567 related articles for article (PubMed ID: 1344978)
41. [Segmental neurofibromatosis in children. Presentation of 43 patients].
Pascual-Castroviejo I; Pascual-Pascual SI; Velázquez-Fragua R; Viaño J; López-Gutiérrez JC
Rev Neurol; 2008 Oct 16-31; 47(8):399-403. PubMed ID: 18937200
[TBL] [Abstract][Full Text] [Related]
42. A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion.
Morava E; Bartsch O; Czako M; Frensel A; Kárteszi J; Kosztolányi GY
Genet Couns; 2003; 14(3):337-42. PubMed ID: 14577679
[TBL] [Abstract][Full Text] [Related]
43. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease.
Hernández-Martín A; Duat-Rodríguez A
Actas Dermosifiliogr; 2016; 107(6):454-64. PubMed ID: 26979265
[TBL] [Abstract][Full Text] [Related]
44. Segmental neurofibromatosis in childhood.
Listernick R; Mancini AJ; Charrow J
Am J Med Genet A; 2003 Aug; 121A(2):132-5. PubMed ID: 12910491
[TBL] [Abstract][Full Text] [Related]
45. Radiology case of the month. Café-au-lait spots. Neurofibromatosis type 1.
Gupta A; Neitzschman HR; Schroder M
J La State Med Soc; 2002; 154(5):221-2. PubMed ID: 12440746
[No Abstract] [Full Text] [Related]
46. Analysis of neurofibromatosis 1 (NF1) lesions by body segment.
Palmer C; Szudek J; Joe H; Riccardi VM; Friedman JM
Am J Med Genet A; 2004 Mar; 125A(2):157-61. PubMed ID: 14981716
[TBL] [Abstract][Full Text] [Related]
47. [The case of neurofibromatosis type ! in a 5-year-old boy].
Przybysz K; Nowak K; Kobielski A; Bolanowski W; Bodalski J
Wiad Lek; 1998; 51 Suppl 4():334-7. PubMed ID: 10731995
[TBL] [Abstract][Full Text] [Related]
48. Neurofibromatosis 1 and osseous fibrous dysplasia in a family.
Schotland HM; Eldridge R; Sommer SS; Malawar M
Am J Med Genet; 1992 Jul; 43(5):815-22. PubMed ID: 1642269
[TBL] [Abstract][Full Text] [Related]
49. Café-au-lait spots in neurofibromatosis type 1 and in healthy control individuals: hyperpigmentation of a different kind?
De Schepper S; Boucneau J; Vander Haeghen Y; Messiaen L; Naeyaert JM; Lambert J
Arch Dermatol Res; 2006 Apr; 297(10):439-49. PubMed ID: 16479403
[TBL] [Abstract][Full Text] [Related]
50. Case of the month. Neurofibromatosis type 1.
Lai M; Flynn S; Cannon TC; Schmucker T; Davis R; Harper R
J Ark Med Soc; 2003 Sep; 100(3):100-1. PubMed ID: 13677142
[TBL] [Abstract][Full Text] [Related]
51. [Type 1 neurofibromatosis in Tunisia: 66 cases].
Gouider R; Azaiz MI; Kchouk M; Lasram L; Ben Osman A; Mrabet A
Ann Dermatol Venereol; 1994; 121(2):185-9. PubMed ID: 7979037
[TBL] [Abstract][Full Text] [Related]
52. Mosaic neurofibromatosis type 1.
Liang C; Schaffer JV
Dermatol Online J; 2008 May; 14(5):6. PubMed ID: 18627742
[TBL] [Abstract][Full Text] [Related]
53. Neurofibromatosis type 1 with overlap Turner syndrome and Klinefelter syndrome.
Hatipoglu N; Kurtoglu S; Kendirci M; Keskin M; Per H
J Trop Pediatr; 2010 Feb; 56(1):69-72. PubMed ID: 19578129
[TBL] [Abstract][Full Text] [Related]
54. Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots.
Brunner HG; Hulsebos T; Steijlen PM; der Kinderen DJ; vd Steen A; Hamel BC
Am J Med Genet; 1993 Jun; 46(4):472-4. PubMed ID: 8357027
[TBL] [Abstract][Full Text] [Related]
55. Multiple halo neurofibromas.
Smith WE; Moseley JC
Arch Dermatol; 1976 Jul; 112(7):987-90. PubMed ID: 820271
[TBL] [Abstract][Full Text] [Related]
56. Diagnostic value of multiple café-au-lait macules for neurofibromatosis 1 in Chinese children.
Yao R; Wang L; Yu Y; Wang J; Shen Y
J Dermatol; 2016 May; 43(5):537-42. PubMed ID: 26458495
[TBL] [Abstract][Full Text] [Related]
57. Autoimmune haemolysis as an unusual cause of anaemia in von Recklinghausen's disease.
Tekin F; Ozutemiz O; Carcurgan S; Ilter T
Neth J Med; 2004 Oct; 62(9):337-9. PubMed ID: 15635820
[TBL] [Abstract][Full Text] [Related]
58. Neurofibromatosis 1: from lab bench to clinic.
Ward BA; Gutmann DH
Pediatr Neurol; 2005 Apr; 32(4):221-8. PubMed ID: 15797177
[TBL] [Abstract][Full Text] [Related]
59. Café au lait macules and juvénile polyps.
Pacheco TR; Scatena LS; Hoffenberg EJ; Gralla J; Lee LA
Pediatr Dermatol; 2007; 24(3):E17-21. PubMed ID: 17509109
[TBL] [Abstract][Full Text] [Related]
60. Multiple café au lait spots in familial patients with MAP2K2 mutation.
Takenouchi T; Shimizu A; Torii C; Kosaki R; Takahashi T; Saya H; Kosaki K
Am J Med Genet A; 2014 Feb; 164A(2):392-6. PubMed ID: 24311457
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
