511 related articles for article (PubMed ID: 15849989)
1. Clinical and genetic significance of unilateral Lisch nodules.
Ceuterick SD; Van Den Ende JJ; Smets RM
Bull Soc Belge Ophtalmol; 2005; (295):49-53. PubMed ID: 15849989
[TBL] [Abstract][Full Text] [Related]
2. [Lisch nodules. Markers for a non-invasive diagnosis in Recklinghausen neurofibromatosis].
Crişan M; Talu S; Florea M; Coprean D; Cosgarea R; Crişan D
Oftalmologia; 2008; 52(4):56-61. PubMed ID: 19354164
[TBL] [Abstract][Full Text] [Related]
3. [Neurofibromatosis type 1: a survey of 195 patients].
Overweg-Plandsoen WC; Weersink RG; Sillevis Smitt JH; Fleury P; van Asperen CJ
Ned Tijdschr Geneeskd; 1997 Mar; 141(13):624-9. PubMed ID: 9127578
[TBL] [Abstract][Full Text] [Related]
4. Eye disorders in neurofibromatosis (NF1).
Kordić R; Sabol Z; Cerovski B; Katusić D; Jukić T
Coll Antropol; 2005; 29 Suppl 1():29-31. PubMed ID: 16193672
[TBL] [Abstract][Full Text] [Related]
5. Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?
Yang CC; Happle R; Chao SC; Yu-Yun Lee J; Chen W
J Am Acad Dermatol; 2008 Mar; 58(3):493-7. PubMed ID: 18280349
[TBL] [Abstract][Full Text] [Related]
6. Bilateral segmental neurofibromatosis with gastric carcinoma.
Kajimoto A; Oiso N; Fukai K; Ishii M
Clin Exp Dermatol; 2007 Jan; 32(1):43-4. PubMed ID: 16939586
[TBL] [Abstract][Full Text] [Related]
7. Partial unilateral lentiginosis with ipsilateral Lisch nodules and axillary freckling.
Chen W; Fan PC; Happle R
Dermatology; 2004; 209(4):321-4. PubMed ID: 15539896
[TBL] [Abstract][Full Text] [Related]
8. [Syndromes 18. Von Recklinghausen's disease].
Baart JA; van Hagen JM
Ned Tijdschr Tandheelkd; 2000 Feb; 107(2):57-9. PubMed ID: 11385791
[TBL] [Abstract][Full Text] [Related]
9. Combined retinal hamartomas leading to the diagnosis of neurofibromatosis type 2.
Grant EA; Trzupek KM; Reiss J; Crow K; Messiaen L; Weleber RG
Ophthalmic Genet; 2008 Sep; 29(3):133-8. PubMed ID: 18766994
[TBL] [Abstract][Full Text] [Related]
10. [Importance of multidisciplinary consultations for children with neurofibromatosis].
Bursztyn J; Rodriguez D
J Fr Ophtalmol; 1999 Nov; 22(9):959-62. PubMed ID: 10609170
[TBL] [Abstract][Full Text] [Related]
11. [Neurofibromatosis type 1 and hypertension in pediatrics: case report].
Demarchi I; Genoni G; Prodam F; Petri A; Busti A; Cortese L; Negro M; Bellone S; Acucella G; Bona G
Minerva Pediatr; 2011 Aug; 63(4):335-9. PubMed ID: 21909069
[TBL] [Abstract][Full Text] [Related]
12. Partial unilateral lentiginosis is mosaic neurofibromatosis type 1 or not?
Yaşar Ş; Ersanli A; Göktay F; Aytekin S; Cebeci D; Güneş P
J Dermatol; 2017 Jan; 44(1):29-35. PubMed ID: 27439996
[TBL] [Abstract][Full Text] [Related]
13. [Neurofibromatosis versus schwannomatosis].
Mautner VF; Schröder S; Pulst SM; Ostertag H; Kluwe L
Fortschr Neurol Psychiatr; 1998 Jun; 66(6):271-7. PubMed ID: 9676422
[TBL] [Abstract][Full Text] [Related]
14. [Lisch nodule in neurofibromatosis type 1].
Abaloun Y; Ajhoun Y
Pan Afr Med J; 2017; 27():218. PubMed ID: 28979620
[TBL] [Abstract][Full Text] [Related]
15. Predictive value of café au lait macules at initial consultation in the diagnosis of neurofibromatosis type 1.
Nunley KS; Gao F; Albers AC; Bayliss SJ; Gutmann DH
Arch Dermatol; 2009 Aug; 145(8):883-7. PubMed ID: 19687418
[TBL] [Abstract][Full Text] [Related]
16. [Managing children with neurofibromatosis type 1: what should we look for?].
Martins CL; Monteiro JP; Farias A; Fernandes R; Fonseca MJ
Acta Med Port; 2007; 20(5):393-400. PubMed ID: 18282435
[TBL] [Abstract][Full Text] [Related]
17. Lisch nodules and skin manifestation in neurofibromatosis type 1.
Otsuka F; Kawashima T; Imakado S; Usuki Y; Hon-Mura S
Arch Dermatol; 2001 Feb; 137(2):232-3. PubMed ID: 11176707
[No Abstract] [Full Text] [Related]
18. Neurological complications involving the central nervous system in neurofibromatosis type 1.
Hsieh HY; Wu T; Wang CJ; Chin SC; Chen YR
Acta Neurol Taiwan; 2007 Jun; 16(2):68-73. PubMed ID: 17685129
[TBL] [Abstract][Full Text] [Related]
19. [Neurofibromatosis].
Wolkenstein P; Decq P
Neurochirurgie; 1998 Nov; 44(4):267-72. PubMed ID: 9864698
[TBL] [Abstract][Full Text] [Related]
20. SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.
Pasmant E; Sabbagh A; Hanna N; Masliah-Planchon J; Jolly E; Goussard P; Ballerini P; Cartault F; Barbarot S; Landman-Parker J; Soufir N; Parfait B; Vidaud M; Wolkenstein P; Vidaud D; France RN
J Med Genet; 2009 Jul; 46(7):425-30. PubMed ID: 19366998
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
