David A Stumpf, MD, PhD - Publications

1977-1985 Neurology & Pediatrics University of Colorado, Boulder, Boulder, CO, United States 
 1985- Neurology Northwestern University Feinberg School of Medicine, Chicago, IL, United States 
biochemistry, mitochondrial disorders, lysosomal disorders

27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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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