ana.410410306. Ann Neurol. 1997. PMID: 9066352

6

Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation.

Simon DK, Pulst SM, Sutton JP, Browne SE, Beal MF, Johns DR. Simon DK, et al. Neurology. 1999 Nov 10;53(8):1787-93. doi: 10.1212/wnl.53.8.1787. Neurology. 1999. PMID: 10563629

7

Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutation.

Austin SA, Vriesendorp FJ, Thandroyen FT, Hecht JT, Jones OT, Johns DR. Austin SA, et al. Neurology. 1998 Nov;51(5):1447-50. doi: 10.1212/wnl.51.5.1447. Neurology. 1998. PMID: 9818878

8

Sensory ataxic neuropathy as the presenting feature of a novel mitochondrial disease.

Fadic R, Russell JA, Vedanarayanan VV, Lehar M, Kuncl RW, Johns DR. Fadic R, et al. Neurology. 1997 Jul;49(1):239-45. doi: 10.1212/wnl.49.1.239. Neurology. 1997. PMID: 9222196

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