Cargando…

Introducing and Implementing Genetic Assessment in Cardio-Obstetrics Clinical Practice: Clinical and Genetic Workup of Patients with Cardiomyopathy

Cardiovascular disease (CVD) during pregnancy varies significantly worldwide, influenced by factors such as access to healthcare, delayed diagnosis, causes, and risk factors. Our study sought to explore the spectrum of CVD present in pregnant women in the United Arab Emirates to better understand th...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mansoori, Ghadeera Al, Mahmeed, Wael Al, Wani, Saleema, Salih, Bashir Taha, Ansari, Tarek El, Farook, Fathima, Farooq, Zenab, Khair, Howaida, Zaręba, Kornelia, Dhahouri, Nahid Al, Raj, Anjana, Foo, Roger S., Ali, Bassam R., Jasmi, Fatma Al, Akawi, Nadia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10252198/ https://www.ncbi.nlm.nih.gov/pubmed/37298070 http://dx.doi.org/10.3390/ijms24119119

Ejemplares similares

Etoricoxib as a treatment of choice for patients with SLCO2A1 mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report
por: Albawa'neh, Areej, et al.
Publicado: (2022)

Case Report: Reinterpretation and Reclassification of ARSB:p.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene
por: Al Dhahouri, Nahid, et al.
Publicado: (2022)

LINS, a modulator of the WNT signaling pathway, is involved in human cognition
por: Akawi, Nadia A, et al.
Publicado: (2013)

Clinical, Biochemical, and Genetic Heterogeneity in Glutaric Aciduria Type II Patients
por: Ali, Amanat, et al.
Publicado: (2021)

Legal Awareness and Practices of Female Genital Mutilation/Cutting (FGM/C) among United Arab Emirates Medical Practitioners
por: Al Awar, Shamsa, et al.
Publicado: (2023)

Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency
por: Ali, Amanat, et al.
Publicado: (2021)

Risk of sexual dysfunctions in breastfeeding females: protocol for a systematic review and meta-analysis
por: Smetanina, Darya, et al.
Publicado: (2023)

Perinatal Outcomes in Foetuses with Increased Nuchal Translucency and Normal Karyotype: A Retrospective Cohort Study from the United Arab Emirates
por: Khair, Howaida, et al.
Publicado: (2023)

Role of Ceramides in the Molecular Pathogenesis and Potential Therapeutic Strategies of Cardiometabolic Diseases: What we Know so Far
por: Shalaby, Youssef M., et al.
Publicado: (2022)

Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
por: Belcher, Ryan, et al.
Publicado: (2021)

Assessment of methylcitrate and methylcitrate to citrate ratio in dried blood spots as biomarkers for inborn errors of propionate metabolism
por: Al-Dirbashi, Osama Y., et al.
Publicado: (2019)

Hunter disease eClinic: interactive, computer-assisted, problem-based approach to independent learning about a rare genetic disease
por: Al-Jasmi, Fatma, et al.
Publicado: (2010)

Pharmaceutical Chaperones and Proteostasis Regulators in the Therapy of Lysosomal Storage Disorders: Current Perspective and Future Promises
por: Mohamed, Fedah E., et al.
Publicado: (2017)

Sotos syndrome and the added value of genetic workup in epilepsy surgery
por: Bättig, Linda, et al.
Publicado: (2021)

Health Care System View of Human Papilloma Virus (HPV) Vaccine Acceptability by Emirati Men
por: Al Shdefat, Suzan, et al.
Publicado: (2022)

Identification Level of Awareness and Knowledge of Emirati Men about HPV
por: Al Shdefat, Suzan, et al.
Publicado: (2022)

Anticoagulation in COVID-19
por: Atallah, Bassam, et al.
Publicado: (2020)

The Association Between Periodontitis and Erectile Dysfunction: A Systematic Review and Meta-Analysis
por: Farook, Fathima, et al.
Publicado: (2021)

Stillbirth Investigations: An Iconographic and Concise Diagnostic Workup in Perinatal Pathology
por: Sergi, Consolato M., et al.
Publicado: (2023)

Pregnant Women’s Perception and Knowledge of the Impact of Obesity on Prenatal Outcomes—A Cross-Sectional Study
por: Khair, Howaida, et al.
Publicado: (2023)

Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research Approaches
por: Gieldon, Laura, et al.
Publicado: (2019)

Response: Sotos Syndrome and the added value of genetic workup in epilepsy surgery
por: Myers, Kenneth A.
Publicado: (2021)

Standardized pre-procedural clinical workup for protected percutaneous coronary intervention
por: Al-Rashid, Fadi, et al.
Publicado: (2022)

SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure
por: Al Zaabi, Nuha, et al.
Publicado: (2017)

Review of Multiple Myeloma Genetics including Effects on Prognosis, Response to Treatment, and Diagnostic Workup
por: Wiedmeier-Nutor, Julia Erin, et al.
Publicado: (2022)

Adapting to the COVID-19 Pandemic at a Quaternary Care Hospital in the Middle East Gulf Region
por: Atallah, Bassam, et al.
Publicado: (2020)

Y Choromosomal Microdeletion Screening in The Workup of Male Infertility and Its Current Status in India
por: Suganthi, Ramaswamy, et al.
Publicado: (2014)

A Case of Escherichia coli Endogenous Panophthalmitis and Orbital Cellulitis With Normal Workup for Primary Focus
por: Hassanin, Fadi F, et al.
Publicado: (2021)

A mutation in KIF7 is responsible for the autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance
por: Ali, Bassam R, et al.
Publicado: (2012)

Cardio-oncology: Shared Genetic, Metabolic, and Pharmacologic Mechanism
por: Zhao, Yiqi, et al.
Publicado: (2023)

Effect of HMGB1 and HBD-3 levels in the diagnosis of sepsis- A comparative descriptive study
por: Mansour, Nourah Al, et al.
Publicado: (2023)

Commentary: Pre-aesthetic workup: Should it be a part of pre-refractive surgery workup?
por: Sachdev, Ritika
Publicado: (2021)

Endoplasmic Reticulum Quality Control Is Involved in the Mechanism of Endoglin-Mediated Hereditary Haemorrhagic Telangiectasia
por: Ali, Bassam R., et al.
Publicado: (2011)

A Randomized Clinical Study of the Plaque Removal Efficacy of a Novel Manual Toothbrush With Micro-Pulse Bristles on Fixed Orthodontic Patients
por: Al Shammari, Abdulsalam, et al.
Publicado: (2022)

Cardiac Workup of Ischemic Stroke
por: Ustrell, Xavier, et al.
Publicado: (2010)

Diagnostic workup for ARDS patients
por: Papazian, Laurent, et al.
Publicado: (2016)

Findings of Cardiovascular Workup of Kidney Transplant Candidates: A Retrospective Study of a Single-Center in Saudi Arabia
por: Arabi, Ziad, et al.
Publicado: (2023)

Molecular and clinical analysis of Ellis-van Creveld syndrome in the United Arab Emirates
por: Ali, Bassam R, et al.
Publicado: (2010)

Comprehensive Laboratory Diagnostic Workup for Patients with Suspected Intraocular Lymphoma including Flow Cytometry, Molecular Genetics and Cytopathology
por: Shumilov, Evgenii, et al.
Publicado: (2022)

Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years
por: Gemelli, Chiara, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_512upphju3k4oh3f5c4n147gtr