117 related articles for article (PubMed ID: 23322702)
1. A new NF1 variant in a patient with atypical manifestations.
Onitilo AA; Engel JM
Am J Med Genet A; 2013 Feb; 161A(2):389-92. PubMed ID: 23322702
[No Abstract] [Full Text] [Related]
2. [Intraductal carcinoma arising in a fibroadenoma].
Hernando Almudí E; Casamayor Franco C; Ligorred Padilla L; Vera J
Cir Esp; 2008 Nov; 84(5):282-3. PubMed ID: 19080916
[No Abstract] [Full Text] [Related]
3. Atypical teratoid rhabdoid tumor in a child with neurofibromatosis 1.
El Kababri M; André N; Carole C; Lena G; Figarella-Branger D; Gentet JC
Pediatr Blood Cancer; 2006 Feb; 46(2):267-8. PubMed ID: 16086409
[No Abstract] [Full Text] [Related]
4. Calcified uterine leiomyoma simulating metastatic disease on bone scan.
Rohrer DG; Williamson BR; Teates CD
South Med J; 1988 May; 81(5):651-2. PubMed ID: 2835820
[TBL] [Abstract][Full Text] [Related]
5. Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 gene.
Stewart W; Traynor JP; Cooke A; Griffiths S; Onen NF; Balsitis M; Shah AA; Upadhyaya M; Tobias ES
Fam Cancer; 2007; 6(1):147-52. PubMed ID: 16944271
[TBL] [Abstract][Full Text] [Related]
6. Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1.
Xiao H; Yuan L; Xu H; Yang Z; Huang F; Song Z; Yang Y; Zeng C; Deng H
J Mol Neurosci; 2018 Aug; 65(4):557-563. PubMed ID: 30046999
[TBL] [Abstract][Full Text] [Related]
7. Identification of a missense mutation causing exon skipping in a neurofibromatosis type 1 patient.
Fu Y; Zhang JQ; Jiang CL; Wang HY
J Dermatol; 2018 Aug; 45(8):986-988. PubMed ID: 29952103
[TBL] [Abstract][Full Text] [Related]
8. Noonan syndrome and neurofibromatosis type I in a family with a novel mutation in NF1.
Nyström AM; Ekvall S; Allanson J; Edeby C; Elinder M; Holmström G; Bondeson ML; Annerén G
Clin Genet; 2009 Dec; 76(6):524-34. PubMed ID: 19845691
[TBL] [Abstract][Full Text] [Related]
9. Neurofibromatosis type 1: New developments in genetics and treatment.
Wilson BN; John AM; Handler MZ; Schwartz RA
J Am Acad Dermatol; 2021 Jun; 84(6):1667-1676. PubMed ID: 32771543
[TBL] [Abstract][Full Text] [Related]
10. Two novel mutations of the NF1 gene in Chinese Han families with type 1 neurofibromatosis.
Cai Y; Fan Z; Liu Q; Li J; Du J; Shen Y; Wang S
J Dermatol Sci; 2005 Aug; 39(2):125-7. PubMed ID: 16005615
[No Abstract] [Full Text] [Related]
11. A new insight into our understanding of neurofibromatosis type 1?
Chimenti S
J Eur Acad Dermatol Venereol; 2004 May; 18(3):261. PubMed ID: 15096131
[No Abstract] [Full Text] [Related]
12. NF1 mutations and molecular testing.
Thomson SA; Fishbein L; Wallace MR
J Child Neurol; 2002 Aug; 17(8):555-61; discussion 571-2, 646-51. PubMed ID: 12403553
[TBL] [Abstract][Full Text] [Related]
13. Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutation.
Kannu P; Nour M; Irving M; Xie J; Loder D; Lai J; Islam O; MacKenzie J; Messiaen L
Clin Genet; 2013 Feb; 83(2):191-4. PubMed ID: 22533502
[No Abstract] [Full Text] [Related]
14. Large number of cutaneous neurofibromas beyond age-appropriate incidence in a patient with a large deletion of NF1.
Yoshida Y; Ehara Y; Kosaki K; Yamamoto O
J Dermatol; 2018 Mar; 45(3):363-364. PubMed ID: 29498099
[No Abstract] [Full Text] [Related]
15. The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.
Jeong SY; Park SJ; Kim HJ
J Korean Med Sci; 2006 Feb; 21(1):107-12. PubMed ID: 16479075
[TBL] [Abstract][Full Text] [Related]
16. Presence of the R1748X mutation in the NF1 gene in a Brazilian patient with ectropion uveae.
Trovó-Marqui AB; Goloni-Bertollo EM; Teixeira MF; Tajara EH
Ophthalmic Res; 2004; 36(6):349-52. PubMed ID: 15627836
[TBL] [Abstract][Full Text] [Related]
17. The neurofibromin 1 type I isoform predominance characterises female population affected by sporadic breast cancer: preliminary data.
Marrero D; Peralta R; Valdivia A; De la Mora A; Romero P; Parra M; Mendoza N; Mendoza M; Rodriguez D; Camacho E; Duarte A; Castelazo G; Vanegas E; Garcia I; Vargas C; Arenas D; Jimenez F; Salcedo M
J Clin Pathol; 2012 May; 65(5):419-23. PubMed ID: 22412049
[TBL] [Abstract][Full Text] [Related]
18. [Analysis of NF1 gene mutations in two sporadic patients with neurofibromatosis type 1].
Zhao X; Zhou Q; Cai L; Zhao Z; Zhang L; Wang P; Zhang G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):489-492. PubMed ID: 30098240
[TBL] [Abstract][Full Text] [Related]
19. Empirically downgrading 10 constitutional missense variants of the NF1 gene based on co-existing truncating variants.
Kluwe L; Mautner VF
Am J Med Genet A; 2021 Feb; 185(2):602-603. PubMed ID: 33231931
[No Abstract] [Full Text] [Related]
20. Neurofibromatosis (Recklinghausen's disease) with gastrointestinal and uterine manifestations: report of a case.
Taylor WI
J Am Osteopath Assoc; 1974 Sep; 74(1):39-42. PubMed ID: 4371358
[No Abstract] [Full Text] [Related]
[Next] [New Search]