Bryan Hainline

  • 1380 Citations
  • 17 h-Index
1980 …2017
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Fingerprint Dive into the research topics where Bryan Hainline is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Inborn Errors Metabolism Medicine & Life Sciences
Zein Medicine & Life Sciences
Pterins Medicine & Life Sciences
Pyruvate Carboxylase Deficiency Disease Medicine & Life Sciences
Hyperammonemia Medicine & Life Sciences
Molybdenum Medicine & Life Sciences
Acyl-CoA Dehydrogenase Medicine & Life Sciences
Liver Transplantation Medicine & Life Sciences

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Publications 1980 2017

  • 1380 Citations
  • 17 h-Index
  • 27 Article
  • 2 Chapter

Medical genetics and biochemistry in diagnosis and management

Hainline, B. & Griffith, C., Mar 31 2017, Practical Hepatic Pathology: A Diagnostic Approach: Second Edition. Elsevier, p. 91-99 9 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Medical Genetics
Biochemistry
2 Citations (Scopus)

221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

Bentler, K., Zhai, S., Elsbecker, S. A., Arnold, G. L., Burton, B. K., Vockley, J., Cameron, C. A., Hiner, S. J., Edick, M. J., Berry, S. A., Thomas, J., Dodge, M., Singh, R., Lakshman, S., Coakley, K., Stembridge, A., Russi, A. S., Phillips, E., Burton, B., Edano, C. & 62 others, Shrestha, S., Hoganson, G., Dwyer, L., Hainline, B., Romie, S., Hainline, S., Asamoah, A., Goodin, K., Rajakaruna, C., Jackson, K., Hamosh, A., Vernon, H., Smith, N., Ahmad, A., Lipinski, S., Feldman, G., Berry, S., Elsbecker, S., Bentler, K., Font-Montgomery, E., Peck, D., Pena, L. D. M., Koeberl, D. D., Jiang, Y. H., Kishnani, P. S., Rizzo, W., Dawson, M., Ambrose, N., Levy, P., Kronn, D., Fong, C. T., D'Aco, K., Hart, T., Erbe, R., Samons, M., Leslie, N., Powers, R., Bartholomew, D., Goff, M., vanCalcar, S., Hansen, J., Arnold, G., Vockley, J., Walsh-Vockley, C., Rhead, W., Dimmock, D., Engelking, P., Bird, C., Swan, A., Schwoerer, J. S., Henry, S., Narumanchi, T. C., Hummel, M., Wilkins, J., Davis-Keppen, L., Stein, Q., Loman, R., Cameron, C., Edick, M. J., Hiner, S. J., Justice, K. & Zhai, S., Sep 1 2016, In : Molecular Genetics and Metabolism. 119, 1-2, p. 75-82 8 p.

Research output: Contribution to journalArticle

Acyl-CoA Dehydrogenase
Inborn Errors Metabolism
Metabolism
Health
Newborn Infant
4 Citations (Scopus)

An atypical case of canavan disease with stroke-like presentation

Delaney, K. E., Kralik, S. F., Hainline, B. & Golomb, M., Feb 1 2015, In : Pediatric Neurology. 52, 2, p. 218-221 4 p.

Research output: Contribution to journalArticle

Canavan Disease
Stroke
Seizures
Magnetic Resonance Imaging
Language Development Disorders

Medical Genetics and Biochemistry in Diagnosis and Management

Hainline, B., 2011, Practical Hepatic Pathology. Elsevier Inc., p. 105-113 9 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Medical Genetics
Biochemistry
10 Citations (Scopus)

Neonatal graves' disease associated with severe metabolic abnormalities

Lewis, K. A., Engle, W., Hainline, B., Johnson, N., Corkins, M. & Eugster, E., Jul 2011, In : Pediatrics. 128, 1

Research output: Contribution to journalArticle

Infant, Newborn, Diseases
Hyperammonemia
Inborn Errors Metabolism
Hyperbilirubinemia
Graves Disease