99 related articles for article (PubMed ID: 23434365)
1. Neurofibromatosis in a toddler with back pain.
Okunoghae E; Starrett E; Gray B
J Pediatr Health Care; 2014; 28(1):88-91. PubMed ID: 23434365
[No Abstract] [Full Text] [Related]
2. Segmentally distributed neurofibromatosis associated with adenocarcinoma of the colon.
Kim SE; Heo EP; Yoon TJ; Kim TH
J Dermatol; 2002 Jun; 29(6):350-3. PubMed ID: 12126071
[TBL] [Abstract][Full Text] [Related]
3. [Neurofibromatosis--easy to see, easy to overlook. Interview by Kjell Arne Bakke].
Farmen M
Tidsskr Sykepl; 1997 Sep; 85(15):30-3. PubMed ID: 9362945
[No Abstract] [Full Text] [Related]
4. Physical signs for the general dental practitioner. Case 39. Café au lait spots due to neurofibromatosis.
Bain S
Dent Update; 2006 Nov; 33(9):572. PubMed ID: 17176744
[No Abstract] [Full Text] [Related]
5. Segmental neurofibromatosis with only macular lesions.
Micali G; Lembo D; Giustini S; Calvieri S
Pediatr Dermatol; 1993 Mar; 10(1):43-5. PubMed ID: 8493167
[TBL] [Abstract][Full Text] [Related]
6. Partial unilateral lentiginosis associated with segmental neurofibromatosis.
Lee WS; Yoo MS; Ahn SK; Won JH
J Dermatol; 1995 Dec; 22(12):958-9. PubMed ID: 8648006
[TBL] [Abstract][Full Text] [Related]
7. Neurofibromatosis of atypical presentation.
Tato BP; Sáez AC; Recuero JL; Dorado MM; Fernández PR; de Paz FS
J Eur Acad Dermatol Venereol; 2005 Sep; 19(5):608-11. PubMed ID: 16164720
[TBL] [Abstract][Full Text] [Related]
8. A case of agminated lentiginosis with multiple café-au-lait macules.
Lee JH; Kim SE; Park K; Son SJ; Song KY
Clin Exp Dermatol; 2007 Nov; 32(6):658-60. PubMed ID: 17725665
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Head and neck manifestations of neurofibromatosis.
Muecke M; Amedee RG
J La State Med Soc; 1994 May; 146(5):183-6. PubMed ID: 8027629
[TBL] [Abstract][Full Text] [Related]
11. [Brown spots on the whole body: the mother has them as well. Neurofibromatosis].
Stiefelhagen P
MMW Fortschr Med; 2013 Nov; 155 Spec No 2():7, 35. PubMed ID: 24734438
[No Abstract] [Full Text] [Related]
12. Psoriasis in a patient with neurofibromatosis.
Celebi S; Kiliç SS; Okan M
Turk J Pediatr; 1999; 41(4):545-9. PubMed ID: 10770127
[TBL] [Abstract][Full Text] [Related]
13. Segmental neurofibromatosis: report of 3 cases.
Mansur AT; Göktay F; Akkaya AD; Güneş P
Cutis; 2011 Jan; 87(1):45-50. PubMed ID: 21323101
[TBL] [Abstract][Full Text] [Related]
14. Neurofibromatosis--review of the literature and case report.
Pastar Z; Lipozencić J; Budimcić D; Tomljanović-Veselski M
Acta Dermatovenerol Croat; 2006; 14(3):167-71. PubMed ID: 17010267
[TBL] [Abstract][Full Text] [Related]
15. Common hyperpigmentation disorders in adults: Part I. Diagnostic approach, café au lait macules, diffuse hyperpigmentation, sun exposure, and phototoxic reactions.
Stulberg DL; Clark N; Tovey D
Am Fam Physician; 2003 Nov; 68(10):1955-60. PubMed ID: 14655804
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Digestive hemorrhage in a patient with multiple neurofibromatosis].
Vagni V; Raparelli L; Mazzarella Farao R
G Chir; 1995; 16(8-9):357-9. PubMed ID: 8645540
[TBL] [Abstract][Full Text] [Related]
18. Christmas tree sign.
Ashkan K; Casey AT
J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):824. PubMed ID: 10567511
[No Abstract] [Full Text] [Related]
19. Segmental neurofibromatosis [NF type - v].
Arfan-ul-Bari ; Simeen-ber-Rahman
J Coll Physicians Surg Pak; 2003 Dec; 13(12):717-8. PubMed ID: 15569561
[TBL] [Abstract][Full Text] [Related]
20. Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype.
Ruggieri M; Polizzi A; Salpietro V; Incorpora G; Nicita F; Pavone P; Falsaperla R; Nucifora C; Granata F; Distefano A; Padua L; Caltabiano R; Lanzafame S; Gabriele AL; Ortensi A; D'Orazi V; Panunzi A; Milone P; Mankad K; Platania N; Albanese V; Pavone V
Neuropediatrics; 2013 Oct; 44(5):239-44. PubMed ID: 23780384
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]