Johns DR - Search Results

1

Rutkove SB, De Girolami U, Preston DC, Freeman R, Nardin RA, Gouras GK, Johns DR, Raynor EM. Rutkove SB, et al. Among authors: johns dr. Muscle Nerve. 1996 Jul;19(7):870-5. doi: 10.1002/(SICI)1097-4598(199607)19:7<870::AID-MUS9>3.0.CO;2-6. Muscle Nerve. 1996. PMID: 8965841

2

Mitochondrial dysfunction and neuromuscular disease.

Nardin RA, Johns DR. Nardin RA, et al. Among authors: johns dr. Muscle Nerve. 2001 Feb;24(2):170-91. doi: 10.1002/1097-4598(200102)24:2<170::aid-mus30>3.0.co;2-0. Muscle Nerve. 2001. PMID: 11180201 Review.

3

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. Among authors: johns dr. Neurology. 1997 Jul;49(1):239-45. doi: 10.1212/wnl.49.1.239. Neurology. 1997. PMID: 9222196

4

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. Among authors: johns dr. Ann Neurol. 1997 Mar;41(3):314-25. doi: 10.1002/ana.410410306. Ann Neurol. 1997. PMID: 9066352

5

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.

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. Among authors: johns dr. Neurology. 1999 Nov 10;53(8):1787-93. doi: 10.1212/wnl.53.8.1787. Neurology. 1999. PMID: 10563629

7

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.

8

Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation.

Tarnopolsky MA, Simon DK, Roy BD, Chorneyko K, Lowther SA, Johns DR, Sandhu JK, Li Y, Sikorska M. Tarnopolsky MA, et al. Among authors: johns dr. Muscle Nerve. 2004 Apr;29(4):537-47. doi: 10.1002/mus.20020. Muscle Nerve. 2004. PMID: 15052619

9

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.

10

The ophthalmologic manifestations of mitochondrial disease.

Johns DR. Johns DR. Semin Ophthalmol. 1995 Dec;10(4):295-302. doi: 10.3109/08820539509063800. Semin Ophthalmol. 1995. PMID: 10160216 Review.

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