Ragge NK - Search Results

1

Dominant coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate.

Ravine D, Ragge NK, Stephens D, Oldridge M, Wilkie AO. Ravine D, et al. Among authors: ragge nk. Am J Med Genet. 1997 Oct 17;72(2):227-36. doi: 10.1002/(sici)1096-8628(19971017)72:2<227::aid-ajmg19>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9382148

2

Dominant inheritance of optic pits.

Ragge NK, Ravine D, Wilkie AO. Ragge NK, et al. Am J Ophthalmol. 1998 Jan;125(1):124-5. doi: 10.1016/s0002-9394(99)80255-4. Am J Ophthalmol. 1998. PMID: 9437334 No abstract available.

3

Anophthalmos, microphthalmos, and Coloboma in the United kingdom: clinical features, results of investigations, and early management.

Shah SP, Taylor AE, Sowden JC, Ragge N, Russell-Eggitt I, Rahi JS, Gilbert CE; Surveillance of Eye Anomalies Special Interest Group. Shah SP, et al. Ophthalmology. 2012 Feb;119(2):362-8. doi: 10.1016/j.ophtha.2011.07.039. Epub 2011 Nov 4. Ophthalmology. 2012. PMID: 22054996

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: ragge nk. 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

Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.

Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM. Ragge NK, et al. J Med Genet. 2003 Jan;40(1):37-41. doi: 10.1136/jmg.40.1.37. J Med Genet. 2003. PMID: 12525540 Free PMC article.

6

Incidence and patterns of detection and management of childhood-onset hereditary retinal disorders in the UK.

Hamblion EL, Moore AT, Rahi JS; British Childhood Onset Hereditary Retinal Disorders Network. Hamblion EL, et al. Br J Ophthalmol. 2012 Mar;96(3):360-5. doi: 10.1136/bjo.2010.201178. Epub 2011 Jun 7. Br J Ophthalmol. 2012. PMID: 21653210

7

Big discs with optic nerve hypoplasia.

Ragge NK, Hoyt WF, Lambert SR. Ragge NK, et al. J Clin Neuroophthalmol. 1991 Jun;11(2):137. J Clin Neuroophthalmol. 1991. PMID: 1832688 No abstract available.

8

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: ragge nk. Hum Mol Genet. 1994 Jun;3(6):885-91. doi: 10.1093/hmg/3.6.885. Hum Mol Genet. 1994. PMID: 7951231

9

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

10

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: ragge nk. 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

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