NS22224/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1986	2
1987	5
1988	1
1989	3
1990	2
1991	5
1992	5
1993	3
1996	2
1998	1
2010	1
2025	0

1

Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma).

Fontaine B, Rouleau GA, Seizinger BR, Menon AG, Jewell AF, Martuza RL, Gusella JF. Fontaine B, et al. Ann N Y Acad Sci. 1991;615:338-43. doi: 10.1111/j.1749-6632.1991.tb37776.x. Ann N Y Acad Sci. 1991. PMID: 2039155 Review.

2

The molecular biology of human glial tumors.

Martuza RL, Seizinger BR, Jacoby LB, Rouleau GA, Gusella JF. Martuza RL, et al. Trends Neurosci. 1988 Jan;11(1):22-7. doi: 10.1016/0166-2236(88)90045-8. Trends Neurosci. 1988. PMID: 2469150 Review. No abstract available.

3

The genomic structure of the human skeletal muscle sodium channel gene.

McClatchey AI, Lin CS, Wang J, Hoffman EP, Rojas C, Gusella JF. McClatchey AI, et al. Hum Mol Genet. 1992 Oct;1(7):521-7. doi: 10.1093/hmg/1.7.521. Hum Mol Genet. 1992. PMID: 1339144

4

Neurofibromatosis type 1 gene mutations in neuroblastoma.

The I, Murthy AE, Hannigan GE, Jacoby LB, Menon AG, Gusella JF, Bernards A. The I, et al. Nat Genet. 1993 Jan;3(1):62-6. doi: 10.1038/ng0193-62. Nat Genet. 1993. PMID: 8490657

5

Monozygotic twins discordant for neurofibromatosis 1.

Kaplan L, Foster R, Shen Y, Parry DM, McMaster ML, O'Leary MC, Gusella JF. Kaplan L, et al. Am J Med Genet A. 2010 Mar;152A(3):601-6. doi: 10.1002/ajmg.a.33271. Am J Med Genet A. 2010. PMID: 20186797 Free PMC article.

6

Physical mapping of a translocation breakpoint in neurofibromatosis.

Fountain JW, Wallace MR, Bruce MA, Seizinger BR, Menon AG, Gusella JF, Michels VV, Schmidt MA, Dewald GW, Collins FS. Fountain JW, et al. Science. 1989 Jun 2;244(4908):1085-7. doi: 10.1126/science.2543076. Science. 1989. PMID: 2543076

7

Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease.

Seizinger BR, Smith DI, Filling-Katz MR, Neumann H, Green JS, Choyke PL, Anderson KM, Freiman RN, Klauck SM, Whaley J, et al. Seizinger BR, et al. Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2864-8. doi: 10.1073/pnas.88.7.2864. Proc Natl Acad Sci U S A. 1991. PMID: 2011596 Free PMC article.

8

Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17.

Menon AG, Ledbetter DH, Rich DC, Seizinger BR, Rouleau GA, Michels VF, Schmidt MA, Dewald G, DallaTorre CM, Haines JL, et al. Menon AG, et al. Genomics. 1989 Aug;5(2):245-9. doi: 10.1016/0888-7543(89)90053-0. Genomics. 1989. PMID: 2507442

9

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Rouleau GA, Seizinger BR, Wertelecki W, Haines JL, Superneau DW, Martuza RL, Gusella JF. Rouleau GA, et al. Am J Hum Genet. 1990 Feb;46(2):323-8. Am J Hum Genet. 1990. PMID: 2105641 Free PMC article.

10

Different gene loci for hyperkalemic and hypokalemic periodic paralysis.

Fontaine B, Trofatter J, Rouleau GA, Khurana TS, Haines J, Brown R, Gusella JF. Fontaine B, et al. Neuromuscul Disord. 1991;1(4):235-8. doi: 10.1016/0960-8966(91)90095-a. Neuromuscul Disord. 1991. PMID: 1822800

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