These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
117 related articles for article (PubMed ID: 24715715)
1. A patient with Cantú syndrome associated with fatal bronchopulmonary dysplasia and pulmonary hypertension. Park JY; Koo SH; Jung YJ; Lim YJ; Chung ML Am J Med Genet A; 2014 Aug; 164A(8):2118-20. PubMed ID: 24715715 [No Abstract] [Full Text] [Related]
2. Pulmonary hypertension secondary to partial pulmonary venous obstruction in a child with Cantu syndrome. Kobayashi D; Cook AL; Williams DA Pediatr Pulmonol; 2010 Jul; 45(7):727-9. PubMed ID: 20575102 [TBL] [Abstract][Full Text] [Related]
3. Short-term follow-up of a Brazilian patient with Cantú syndrome. Graziadio C; Rosa RF; Rosa RC; Zen PR; Flores JA; Paskulin GA Am J Med Genet A; 2011 May; 155A(5):1184-8. PubMed ID: 21465652 [No Abstract] [Full Text] [Related]
4. Cantú syndrome as a rare cause of pericardial effusion in a young woman. Jesani H; Elangovan S; Zaidi A Br J Hosp Med (Lond); 2019 Dec; 80(12):732-733. PubMed ID: 31822179 [No Abstract] [Full Text] [Related]
5. Aortic aneurysm and craniosynostosis in a family with Cantu syndrome. Hiraki Y; Miyatake S; Hayashidani M; Nishimura Y; Matsuura H; Kamada M; Kawagoe T; Yunoki K; Okamoto N; Yofune H; Nakashima M; Tsurusaki Y; Satisu H; Murakami A; Miyake N; Nishimura G; Matsumoto N Am J Med Genet A; 2014 Jan; 164A(1):231-6. PubMed ID: 24352916 [TBL] [Abstract][Full Text] [Related]
6. A familial case of Cantu craniofaciofronto digital syndrome. Garcia-Gonzalez CL; Garcia-Cruz D; Garcia-Cruz MO; Castañeda-Cisneros G; Garcia-Ortiz JE; Orozco-Gutiérrez MH; Sanchez-Corona J Clin Dysmorphol; 2012 Jul; 21(3):162-166. PubMed ID: 22504422 [No Abstract] [Full Text] [Related]
7. Novel variants of ABCC9 in Japanese children with Cantú syndrome. Kubota K; Yamamoto T; Miyatake S; Matsumoto N; Fukao T Pediatr Int; 2020 Mar; 62(3):410-412. PubMed ID: 32198910 [No Abstract] [Full Text] [Related]
8. Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9. Czeschik JC; Voigt C; Goecke TO; Lüdecke HJ; Wagner N; Kuechler A; Wieczorek D Am J Med Genet A; 2013 Feb; 161A(2):295-300. PubMed ID: 23307537 [TBL] [Abstract][Full Text] [Related]
10. Cantú syndrome resulting from activating mutation in the KCNJ8 gene. Cooper PE; Reutter H; Woelfle J; Engels H; Grange DK; van Haaften G; van Bon BW; Hoischen A; Nichols CG Hum Mutat; 2014 Jul; 35(7):809-13. PubMed ID: 24700710 [TBL] [Abstract][Full Text] [Related]
11. Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition. Brownstein CA; Towne MC; Luquette LJ; Harris DJ; Marinakis NS; Meinecke P; Kutsche K; Campeau PM; Yu TW; Margulies DM; Agrawal PB; Beggs AH Eur J Med Genet; 2013 Dec; 56(12):678-82. PubMed ID: 24176758 [TBL] [Abstract][Full Text] [Related]
12. Aortic and pulmonary artery dilatation in Cantu syndrome: expanding the phenotype. Chew YR; Lim JY; Teoh OH; Chen CK; Foo R; Lai AH; Jamuar SS Clin Dysmorphol; 2019 Jul; 28(3):167-169. PubMed ID: 30921097 [No Abstract] [Full Text] [Related]
14. Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndrome. Rosser EM; Kaariainen H; Hurst JA; Baraitser M; Hall CM; Clayton P; Leonard JV Clin Dysmorphol; 1998 Apr; 7(2):79-85. PubMed ID: 9571276 [TBL] [Abstract][Full Text] [Related]
15. Cantú syndrome, the changing phenotype: a report of the two oldest Dutch patients. Roessler HI; Volker-Touw CML; Terhal PA; van Haaften G; van Haelst MM Clin Dysmorphol; 2018 Jul; 27(3):78-83. PubMed ID: 29595750 [No Abstract] [Full Text] [Related]
16. De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder. Afifi HH; Abdel-Hamid MS; Eid MM; Mostafa IS; Abdel-Salam GM Pediatr Dermatol; 2016; 33(2):e109-13. PubMed ID: 26871653 [TBL] [Abstract][Full Text] [Related]
17. Glibenclamide treatment in a Cantú syndrome patient with a pathogenic ABCC9 gain-of-function variant: Initial experience. Ma A; Gurnasinghani S; Kirk EP; McClenaghan C; Singh GK; Grange DK; Pandit C; Zhu Y; Roscioli T; Elakis G; Buckley M; Mehta B; Roberts P; Mervis J; Biggin A; Nichols CG Am J Med Genet A; 2019 Aug; 179(8):1585-1590. PubMed ID: 31175705 [TBL] [Abstract][Full Text] [Related]
19. Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations. Grange DK; Lorch SM; Cole PL; Singh GK Am J Med Genet A; 2006 Aug; 140(15):1673-80. PubMed ID: 16835932 [TBL] [Abstract][Full Text] [Related]
20. Cantú syndrome: report of nine new cases and expansion of the clinical phenotype. Scurr I; Wilson L; Lees M; Robertson S; Kirk E; Turner A; Morton J; Kidd A; Shashi V; Stanley C; Berry M; Irvine AD; Goudie D; Turner C; Brewer C; Smithson S Am J Med Genet A; 2011 Mar; 155A(3):508-18. PubMed ID: 21344641 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]