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300 related items for PubMed ID: 17914491
1. 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 [Abstract] [Full Text] [Related]
3. [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 [Abstract] [Full Text] [Related]
4. [Von Recklinghausen disease and hepatic neurofibromatosis]. Guzman Toro F, Hinestroza D, Colmenares D. G E N; 1995; 49(4):303-6. PubMed ID: 8762661 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. 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 [Abstract] [Full Text] [Related]
10. 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 01; 125A(2):157-61. PubMed ID: 14981716 [Abstract] [Full Text] [Related]
11. Lisch nodules and skin manifestation in neurofibromatosis type 1. Otsuka F, Kawashima T, Imakado S, Usuki Y, Hon-Mura S. Arch Dermatol; 2001 Feb 01; 137(2):232-3. PubMed ID: 11176707 [No Abstract] [Full Text] [Related]
14. Hyperpigmented spots at fundus examination: a new ocular sign in Neurofibromatosis Type I. Moramarco A, Mallone F, Sacchetti M, Lucchino L, Miraglia E, Roberti V, Lambiase A, Giustini S. Orphanet J Rare Dis; 2021 Mar 23; 16(1):147. PubMed ID: 33757576 [Abstract] [Full Text] [Related]
15. The absence that makes the difference: choroidal abnormalities in Legius syndrome. Tucci A, Saletti V, Menni F, Cesaretti C, Scuvera G, Esposito S, Melloni G, Esposito S, Milani D, Cereda C, Cigada M, Tresoldi L, Viola F, Natacci F. J Hum Genet; 2017 Nov 23; 62(11):1001-1004. PubMed ID: 28747691 [Abstract] [Full Text] [Related]
16. Vitamin D deficiency associated with number of neurofibromas in neurofibromatosis 1. Lammert M, Friedman JM, Roth HJ, Friedrich RE, Kluwe L, Atkins D, Schooler T, Mautner VF. J Med Genet; 2006 Oct 23; 43(10):810-3. PubMed ID: 16571643 [Abstract] [Full Text] [Related]
18. Atypical hematologic and renal manifestations in neurofibromatosis type I: coincidence or pathophysiological link? Van-Gils J, Harambat J, Jubert C, Vidaud D, Llanas B, Perel Y, Lacombe D, Goizet C. Eur J Med Genet; 2014 Oct 23; 57(11-12):639-42. PubMed ID: 25234363 [Abstract] [Full Text] [Related]
19. Lisch nodules: a diagnostic sign for Von Recklinghausen's neurofibromatosis. Norman RA. J Am Optom Assoc; 1983 Jun 23; 54(6):533-5. PubMed ID: 6409954 [Abstract] [Full Text] [Related]
20. 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 23; 297(10):439-49. PubMed ID: 16479403 [Abstract] [Full Text] [Related] Page: [Next] [New Search]