Results 201 to 210 of about 266,382 (322)

Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy.

JACC Clinical Electrophysiology, 2018
A. Wilde, A. Amin
semanticscholar   +1 more source

Sudden unexpected infant death, sudden unexplained death in childhood, and sudden unexpected death in epilepsy

Developmental Medicine &Child Neurology, Volume 67, Issue 6, Page 734-739, June 2025.
Abstract Sudden deaths in infants and children represent a profound and tragic event that continues to challenge researchers despite extensive investigation over several decades. The predominant phenotype, sudden infant death syndrome (SIDS), has evolved into the broader category of sudden unexpected infant death (SUID).
Suvasini Sharma, Robyn Whitney, Sayoni Roy Chowdhury, Rajesh Ramachandrannair   +3 more
wiley   +1 more source

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.

, 1997
John Burn, A. John Camm, Melanie J. Davies, L. Peltonen, Peter J. Schwartz, Hugh Watkins   +5 more
openalex   +1 more source

Apparent Ventricular Bigeminy in the Congenital Long QT Syndrome: What is the Mechanism? [PDF]

, 2000
Yen‐Bin Liu, Wen‐Jone Chen, Yuan‐Teh Lee   +2 more
openalex   +1 more source

ABCB1, SLC22A1, COMT, and OPRM1 genotypes: Study of their influence on plasma methadone levels and clinical response to methadone maintenance treatment in opioid use disorder

Fundamental &Clinical Pharmacology, Volume 39, Issue 3, June 2025.
Abstract Background Opioid use disorder (OUD) is an emerging and global public health concern, and its management remains inadequate, notably due to a lack of biomarkers, except for the CYP2B6 genetic polymorphisms. Objectives Hence, the aim of this study was to assess the influence of genetic polymorphisms of ABCB1, SLC22A1, COMT, and OPRM1 on ...
Abd El Kader Ait Tayeb, Edouard‐Jules Laforgue, Benoit Schreck, Marie Grall‐Bronnec, Jean‐Benoit Hardouin, Juliette Leboucher, OPAL Group, Caroline Victorri‐Vigneau, Céline Verstuyft   +8 more
wiley   +1 more source

Evaluation of Autonomic Nervous Activity in Patients With Congenital Long QT Syndrome by an Analysis of RR Variability

, 1996
Hiroshi Morita, Hiroshi Yamanari, Tohru Ohe   +2 more
openalex   +2 more sources

Acquired Genotype-Positive Long QT Syndrome After Pediatric Heart Transplantation. [PDF]

Pediatr Transplant
Barresi NV, Sebastian J, Arora G, Feingold B.   +3 more
europepmc   +1 more source

Long QT syndrome: Genetic implications and drug influence [PDF]

, 2008
Gojković-Bukarica Ljiljana, Savić Nataša   +1 more
core   +1 more source

Acute Effects of Four Major Trace Amines on Zebrafish Behavioral, Neurochemical, and Neuroendocrine Responses

Journal of Neurochemistry, Volume 169, Issue 6, June 2025.
A trace amine beta‐phenylethylamine is anxiolytic and reduces brain acetylcholine at 12 μg/L, but elevates anxiety and cortisol levels at 1000 μg/L. Acute tryptamine at 7 mg/L is anxiogenic, reduces shoaling and social interaction, but elevates brain acetylcholine and cortisol levels. Acute tyramine at 15 μg/L, and octopamine at 125, 500, and 1500 μg/L,
Thalia M. Quintanilha, Pietra M. Costa, Ana L. S. Cardoso, Gabrieli S. Battú, Leonardo M. Bastos, Bruno P. dos Santos, Talise E. Müller, Tiago F. de Oliveira, Angelo Piato, Allan V. Kalueff, Murilo S. de Abreu   +10 more
wiley   +1 more source

A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT syndrome

, 1998
Hiroyuki Yamagishi, Michiko Furutani, Mitsuhiro Kamisago, Yoshiyuki Morikawa, Yoshifumi Kojima, Yoshiaki Hino, Yoshiyuki Furutani, Misa Kimura, Shin‐ichiro Imamura, Atsuyoshi Takao, Kazuo Momma, Rumiko Matsuoka   +11 more
openalex   +1 more source