Pulst SM - Search Results

1

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

2

Familial spinal neurofibromatosis: clinical and DNA linkage analysis.

Pulst SM, Riccardi VM, Fain P, Korenberg JR. Pulst SM, et al. Neurology. 1991 Dec;41(12):1923-7. doi: 10.1212/wnl.41.12.1923. Neurology. 1991. PMID: 1745350

3

Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia.

Pulst SM, Pribyl T, Barker DF, Riccardi VM, Ren M, Yaari H, Korenberg JR. Pulst SM, et al. Am J Med Genet. 1991 Jul 1;40(1):84-7. doi: 10.1002/ajmg.1320400117. Am J Med Genet. 1991. PMID: 1909491

4

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

5

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

6

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

7

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

8

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

9

Ocular abnormalities in neurofibromatosis 2.

Ragge NK, Baser ME, Klein J, Nechiporuk A, Sainz J, Pulst SM, Riccardi VM. Ragge NK, et al. Among authors: pulst sm. Am J Ophthalmol. 1995 Nov;120(5):634-41. doi: 10.1016/s0002-9394(14)72210-x. Am J Ophthalmol. 1995. PMID: 7485365

10

Spinal tumors in patients with neurofibromatosis type 2: MR imaging study of frequency, multiplicity, and variety.

Mautner VF, Tatagiba M, Lindenau M, Fünsterer C, Pulst SM, Baser ME, Kluwe L, Zanella FE. Mautner VF, et al. Among authors: pulst sm. AJR Am J Roentgenol. 1995 Oct;165(4):951-5. doi: 10.2214/ajr.165.4.7676998. AJR Am J Roentgenol. 1995. PMID: 7676998

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