168 related articles for article (PubMed ID: 37373745)
1. Heart Disease Characterization and Myocardial Strain Analysis in Patients with
Latorre-Pellicer A; Trujillano L; Del Rincón J; Peña-Marco M; Gil-Salvador M; Lucia-Campos C; Arnedo M; Puisac B; Ramos FJ; Ayerza-Casas A; Pié J
J Clin Med; 2023 Jun; 12(12):. PubMed ID: 37373745
[TBL] [Abstract][Full Text] [Related]
2. A Novel Multi-Exon Deletion of
Liu Y; Ding H; Yan T; Liu L; Yu L; Huang Y; Li F; Zeng Y; Huang W; Zhang Y; Yin A
Front Genet; 2021; 12():690216. PubMed ID: 34373684
[No Abstract] [Full Text] [Related]
3. Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation.
Abbassi M; Bourmtane A; Sayel H; El Mouhi H; Jalte M; Elasri YA; Askander O; El Fahime E; Bouguenouch L
Mol Biol Rep; 2023 Nov; 50(11):9121-9128. PubMed ID: 37747683
[TBL] [Abstract][Full Text] [Related]
4. PACS1-Neurodevelopmental disorder: clinical features and trial readiness.
Van Nuland A; Reddy T; Quassem F; Vassalli JD; Berg AT
Orphanet J Rare Dis; 2021 Sep; 16(1):386. PubMed ID: 34517877
[TBL] [Abstract][Full Text] [Related]
5. Schuurs-Hoeijmakers Syndrome (
Tenorio-Castaño J; Morte B; Nevado J; Martinez-Glez V; Santos-Simarro F; García-Miñaúr S; Palomares-Bralo M; Pacio-Míguez M; Gómez B; Arias P; Alcochea A; Carrión J; Arias P; Almoguera B; López-Grondona F; Lorda-Sanchez I; Galán-Gómez E; Valenzuela I; Méndez Perez MP; Cuscó I; Barros F; Pié J; Ramos S; Ramos FJ; Kuechler A; Tizzano E; Ayuso C; Kaiser FJ; Pérez-Jurado LA; Carracedo Á; The ENoD-Ciberer Consortium ; The Side Consortium ; Lapunzina P
Genes (Basel); 2021 May; 12(5):. PubMed ID: 34068396
[TBL] [Abstract][Full Text] [Related]
6. A Novel PACS1 Variant Associated With Schuurs-Hoeijmakers Syndrome Phenotype in an Indigenous Descendant in Brazil: A Case Report.
Lucena PH; Nonaka C; Armani-Franceschi G; Carneiro P; Sales H; Lucena M; Bandeira ID; Solano B; Lucena R
Cureus; 2022 Oct; 14(10):e30486. PubMed ID: 36415352
[TBL] [Abstract][Full Text] [Related]
7. Molecular Basis of the Schuurs-Hoeijmakers Syndrome: What We Know about the Gene and the PACS-1 Protein and Novel Therapeutic Approaches.
Arnedo M; Ascaso Á; Latorre-Pellicer A; Lucia-Campos C; Gil-Salvador M; Ayerza-Casas A; Pablo MJ; Gómez-Puertas P; Ramos FJ; Bueno-Lozano G; Pié J; Puisac B
Int J Mol Sci; 2022 Aug; 23(17):. PubMed ID: 36077045
[TBL] [Abstract][Full Text] [Related]
8. First Report of Mexican Patients with
Corona-Rivera JR; Zenteno JC; López-Pérez LG; Yokoyama-Rebollar E; Villarroel CE; Barragán-Arévalo T; Montes-Almanza LÁ; Zepeda-Romero LC; Morales-Domínguez GE; Peña-Padilla C; Bobadilla-Morales L; Corona-Rivera A
Mol Syndromol; 2023 Apr; 14(2):143-151. PubMed ID: 37064331
[TBL] [Abstract][Full Text] [Related]
9. Schuurs-Hoeijmakers syndrome in two patients from Japan.
Hoshino Y; Enokizono T; Imagawa K; Tanaka R; Suzuki H; Fukushima H; Arai J; Sumazaki R; Uehara T; Takenouchi T; Kosaki K
Am J Med Genet A; 2019 Mar; 179(3):341-343. PubMed ID: 30588754
[TBL] [Abstract][Full Text] [Related]
10. Do PACS1 variants impeding adaptor protein binding predispose to syndromic intellectual disability?
Moller-Hansen A; Hejla D; Lee HK; Lyles JB; Yang Y; Chen K; Li WL; Thomas G; Boerkoel CF
Am J Med Genet A; 2023 Aug; 191(8):2181-2187. PubMed ID: 37141437
[TBL] [Abstract][Full Text] [Related]
11. Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature.
Seto MT; Bertoli-Avella AM; Cheung KW; Chan KY; Yeung KS; Fung JL; Beetz C; Bauer P; Luk HM; Lo IF; Lee CP; Chung BH; Kan AS
Am J Med Genet A; 2021 Feb; 185(2):384-389. PubMed ID: 33166031
[TBL] [Abstract][Full Text] [Related]
12. Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.
De Backer J
Verh K Acad Geneeskd Belg; 2009; 71(6):335-71. PubMed ID: 20232788
[TBL] [Abstract][Full Text] [Related]
13. Schuurs-Hoeijmakers syndrome in a patient from India.
Dutta AK
Am J Med Genet A; 2019 Apr; 179(4):522-524. PubMed ID: 30690871
[TBL] [Abstract][Full Text] [Related]
14. Schuurs-Hoeijmakers syndrome in a patient from Iraq - Kirkuk.
Abdulqader SA; Wli WA; Qaryaqos SH
Clin Case Rep; 2021 Oct; 9(10):e04897. PubMed ID: 34631081
[TBL] [Abstract][Full Text] [Related]
15. Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis.
Sakaguchi Y; Yoshihashi H; Uehara T; Miyama S; Kosaki K; Takenouchi T
Am J Med Genet A; 2021 Mar; 185(3):884-888. PubMed ID: 33369122
[TBL] [Abstract][Full Text] [Related]
16. Acute changes in myocardial systolic function in preterm infants undergoing patent ductus arteriosus ligation: a tissue Doppler and myocardial deformation study.
El-Khuffash AF; Jain A; Dragulescu A; McNamara PJ; Mertens L
J Am Soc Echocardiogr; 2012 Oct; 25(10):1058-67. PubMed ID: 22889993
[TBL] [Abstract][Full Text] [Related]
17. [Echocardiographic evaluation in unoperated congenital heart disease in adults].
Geibel A
Herz; 1999 Jun; 24(4):276-92. PubMed ID: 10444707
[TBL] [Abstract][Full Text] [Related]
18. Basal Left Ventricular Dilatation and Reduced Contraction in Patients With Mitral Valve Prolapse Can Be Secondary to Annular Dilatation: Preoperative and Postoperative Speckle-Tracking Echocardiographic Study on Left Ventricle and Mitral Valve Annulus Interaction.
Fukuda S; Song JK; Mahara K; Kuwaki H; Jang JY; Takeuchi M; Sun BJ; Kim YJ; Miyamoto T; Oginosawa Y; Sonoda S; Eto M; Nishimura Y; Takanashi S; Levine RA; Otsuji Y
Circ Cardiovasc Imaging; 2016 Oct; 9(10):. PubMed ID: 27729364
[TBL] [Abstract][Full Text] [Related]
19. Predictors of transient left ventricular dysfunction following transcatheter patent ductus arteriosus closure in pediatric age.
Agha HM; Hamza HS; Kotby A; Ganzoury MEL; Soliman N
J Saudi Heart Assoc; 2017 Oct; 29(4):244-251. PubMed ID: 28983167
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]