224 related articles for article (PubMed ID: 2511319)
1. A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.
Huson SM; Compston DA; Harper PS
J Med Genet; 1989 Nov; 26(11):712-21. PubMed ID: 2511319
[TBL] [Abstract][Full Text] [Related]
2. Von Recklinghausen neurofibromatosis. A clinical and population study in south-east Wales.
Huson SM; Harper PS; Compston DA
Brain; 1988 Dec; 111 ( Pt 6)():1355-81. PubMed ID: 3145091
[TBL] [Abstract][Full Text] [Related]
3. [Neurofibromatosis--an inborn genetic disorder with susceptibility to neoplasia].
Karwacki MW; Woźniak W
Med Wieku Rozwoj; 2006; 10(3 Pt 2):923-48. PubMed ID: 17401183
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.
Charrow J; Listernick R; Ward K
Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833
[TBL] [Abstract][Full Text] [Related]
6. A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.
Huson SM; Compston DA; Clark P; Harper PS
J Med Genet; 1989 Nov; 26(11):704-11. PubMed ID: 2511318
[TBL] [Abstract][Full Text] [Related]
7. High frequencies of plexiform neurofibromas, mental retardation, learning difficulties, and scoliosis in Brazilian patients with neurofibromatosis type 1.
Trovó-Marqui AB; Goloni-Bertollo EM; Valério NI; Pavarino-Bertelli EC; Muniz MP; Teixeira MF; Antonio JR; Tajara EH
Braz J Med Biol Res; 2005 Sep; 38(9):1441-7. PubMed ID: 16138229
[TBL] [Abstract][Full Text] [Related]
8. Diagnostic outcome in children with multiple café au lait spots.
Korf BR
Pediatrics; 1992 Dec; 90(6):924-7. PubMed ID: 1344978
[TBL] [Abstract][Full Text] [Related]
9. Familial multiple cafe au lait spots.
Arnsmeier SL; Riccardi VM; Paller AS
Arch Dermatol; 1994 Nov; 130(11):1425-6. PubMed ID: 7979446
[TBL] [Abstract][Full Text] [Related]
10. Neurofibromatosis.
Wander JV; Das Gupta TK
Curr Probl Surg; 1977 Feb; 14(2):1-81. PubMed ID: 405178
[No Abstract] [Full Text] [Related]
11. Bone abnormalities occurring in the follow-up of the patients with neurofibromatosis type 1.
Georgescu EF; Stănescu L; Georgescu AC; Dumitrescu D; Foarfă C; Călin G
Rom J Morphol Embryol; 2007; 48(3):249-56. PubMed ID: 17914491
[TBL] [Abstract][Full Text] [Related]
12. [Unusual clinical manifestations of type 1 neurofibromatosis].
Komlósi K; Polgár N; Hadzsiev K; Ottóffy G; Illés T; Dóczi T; Melegh B
Orv Hetil; 2011 Dec; 152(49):1965-70. PubMed ID: 22106164
[TBL] [Abstract][Full Text] [Related]
13. Pathophysiology of neurofibromatosis. IV. Dermatologic insights into heterogeneity and pathogenesis.
Riccardi VM
J Am Acad Dermatol; 1980 Aug; 3(2):157-66. PubMed ID: 6774000
[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. Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients.
Ars E; Kruyer H; Morell M; Pros E; Serra E; Ravella A; Estivill X; Lázaro C
J Med Genet; 2003 Jun; 40(6):e82. PubMed ID: 12807981
[No Abstract] [Full Text] [Related]
16. Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): a follow-up study.
Fois A; Calistri L; Balestri P; Vivarelli R; Bartalini G; Mancini L; Berardi A; Vanni M
Eur J Pediatr; 1993 Jun; 152(6):500-4. PubMed ID: 8335018
[TBL] [Abstract][Full Text] [Related]
17. A clinical study of type 1 neurofibromatosis in north west England.
McGaughran JM; Harris DI; Donnai D; Teare D; MacLeod R; Westerbeek R; Kingston H; Super M; Harris R; Evans DG
J Med Genet; 1999 Mar; 36(3):197-203. PubMed ID: 10204844
[TBL] [Abstract][Full Text] [Related]
18. Von Recklinghausen neurofibromatosis. Incidence of iris hamartomata.
Lewis RA; Riccardi VM
Ophthalmology; 1981 Apr; 88(4):348-54. PubMed ID: 6789269
[TBL] [Abstract][Full Text] [Related]
19. [Thoracic findings in neurofibromatosis].
Camsari G; Gür A; Ozkan G; Bakan ND; Zengin F; Külcü A
Tuberk Toraks; 2006; 54(3):267-72. PubMed ID: 17001545
[TBL] [Abstract][Full Text] [Related]
20. Neurofibromatosis in childhood: a review of 25 cases.
Pollnitz R
Med J Aust; 1976 Jul; 2(2):49-52. PubMed ID: 824536
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
