Results 101 to 110 of about 45,322 (267)

A Case of AL Amyloidosis With Hepatomegaly as the Main Clinical Manifestation

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Light chain (AL) amyloidosis presenting predominantly with hepatomegaly is a rare and frequently misdiagnosed condition. While clinical features are non‐specific, elevated ALP/GGT should raise suspicion. A liver biopsy remains the gold standard for diagnosis.
Shuchen Dong   +5 more
wiley   +1 more source

Superior vena cava syndrome [PDF]

open access: yesQJM: An International Journal of Medicine, 2019
K Horiuchi   +3 more
openaire   +3 more sources

An Unusual Case of Superior Vena Cava Syndrome Caused by the Intravascular Invasion of an Invasive Thymoma [PDF]

open access: diamond, 2013
Hyung Joon Kim   +9 more
openalex   +1 more source

Superior vena cava syndrome and pacemaker leads. Explant by mechanical dissection system of extraction and percutaneous recanalization with stents for new device implantation

open access: gold, 2023
Elkin González Villegas   +8 more
openalex   +2 more sources

Zero Fluoroscopy Ablation of Arrhythmias in Patients With Congenital Heart Disease

open access: yesJournal of Arrhythmia, Volume 41, Issue 6, December 2025.
Zero‐fluoroscopy radiofrequency ablation using 3D electroanatomic mapping was performed in 42 patients with mild, moderate, or great complexity congenital heart disease. Acute success was 100%, with no complications and minimal recurrence over 48 months. This approach eliminates radiation exposure while maintaining safety and efficacy across select yet
Shailendra Upadhyay   +4 more
wiley   +1 more source

Iatrogenic Superior Vena Cava Syndrome after Cardiopulmonary Bypass Diagnosed by Intraoperative Echocardiography [PDF]

open access: gold, 2020
Matthew Ellison   +7 more
openalex   +1 more source

New cases expand the genotype, phenotype and therapeutic landscape of H syndrome

open access: yes
British Journal of Haematology, EarlyView.
Clément Triaille   +10 more
wiley   +1 more source

Prenatal Diagnosis of Joubert Syndrome 23 With Left Isomerism: A Novel Phenotype Associated With Pathogenic KIAA0586 Variant

open access: yesPrenatal Diagnosis, Volume 45, Issue 13, Page 1783-1786, December 2025.
Abstract Joubert syndrome is a rare autosomal recessive ciliopathy defined by the “molar tooth” sign caused by cerebellar vermis hypoplasia and abnormal superior cerebellar peduncles. Over 40 genes are known to cause the disorder, including KIAA0586, which encodes the centrosomal protein TALPID3, essential for ciliogenesis and Hedgehog signaling ...
Tamara Casteleyn   +6 more
wiley   +1 more source

A Utilização de Endopróteses na Síndrome da Veia Cava Superior por Neoplasia do Pulmão.

open access: yesActa Médica Portuguesa, 1998
We present six cases of superior vena cava syndrome caused by a malignant tumor that were treated by percutaneous endoprostheses. The technique is described and the results evaluated.
J M Pisco   +6 more
doaj   +1 more source

What's Your Diagnosis? Large Mediastinal Mass in a Dog

open access: yes
Veterinary Clinical Pathology, EarlyView.
Rosane O. Cruz   +7 more
wiley   +1 more source

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