Cargando…

Y Chromosome in Tumer syndrome; a case report

Detalles Bibliográficos
Autores principales:	Taliana, N, Grech, V, Said, E, DeGiovanni, JV
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Images in Paediatric Cardiology 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270033/ https://www.ncbi.nlm.nih.gov/pubmed/28405210

Ejemplares similares

DiGeorge phenotype in the absence of 22q11 deletion – a case report
por: Taliana, N, et al.
Publicado: (2017)

Delayed Amplatzer device closure of atrial septal defect for persistent cyanosis after surgical correction of severe pulmonary stenosis in early infancy
por: Falzon, A, et al.
Publicado: (2004)

“Bendy” stents help negotiate hairpin intracardiac curves
por: Bugeja, J, et al.
Publicado: (2015)

Right ventricular outflow tract stenting – effective palliation for Fallot’s tetralogy
por: Bugeja, J, et al.
Publicado: (2015)

3 year old with chronic wet cough: Intralobar Bronchopulmonary sequestration
por: Micallef, SP, et al.
Publicado: (2016)

The rarest aortic arch anomaly a case report of asymptomatic isolation of the subclavian artery
por: Taliana, N, et al.
Publicado: (2017)

Flipper coil closure of patent ductus arteriosus
por: Grech, V, et al.
Publicado: (2007)

Cardiac catheter assessment of congenital heart disease prior to total cavopulmonary connection
por: DeGiovanni, JV, et al.
Publicado: (2005)

Patent arterial duct occlusion with two Amplatzer Duct Occluder devices
por: Grech, V, et al.
Publicado: (2011)

Aortic stenting for neonatal coarctation of the aorta - when should this be considered?
por: Bugeja, J, et al.
Publicado: (2016)

Genome analysis of Limosilactobacillus fermentum JN2019 applied to tumeric fermentation for animal feed
por: Yoo, Heeseop, et al.
Publicado: (2021)

Use of stents for correction of pulmonary artery branch stenosis
por: Mercieca, V, et al.
Publicado: (2004)

Amplatzer device closure of an inferior venosus atrial septal defect after surgical closure of a secundum atrial septal defect
por: Falzon, A, et al.
Publicado: (2004)

How to achieve balloon stability in aortic valvuloplasty using rapid ventricular pacing
por: Mehta, C, et al.
Publicado: (2004)

Late presentation and successful treatment of classical scimitar syndrome
por: Grech, V, et al.
Publicado: (2003)

Amplatzer ASO device closure of secundum atrial septal defects and patent foramen ovale
por: Grech, V, et al.
Publicado: (2003)

Transcatheter closure of right coronary artery fistula to the right ventricle
por: Haweleh, A. Abu, et al.
Publicado: (2018)

Management of an absent pulse following arterial catheterization
por: DeGiovanni, JV
Publicado: (2002)

Gonadal dysgenesis in Turner syndrome with Y-chromosome mosaicism: Two case reports
por: Leng, Xue-Fei, et al.
Publicado: (2020)

Stent implantation for coarctation facilitated by the anterograde trans-septal approach
por: Sreeram, N, et al.
Publicado: (2005)

A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report
por: Sheth, Frenny, et al.
Publicado: (2009)

Kallmann Syndrome and X-linked Ichthyosis Caused by Translocation Between Chromosomes X and Y: A Case Report
por: Sait, Haseena, et al.
Publicado: (2021)

Compression of the Superior Vena Cava by an Interatrial Septal Lipoma: A Case Report
por: Grech, R., et al.
Publicado: (2013)

X-derived marker chromosome in patient with mosaic Turner syndrome and Dandy-Walker syndrome: a case report
por: Telepova, Alena S., et al.
Publicado: (2017)

Whole-genome sequencing analysis of Y chromosome microdeletion: a case report
por: Gao, Zhixiang, et al.
Publicado: (2020)

Infective endocarditis complicating COVID-19 pneumonia: a case report
por: Spinoni, Enrico Guido, et al.
Publicado: (2020)

Coronary sinus for cardiac resynchronization therapy: leave it alone and go for the branch! a case report
por: Dell’Era, Gabriele, et al.
Publicado: (2022)

Interim prostacyclin therapy for an isolated disconnected pulmonary artery: a case report
por: Grech, Victor, et al.
Publicado: (2010)

Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report
por: Censani, Marisa, et al.
Publicado: (2013)

Case report: Neonatal pancreatitis, chromosomal abnormality and duodenal stenosis in a newborn. A new syndrome?
por: Ladipo-Ajayi, Oluwaseun, et al.
Publicado: (2020)

Chromosome Y as a marker for sex discrepancies in patients with organ transplants: a case report
por: Balaguer, Nuria, et al.
Publicado: (2021)

Multiple cardiac metastases from urothelial carcinoma case report
por: Grech, Neil, et al.
Publicado: (2022)

Chromosomal Abnormalities in Syndromic Orofacial Clefts: Report of Three Children
por: Shenoy, Rathika Damodara, et al.
Publicado: (2018)

Lane‐Hamilton syndrome
por: Grech, Audrey K., et al.
Publicado: (2023)

Ring Chromosome 18: A Case Report
por: Heydari, Shermineh, et al.
Publicado: (2014)

A Case of Weill-Marchesani Syndrome with Inversion of Chromosome 15
por: Chung, Jae Lim, et al.
Publicado: (2007)

Case report: A rare case of eccrine carcinoma
por: Kshirsagar, Ashok Y., et al.
Publicado: (2015)

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report
por: VAHIDI MEHRJARDI, Mohammad Yahya, et al.
Publicado: (2016)

A Case of Advanced Glaucoma with Increased Episcleral Venous Pressure in a 17-Year-Old with Eisenmenger Syndrome
por: Grech, Leanne, et al.
Publicado: (2017)

Chromosomal Microarray Testing in NEC: A Case Report
por: Burjonrappa, Sathyaprasad C, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_g9aredofarmc0cnnsra6uask7s