Results 171 to 180 of about 169,795 (221)

Clinical progress note: Management of the hospitalized patient who uses methamphetamine

open access: yes
Journal of Hospital Medicine, Volume 20, Issue 4, Page 380-384, April 2025.
Alexander A. Logan   +2 more
wiley   +1 more source

Advances and Challenges in Quizartinib‐Based FLT3 Inhibition for Acute Myeloid Leukemia: Mechanisms of Resistance and Prospective Combination Therapies

open access: yesEuropean Journal of Haematology, Volume 114, Issue 4, Page 584-595, April 2025.
ABSTRACT FLT3 mutations are among the most common genetic alterations in acute myeloid leukemia (AML) and are associated with poor prognosis. Significant advancements have been made in developing FLT3 inhibitors (FLT3Is), such as quizartinib, which have improved treatment outcomes in both newly diagnosed and relapsed/refractory AML.
Antonella Bruzzese   +10 more
wiley   +1 more source

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

open access: bronze, 2000
Kirsi Piippo   +11 more
openalex   +1 more source

Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome [PDF]

open access: bronze, 2001
Toshio Itoh   +18 more
openalex   +1 more source

The Role of Infarct Border Zone Remodelling in Ventricular Arrhythmias: Bridging Basic Research and Clinical Applications

open access: yesJournal of Cellular and Molecular Medicine, Volume 29, Issue 7, April 2025.
ABSTRACT Patients who experience post‐myocardial infarction (MI) and present with a left ventricular ejection fraction of less than 35% are classified as being at high risk for sudden cardiac death due to ventricular arrhythmias (VAs). The expansion of scar tissue and the extension of the infarct border zone (IBZ) following MI play critical roles in ...
Jin Ma   +3 more
wiley   +1 more source

Characterisation of sleep apneas and respiratory circuitry in mice lacking CDKL5

open access: yesJournal of Sleep Research, Volume 34, Issue 2, April 2025.
Summary CDKL5 deficiency disorder is a rare genetic disease caused by mutations in the CDKL5 gene. Central apneas during wakefulness have been reported in patients with CDKL5 deficiency disorder. Studies on CDKL5‐knockout mice, a CDKL5 deficiency disorder model, reported sleep apneas, but it is still unclear whether these events are central (central ...
Gabriele Matteoli   +12 more
wiley   +1 more source

Cycle Length‐Associated Modulation of the Regional Dispersion of Ventricular Repolarization in a Canine Model of Long QT Syndrome [PDF]

open access: bronze, 2001
Masaomi Chinushi   +5 more
openalex   +1 more source

Phase 2 Early Afterdepolarization as a Trigger of Polymorphic Ventricular Tachycardia in Acquired Long-QT Syndrome [PDF]

open access: bronze, 2001
Gan‐Xin Yan   +5 more
openalex   +1 more source

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