Kittichate Visuttijai
Goeteborg, O, Sweden
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 26 publications
A novel myopathy with autophagic vacuoles associated with biallelic variants in CLN8.
Journal: Brain pathology (Zurich, Switzerland)
Published: May 20, 2026
Dysregulation of glycogen metabolism in cardiomyopathy caused by glycogenin-1 (GYG1) missense variants.
Journal: The Journal of clinical endocrinology and metabolism
Published: March 26, 2026
Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiency.
Journal: Acta neuropathologica
Published: October 02, 2024
Histopathological Evaluation of Somatostatin Receptor 2 Expression in Myocarditis-Rationale for the Diagnostic Use of Somatostatin Receptor Imaging.
Journal: Diagnostics (Basel, Switzerland)
Published: September 26, 2024
Abnormal expression of myosin heavy chains in early postnatal stages of spinal muscular atrophy type I at single fibre level.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: June 15, 2024
A novel homozygous pathogenic missense variant in COX6B1: Further delineation of the phenotype.
Journal: American journal of medical genetics. Part A
Published: February 21, 2024
Proteomic profiling of polyglucosan bodies associated with glycogenin-1 deficiency in skeletal muscle.
Journal: Neuropathology and applied neurobiology
Published: January 29, 2024
Potential Natural Products Regulation of Molecular Signaling Pathway in Dermal Papilla Stem Cells.
Journal: Molecules (Basel, Switzerland)
Published: May 25, 2023
Chitooligosaccharide prevents vascular endothelial cell apoptosis by attenuation of endoplasmic reticulum stress via suppression of oxidative stress through Nrf2-SOD1 up-regulation.
Journal: Pharmaceutical biology
Published: October 27, 2022
Structural modification of resveratrol analogue exhibits anticancer activity against lung cancer stem cells via suppression of Akt signaling pathway.
Journal: BMC complementary medicine and therapies
Published: October 05, 2022
Ribonuclease inhibitor 1 (RNH1) deficiency cause congenital cataracts and global developmental delay with infection-induced psychomotor regression and anemia.
Journal: European journal of human genetics : EJHG
Published: September 05, 2022
Last Updated: 09/26/2026