Blake D - Search Results

1

Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processing.

Van Coster RN, De Vivo DC, Blake D, Lombes A, Barrett R, DiMauro S. Van Coster RN, et al. Among authors: blake d. Neurology. 1991 Nov;41(11):1815-21. doi: 10.1212/wnl.41.11.1815. Neurology. 1991. PMID: 1944914 Review.

2

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.

Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE, et al. Hirano M, et al. Among authors: blake dm. Neurology. 1994 Apr;44(4):721-7. doi: 10.1212/wnl.44.4.721. Neurology. 1994. PMID: 8164833

3

Clinical syndromes associated with ragged red fibers.

Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC. Rowland LP, et al. Among authors: blake dm. Rev Neurol (Paris). 1991;147(6-7):467-73. Rev Neurol (Paris). 1991. PMID: 1962052

4

Multifocal motor neuropathy with conduction block: is it a distinct clinical entity?

Lange DJ, Trojaborg W, Latov N, Hays AP, Younger DS, Uncini A, Blake DM, Hirano M, Burns SM, Lovelace RE, et al. Lange DJ, et al. Among authors: blake dm. Neurology. 1992 Mar;42(3 Pt 1):497-505. doi: 10.1212/wnl.42.3.497. Neurology. 1992. PMID: 1549208

5

Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.

Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Wilhelmsen KC, et al. Among authors: blake dm. Ann Neurol. 1996 Apr;39(4):507-20. doi: 10.1002/ana.410390413. Ann Neurol. 1996. PMID: 8619529 Review.

6

A comparative study of the cerebrovascular complications of cocaine: alkaloidal versus hydrochloride--a review.

Levine SR, Brust JC, Futrell N, Brass LM, Blake D, Fayad P, Schultz LR, Millikan CH, Ho KL, Welch KM. Levine SR, et al. Among authors: blake d. Neurology. 1991 Aug;41(8):1173-7. doi: 10.1212/wnl.41.8.1173. Neurology. 1991. PMID: 1866000 Review.

7

Persistent and transient "conduction block" in motor neuron diseases.

Lange DJ, Trojaborg W, McDonald TD, Blake DM. Lange DJ, et al. Among authors: blake dm. Muscle Nerve. 1993 Sep;16(9):896-903. doi: 10.1002/mus.880160903. Muscle Nerve. 1993. PMID: 8355720

8

X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.

Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaño P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, Hirano M. Quinzii CM, et al. Among authors: blake dm. Am J Hum Genet. 2008 Jan;82(1):208-13. doi: 10.1016/j.ajhg.2007.09.013. Am J Hum Genet. 2008. PMID: 18179901 Free PMC article.

9

Eimeria of chickens: the changing face of an old foe.

Blake DP. Blake DP. Avian Pathol. 2025 Jan 2:1-12. doi: 10.1080/03079457.2024.2441180. Online ahead of print. Avian Pathol. 2025. PMID: 39743984 Review.

10

Divers treated in Townsville, Australia: worse symptoms lead to poorer outcomes.

Blake DF, Crowe M, Lindsay D, Turk R, Mitchell SJ, Pollock NW. Blake DF, et al. Diving Hyperb Med. 2024 Dec 20;54(4):308-319. doi: 10.28920/dhm54.4.308-319. Diving Hyperb Med. 2024. PMID: 39675739

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