These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
75 related articles for article (PubMed ID: 2516454)
1. Neurofibromatosis in Gothenburg, Sweden. IV. Genetic analyses. Samuelsson B; Akesson HO Neurofibromatosis; 1989; 2(2):107-15. PubMed ID: 2516454 [TBL] [Abstract][Full Text] [Related]
2. Neurofibromatosis in Gothenburg, Sweden. I. Background, study design and epidemiology. Samuelsson B; Samuelsson S Neurofibromatosis; 1989; 2(1):6-22. PubMed ID: 2517025 [TBL] [Abstract][Full Text] [Related]
3. Neurofibromatosis. A clinical and genetic study of 96 cases in Gothenburg, Sweden. Samuelsson B; Axelsson R Acta Derm Venereol Suppl (Stockh); 1981; 95():67-71. PubMed ID: 6807042 [TBL] [Abstract][Full Text] [Related]
4. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
5. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate. Piver MS Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011 [TBL] [Abstract][Full Text] [Related]
6. Paternal origin of new mutations in von Recklinghausen neurofibromatosis. Jadayel D; Fain P; Upadhyaya M; Ponder MA; Huson SM; Carey J; Fryer A; Mathew CG; Barker DF; Ponder BA Nature; 1990 Feb; 343(6258):558-9. PubMed ID: 2105472 [TBL] [Abstract][Full Text] [Related]
7. [The classification of atypical forms of neurofibromatosis]. Theiler R; Stocker H; Boltshauser E Schweiz Med Wochenschr; 1991 Mar; 121(13):446-55. PubMed ID: 1903213 [TBL] [Abstract][Full Text] [Related]
8. Neurofibromatosis in Gothenburg, Sweden. II. Intellectual compromise. Samuelsson B; Riccardi VM Neurofibromatosis; 1989; 2(2):78-83. PubMed ID: 2516460 [TBL] [Abstract][Full Text] [Related]
9. Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal-recessive inheritance and complete penetrance. Genĉík A Dev Ophthalmol; 1989; 16():76-115. PubMed ID: 2676634 [TBL] [Abstract][Full Text] [Related]
10. [Genetic counseling in neurofibromatosis. Apropos of a study of 53 families]. Toutain A; Kaplan J; Briard ML; Frézal J J Genet Hum; 1988 Jun; 36(3):163-71. PubMed ID: 3137311 [TBL] [Abstract][Full Text] [Related]
11. Neurofibromatosis in Gothenburg, Sweden. III. Psychiatric and social aspects. Samuelsson B; Riccardi VM Neurofibromatosis; 1989; 2(2):84-106. PubMed ID: 2516461 [TBL] [Abstract][Full Text] [Related]
12. [Ophthalmologic differentiation of various forms of neurofibromatosis]. Mautner VF; Hazim W; Guthoff R Ophthalmologe; 1993 Aug; 90(4):391-3. PubMed ID: 8374240 [TBL] [Abstract][Full Text] [Related]
13. A genetic linkage study in 15 families of individuals with von Recklinghausen neurofibromatosis. Dunn BG; Ferrell RE; Riccardi VM Am J Med Genet; 1985 Oct; 22(2):403-7. PubMed ID: 3931478 [TBL] [Abstract][Full Text] [Related]
14. Discounting an adverse maternal effect on severity of neurofibromatosis. Riccardi VM; Wald JS Pediatrics; 1987 Mar; 79(3):386-93. PubMed ID: 3103092 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study. Brito D; Richard P; Komajda M; Madeira H Rev Port Cardiol; 2008 Feb; 27(2):147-73. PubMed ID: 18488914 [TBL] [Abstract][Full Text] [Related]
18. Linkage analysis of Von Recklinghausen neurofibromatosis: chromosomes 4 and 19. Dietz JN; Robbins T; Cannon LA; Schwartz CE; Carey JC; Johnson JP; Kivlin J; Skolnick MH Genet Epidemiol; 1986; 3(5):313-21. PubMed ID: 3096816 [TBL] [Abstract][Full Text] [Related]
19. Paternal age and sporadic neurofibromatosis 1: a case-control study and consideration of the methodologic issues. Bunin GR; Needle M; Riccardi VM Genet Epidemiol; 1997; 14(5):507-16. PubMed ID: 9358268 [TBL] [Abstract][Full Text] [Related]
20. Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA. de Raedt T; Cools J; Debiec-Rychter M; Brems H; Mentens N; Sciot R; Himpens J; de Wever I; Schöffski P; Marynen P; Legius E Gastroenterology; 2006 Dec; 131(6):1907-12. PubMed ID: 17087943 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]