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期刊名:Journal of medical cases

缩写:J MED CASES

ISSN:1923-4155

e-ISSN:1923-4163

IF/分区:0.5/Q3

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共收录本刊相关文章索引433
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Eugen Enesi,Vojsava Leka,Gentian Huti et al. Eugen Enesi et al.
Stroke during pregnancy is uncommon but poses a significant threat to both mother and fetus, requiring rapid, carefully balanced interventions. We describe a 46-year-old woman at 24 weeks' gestation who presented with sudden speech difficul...
Ibrahim Alharbi,Danah Khalid Alharbi,Razan Abdelrahim et al. Ibrahim Alharbi et al.
A 10-year-old Saudi girl with a homozygous GLIS3 gene deletion presented with the classic triad of neonatal diabetes mellitus, congenital hypothyroidism, and congenital glaucoma. During routine surveillance, an incidental complex left renal...
Alert Drishti,Entela Shkodrani,Rudin Domi et al. Alert Drishti et al.
Acetaminophen and ibuprofen are among the most used analgesic-antipyretic agents worldwide, yet their combined overdose can become life-threatening, particularly when medical care is delayed. We report the case of a 29-year-old woman who pr...
Laurianne Giraudeau,Bruno Meymandi-Nejad,Philippe Alessi et al. Laurianne Giraudeau et al.
Multilocular odontogenic keratocyst (MOK) is a benign odontogenic lesion with significant aggressive behavior and a high risk of recurrence. Its occurrence in the symphyseal region is rare, with the posterior mandible being the usual site o...
Pavel Stanchev,Ekaterina Babadzhanova,Boris Tilov et al. Pavel Stanchev et al.
Thyrotoxicosis refers to the clinical state resulting from elevated thyroid hormone levels and may occur with or without underlying hyperthyroidism. Recognizing non-thyroidal and iatrogenic causes is essential for accurate diagnosis and man...
Nikolina Musulin,Sonja Krofak,Aleksandra Jokic et al. Nikolina Musulin et al.
Budd-Chiari syndrome (BCS) is a rare hepatic vascular disorder frequently associated with prothrombotic conditions such as myeloproliferative neoplasms. Pregnancy and assisted reproductive technologies further increase thrombotic and portal...
Ella Lahart,Linda Akbarshahi,Jacob Tadros et al. Ella Lahart et al.
Vertebral artery dissection (VAD) is an uncommon but critical cause of ischemic stroke in young adults. While some cases of VAD are associated with trauma, many occur spontaneously or without clearly identifiable precipitating events. This ...
Nazish Tarar,Hannah Walsh,Katherine Sadaniantz et al. Nazish Tarar et al.
Takotsubo cardiomyopathy (TCM) is characterized by transient left ventricular (LV) dysfunction that classically presents as apical ballooning with basal hyperkinesis. A recognized variant, reverse TCM, conversely is characterized by basal a...
Bassil Leghrouz,Tariq Hindi,Ihab Hilo et al. Bassil Leghrouz et al.
Nephronophthisis is a rare genetic disorder affecting the kidneys and is one of the leading causes of end-stage kidney disease in children. The Bombay blood group is an extremely rare blood type that poses serious clinical challenges, parti...
Samantha A Currier,Lance M Relland,Joseph D Tobias Samantha A Currier
Miller-Dieker syndrome (MDS), also known as Miller-Dieker lissencephaly syndrome or chromosome 17p13.3 deletion syndrome, is a rare chromosomal disorder (microdeletion syndrome) characterized by lissencephaly, altered facial features, and n...