Sims KB - Search Results

1

Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase.

Murphy DL, Sims KB, Karoum F, Garrick NA, de la Chapelle A, Sankila EM, Norio R, Breakefield XO. Murphy DL, et al. Among authors: sims kb. J Neural Transm Gen Sect. 1991;83(1-2):1-12. doi: 10.1007/BF01244447. J Neural Transm Gen Sect. 1991. PMID: 2018626

2

Marked amine and amine metabolite changes in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase.

Murphy DL, Sims KB, Karoum F, de la Chapelle A, Norio R, Sankila EM, Breakefield XO. Murphy DL, et al. Among authors: sims kb. J Neurochem. 1990 Jan;54(1):242-7. doi: 10.1111/j.1471-4159.1990.tb13307.x. J Neurochem. 1990. PMID: 2293615

3

Abnormal protein in the cerebrospinal fluid of patients with a submicroscopic X-chromosomal deletion associated with Norrie disease: preliminary report.

Joy JE, Poglod R, Murphy DL, Sims KB, de la Chapelle A, Sankila EM, Norio R, Merril CR. Joy JE, et al. Among authors: sims kb. Appl Theor Electrophor. 1991;2(1):3-5. Appl Theor Electrophor. 1991. PMID: 1932207

4

Are MAO-A deficiency states in the general population and in putative high-risk populations highly uncommon?

Murphy DL, Sims K, Eisenhofer G, Greenberg BD, George T, Berlin F, Zametkin A, Ernst M, Breakefield XO. Murphy DL, et al. J Neural Transm Suppl. 1998;52:29-38. doi: 10.1007/978-3-7091-6499-0_4. J Neural Transm Suppl. 1998. PMID: 9564605

5

Monoamine oxidase deficiency in males with an X chromosome deletion.

Sims KB, de la Chapelle A, Norio R, Sankila EM, Hsu YP, Rinehart WB, Corey TJ, Ozelius L, Powell JF, Bruns G, et al. Sims KB, et al. Neuron. 1989 Jan;2(1):1069-76. doi: 10.1016/0896-6273(89)90231-6. Neuron. 1989. PMID: 2483108

6

Norrie disease gene is distinct from the monoamine oxidase genes.

Sims KB, Ozelius L, Corey T, Rinehart WB, Liberfarb R, Haines J, Chen WJ, Norio R, Sankila E, de la Chapelle A, et al. Sims KB, et al. Am J Hum Genet. 1989 Sep;45(3):424-34. Am J Hum Genet. 1989. PMID: 2773935 Free PMC article.

7

Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.

Collins FA, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE. Collins FA, et al. Among authors: sims kb. Am J Med Genet. 1992 Jan 1;42(1):127-34. doi: 10.1002/ajmg.1320420126. Am J Med Genet. 1992. PMID: 1308352

8

Physical fine-mapping of a deletion spanning the Norrie gene.

Diergaarde PJ, Wieringa B, Bleeker-Wagemakers EM, Sims KB, Breakefield XO, Ropers HH. Diergaarde PJ, et al. Among authors: sims kb. Hum Genet. 1989 Dec;84(1):22-6. doi: 10.1007/BF00210665. Hum Genet. 1989. PMID: 2606473

9

Characterization of a YAC containing part or all of the Norrie disease locus.

Chen ZY, Sims KB, Coleman M, Donnai D, Monaco A, Breakefield XO, Davies KE, Craig IW. Chen ZY, et al. Among authors: sims kb. Hum Mol Genet. 1992 Jun;1(3):161-4. doi: 10.1093/hmg/1.3.161. Hum Mol Genet. 1992. PMID: 1303171

10

Molecular genetics of the monoamine oxidases.

Hsu YP, Powell JF, Sims KB, Breakefield XO. Hsu YP, et al. Among authors: sims kb. J Neurochem. 1989 Jul;53(1):12-8. doi: 10.1111/j.1471-4159.1989.tb07289.x. J Neurochem. 1989. PMID: 2656914 Review. No abstract available.

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