D. Stumpf

发表

B- and T-cell markers in opsoclonus–myoclonus syndrome: Immunophenotyping of CSF lymphocytes

S. Verhulst, M. Nigro, M. Pranzatelli, 2004, Neurology.

B- and T-cell markers in opsoclonus–myoclonus syndrome

S. Verhulst, M. Nigro, M. Pranzatelli, 2004, Neurology.

Symptoms of B12 deficiency can occur in women of childbearing age supplemented with folate

D. Stumpf, 2003, Neurology.

Seizures, anticonvulsants, and pregnancy.

D. Stumpf, M. Frost, 1978, American journal of diseases of children.

The effect of malate on propionate mitochondrial toxicity.

D. Stumpf, T. Matsuishi, K. Chrislip, 1991, Biochemical medicine and metabolic biology.

Adrenoleukodystrophy: Failure of Immunosuppression to Prevent Neurological Progression

H. Schaumburg, D. Stumpf, M. Frost, 1981 .

Brain mitochondrial metabolism in experimental thiamine deficiency

J. Parks, W. Parker, D. Stumpf, 1984, Neurology.

Inhibitory effects of sodium valproate on oxidative phosphorylation

J. Parks, B. Chir., D. Stumpf, 1981, Neurology.

Salicylate-induced loose coupling: protonmotive force measurements.

W. Parker, D. Stumpf, R. Haas, 1985, Biochemical pharmacology.

Effects of octanoate on rat brain and liver mitochondria

W. Parker, D. Stumpf, R. Haas, 1983, Neurology.

Carnitine deficiency with valproate therapy.

W. Parker, D. Stumpf, R. Haas, 1983, The Journal of pediatrics.

Propionate Inhibition of Succinate: CoA Ligase (GDP) and the Citric Acid Cycle in Mitochondria

J. Parks, D. Stumpf, L. Eguren, 1980, Pediatric Research.

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

D. Stumpf, T. Matsuishi, K. Chrislip, 1991, Biochemical medicine and metabolic biology.

Carnitine deficiency, organic acidemias, and Reye's syndrome

C. Angelini, W. Parker, D. Stumpf, 1985, Neurology.

Urea cycle regulation

J. Parks, D. Stumpf, 1980, Neurology.

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

D. Bettis, R. Sokol, M. Traber, 1988, The Journal of laboratory and clinical medicine.

Loosely coupled mitochondrial oxidative phosphorylation induced by protoporphyrin.

J. Parks, W. W. Bullen, D. Stumpf, 1979, Biochemical medicine.

Reye syndrome: an international perspective

D. Stumpf, 1995, Brain and Development.

Human α‐tocopherol transfer protein: Gene structure and mutations in familial vitamin E deficiency

W. Hung, T. Siddique, M. Ahmed, 1996 .

Visual hallucinations in a blind epileptic

C. Filley, G. Wilkening, D. Stumpf, 1983 .

The infant with anencephaly

R. Cranford, R. Poland, J. Queenan, 1990 .

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

A. Crocker, M. Lafrance, J. Austin, 1973, American journal of diseases of children.

Studies in globoid (Krabbe) leukodystrophy (GLD). V. Controlled enzymic studies in ten human cases.

R. Brady, D. Armstrong, K. Suzuki, 1970, Archives of neurology.

A monospecific antibody to human sulfatase A. Preparation, characterization and significance.

E. Neuwelt, J. Austin, D. Stumpf, 1971, Biochimica et biophysica acta.

Metachromatic leukodystrophy (MLD). X. Immunological studies of the abnormal sulfatase A.

E. Neuwelt, J. Austin, D. Stumpf, 1971, Archives of neurology.

Friedreich's disease

J. Parks, W. Parker, D. Stumpf, 1983, Neurology.

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

J. Parks, S. Goodman, R. Matalon, 1984, The Journal of pediatrics.

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

M. Norenberg, E. McCabe, S. Goodman, 1982, The Journal of pediatrics.

Metachromatic leukodystrophy (MLD). IX. Qualitative and quantitative differences in urinary arylsulfatase A in different forms of MLD.

J. Austin, D. Stumpf, 1971, Archives of neurology.

Recent Advances in Metachromatic Leukodystrophy

E. Neuwelt, J. Austin, D. Stumpf, 1972 .

Metachromatic leukodystrophy (MLD). 8. MLD in adults; diagnosis and pathogenesis.

S. Fouch, D. Armstrong, J. Austin, 1968, Archives of neurology.

Friedreich's disease

D. Bettis, C. Angelini, R. Sokol, 1987, Neurology.

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

J. Parks, D. Stumpf, R. Haas, 1982, Biochemical medicine.

Systemic lymphoma mimicking acute disseminated encephalomyelitis.

A. Bassuk, D. Burrowes, G. Keating, 2004, Pediatric neurology.

Malignant atrophie papulosis (Kohlmeier‐Degos disease) in childhood

G. Myers, D. Stumpf, F. Horner, 1976, Neurology.

Friedreich'S Ataxia: I. Normal pyruvate dehydrogenase complex activity in platelets

J. Parks, D. Stumpf, 1978, Annals of neurology.

The inherited ataxias.

D. Stumpf, 1985, Neurologic clinics.

Human mitochondrial electron transport chain: assay of succinate: cytochrome c reductase in leukocytes, platelets and cultured fibroblasts.

J. Parks, D. Stumpf, 1981, Biochemical medicine.

The Winchester syndrome and mucopolysaccharide metabolism

D. Stumpf, 1975 .

Defective sulfatide synthesis in Krabbe's disease (globoid leukodystrophy).

D. Armstrong, J. Austin, D. Stumpf, 1967, Transactions of the American Neurological Association.

Protonmotive force in muscle mitochondria

J. Parks, R. Eilert, D. Stumpf, 1982, Muscle & nerve.

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria.

I. Dianzani, R. Schutgens, K. Gibson, 1991, The Journal of pediatrics.

Werdnig Hoffman's disease (spinal muscular atrophy type I): A clinical study of 25 Saudi nationals in Al-Khobar.

G. Gascon, S. Al-Rajeh, O. Bademosi, 1992, Annals of Saudi medicine.

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

W. Hung, T. Siddique, M. Ahmed, 1996, Annals of neurology.

Professor Yukio Fukuyama.

D. Stumpf, 2015, Pediatric neurology.

Subcellular distribution of two enzyme systems which degrade 3'-phosphoadenosine 5'-phosphosulfate ("active sulfate").

D. Armstrong, J. Austin, D. Stumpf, 1969, Biochimica et Biophysica Acta.

Properties and sub-cellular distribution of two sulfatases which degrade adenosine 5'-phosphosulfate.

D. Armstrong, B. Bachhawat, J. Austin, 1970, Biochimica et biophysica acta.

Friedreich's disease: a metabolic cardiomyopathy.

D. Stumpf, 1982, American heart journal.

L-Carnitine Reduces Brain Injury after Hypoxia-Ischemia in Newborn Rats

M. Wainwright, D. Stumpf, Justin C. Brown, 2003, Pediatric Research.

The founding of pediatric neurology in America.

D. Stumpf, 1981, Bulletin of the New York Academy of Medicine.

Dr Charles F. Barlow, Bronson Crothers Professor of Neurology

D. Stumpf, 1992, Journal of child neurology.

Book Review: Randolph K. Byers, MD, 1896-1988

C. F. Barlow, D. Stumpf, 1990 .

Bilirubin increases mitochondrial inner membrane conductance.

J. Parks, D. Stumpf, L. Eguren, 1985, Biochemical medicine.

Brain Death in Children Task Force Guidelines

D. Stumpf, 1989 .

The metabolic consequences of experimental intraventricular hemorrhage

M. Pranzatelli, D. Stumpf, 1985, Neurology.