123 related articles for article (PubMed ID: 11015700)
21. [Neurofibromatosis: the most frequent hereditary tumor predisposition syndrome].
Wimmer K
Wien Med Wochenschr; 2005 Jun; 155(11-12):273-80. PubMed ID: 16035388
[TBL] [Abstract][Full Text] [Related]
22. Genetic and clinical considerations in six cases with neurofibromatosis type 1.
Buteică E; Stoicescu I; Burada F; Stănoiu B
Rom J Morphol Embryol; 2007; 48(3):243-8. PubMed ID: 17914490
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of the neurofibromatoses.
Pulst SM
Clin Perinatol; 1990 Dec; 17(4):829-44. PubMed ID: 1981029
[TBL] [Abstract][Full Text] [Related]
24. The R1947X mutation of NF1 causing autosomal dominant neurofibromatosis type 1 in a Chinese family.
Yang Q; Huang C; Yang X; Feng Y; Wang Q; Liu M
J Genet Genomics; 2008 Feb; 35(2):73-6. PubMed ID: 18407053
[TBL] [Abstract][Full Text] [Related]
25. Neurofibromatosis 1 in childhood.
North KN
Semin Pediatr Neurol; 1998 Dec; 5(4):231-42. PubMed ID: 9874851
[TBL] [Abstract][Full Text] [Related]
26. [Clinical diagnosis of neurofibromatosis type 1].
Wolkenstein P; Zeller J
Presse Med; 1999 Dec; 28(39):2174-80. PubMed ID: 10629698
[TBL] [Abstract][Full Text] [Related]
27. Exonic deletions in the NF1 gene in patients with neurofibromatosis type I from the lower Silesian region of Poland.
Laczmańska I; Szczepaniak M; Jakubiak A; Stembalska A
Adv Clin Exp Med; 2014; 23(4):517-21. PubMed ID: 25166435
[TBL] [Abstract][Full Text] [Related]
28. Ten novel mutations in the human neurofibromatosis type 1 (NF1) gene in Italian patients.
Origone P; De Luca A; Bellini C; Buccino A; Mingarelli R; Costabel S; La Rosa C; Garrè C; Coviello DA; Ajmar F; Dallapiccola B; Bonioli E
Hum Mutat; 2002 Jul; 20(1):74-5. PubMed ID: 12112660
[TBL] [Abstract][Full Text] [Related]
29. Molecular genetics of neurofibromatosis type 1 (NF1).
Shen MH; Harper PS; Upadhyaya M
J Med Genet; 1996 Jan; 33(1):2-17. PubMed ID: 8825042
[TBL] [Abstract][Full Text] [Related]
30. Neurofibromatosis type 1.
Boyd KP; Korf BR; Theos A
J Am Acad Dermatol; 2009 Jul; 61(1):1-14; quiz 15-6. PubMed ID: 19539839
[TBL] [Abstract][Full Text] [Related]
31. Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis.
Burkitt Wright EM; Sach E; Sharif S; Quarrell O; Carroll T; Whitehouse RW; Upadhyaya M; Huson SM; Evans DG
J Med Genet; 2013 Sep; 50(9):606-13. PubMed ID: 23812910
[TBL] [Abstract][Full Text] [Related]
32. Familial café au lait spots: a variant of neurofibromatosis type 1.
Abeliovich D; Gelman-Kohan Z; Silverstein S; Lerer I; Chemke J; Merin S; Zlotogora J
J Med Genet; 1995 Dec; 32(12):985-6. PubMed ID: 8825931
[TBL] [Abstract][Full Text] [Related]
33. Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphisms.
Gasparini P; D'Agruma L; Pio de Cillis G; Balestrazzi P; Mingarelli R; Zelante L
Hum Genet; 1996 Apr; 97(4):492-5. PubMed ID: 8834249
[TBL] [Abstract][Full Text] [Related]
34. [Phenotypic and genetic features in neurofibromatosis type 1 in children].
Duat Rodríguez A; Martos Moreno GÁ; Martín Santo-Domingo Y; Hernández Martín A; Espejo-Saavedra Roca JM; Ruiz-Falcó Rojas ML; Argente J
An Pediatr (Barc); 2015 Sep; 83(3):173-82. PubMed ID: 25541118
[TBL] [Abstract][Full Text] [Related]
35. Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform.
Calì F; Chiavetta V; Ruggeri G; Piccione M; Selicorni A; Palazzo D; Bonsignore M; Cereda A; Elia M; Failla P; Figura MG; Fiumara A; Maitz S; Luana Mandarà GM; Mattina T; Ragalmuto A; Romano C; Ruggieri M; Salluzzo R; Saporoso A; Schepis C; Sorge G; Spanò M; Tortorella G; Romano V
Eur J Med Genet; 2017 Feb; 60(2):93-99. PubMed ID: 27838393
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. [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]
38. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots and Freckling. Part II. Other Skin Manifestations Characteristic of NF1. NF1 and Cancer.
Hernández-Martín A; Duat-Rodríguez A
Actas Dermosifiliogr; 2016; 107(6):465-73. PubMed ID: 26956402
[TBL] [Abstract][Full Text] [Related]
39. Café-au-lait Macules and Neurofibromatosis Type 1: A Review of the Literature.
Bernier A; Larbrisseau A; Perreault S
Pediatr Neurol; 2016 Jul; 60():24-29.e1. PubMed ID: 27212418
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]