| Year |
Citation |
Score |
| 2004 |
Pranzatelli MR, Travelstead AL, Tate ED, Allison TJ, Moticka EJ, Franz DN, Nigro MA, Parke JT, Stumpf DA, Verhulst SJ. B- and T-cell markers in opsoclonus-myoclonus syndrome: immunophenotyping of CSF lymphocytes. Neurology. 62: 1526-32. PMID 15136676 DOI: 10.1212/Wnl.62.9.1526 |
0.571 |
|
| 2004 |
Pranzatelli MR, Travelstead AL, Tate ED, Allison TJ, Moticka EJ, Franz DN, Nigro MA, Parke JT, Stumpf DA, Verhulst SJ. B- and t-cell markers in opsoclonus-myoclonus syndrome: immunophenotyping of CSF lymphocytes American Journal of Ophthalmology. 138: 319. DOI: 10.1016/J.Ajo.2004.06.052 |
0.562 |
|
| 1996 |
Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T, Ahmed. Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency. Annals of Neurology. 39: 295-300. PMID 8602747 DOI: 10.1002/Ana.410390305 |
0.672 |
|
| 1991 |
Matsuishi T, Stumpf DA, Seliem M, Eguren LA, Chrislip K. Propionate mitochondrial toxicity in liver and skeletal muscle: acyl CoA levels. Biochemical Medicine and Metabolic Biology. 45: 244-53. PMID 1883630 DOI: 10.1016/0885-4505(91)90027-I |
0.529 |
|
| 1991 |
Matsuishi T, Stumpf DA, Chrislip K. The effect of malate on propionate mitochondrial toxicity. Biochemical Medicine and Metabolic Biology. 46: 177-84. PMID 1782009 DOI: 10.1016/0885-4505(91)90065-S |
0.505 |
|
| 1990 |
Stumpf DA, Barlow CF. Book Review: Randolph K. Byers, MD, 1896-1988 Journal of Child Neurology. 5: 170-171. DOI: 10.1177/088307389000500225 |
0.551 |
|
| 1985 |
Stumpf DA, Eguren LA, Parks JK. Bilirubin increases mitochondrial inner membrane conductance. Biochemical Medicine. 34: 226-9. PMID 4084246 DOI: 10.1016/0006-2944(85)90115-2 |
0.31 |
|
| 1985 |
Haas R, Parker WD, Stumpf D, Eguren LA. Salicylate-induced loose coupling: protonmotive force measurements. Biochemical Pharmacology. 34: 900-2. PMID 3977963 DOI: 10.1016/0006-2952(85)90774-9 |
0.386 |
|
| 1985 |
Stumpf DA, Parker WD, Angelini C. Carnitine deficiency, organic acidemias, and Reye's syndrome. Neurology. 35: 1041-5. PMID 3892364 DOI: 10.1212/Wnl.35.7.1041 |
0.481 |
|
| 1984 |
Parker WD, Haas R, Stumpf DA, Parks J, Eguren LA, Jackson C. Brain mitochondrial metabolism in experimental thiamine deficiency. Neurology. 34: 1477-81. PMID 6493495 DOI: 10.1212/Wnl.34.11.1477 |
0.608 |
|
| 1983 |
Parker WD, Haas R, Stumpf DA, Eguren LA. Effects of octanoate on rat brain and liver mitochondria. Neurology. 33: 1374-7. PMID 6684238 DOI: 10.1212/Wnl.33.10.1374 |
0.587 |
|
| 1983 |
Stumpf DA, Parks JK, Parker WD. Friedreich's disease: IV. Reduced mitochondrial malic enzyme activity in heterozygotes. Neurology. 33: 780-3. PMID 6682522 DOI: 10.1212/Wnl.33.6.780 |
0.496 |
|
| 1983 |
Stumpf DA, Parker WD, Haas R. Carnitine deficiency with valproate therapy. The Journal of Pediatrics. 103: 175-6. PMID 6408234 DOI: 10.1016/S0022-3476(83)80831-2 |
0.401 |
|
| 1983 |
Filley CM, Stumpf DA, Wilkening G. Visual hallucinations in a blind epileptic* Neuro-Ophthalmology. 3: 167-170. DOI: 10.3109/01658108309009734 |
0.478 |
|
| 1982 |
Stumpf DA, Parks JK, Eguren LA, Haas R. Friedreich ataxia: III. Mitochondrial malic enzyme deficiency. Neurology. 32: 221-7. PMID 7199631 DOI: 10.1212/Wnl.32.3.221 |
0.546 |
|
| 1982 |
Bergen BJ, Stumpf DA, Haas R, Parks JK, Eguren LA. A mechanism of toxicity of isovaleric acid in rat liver mitochondria. Biochemical Medicine. 27: 154-60. PMID 7082321 DOI: 10.1016/0006-2944(82)90017-5 |
0.488 |
|
| 1982 |
Stumpf DA, Haas R, Eguren LA, Parks JK, Eilert RE. Protonmotive force in muscle mitochondria. Muscle & Nerve. 5: 14-9. PMID 6276744 DOI: 10.1002/Mus.880050104 |
0.475 |
|
| 1981 |
Stumpf DA, Hayward A, Haas R, Frost M, Schaumburg HH. Adrenoleukodystrophy: Failure of Immunosuppression to Prevent Neurological Progression Jama Neurology. 38: 48-49. PMID 7458724 DOI: 10.1001/Archneur.1981.00510010074014 |
0.467 |
|
| 1981 |
Haas R, Stumpf DA, Parks JK, Eguren L. Inhibitory effects of sodium valproate on oxidative phosphorylation. Neurology. 31: 1473-6. PMID 6796903 DOI: 10.1212/Wnl.31.11.1473 |
0.504 |
|
| 1981 |
Stumpf DA, Parks JK. Human mitochondrial electron transport chain: assay of succinate: cytochrome c reductase in leukocytes, platelets and cultured fibroblasts. Biochemical Medicine. 25: 234-8. PMID 6269538 DOI: 10.1016/0006-2944(81)90080-6 |
0.309 |
|
| 1980 |
Stumpf DA, Parks JK. Urea cycle regulation: I. Coupling of ornithine metabolism to mitochondrial oxidative phosphorylation. Neurology. 30: 178-83. PMID 7188796 DOI: 10.1212/Wnl.30.2.178 |
0.325 |
|
| 1980 |
Stumpf DA, McAfee J, Parks JK, Eguren L. Propionate inhibition of succinate:CoA ligase (GDP) and the citric acid cycle in mitochondria. Pediatric Research. 14: 1127-31. PMID 6780967 DOI: 10.1203/00006450-198010000-00008 |
0.302 |
|
| 1979 |
Stumpf DA, McCabe ER, Parks JK, Bullen WW, Schiff S. Loosely coupled mitochondrial oxidative phosphorylation induced by protoporphyrin. Biochemical Medicine. 21: 182-9. PMID 465014 DOI: 10.1016/0006-2944(79)90070-X |
0.326 |
|
| 1976 |
Horner FA, Myers GJ, Stumpf DA, Oseroff BJ, Choi BH. Malignant atrophic papulosis (Kohlmeier-Degos disease) in childhood. Neurology. 26: 317-21. PMID 944388 DOI: 10.1212/Wnl.26.4.317 |
0.599 |
|
| 1973 |
Stumpf DA, Austin JH, Crocker AC, LaFrance M. Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues. American Journal of Diseases of Children (1960). 126: 747-55. PMID 4271367 DOI: 10.1001/Archpedi.1973.02110190597003 |
0.516 |
|
| 1971 |
Stumpf D, Austin J. Metachromatic Leukodystrophy (MLD): IX. Qualitative and Quantitative Differences in Urinary Arylsulfatase A in Different Forms of MLD Jama Neurology. 24: 117-124. PMID 5540376 DOI: 10.1001/Archneur.1971.00480320045004 |
0.506 |
|
| 1970 |
Austin J, Suzuki K, Armstrong D, Brady R, Bachhawat BK, Schlenker J, Stumpf D. Studies in Globoid (Krabbe) Leukodystrophy (GLD): V. Controlled Enzymic Studies in Ten Human Cases Jama Neurology. 23: 502-512. PMID 5478272 DOI: 10.1001/Archneur.1970.00480300024003 |
0.508 |
|
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