Results 151 to 160 of about 67,248 (260)

Embolization by Gelatin Sponge for Tract Closure After Inappropriate Procedure of Percutaneous Endoscopic Gastrostomy: Safe Management of Hepatic Injury After Transhepatic Placement

open access: yesDEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Placement of percutaneous endoscopic gastrostomy (PEG) is generally safe and well‐tolerated. Transhepatic insertion of PEG tubes is an extremely rare but serious complication. Optimal management strategies for safe removal of PEG tubes remain unclear.
Hiroshi Yukimoto   +9 more
wiley   +1 more source

Clinical outcomes after nondiagnostic prenatal exome sequencing: Need for balancing reassurance and residual risks in genetic counseling

open access: yesJournal of Genetic Counseling, Volume 35, Issue 2, April 2026.
Abstract The clinical application of prenatal exome sequencing (pES) for fetal structural anomalies is relatively new. Although a prenatal genetic diagnosis has been shown to have high clinical and personal utility for families, nearly 70% of pregnancies undergoing pES will receive nondiagnostic results.
Sophie Albert   +4 more
wiley   +1 more source

Hemihepatectomia derecha en un hemangioma gigante: presentación de caso

open access: yesRevista Médica Electrónica
El hemangioma hepático es el tumor benigno más frecuente del hígado, y su diagnóstico casi siempre es incidental por ecosonograma abdominal. Generalmente son asintomáticos excepto si son gigantes, que los síntomas serían por el efecto de masa.
Roxana Ávalos García   +3 more
doaj  

Glycogen Storage Disease in Twins: When Two Lives Reflect One Silent Battle. [PDF]

open access: yesClin Case Rep
Shah RK   +10 more
europepmc   +1 more source

Mitochondrial DNA Depletion Syndrome 1 (MTDPS1)—A Novel Cause of Premature Ovarian Insufficiency

open access: yesClinical Genetics, Volume 109, Issue 4, Page 784-787, April 2026.
We describe a woman with MNGIE due to a novel homozygous TYMP nonsense variant and propose MNGIE as the cause of her premature ovarian insufficiency—a rarely reported association—highlighting the need to consider mitochondrial disease in unexplained POI, especially in atypical, consanguineous presentations. ABSTRACT Mitochondrial DNA depletion syndrome
Michael Matheou   +3 more
wiley   +1 more source

Prevalence and Diagnostic Challenge of Hemophagocytic Lymphohistiocytosis Syndrome in Critically Ill Patients

open access: yesEuropean Journal of Haematology, Volume 116, Issue 4, Page 380-390, April 2026.
ABSTRACT Background Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome. It is a severe condition with a challenging diagnosis in the intensive care unit (ICU), for which current recommendations rely on fulfilling five of eight HLH‐2004 criteria.
Claire Queffeulou   +4 more
wiley   +1 more source

Clinico-Etiological Study of Purpura Fulminans: Experience from a Tertiary-Care Children Hospital. [PDF]

open access: yesIndian Dermatol Online J
Kalam S   +4 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy