Martuza RL - Search Results

1

Neurofibromatosis type 2 appears to be a genetically homogeneous disease.

Narod SA, Parry DM, Parboosingh J, Lenoir GM, Ruttledge M, Fischer G, Eldridge R, Martuza RL, Frontali M, Haines J, et al. Narod SA, et al. Among authors: martuza rl. Am J Hum Genet. 1992 Sep;51(3):486-96. Am J Hum Genet. 1992. PMID: 1496982 Free PMC article.

2

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. Among authors: martuza rl. Am J Hum Genet. 1990 Feb;46(2):323-8. Am J Hum Genet. 1990. PMID: 2105641 Free PMC article.

3

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

Martuza RL, Eldridge R. Martuza RL, et al. N Engl J Med. 1988 Mar 17;318(11):684-8. doi: 10.1056/NEJM198803173181106. N Engl J Med. 1988. PMID: 3125435 Review. No abstract available.

4

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22.

Rouleau GA, Wertelecki W, Haines JL, Hobbs WJ, Trofatter JA, Seizinger BR, Martuza RL, Superneau DW, Conneally PM, Gusella JF. Rouleau GA, et al. Among authors: martuza rl. Nature. 1987 Sep 17-23;329(6136):246-8. doi: 10.1038/329246a0. Nature. 1987. PMID: 2888021

5

Advances in neurofibromatosis 2 (NF2): a workshop report.

Lim DJ, Rubenstein AE, Evans DG, Jacks T, Seizinger BG, Baser ME, Beebe D, Brackmann DE, Chiocca EA, Fehon RG, Giovannini M, Glazer R, Gusella JF, Gutmann DH, Korf B, Lieberman F, Martuza R, McClatchey AI, Parry DM, Pulst SM, Ramesh V, Ramsey WJ, Ratner N, Rutkowski JL, Ruttledge M, Weinstein DE. Lim DJ, et al. J Neurogenet. 2000 Jun;14(2):63-106. doi: 10.3109/01677060009083477. J Neurogenet. 2000. PMID: 10992163 Review. No abstract available.

6

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

Fontaine B, Rouleau GA, Seizinger B, Jewell AF, Hanson MP, Martuza RL, Gusella JF. Fontaine B, et al. Among authors: martuza rl. Am J Hum Genet. 1990 Nov;47(5):823-7. Am J Hum Genet. 1990. PMID: 2220822 Free PMC article.

7

Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putative 'tumor progression' locus.

Menon AG, Rutter JL, von Sattel JP, Synder H, Murdoch C, Blumenfeld A, Martuza RL, von Deimling A, Gusella JF, Houseal TW. Menon AG, et al. Among authors: martuza rl. Oncogene. 1997 Feb 6;14(5):611-6. doi: 10.1038/sj.onc.1200853. Oncogene. 1997. PMID: 9053860

8

Bilateral acoustic neurofibromatosis (neurofibromatosis 2): a disorder distinct from von Recklinghausen's neurofibromatosis (neurofibromatosis 1).

Flexon PB, Nadol JB Jr, Schuknecht HF, Montgomery WW, Martuza RL. Flexon PB, et al. Among authors: martuza rl. Ann Otol Rhinol Laryngol. 1991 Oct;100(10):830-4. doi: 10.1177/000348949110001008. Ann Otol Rhinol Laryngol. 1991. PMID: 1952650 Review.

9

Models for inherited susceptibility to cancer in the nervous system: a molecular-genetic approach to neurofibromatosis.

Seizinger BR, Martuza RL, Rouleau G, Breakefield XO, Gusella JF. Seizinger BR, et al. Among authors: martuza rl. Dev Neurosci. 1987;9(3):144-53. doi: 10.1159/000111618. Dev Neurosci. 1987. PMID: 3119309 Review.

10

Treatment of schwannomas with an oncolytic recombinant herpes simplex virus in murine models of neurofibromatosis type 2.

Messerli SM, Prabhakar S, Tang Y, Mahmood U, Giovannini M, Weissleder R, Bronson R, Martuza R, Rabkin S, Breakefield XO. Messerli SM, et al. Hum Gene Ther. 2006 Jan;17(1):20-30. doi: 10.1089/hum.2006.17.20. Hum Gene Ther. 2006. PMID: 16409122

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