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Items: 1 to 20 of 107

1.

Neurofibromatosis type 1 complicated by atypical coarctation of the thoracic aorta.

Kimura M, Kakizaki S, Kawano K, Sato S, Kure S.

Case Rep Pediatr. 2013;2013:458543. doi: 10.1155/2013/458543.

2.

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. doi: 10.1016/j.pediatrneurol.2016.03.003. Review.

PMID:
27212418
3.

[Neurofibromatosis type 1 and hypertension in pediatrics: case report].

Demarchi I, Genoni G, Prodam F, Petri A, Busti A, Cortese L, Negro M, Bellone S, Acucella G, Bona G.

Minerva Pediatr. 2011 Aug;63(4):335-9. Italian.

PMID:
21909069
4.

[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 Sep-Oct;20(5):393-400. Portuguese.

5.

Renal artery stenosis due to neurofibromatosis type 1: case report and literature review.

Duan L, Feng K, Tong A, Liang Z.

Eur J Med Res. 2014 Mar 28;19:17. doi: 10.1186/2047-783X-19-17. Review.

6.

Clinical and genetic significance of unilateral Lisch nodules.

Ceuterick SD, Van Den Ende JJ, Smets RM.

Bull Soc Belge Ophtalmol. 2005;(295):49-53.

PMID:
15849989
7.

Café-au-lait macules and intertriginous freckling in piebaldism: clinical overlap with neurofibromatosis type 1 and Legius syndrome.

Stevens CA, Chiang PW, Messiaen LM.

Am J Med Genet A. 2012 May;158A(5):1195-9. doi: 10.1002/ajmg.a.35297.

PMID:
22438235
8.

[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. Romanian.

PMID:
19354164
9.

[Developmental manifestation in children with neurofibromatosis type 1].

Cohen R, Shuper A.

Harefuah. 2010 Jan;149(1):49-52, 61. Review. Hebrew.

PMID:
20422842
10.
11.

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. doi: 10.1016/j.jaad.2007.03.013.

PMID:
18280349
12.

Neurofibromatosis type 1-associated hypertension secondary to coarctation of the thoracic aorta.

Mavani G, Kesar V, Devita MV, Rosenstock JL, Michelis MF, Schwimmer JA.

Clin Kidney J. 2014 Aug;7(4):394-5. doi: 10.1093/ckj/sfu054.

13.

Synchronous multiple colonic adenocarcinomas arising in patient with neurofibromatosis type 1.

Kim IY, Cho MY, Kim YW.

Ann Surg Treat Res. 2014 Sep;87(3):156-60. doi: 10.4174/astr.2014.87.3.156.

14.

Iris hamartomas (Lisch nodules) in a case of segmental neurofibromatosis.

Weleber RG, Zonana J.

Am J Ophthalmol. 1983 Dec;96(6):740-3.

PMID:
6419615
15.

Clinical and genetic aspects of neurofibromatosis 1.

Jett K, Friedman JM.

Genet Med. 2010 Jan;12(1):1-11. doi: 10.1097/GIM.0b013e3181bf15e3. Review.

PMID:
20027112
16.

A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.

Gabriele AL, Ruggieri M, Patitucci A, Magariello A, Conforti FL, Mazzei R, Muglia M, Ungaro C, Di Palma G, Citrigno L, Sproviero W, Gambardella A, Quattrone A.

Childs Nerv Syst. 2011 Apr;27(4):635-8. doi: 10.1007/s00381-010-1282-z.

PMID:
20927530
17.

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. doi: 10.1111/1346-8138.13169.

PMID:
26458495
18.

Bilateral segmental neurofibromatosis with gastric carcinoma.

Kajimoto A, Oiso N, Fukai K, Ishii M.

Clin Exp Dermatol. 2007 Jan;32(1):43-4.

PMID:
16939586
19.

Eye disorders in neurofibromatosis (NF1).

Kordić R, Sabol Z, Cerovski B, Katusić D, Jukić T.

Coll Antropol. 2005;29 Suppl 1:29-31.

PMID:
16193672
20.

Neurofibromatosis 1 in childhood.

North KN.

Semin Pediatr Neurol. 1998 Dec;5(4):231-42. Review.

PMID:
9874851
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