Results 91 to 100 of about 17,456 (195)

A rare case of paradoxical left sided endocarditis through patent foramen ovale

Marshall Journal of Medicine, 2017
A 36 -year old woman IV drug abuser admitted with Right-Sided Infective Endocarditis (RSIE) as demonstrated by transthoracic echocardiogram. Patient was admitted 8 weeks later with recurrence of symptoms, moreover signs of systemic embolization were ...
George M. Yousef , Paul I. Okhumale, Haytham Aljoudi,, Silvestre Cansino   +3 more
doaj   +1 more source

Health Care Utilization in Adults With Congenital Heart Disease: Population‐Based Findings

Birth Defects Research, Volume 118, Issue 6, June 2026.
ABSTRACT Background Population‐based data on healthcare utilization in adults with congenital heart disease (CHD) are limited. We examined utilization patterns in a multi‐site, population‐based U.S. cohort of adults with CHD. Methods This retrospective cohort linked health and administrative records from five regions (Colorado, North Carolina, Utah ...
Tessa L. Crume, Amber D. Khanna, Alexandra Tillman, George K. Lui, Aida S. Soim, Daphne T. Hsu, Kristin Sommerhalter, Anaclare Sullivan, Jennifer S. Li, Alfred D′Ottavio II, Wendy M. Book, Cheryl Raskind‐Hood, Kevin Whitehead, Nelangi Pinto, Marcia L. Feldkamp, Matthew R. Reeder, Sergey Krikov, Lorenzo D. Botto   +17 more
wiley   +1 more source

Trametinib Therapy for Hypertrophic Cardiomyopathy and Pulmonary Hypertension in a Child With RAF1‐Related Noonan Syndrome (p.Ser257Leu): A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This case describes a female infant with RAF1‐related Noonan syndrome who developed severe hypertrophic obstructive cardiomyopathy, pulmonary hypertension, and cardiorespiratory failure that responded to trametinib treatment but ultimately progressed to death following dose tapering and discontinuation of therapy. To the best of our knowledge,
C. Noah Nilsson, Othman A. Aljohani, Michael A. Smith, Rachelle Durand, Inger Norlyk Sheyanth, Hythem Nawaytou, Elliot Stieglitz, Russel Valle, Sanjeev A. Datar   +8 more
wiley   +1 more source

A Case Report on Meningitis Complicated by Acute Ischemic Stroke and Failed Thrombolysis

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Ischemic stroke is one of the rare but grave complications of meningitis with poor outcomes and long‐term sequelae, and the role of thrombolysis with infection‐related stroke remains uncertain. This case report documents a 52‐year‐old man presented with fever, headache, vomiting, and altered sensorium, and on examination he had neck rigidity ...
Sonam Dema, Dechen Choden, Sonam Wangmo
wiley   +1 more source

Comparison of medical treatments in cryptogenic stroke patients with patent foramen ovale: A randomized clinical trial

Journal of Research in Medical Sciences, 2013
Background: This randomized clinical trial compared rates of stroke or transient ischemic attack recurrence or death in patients with cryptogenic stroke and patent foramen ovale (PFO) who received medical treatment with aspirin or warfarin. Materials and
Abdolhamid Shariat, Ehsan Yaghoubi, Mohsen Farazdaghi, Kamran Aghasadeghi, Afshin Borhani Haghighi   +4 more
doaj  

Pregnancy Outcomes and Postnatal Health From Transferred Mosaic Embryos Following Preimplantation Genetic Testing for Aneuploidy

iNew Medicine, Volume 2, Issue 2, June 2026.
This illustration synthesizes the methods and conclusion of this study, demonstrating that the transfer of mosaic embryos following reimplantation genetic testing for aneuploidy does not increase the risk to postnatal health. ABSTRACT Next‐generation sequencing (NGS) has increased the detection of mosaic embryos during preimplantation genetic testing ...
Lili Chen, Dehuan Huang, Jingcheng Sang, Yiqi Yin, Caiyun Wu, Yan Hao, Dawei Chen, Zhiguo Zhang, Yunxia Cao, Ri‐Cheng Chian, Ping Zhou   +10 more
wiley   +1 more source

Optimizing Skull Base Anatomy Education: Qualitative Insights From Learner Interaction With 2D, Monoscopic 3D, and Virtual Reality Models

Laryngoscope Investigative Otolaryngology, Volume 11, Issue 3, June 2026.
ABSTRACT Objective Several models are currently employed to teach anatomy to medical students and residents, including cadaveric, two‐dimensional (2D), monoscopic three‐dimensional (3D), and virtual reality (VR) models. While many studies have focused on measuring how much and how quickly each model can help residents and medical students attain and ...
Elizabeth N. Liao, Nina W. Zhao, Kendyl Naugle, Katrin Jaradeh, Roberto Rodriguez Rubio, Ivan El‐Sayed   +5 more
wiley   +1 more source

Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome

Molecular Genetics &Genomic Medicine, Volume 14, Issue 6, June 2026.
A novel de novo NSD2 variant (c.2137G>C, p.Gly713Arg) was identified in a Chinese patient presenting with a syndromic developmental disorder. RNA analysis from patient‐derived material revealed that this missense variant induces aberrant splicing of NSD2 transcripts, resulting in a frameshift and likely a loss‐of‐function protein product.
Shixuan Xu, Guoqiang Li, Yimin He, Yiyao Chen, Lu‐lu Li, Niu Li, Shuyuan Li, Jian Wang   +7 more
wiley   +1 more source

A correlative study between white matter lesions of migraine and patent foramen ovale

Chinese Journal of Contemporary Neurology and Neurosurgery, 2014
Migraine is a kind of common primary headache, which seriously damages human health and quality of life. Recent studies show there is a high incidence of white matter lesions (WML) in migraineurs, which is independent of other risk factors for ...
Qiang ZHANG, Guo-gang LUO
doaj  

X‐Linked Intellectual Developmental Disorder‐93 Caused by BRWD3 Mutation in Females: A Case Report and Literature Review

Molecular Genetics &Genomic Medicine, Volume 14, Issue 6, June 2026.
A case of MRX93 in a 1‐year‐and‐3‐month‐old girl was reported, in whom a heterozygous deletion from exon 21 to exon 30 in the BRWD3 gene occurred. We conducted a literature review to explore the clinical phenotypes and genetic characteristics of MRX93 in females. ABSTRACT Objective To report the clinical manifestations and genetic diagnosis of a female
Yang Xiu, Yige Zhang, Yake Jiao, Wei Wang, Yanyan Hu   +4 more
wiley   +1 more source