Pulst SM - Search Results

1

Loss of alleles in vestibular schwannomas: use of microsatellite markers on chromosome 22.

Sainz J, Baser ME, Ragge NK, Nelson RA, Pulst SM. Sainz J, et al. Among authors: pulst sm. Arch Otolaryngol Head Neck Surg. 1993 Dec;119(12):1285-8. doi: 10.1001/archotol.1993.01880240015003. Arch Otolaryngol Head Neck Surg. 1993. PMID: 17431981

2

Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas.

Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM. Sainz J, et al. Among authors: pulst sm. Hum Mol Genet. 1994 Jun;3(6):885-91. doi: 10.1093/hmg/3.6.885. Hum Mol Genet. 1994. PMID: 7951231

3

Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas.

Sainz J, Figueroa K, Baser ME, Pulst SM. Sainz J, et al. Among authors: pulst sm. Hum Genet. 1996 Jan;97(1):121-3. doi: 10.1007/BF00218846. Hum Genet. 1996. PMID: 8557252

4

Phenotypic variability in monozygotic twins with neurofibromatosis 2.

Baser ME, Ragge NK, Riccardi VM, Janus T, Gantz B, Pulst SM. Baser ME, et al. Among authors: pulst sm. Am J Med Genet. 1996 Sep 6;64(4):563-7. doi: 10.1002/(SICI)1096-8628(19960906)64:4<563::AID-AJMG7>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8870923

5

Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations.

Baser ME, Mautner VF, Ragge NK, Nechiporuk A, Riccardi VM, Klein J, Sainz J, Pulst SM. Baser ME, et al. Among authors: pulst sm. Neurology. 1996 Nov;47(5):1269-77. doi: 10.1212/wnl.47.5.1269. Neurology. 1996. PMID: 8909442

6

High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons.

Sainz J, Figueroa K, Baser ME, Mautner VF, Pulst SM. Sainz J, et al. Among authors: pulst sm. Hum Mol Genet. 1995 Jan;4(1):137-9. doi: 10.1093/hmg/4.1.137. Hum Mol Genet. 1995. PMID: 7711726 No abstract available.

7

CA-repeat polymorphism at the D22S430 locus adjacent to NF2.

Sainz J, Nechiporuk A, Kim UJ, Simon MI, Pulst SM. Sainz J, et al. Among authors: pulst sm. Hum Mol Genet. 1993 Dec;2(12):2203. doi: 10.1093/hmg/2.12.2203. Hum Mol Genet. 1993. PMID: 8111404 No abstract available.

8

A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes.

Scoles DR, Baser ME, Pulst SM. Scoles DR, et al. Among authors: pulst sm. Neurology. 1996 Aug;47(2):544-6. doi: 10.1212/wnl.47.2.544. Neurology. 1996. PMID: 8757035

9

Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomas.

Huynh DP, Mautner V, Baser ME, Stavrou D, Pulst SM. Huynh DP, et al. Among authors: pulst sm. J Neuropathol Exp Neurol. 1997 Apr;56(4):382-90. doi: 10.1097/00005072-199704000-00007. J Neuropathol Exp Neurol. 1997. PMID: 9100669

10

Dinucleotide repeat polymorphism at the D22S351 locus.

Sainz J, Rasmussen M, Nechiporuk A, Vissing H, Cheng X, Korenberg JR, Pulst SM. Sainz J, et al. Among authors: pulst sm. Hum Mol Genet. 1993 Oct;2(10):1749. doi: 10.1093/hmg/2.10.1749. Hum Mol Genet. 1993. PMID: 8268946 No abstract available.

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