Barbara K Burton

  • 6056 Citations
1973 …2019
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Research Output 1973 2019

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2018
1 Citation (Scopus)

Cardiopulmonary exercise testing reflects improved exercise capacity in response to treatment in morquio a patients: Results of a 52-week pilot study of two different doses of elosulfase alfa

Berger, K. I., Burton, B. K., Lewis, G. D., Tarnopolsky, M., Harmatz, P. R., Mitchell, J. J., Muschol, N., Jones, S. A., Sutton, V. R., Pastores, G. M., Lau, H., Sparkes, R. & Shaywitz, A. J., Jan 1 2018, JIMD Reports. Springer, p. 9-17 9 p. (JIMD Reports; vol. 42).

Research output: Chapter in Book/Report/Conference proceedingChapter

Exercise
Stairs
Testing
Oxygen
Enzyme Replacement Therapy
2016

Inherited Metabolic Disorders

Burton, BK., 2016, Avery's Neonatology: Pathophysiology and Management of the Newborn, 7th Ed. MacDonald, MG. & Seshia, MMK. (eds.). Philadelphia: Wolters Kluwer, p. 740-9

Research output: Chapter in Book/Report/Conference proceedingChapter

2014
18 Citations (Scopus)

Enzyme replacement therapy in mucopolysaccharidosis ii patients under 1 year of age

Lampe, C., Atherton, A., Burton, B. K., Descartes, M., Giugliani, R., Horovitz, D. D. G., Kyosen, S. O., Magalhães, T. S. P. C., Martins, A. M., Mendelsohn, N. J., Muenzer, J. & Smith, L. D., Jan 1 2014, JIMD Reports. Springer, p. 99-113 15 p. (JIMD Reports; vol. 14).

Research output: Chapter in Book/Report/Conference proceedingChapter

Mucopolysaccharidoses
Enzyme Replacement Therapy
Mucopolysaccharidosis II
Enzymes
Siblings
2010

Sapropterin treatment of phenylketonuria

Burton, BK., 2010, Small Molecule Therapy for Genetic Disease. Thoene, JG. (ed.). New York: Cambridge University Press, p. 76-85

Research output: Chapter in Book/Report/Conference proceedingChapter

2008

Enzyme deficiency diseases

Burton, BK., 2008, Dermatology, 2nd. Ed.. Bolognia, JL., Torizzo, JL. & Rapini, RR. (eds.). Oxford: Elsevier, p. 863-868

Research output: Chapter in Book/Report/Conference proceedingChapter

2005

Amino acid and organic acid disorders

Burton, BK. & Charrow, J., 2005, Pediatrics: Just the Facts. Green, T., Franklin, W. & Tanz, RR. (eds.). New York: McGraw-Hill, p. 336-40

Research output: Chapter in Book/Report/Conference proceedingChapter

Carbohydrate metabolism

Burton, BK. & Charrow, J., 2005, Pediatrics: Just the Facts. Green, T., Franklin, W. & Tanz, RR. (eds.). New York: McGraw-Hill, p. 341-3

Research output: Chapter in Book/Report/Conference proceedingChapter

Chromosome abnormalites

Burton, BK. & Tanz, RR., 2005, Pediatrics: Just the Facts. Green, T. & Franklin, W. (eds.). New York: McGraw-Hill, p. 333-5

Research output: Chapter in Book/Report/Conference proceedingChapter

Fatty acid oxidation disorders

Burton, BK., 2005, Pediatrics: Just the Facts. Green, T., Franklin, W. & Tanz, RR. (eds.). New York: McGraw-Hill

Research output: Chapter in Book/Report/Conference proceedingChapter

Inherited metabolic disorders

Burton, BK., 2005, Neonatology: Pathophysiology and Management of the Newborn, 6th Ed. MacDonald, MG., Seshie, MMK. & Mullett, MD. (eds.). Philadelphia: Lippincott, Williams and Wilkins, p. 965-980

Research output: Chapter in Book/Report/Conference proceedingChapter

Newborn screening

Burton, BK., 2005, Pediatrics: Just the Facts. Green, T., Franklin, W. & Tanz, RR. (eds.). New York: McGraw-Hill, p. 349-50

Research output: Chapter in Book/Report/Conference proceedingChapter

Other important single gene disorders

Burton, BK. & Charrow, J., 2005, Pediatrics: Just the Facts. Green, T., Franklin, W. & Tanz, RR. (eds.). New York: McGraw-Hill, p. 345-9

Research output: Chapter in Book/Report/Conference proceedingChapter

Submicroscopic chromosome anomalies ( contiguous gene syndromes)

Burton, BK., 2005, Pediatrics: Just the Facts. Green, T., Franklin, W. & Tanz, RR. (eds.). New York: McGraw-Hill, p. 335-6

Research output: Chapter in Book/Report/Conference proceedingChapter

2003

Enzyme deficiency diseases

Burton, BK., 2003, Dermatology. Bolognia, JL., Jorizzo, JL. & Rapini, RP. (eds.). Philadelphia: Mosby, p. 893-9

Research output: Chapter in Book/Report/Conference proceedingChapter

2000
22 Citations (Scopus)

Urea cycle disorders

Burton, BK., 2000, Clinics in Liver Disease. Bezerra, JA. & Balistreri, WF. (eds.). Philadelphia: W.B.Saunders, p. 815-830

Research output: Chapter in Book/Report/Conference proceedingChapter

1999

Inherited metabolic disorders

Burton, BK., 1999, Neonatology, 5th Ed. Avery, GB., Fletcher, MA. & MacDonald, MG. (eds.). Philadelphia: JB Lippincott, p. 962-998

Research output: Chapter in Book/Report/Conference proceedingChapter

1998

Management of the pregnancy complicated by fetal cardiac defects

Cusick, W., Burton, BK. & Buttino, L., 1998, Cardiac Problems in Pregnancy, 3rd Ed. Eikayam, U. & Gleicher, N. (eds.). New York: Wiley-Liss, p. 725-32

Research output: Chapter in Book/Report/Conference proceedingChapter

Patient counseling, ethical and legal issues

Burton, BK., 1998, Interventional Ultrasound in Obstetrics and Gynecology. Santolaya-Forgas, J. & Lemery, D. (eds.). Oxford: Blackwell Scientific Press, p. 3-11

Research output: Chapter in Book/Report/Conference proceedingChapter

1994

Inherited metabolic disorders

Burton, BK., 1994, Neonatology, 4th Ed. Avery, GB., Fletcher, MA. & MacDonald, MG. (eds.). Philadelphia: JB Lippincott, p. 726-43

Research output: Chapter in Book/Report/Conference proceedingChapter

1992

Unexplained elevated MSAFP and adverse perinatal outcome

Burton, BK., 1992, Maternal Serum Screening for Fetal Genetic Disorders. Elias, S. & Simpson, JL. (eds.). New York: Churchill-Livingstone, p. 109-119

Research output: Chapter in Book/Report/Conference proceedingChapter

1987

Maternal serum alpha-fetoprotein

Nelson, LH., Burton, BK. & Sowers, S., 1987, Diagnostic Ultrasound Applied to Obstetrics and Gynecology. Sabbagha, RE. (ed.). Philadelphia: Lippincott, p. 252-63

Research output: Chapter in Book/Report/Conference proceedingChapter

1986

Biological and biochemical pitfalls in the prenatal diagnosis of inborn errors of metabolism

Burton, BK. & Nadler, HL., 1986, Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment. Milunsky, A. (ed.). New York: Plenum, p. 437-51

Research output: Chapter in Book/Report/Conference proceedingChapter

1982
2 Citations (Scopus)

The clinical significance of low maternal serum alpha-fetoprotein in obstetric practice

Sowers, SG. & Burton, BK., 1982, Annual Review of Birth Defects 1981. Nyhan, WL. & Jones, K. (eds.). New York: Alan R. Liss, p. 181-4

Research output: Chapter in Book/Report/Conference proceedingChapter

1980

Genetics

Nadler, HL. & Burton, BK., 1980, Fetal and Maternal Medicine. Kretchmer, N. & Quilligan, EJ. (eds.). New York: Wiley & Sons, p. 59-107

Research output: Chapter in Book/Report/Conference proceedingChapter

Genetics in surgery

Nadler, HL. & Burton, BK., 1980, Swenson's Pediatric Surgery. Raffensperger, J. (ed.). New York: Appleton-Century-Crofts, p. 85-103

Research output: Chapter in Book/Report/Conference proceedingChapter

1979

Biochemical and biologic pitfalls in the use of cell culture for prenatal diagnosis.

Burton, BK., Gerbie, AB. & Nadler, HL., 1979, Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment. Milunsky, A. (ed.). New York: Plenum, p. 369-77

Research output: Chapter in Book/Report/Conference proceedingChapter

8 Citations (Scopus)

Empiric recurrence risks for congenital hydrocephalus

Burton, BK., 1979, Birth Defects: Orginal Articles Series. New York: Elsevier, p. 107-115

Research output: Chapter in Book/Report/Conference proceedingChapter

Screening the newborn for genetic and metabolic disorders

Burton, BK. & Nadler, HL., 1979, Pediatric Update: Review for Physicians. Moss, A. (ed.). New York: Elsevier, p. 131-142

Research output: Chapter in Book/Report/Conference proceedingChapter

1978

Enzymes in the amniotic fluid and the prenatal diagnosis of inborn errors of metabolism

Burton, BK., Gerbie, AB. & Nadler, HL., 1978, Amniotic Fluid: Research and Clinical Application, 2nd Ed. Fairweather, DVI. & Eskes, TKAB. (eds.). Amsterdam: Excerpta Medica, p. 225-245

Research output: Chapter in Book/Report/Conference proceedingChapter

1973

Enzymes in the amniotic fluid and the prenatal diagnosis of inborn errors of metabolism

Nadler, HL. & Burton, BK., 1973, Amniotic Fluid. Fairweather, DVI. & Eskes, TKAB. (eds.). Amsterdam: Excerpta Medica, p. 223-261

Research output: Chapter in Book/Report/Conference proceedingChapter