164 related articles for article (PubMed ID: 33305557)
1. Primary pulmonary lymphangiectasia in Noonan syndrome: apropos of an extremely rare manifestation and a brief literature review.
Dendrinou GE; Zagarelos P; Sofronas A; Katsenos S
Monaldi Arch Chest Dis; 2020 Dec; 90(4):. PubMed ID: 33305557
[TBL] [Abstract][Full Text] [Related]
2. A case of Noonan syndrome with pulmonary and abdominal lymphangiectasia.
Oztürk S; Cefle K; Palanduz S; Erten NB; Karan MA; Tasçioglu C; Umman S; Falay O; Vatansever S; Güler K; Cantez S
Int J Clin Pract; 2000 May; 54(4):274-6. PubMed ID: 10912323
[TBL] [Abstract][Full Text] [Related]
3. Noonan syndrome.
Roberts AE; Allanson JE; Tartaglia M; Gelb BD
Lancet; 2013 Jan; 381(9863):333-42. PubMed ID: 23312968
[TBL] [Abstract][Full Text] [Related]
4. Twin infant with lymphatic dysplasia diagnosed with Noonan syndrome by molecular genetic testing.
Mathur D; Somashekar S; Navarrete C; Rodriguez MM
Fetal Pediatr Pathol; 2014 Aug; 33(4):253-7. PubMed ID: 24754368
[TBL] [Abstract][Full Text] [Related]
5. Pulmonary lymphangiectasis in Noonan syndrome.
Hernandez RJ; Stern AM; Rosenthal A
AJR Am J Roentgenol; 1980 Jan; 134(1):75-80. PubMed ID: 6766041
[TBL] [Abstract][Full Text] [Related]
6. Lymphoscintigraphy. Pulmonary lymphangiectasia.
Sty JR; Thomas JP; Wolff MH; Litwin SB
Clin Nucl Med; 1984 Dec; 9(12):716. PubMed ID: 6509845
[TBL] [Abstract][Full Text] [Related]
7. [Cochlear implantation in a patient with Noonan syndrome caused by a variant in
Hu L; Chen J; Xin Y; Fang X; Jiao Y
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Sep; 35(9):839-842. PubMed ID: 34628841
[No Abstract] [Full Text] [Related]
8. [Pulmonary lymphangiectasis with spontaneous chylothorax in Noonan syndrome].
Sailer M; Unsinn K; Fink C; Covi B; Gassner I
Klin Padiatr; 1995; 207(5):302-4. PubMed ID: 7500608
[TBL] [Abstract][Full Text] [Related]
9. Lymphoscintigraphy and lymphangiography of lymphangiectasia.
Howarth D; Gloviczki P
J Nucl Med; 1998 Sep; 39(9):1635-8. PubMed ID: 9744359
[TBL] [Abstract][Full Text] [Related]
10. Abnormalities of pubertal development and gonadal function in Noonan syndrome.
Patti G; Scaglione M; Maiorano NG; Rosti G; Divizia MT; Camia T; De Rose EL; Zucconi A; Casalini E; Napoli F; Di Iorgi N; Maghnie M
Front Endocrinol (Lausanne); 2023; 14():1213098. PubMed ID: 37576960
[TBL] [Abstract][Full Text] [Related]
11. Diagnosis of secondary pulmonary lymphangiectasia in congenital heart disease: a novel role for chest ultrasound and prognostic implications.
Lam CZ; Bhamare TA; Gazzaz T; Manson D; Humpl T; Seed M
Pediatr Radiol; 2017 Oct; 47(11):1441-1451. PubMed ID: 28631156
[TBL] [Abstract][Full Text] [Related]
12. Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment.
Linglart L; Gelb BD
Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):73-80. PubMed ID: 32022400
[TBL] [Abstract][Full Text] [Related]
13. Noonan syndrome: introduction and basic clinical features.
Rohrer T
Horm Res; 2009 Dec; 72 Suppl 2():3-7. PubMed ID: 20029230
[TBL] [Abstract][Full Text] [Related]
14. Coronary artery disease in adults with Noonan syndrome: Case series and literature review.
Ly R; Soulat G; Iserin L; Ladouceur M
Arch Cardiovasc Dis; 2021; 114(8-9):598-605. PubMed ID: 34535417
[TBL] [Abstract][Full Text] [Related]
15. Variable phenotypic expression in a large Noonan syndrome family segregating a novel SOS1 mutation.
van Trier DC; Rinne T; Noordam K; Draaisma JM; van der Burgt I
Am J Med Genet A; 2017 Nov; 173(11):2968-2972. PubMed ID: 28884940
[TBL] [Abstract][Full Text] [Related]
16. Congenital pulmonary lymphangiectasia in a newborn: a response to autologous blood therapy.
Akcakus M; Koklu E; Bilgin M; Kurtoglu S; Altunay L; Canpolat M; Budak N
Neonatology; 2007; 91(4):256-9. PubMed ID: 17568156
[TBL] [Abstract][Full Text] [Related]
17. Constrictive pericarditis simulating intestinal lymphangiectasia in a patient with the Noonan syndrome.
O'Sullivan T; Hally M; Cronin CC; Bashyam M; Mitchell TH
Ir J Med Sci; 1993 May; 162(5):180-1. PubMed ID: 8335455
[TBL] [Abstract][Full Text] [Related]
18. [A patient with Noonan syndrome].
Bins A; Gortzak RA
Ned Tijdschr Tandheelkd; 2013 Dec; 120(12):671-5. PubMed ID: 24555250
[TBL] [Abstract][Full Text] [Related]
19. Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene.
Mercadante F; Piro E; Busè M; Salzano E; Ferrara A; Serra G; Passarello C; Corsello G; Piccione M
Ital J Pediatr; 2022 Aug; 48(1):152. PubMed ID: 35986401
[TBL] [Abstract][Full Text] [Related]
20. A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature.
Nemcikova M; Vejvalkova S; Fencl F; Sukova M; Krepelova A
Eur J Pediatr; 2016 Apr; 175(4):587-92. PubMed ID: 26518681
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
