119 related articles for article (PubMed ID: 8909442)
1. 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
Neurology; 1996 Nov; 47(5):1269-77. PubMed ID: 8909442
[TBL] [Abstract][Full Text] [Related]
2. Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigree.
Sainio M; Strachan T; Blomstedt G; Salonen O; Setälä K; Palotie A; Palo J; Pyykkö I; Peltonen L; Jääskeläinen J
Neurology; 1995 Jul; 45(7):1314-22. PubMed ID: 7617190
[TBL] [Abstract][Full Text] [Related]
3. Phenotypic variability in two families with novel splice-site and frameshift NF2 mutations.
Mautner VF; Baser ME; Kluwe L
Hum Genet; 1996 Aug; 98(2):203-6. PubMed ID: 8698343
[TBL] [Abstract][Full Text] [Related]
4. Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers.
Ruttledge MH; Narod SA; Dumanski JP; Parry DM; Eldridge R; Wertelecki W; Parboosingh J; Faucher MC; Lenoir GM; Collins VP
Neurology; 1993 Sep; 43(9):1753-60. PubMed ID: 8414026
[TBL] [Abstract][Full Text] [Related]
5. Ocular abnormalities in neurofibromatosis 2.
Ragge NK; Baser ME; Klein J; Nechiporuk A; Sainz J; Pulst SM; Riccardi VM
Am J Ophthalmol; 1995 Nov; 120(5):634-41. PubMed ID: 7485365
[TBL] [Abstract][Full Text] [Related]
6. 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
Am J Hum Genet; 1992 Sep; 51(3):486-96. PubMed ID: 1496982
[TBL] [Abstract][Full Text] [Related]
7. Neurofibromatosis 2 in the pediatric age group.
Mautner VF; Tatagiba M; Guthoff R; Samii M; Pulst SM
Neurosurgery; 1993 Jul; 33(1):92-6. PubMed ID: 8355853
[TBL] [Abstract][Full Text] [Related]
8. [Type 2 neurofibromatosis without acoustic neuroma].
Mautner VF; Lindenau M; Köppen J; Hazim W; Kluwe L
Zentralbl Neurochir; 1995; 56(2):83-7. PubMed ID: 7639047
[TBL] [Abstract][Full Text] [Related]
9. Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity.
Parry DM; Eldridge R; Kaiser-Kupfer MI; Bouzas EA; Pikus A; Patronas N
Am J Med Genet; 1994 Oct; 52(4):450-61. PubMed ID: 7747758
[TBL] [Abstract][Full Text] [Related]
10. Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene.
Sestini R; Vivarelli R; Balestri P; Ammannati F; Montali E; Papi L
Hum Genet; 2000 Oct; 107(4):366-71. PubMed ID: 11129337
[TBL] [Abstract][Full Text] [Related]
11. Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients.
Ruggieri M; Iannetti P; Polizzi A; La Mantia I; Spalice A; Giliberto O; Platania N; Gabriele AL; Albanese V; Pavone L
Neuropediatrics; 2005 Feb; 36(1):21-34. PubMed ID: 15776319
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic variability in monozygotic twins with neurofibromatosis 2.
Baser ME; Ragge NK; Riccardi VM; Janus T; Gantz B; Pulst SM
Am J Med Genet; 1996 Sep; 64(4):563-7. PubMed ID: 8870923
[TBL] [Abstract][Full Text] [Related]
13. Misleading linkage results in an NF2 presymptomatic test owing to mosaicism.
Bijlsma EK; Wallace AJ; Evans DG
J Med Genet; 1997 Nov; 34(11):934-6. PubMed ID: 9391890
[TBL] [Abstract][Full Text] [Related]
14. Diagnosis, Management, and New Therapeutic Options in Childhood Neurofibromatosis Type 2 and Related Forms.
Ruggieri M; Praticò AD; Evans DG
Semin Pediatr Neurol; 2015 Dec; 22(4):240-58. PubMed ID: 26706012
[TBL] [Abstract][Full Text] [Related]
15. [Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type II].
Cui YX; Xia XY; Huang TT; Wei L; Fan XB; Yao B; Ge YF; Li XJ; Huang YF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):688-91. PubMed ID: 21154335
[TBL] [Abstract][Full Text] [Related]
16. Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study.
Evans DG; Mason S; Huson SM; Ponder M; Harding AE; Strachan T
J Neurol Neurosurg Psychiatry; 1997 Apr; 62(4):361-6. PubMed ID: 9120449
[TBL] [Abstract][Full Text] [Related]
17. Further genotype--phenotype correlations in neurofibromatosis 2.
Selvanathan SK; Shenton A; Ferner R; Wallace AJ; Huson SM; Ramsden RT; Evans DG
Clin Genet; 2010 Feb; 77(2):163-70. PubMed ID: 19968670
[TBL] [Abstract][Full Text] [Related]
18. [A case of neurofibromatosis type 2 (NF2) presenting with late-onset axonal polyneuropathy].
Iseki C; Takahashi Y; Wada M; Kawanami T; Kurita K; Kato T
Rinsho Shinkeigaku; 2009 Jul; 49(7):419-23. PubMed ID: 19715170
[TBL] [Abstract][Full Text] [Related]
19. Neurofibromatosis type 2 in an infant with multiple plexiform schwannomas as first symptom.
Miyakawa T; Kamada N; Kobayashi T; Hirano K; Fujii K; Sasahara Y; Nagai Y; Shinkai H
J Dermatol; 2007 Jan; 34(1):60-4. PubMed ID: 17204104
[TBL] [Abstract][Full Text] [Related]
20. Mutations and allelic loss of the NF2 gene in neurofibromatosis 2-associated skin tumors.
Kluwe L; Friedrich RE; Hagel C; Lindenau M; Mautner VF
J Invest Dermatol; 2000 May; 114(5):1017-21. PubMed ID: 10771486
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
