Swoboda KJ - Search Results

1

Clinical and therapeutic observations in aromatic L-amino acid decarboxylase deficiency.

Swoboda KJ, Hyland K, Goldstein DS, Kuban KC, Arnold LA, Holmes CS, Levy HL. Swoboda KJ, et al. Neurology. 1999 Oct 12;53(6):1205-11. doi: 10.1212/wnl.53.6.1205. Neurology. 1999. PMID: 10522874

2

Frontal abnormalities in a patient with obsessive-compulsive disorder: the role of structural lesions in obsessive-compulsive behavior.

Swoboda KJ, Jenike MA. Swoboda KJ, et al. Neurology. 1995 Dec;45(12):2130-4. doi: 10.1212/wnl.45.12.2130. Neurology. 1995. PMID: 8848180 Review.

3

Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency.

Hyland K, Nygaard TG, Trugman JM, Swoboda KJ, Arnold LA, Sparagana SP. Hyland K, et al. Among authors: swoboda kj. J Inherit Metab Dis. 1999 May;22(3):213-5. doi: 10.1023/a:1005532610051. J Inherit Metab Dis. 1999. PMID: 10384370 No abstract available.

4

Sources and physiological significance of plasma dopamine sulfate.

Goldstein DS, Swoboda KJ, Miles JM, Coppack SW, Aneman A, Holmes C, Lamensdorf I, Eisenhofer G. Goldstein DS, et al. Among authors: swoboda kj. J Clin Endocrinol Metab. 1999 Jul;84(7):2523-31. doi: 10.1210/jcem.84.7.5864. J Clin Endocrinol Metab. 1999. PMID: 10404831

5

Diagnosis and treatment of neurotransmitter-related disorders.

Swoboda KJ, Hyland K. Swoboda KJ, et al. Neurol Clin. 2002 Nov;20(4):1143-61, viii. doi: 10.1016/s0733-8619(02)00018-x. Neurol Clin. 2002. PMID: 12616685 Review.

6

Aromatic L-amino acid decarboxylase deficiency: overview of clinical features and outcomes.

Swoboda KJ, Saul JP, McKenna CE, Speller NB, Hyland K. Swoboda KJ, et al. Ann Neurol. 2003;54 Suppl 6:S49-55. doi: 10.1002/ana.10631. Ann Neurol. 2003. PMID: 12891654

7

Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.

Smith SE, Kinney HC, Swoboda KJ, Levy HL. Smith SE, et al. Among authors: swoboda kj. Mol Genet Metab. 2006 Jun;88(2):138-45. doi: 10.1016/j.ymgme.2006.02.007. Epub 2006 Mar 30. Mol Genet Metab. 2006. PMID: 16574454

8

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.

Swoboda KJ, Soong B, McKenna C, Brunt ER, Litt M, Bale JF Jr, Ashizawa T, Bennett LB, Bowcock AM, Roach ES, Gerson D, Matsuura T, Heydemann PT, Nespeca MP, Jankovic J, Leppert M, Ptácek LJ. Swoboda KJ, et al. Neurology. 2000 Jul 25;55(2):224-30. doi: 10.1212/wnl.55.2.224. Neurology. 2000. PMID: 10908896

9

Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders.

Rosewich H, Sweney MT, DeBrosse S, Ess K, Ozelius L, Andermann E, Andermann F, Andrasco G, Belgrade A, Brashear A, Ciccodicola S, Egan L, George AL Jr, Lewelt A, Magelby J, Merida M, Newcomb T, Platt V, Poncelin D, Reyna S, Sasaki M, Sotero de Menezes M, Sweadner K, Viollet L, Zupanc M, Silver K, Swoboda K. Rosewich H, et al. Neurol Genet. 2017 Mar 2;3(2):e139. doi: 10.1212/NXG.0000000000000139. eCollection 2017 Apr. Neurol Genet. 2017. PMID: 28293679 Free PMC article.

10

Maximizing the Benefit of Life-Saving Treatments for Pompe Disease, Spinal Muscular Atrophy, and Duchenne Muscular Dystrophy Through Newborn Screening: Essential Steps.

Baker M, Griggs R, Byrne B, Connolly AM, Finkel R, Grajkowska L, Haidet-Phillips A, Hagerty L, Ostrander R, Orlando L, Swoboda K, Watson M, Howell RR. Baker M, et al. JAMA Neurol. 2019 Aug 1;76(8):978-983. doi: 10.1001/jamaneurol.2019.1206. JAMA Neurol. 2019. PMID: 31107518

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