Results 261 to 270 of about 125,690 (294)

Single‐Cell Transcriptomic Reveals the Involvement of Cell–Cell Junctions in the Early Development of Hypertrophic Cardiomyopathy

open access: gold
Dingchen Wang   +10 more
openalex   +1 more source

Isorhythmic atrioventricular dissociation during anaesthesia in a cat

open access: yesVeterinary Record Case Reports, Volume 13, Issue 4, December 2025.
Abstract A 10‐year‐old, male, neutered domestic shorthair cat with suspected hypertrophic cardiomyopathy was referred for cystotomy to remove uroliths present in its urinary bladder. Fifteen minutes after induction of general anaesthesia, atrioventricular dissociation was noted on the electrocardiogram with similar atrial and ventricular firing rates ...
Gemma Padrosa Sala   +3 more
wiley   +1 more source

Management of Malignant Arrhythmia in Apical Hypertrophic Cardiomyopathy: A Case Report. [PDF]

open access: yesAm J Case Rep
Acharya R   +5 more
europepmc   +1 more source

Resolution of pancytopenia in a dog infected with Bartonella rochalimae in association with antibiotic therapy

open access: yesVeterinary Record Case Reports, Volume 13, Issue 4, December 2025.
Abstract Fever, non‐regenerative anaemia and leukopenia were documented in a 7‐year‐old, entire, male Akita Inu dog. The serum biochemistry and urinalysis were unremarkable. Tests for infectious agents were negative, except for SNAP 4Dx seropositive for Anaplasma phagocytophilum or A. platys. PCR for Anaplasma spp. was negative.
Clàudia Viñeta   +4 more
wiley   +1 more source

Mitochondrial Dysfunction Contributes to Decompensation in a Zebrafish Model of Isoproterenol‐Induced Heart Failure

open access: yesActa Physiologica, Volume 241, Issue 12, December 2025.
ABSTRACT Aim Heart failure is a clinical syndrome where the heart's structural or functional impairment leads to inadequate blood flow to meet the body's metabolic demands. Mitochondrial dysfunction is increasingly recognized as a central contributor underlying the contractile impairment observed in the failing heart.
Manuel Vicente   +6 more
wiley   +1 more source

Long‐Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History Comparisons

open access: yesAnnals of Clinical and Translational Neurology, Volume 12, Issue 11, Page 2335-2348, November 2025.
ABSTRACT Objectives This ongoing, open‐label extension study is evaluating the long‐term safety, tolerability, and efficacy of givinostat, a Class I and II histone deacetylase inhibitor, in patients with Duchenne muscular dystrophy (DMD). Methods The recruited patients completed one of two prior clinical studies (one Phase 2 and one Phase 3 [EPIDYS ...
Craig M. McDonald   +74 more
wiley   +1 more source

Diagnostic Ambiguity in Apical Hypertrophic Cardiomyopathy: Case-Based Insights and Review of Evolving Criteria. [PDF]

open access: yesJACC Case Rep
Li-Jedras M   +5 more
europepmc   +1 more source

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