Baser ME - Search Results

1

The neuroimaging and clinical spectrum of neurofibromatosis 2.

Mautner VF, Lindenau M, Baser ME, Hazim W, Tatagiba M, Haase W, Samii M, Wais R, Pulst SM. Mautner VF, et al. Among authors: baser me. Neurosurgery. 1996 May;38(5):880-5; discussion 885-6. doi: 10.1097/00006123-199605000-00004. Neurosurgery. 1996. PMID: 8727812

2

Vestibular schwannoma growth in patients with neurofibromatosis Type 2: a longitudinal study.

Mautner VF, Baser ME, Thakkar SD, Feigen UM, Friedman JM, Kluwe L. Mautner VF, et al. Among authors: baser me. J Neurosurg. 2002 Feb;96(2):223-8. doi: 10.3171/jns.2002.96.2.0223. J Neurosurg. 2002. PMID: 11838794

3

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: baser me. AJR Am J Roentgenol. 1995 Oct;165(4):951-5. doi: 10.2214/ajr.165.4.7676998. AJR Am J Roentgenol. 1995. PMID: 7676998

4

Skin abnormalities in neurofibromatosis 2.

Mautner VF, Lindenau M, Baser ME, Kluwe L, Gottschalk J. Mautner VF, et al. Among authors: baser me. Arch Dermatol. 1997 Dec;133(12):1539-43. Arch Dermatol. 1997. PMID: 9420538

5

Phenotypic variability in two families with novel splice-site and frameshift NF2 mutations.

Mautner VF, Baser ME, Kluwe L. Mautner VF, et al. Among authors: baser me. Hum Genet. 1996 Aug;98(2):203-6. doi: 10.1007/s004390050191. Hum Genet. 1996. PMID: 8698343

6

Phenotypic variability in monozygotic twins with neurofibromatosis 2.

Baser ME, Ragge NK, Riccardi VM, Janus T, Gantz B, Pulst SM. Baser ME, et al. 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

7

Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypes.

Kluwe L, Bayer S, Baser ME, Hazim W, Haase W, Fünsterer C, Mautner VF. Kluwe L, et al. Among authors: baser me. Hum Genet. 1996 Nov;98(5):534-8. doi: 10.1007/s004390050255. Hum Genet. 1996. PMID: 8882871

8

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. Neurology. 1996 Nov;47(5):1269-77. doi: 10.1212/wnl.47.5.1269. Neurology. 1996. PMID: 8909442

9

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: baser me. Hum Genet. 1996 Jan;97(1):121-3. doi: 10.1007/BF00218846. Hum Genet. 1996. PMID: 8557252

10

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: baser me. Neurology. 1996 Aug;47(2):544-6. doi: 10.1212/wnl.47.2.544. Neurology. 1996. PMID: 8757035

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