138 related articles for article (PubMed ID: 37414129)
1. Ocular ischemic syndrome in neurofibromatosis type 1 treated with corticosteroids.
Zhang DL; Listernick RH; Rahmani S
J AAPOS; 2023 Aug; 27(4):239-242. PubMed ID: 37414129
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis and clinical course of ocular ischemic syndrome with retinal vascular abnormalities due to unilateral ocular artery and internal carotid artery stenosis in a child with neurofibromatosis type 1: a case report.
Sakai H; Kawata K; Masuoka J; Nishimura T; Enaida H
BMC Ophthalmol; 2020 Oct; 20(1):426. PubMed ID: 33097012
[TBL] [Abstract][Full Text] [Related]
3. An update on choroidal abnormalities and retinal microvascular changes in neurofibromatosis type 1.
Mallone F; Lucchino L; Giustini S; Lambiase A; Moramarco A
Orphanet J Rare Dis; 2022 Jun; 17(1):223. PubMed ID: 35698197
[TBL] [Abstract][Full Text] [Related]
4. [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. PubMed ID: 21909069
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Lisch nodule in neurofibromatosis type 1].
Abaloun Y; Ajhoun Y
Pan Afr Med J; 2017; 27():218. PubMed ID: 28979620
[TBL] [Abstract][Full Text] [Related]
7. Retinal cafe-au-lait macules: A rare retinal finding in a patient with neurofibromatosis type 1.
Venkatesh R; Jain K; Pereira A; Jain SD; Aseem A; Mahendradas P; Yadav NK
Indian J Ophthalmol; 2019 Dec; 67(12):2101-2103. PubMed ID: 31755475
[TBL] [Abstract][Full Text] [Related]
8. ISCHEMIC RETINOPATHY IN NEUROFIBROMATOSIS TYPE 1.
Dansingani KK; Jung JJ; Belinsky I; Marr BP; Freund KB
Retin Cases Brief Rep; 2015; 9(4):290-4. PubMed ID: 26252734
[TBL] [Abstract][Full Text] [Related]
9. Neurofibromatosis Type 1 Vasculopathy Presenting as Branch Retinal Vein Occlusion: Case Report and Review of the Literature.
Özdemir Zeydanlı E; Özdek Ş
Turk J Ophthalmol; 2023 Dec; 53(6):390-394. PubMed ID: 38008934
[TBL] [Abstract][Full Text] [Related]
10. Ocular Ischemic Syndrome due to Internal Carotid Artery Occlusion with Neurofibromatosis Type 1.
Kawamura K; Kimiwada T; Sato K; Nitta F; Hayashi T; Shirane R; Tominaga T
J Stroke Cerebrovasc Dis; 2022 Jun; 31(6):106410. PubMed ID: 35349882
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 18280349
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.
Vannelli S; Buganza R; Runfola F; Mussinatto I; Andreacchio A; de Sanctis L
Ital J Pediatr; 2020 May; 46(1):58. PubMed ID: 32393377
[TBL] [Abstract][Full Text] [Related]
14. A novel NF1 mutation in a pediatric patient with renal artery aneurysm.
Chillura I; Restivo GA; Callari S; Cibella S; D'Alessandro MM; Corrado C; Vallone M; Antona V; Corsello G
Ital J Pediatr; 2022 Nov; 48(1):186. PubMed ID: 36411470
[TBL] [Abstract][Full Text] [Related]
15. Eye disorders in neurofibromatosis (NF1).
Kordić R; Sabol Z; Cerovski B; Katusić D; Jukić T
Coll Antropol; 2005; 29 Suppl 1():29-31. PubMed ID: 16193672
[TBL] [Abstract][Full Text] [Related]
16. Neurofibromatosis, stroke and basilar impression. Case report.
Piovesan EJ; Scola RH; Werneck LC; Zétola VH; Nóvak EM; Iwamoto FM; Piovesan LM
Arq Neuropsiquiatr; 1999 Jun; 57(2B):484-8. PubMed ID: 10450358
[TBL] [Abstract][Full Text] [Related]
17. [Clinical diagnosis of neurofibromatosis type 1].
Wolkenstein P; Zeller J
Presse Med; 1999 Dec; 28(39):2174-80. PubMed ID: 10629698
[TBL] [Abstract][Full Text] [Related]
18. Partial unilateral lentiginosis is mosaic neurofibromatosis type 1 or not?
Yaşar Ş; Ersanli A; Göktay F; Aytekin S; Cebeci D; Güneş P
J Dermatol; 2017 Jan; 44(1):29-35. PubMed ID: 27439996
[TBL] [Abstract][Full Text] [Related]
19. Early-onset stroke in two siblings with Neurofibromatosis type 1.
Rukavina K; Töpper R; Kunze A; Hess A; Glatzel M; Valdueza JM; Farschtschi S; Hagel C
Eur J Med Genet; 2019 Oct; 62(10):103710. PubMed ID: 31279841
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]