Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 47

1.

Professor Yukio Fukuyama.

Stumpf DA.

Pediatr Neurol. 2015 Jul;53(1):1-2. doi: 10.1016/j.pediatrneurol.2015.01.015. Epub 2015 Apr 6. No abstract available.

PMID:
25959285
2.

A tribute and toast on the occasion of the retirement of Professor Shaul Harel, MD.

Constantini S, Rosman NP, Evrard P, Velickovic Perat M, Stumpf DA, Dubowitz V.

J Child Neurol. 2010 May;25(5):637-43. doi: 10.1177/0883073809357470. Epub 2010 Mar 5. No abstract available.

PMID:
20207614
3.

B- and T-cell markers in opsoclonus-myoclonus syndrome: immunophenotyping of CSF lymphocytes.

Pranzatelli MR, Travelstead AL, Tate ED, Allison TJ, Moticka EJ, Franz DN, Nigro MA, Parke JT, Stumpf DA, Verhulst SJ.

Neurology. 2004 May 11;62(9):1526-32.

PMID:
15136676
4.

Systemic lymphoma mimicking acute disseminated encephalomyelitis.

Bassuk AG, Keating GF, Stumpf DA, Burrowes DM, Stack C.

Pediatr Neurol. 2004 Feb;30(2):129-31.

PMID:
14984907
5.

L-carnitine reduces brain injury after hypoxia-ischemia in newborn rats.

Wainwright MS, Mannix MK, Brown J, Stumpf DA.

Pediatr Res. 2003 Nov;54(5):688-95. Epub 2003 Aug 6.

PMID:
12904603
6.

Symptoms of B(12) deficiency can occur in women of childbearing age supplemented with folate.

Stumpf DA.

Neurology. 2003 Jan 28;60(2):353; author reply 353. No abstract available.

PMID:
12552069
7.

Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency.

Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T, Ahmed.

Ann Neurol. 1996 Mar;39(3):295-300.

PMID:
8602747
8.

Reye syndrome: an international perspective.

Stumpf DA.

Brain Dev. 1995;17 Suppl:77-8. Review.

PMID:
8882577
9.

Dr Charles F. Barlow, Bronson Crothers professor of neurology.

Stumpf DA.

J Child Neurol. 1992 Jan;7(1):61-5. No abstract available.

PMID:
1552153
10.

The effect of malate on propionate mitochondrial toxicity.

Matsuishi T, Stumpf DA, Chrislip K.

Biochem Med Metab Biol. 1991 Oct;46(2):177-84.

PMID:
1782009
11.

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria.

Gibson KM, Sherwood WG, Hoffman GF, Stumpf DA, Dianzani I, Schutgens RB, Barth PG, Weismann U, Bachmann C, Schrynemackers-Pitance P, et al.

J Pediatr. 1991 Jun;118(6):885-90.

PMID:
1710267
12.

Propionate mitochondrial toxicity in liver and skeletal muscle: acyl CoA levels.

Matsuishi T, Stumpf DA, Seliem M, Eguren LA, Chrislip K.

Biochem Med Metab Biol. 1991 Apr;45(2):244-53.

PMID:
1883630
13.

Isolated vitamin E deficiency in the absence of fat malabsorption--familial and sporadic cases: characterization and investigation of causes.

Sokol RJ, Kayden HJ, Bettis DB, Traber MG, Neville H, Ringel S, Wilson WB, Stumpf DA.

J Lab Clin Med. 1988 May;111(5):548-59.

PMID:
3361234
14.

Acute ataxia.

Stumpf DA.

Pediatr Rev. 1987 Apr;8(10):303-6. Review. No abstract available.

PMID:
3332333
15.

Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorption.

Stumpf DA, Sokol R, Bettis D, Neville H, Ringel S, Angelini C, Bell R.

Neurology. 1987 Jan;37(1):68-74.

PMID:
3796840
16.

Bilirubin increases mitochondrial inner membrane conductance.

Stumpf DA, Eguren LA, Parks JK.

Biochem Med. 1985 Oct;34(2):226-9.

PMID:
4084246
17.

The metabolic consequences of experimental intraventricular hemorrhage.

Pranzatelli MR, Stumpf DA.

Neurology. 1985 Sep;35(9):1299-303.

PMID:
4022375
18.

Carnitine deficiency, organic acidemias, and Reye's syndrome.

Stumpf DA, Parker WD Jr, Angelini C.

Neurology. 1985 Jul;35(7):1041-5. Review.

PMID:
3892364
19.

The inherited ataxias.

Stumpf DA.

Pediatr Neurol. 1985 May-Jun;1(3):129-33. Review.

PMID:
3916902
20.

The inherited ataxias.

Stumpf DA.

Neurol Clin. 1985 Feb;3(1):47-57. Review.

PMID:
3921817
21.

Anticonvulsant use during pregnancy.

Stumpf DA.

Clin Ther. 1985;7(2):258-65.

PMID:
3986865
22.

Brain mitochondrial metabolism in experimental thiamine deficiency.

Parker WD Jr, Haas R, Stumpf DA, Parks J, Eguren LA, Jackson C.

Neurology. 1984 Nov;34(11):1477-81.

PMID:
6493495
23.

A microchamber for polarographic assay.

Haas RH, Stumpf DA.

Biochem Med. 1984 Aug;32(1):138-43.

PMID:
6497867
24.

Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid.

Matalon R, Stumpf DA, Michals K, Hart RD, Parks JK, Goodman SI.

J Pediatr. 1984 Jan;104(1):65-9.

PMID:
6418873
25.

[Mitochondrial disorders].

Stumpf DA.

Rinsho Shinkeigaku. 1983 Dec;23(12):1046-55. Review. Japanese. No abstract available.

PMID:
6375929
26.

Effects of octanoate on rat brain and liver mitochondria.

Parker WD Jr, Haas R, Stumpf DA, Eguren LA.

Neurology. 1983 Oct;33(10):1374-7.

PMID:
6684238
27.

Carnitine deficiency with valproate therapy.

Stumpf DA, Parker WD, Haas R.

J Pediatr. 1983 Jul;103(1):175-6. No abstract available.

PMID:
6408234
28.

Friedreich's disease: IV. Reduced mitochondrial malic enzyme activity in heterozygotes.

Stumpf DA, Parks JK, Parker WD.

Neurology. 1983 Jun;33(6):780-3.

PMID:
6682522
29.

Friedreich's disease: a metabolic cardiomyopathy.

Stumpf DA.

Am Heart J. 1982 Oct;104(4 Pt 1):887-8. No abstract available.

PMID:
7124609
30.

Glutaric acidemia type II: clinical, biochemical, and morphologic considerations.

Goodman SI, Stene DO, McCabe ER, Norenberg MD, Shikes RH, Stumpf DA, Blackburn GK.

J Pediatr. 1982 Jun;100(6):946-50. No abstract available.

PMID:
7086597
31.

A mechanism of toxicity of isovaleric acid in rat liver mitochondria.

Bergen BJ, Stumpf DA, Haas R, Parks JK, Eguren LA.

Biochem Med. 1982 Apr;27(2):154-60. No abstract available.

PMID:
7082321
32.

Friedreich ataxia: III. Mitochondrial malic enzyme deficiency.

Stumpf DA, Parks JK, Eguren LA, Haas R.

Neurology. 1982 Mar;32(3):221-7.

PMID:
7199631
33.

Protonmotive force in muscle mitochondria.

Stumpf DA, Haas R, Eguren LA, Parks JK, Eilert RE.

Muscle Nerve. 1982 Jan;5(1):14-9.

PMID:
6276744
34.

The founding of pediatric neurology in America.

Stumpf DA.

Bull N Y Acad Med. 1981 Nov;57(9):804-16. No abstract available.

35.

Inhibitory effects of sodium valproate on oxidative phosphorylation.

Haas R, Stumpf DA, Parks JK, Eguren L.

Neurology. 1981 Nov;31(11):1473-6.

PMID:
6796903
36.

Classics in neurology.

Stumpf DA.

Neurology. 1981 May;31(5):529. No abstract available.

PMID:
7015162
37.
38.

Adrenoleukodystrophy. Failure of immunosuppression to prevent neurological progression.

Stumpf DA, Hayward A, Haas R, Frost M, Schaumburg HH.

Arch Neurol. 1981 Jan;38(1):48-9.

PMID:
7458724
39.

Propionate inhibition of succinate:CoA ligase (GDP) and the citric acid cycle in mitochondria.

Stumpf DA, McAfee J, Parks JK, Eguren L.

Pediatr Res. 1980 Oct;14(10):1127-31.

PMID:
6780967
40.
41.

Friedreich ataxia. II. Normal kinetics of lipoamide dehydrogenase.

Stumpf DA, Parks JK.

Neurology. 1979 Jun;29(6):820-6.

PMID:
221857
42.

Loosely coupled mitochondrial oxidative phosphorylation induced by protoporphyrin.

Stumpf DA, McCabe ER, Parks JK, Bullen WW, Schiff S.

Biochem Med. 1979 Apr;21(2):182-9. No abstract available.

PMID:
465014
43.

Friedreich's ataxia: I. Normal pyruvate dehydrogenase complex activity in platelets.

Stumpf DA, Parks JK.

Ann Neurol. 1978 Oct;4(4):366-8. No abstract available.

PMID:
727741
44.

Seizures, anticonvulsants, and pregnancy.

Stumpf DA, Frost M.

Am J Dis Child. 1978 Aug;132(8):746-8. Review. No abstract available.

PMID:
356585
45.

Malignant atrophic papulosis (Kohlmeier-Degos disease) in childhood.

Horner FA, Myers GJ, Stumpf DA, Oseroff BJ, Choi BH.

Neurology. 1976 Apr;26(4):317-21.

PMID:
944388
46.

Letter: The Winchester syndrome and mucopolysaccharide metabolism.

Stumpf DA.

J Pediatr. 1975 Apr;86(4):646-7. No abstract available.

PMID:
123957
47.

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues.

Stumpf DA, Austin JH, Crocker AC, LaFrance M.

Am J Dis Child. 1973 Dec;126(6):747-55. No abstract available.

PMID:
4271367

Supplemental Content

Loading ...
Support Center