Phenothiazine Derivatives and Their Impact on the Apoptosis Processes: A Review
Journal of Applied Toxicology, Volume 46, Issue 1, Page 42-60, January 2026.ABSTRACT Phenothiazine derivatives have been used for decades as antipsychotic drugs in multiple mental health and physical conditions treatment (schizophrenia, mania in bipolar disorder, and psychosis). Epidemiological studies have shown that people with schizophrenia are less likely to suffer from cancer, which indicates the ability of antipsychotics
Michał Otręba +4 more
wiley +1 more source
Treatable Neonatal Molybdenum Cofactor Deficiency: Rapid Demise Despite Rapid Biochemical Diagnosis
JIMD Reports, Volume 67, Issue 1, January 2026.ABSTRACT Molybdenum cofactor deficiency (MoCD) is an inborn error of metabolism included in the differential for refractory neonatal seizures. The prognosis is guarded, with a median reported age of death between 2.4 and 3.0 years. Mortality is primarily due to seizures and lower respiratory tract infections.
Molly M. Crenshaw +11 more
wiley +1 more source
Impact of Drug Induced Long QT Syndrome: A Systematic Review
, 2018 Karuppiah Arunachalam +4 more
openalex +2 more sources
Is There a Role for Implantable Cardioverter Defibrillators in Long QT Syndrome? [PDF]
, 2002 Arthur A.M. Wilde
openalex +1 more source
Movement Disorders Clinical Practice, Volume 13, Issue 1, Page 44-59, January 2026.Abstract Background Pregnancy after a Parkinson's diagnosis presents complex challenges. Due to the paucity of literature, there is no evidence‐based guidelines and protocols for preconception care, management of pregnancy, childbirth and the postpartum period in women with early‐onset Parkinson's disease (PD).
Alexander C. Lehn +18 more
wiley +1 more source
Genotype‐Specific Risk Stratification and Management of Patients with Long QT Syndrome
, 2013 Alon Barsheshet +2 more
openalex +2 more sources
Effect of physical training on ventricular repolarization in type 1 long QT syndrome: a pilot study in asymptomatic carriers of the G589D KCNQ1 mutation [PDF]
, 2006 Merja Perhonen
openalex +1 more source
A Novel A‐Kinase‐Anchoring Protein 9 Variant in Premature Coronary Artery Disease: A Case Series
Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.AKAP9 Q2136E mutation disrupts AKAP9–PRKAR2A interaction and may contribute to early‐onset CAD. ABSTRACT Background Familial premature coronary artery disease (CAD) is often associated with genetic variants. This study investigated potential causal variants in a Chinese pedigree with premature CAD. Methods In total, nine family members were included in
Yuemiao Jiao +7 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.First Chinese neonatal cases of systemic PHA1B from novel compound‐heterozygous SCNN1B variants (c.585+2T>C; c.1544T>C) presented with life‐threatening hyperkalemia and hyponatremia unresponsive to steroids. Early genetic testing enabled targeted sodium supplementation and potassium‐binding therapy, normalizing electrolytes and underscoring SCNN1B ...
Zhiping Wang, Lijuan Long, Hongjuan Bi
wiley +1 more source
Assessment of Microvolt T‐Wave Alternans in High‐Risk Patients with the Congenital Long‐QT Syndrome [PDF]
, 2009 Jörn Schmitt +6 more
openalex +1 more source