Korson M - Search Results

1

Central apnea in a child with congenital autonomic dysfunction and universal pain loss.

Hansen A, Guerina N, Lerman-Sagie T, Korson M. Hansen A, et al. Among authors: korson m. J Child Neurol. 1996 Mar;11(2):162-4. doi: 10.1177/088307389601100219. J Child Neurol. 1996. PMID: 8881995 No abstract available.

2

Infantile onset of hereditary ascending spastic paralysis with bulbar involvement.

Lerman-Sagie T, Filiano J, Smith DW, Korson M. Lerman-Sagie T, et al. Among authors: korson m. J Child Neurol. 1996 Jan;11(1):54-7. doi: 10.1177/088307389601100114. J Child Neurol. 1996. PMID: 8745388

3

Clinical approach to genetic cardiomyopathy in children.

Schwartz ML, Cox GF, Lin AE, Korson MS, Perez-Atayde A, Lacro RV, Lipshultz SE. Schwartz ML, et al. Among authors: korson ms. Circulation. 1996 Oct 15;94(8):2021-38. doi: 10.1161/01.cir.94.8.2021. Circulation. 1996. PMID: 8873681 Review.

4

Perioperative white matter degeneration and death in a patient with a defect in mitochondrial oxidative phosphorylation.

Casta A, Quackenbush EJ, Houck CS, Korson MS. Casta A, et al. Among authors: korson ms. Anesthesiology. 1997 Aug;87(2):420-5. doi: 10.1097/00000542-199708000-00030. Anesthesiology. 1997. PMID: 9286907 No abstract available.

5

Recommendations for the Management of Strokelike Episodes in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes.

Koenig MK, Emrick L, Karaa A, Korson M, Scaglia F, Parikh S, Goldstein A. Koenig MK, et al. Among authors: korson m. JAMA Neurol. 2016 May 1;73(5):591-4. doi: 10.1001/jamaneurol.2015.5072. JAMA Neurol. 2016. PMID: 26954033 Review.

6

Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneys.

North KN, Hoppel CL, De Girolami U, Kozakewich HP, Korson MS. North KN, et al. Among authors: korson ms. J Pediatr. 1995 Sep;127(3):414-20. doi: 10.1016/s0022-3476(95)70073-0. J Pediatr. 1995. PMID: 7658272 Review.

7

Oxidative phosphorylation defect associated with primary adrenal insufficiency.

North K, Korson MS, Krawiecki N, Shoffner JM, Holm IA. North K, et al. Among authors: korson ms. J Pediatr. 1996 May;128(5 Pt 1):688-92. doi: 10.1016/s0022-3476(96)80136-3. J Pediatr. 1996. PMID: 8627443

8

New England Consortium: a model for medical evaluation of expanded newborn screening with tandem mass spectrometry.

Albers S, Waisbren SE, Ampola MG, Brewster TG, Burke LW, Demmer LA, Filiano J, Greenstein RM, Ingham CL, Korson MS, Marsden D, Schwartz RC, Seashore MR, Shih VE, Levy HL. Albers S, et al. Among authors: korson ms. J Inherit Metab Dis. 2001 Apr;24(2):303-4. doi: 10.1023/a:1010391623104. J Inherit Metab Dis. 2001. PMID: 11405349 No abstract available.

9

Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.

Cox GF, Souri M, Aoyama T, Rockenmacher S, Varvogli L, Rohr F, Hashimoto T, Korson MS. Cox GF, et al. Among authors: korson ms. J Pediatr. 1998 Aug;133(2):247-53. doi: 10.1016/s0022-3476(98)70228-8. J Pediatr. 1998. PMID: 9709714

10

Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management.

North KN, Korson MS, Gopal YR, Rohr FJ, Brazelton TB, Waisbren SE, Warman ML. North KN, et al. Among authors: korson ms. J Pediatr. 1995 Jun;126(6):916-22. doi: 10.1016/s0022-3476(95)70208-3. J Pediatr. 1995. PMID: 7539836

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