Results 171 to 180 of about 5,054,451 (380)

Modified colorimetry of free fatty acids in plasma in the presence of valproic acid. [PDF]

, 1985
F. X. Coudé, G Grimber
openalex   +1 more source

Angioedema induced by valproic acid

Indian Journal of Psychiatry, 2021
Asli Kazgan, Sevler Yildiz
openaire   +3 more sources

Diligent family history to detect a mitochondrial disorder in disguise: Lessons from a case of myoclonic epilepsy

Annals of Movement Disorders
Mitochondrial disorders often present with ataxia, myoclonus, and epilepsy. Valproic acid may be selected for treating myoclonus if it is the presenting feature.
Suvorit S. Bhowmick, Radhay Parikh, Pratishtha Shrivastav   +2 more
doaj   +1 more source

EFFECTS OF VALPROIC ACID (DEPAKENE) ON KETOGENESIS (K), GLUCONEOGENESIS (G), AND UREAGENESIS (U) BY RAT HEPATOCYTES [PDF]

, 1984
Daniel E. Hale, Barbara E. Corkey, Charles A. Stanley   +2 more
openalex   +1 more source

VALPROIC ACID TOXICITY INDUCED BY LACOSAMIDE: A RARE CASE REPORT [PDF]

, 2017
Valproic acid is commonly used in the treatment of both focal and generalized epilepsies and is often tolerated well.Valproic acid is usually tolerated well, but serious complications, including hepatotoxicity and hyperammonemic encephalopathy, may occur.
Chandran, Chanshi, Kumar, Karthika Ashok, Reghu, Remya   +2 more
core   +1 more source

SUPPRESSION OF GROWTH HORMONE AND THYROID HORMONE ASSOCIATED WITH VALPROIC ACID THERAPY [PDF]

, 1987
Carol A. Huseman, Richard Torkelson
openalex   +1 more source

Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel ROGDI Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz Syndrome

Clinical Genetics, Volume 107, Issue 6, Page 705-707, June 2025.
We characterized a novel ROGDI variant (NM_024589.3:c.646‐2A>G) identified in a family case of Kohlschütter‐Tönz Syndrome. This variant disrupts a canonical acceptor splice site, in intron 8. By combining RT‐PCR and targeted long‐read cDNA sequencing.
Miriam Essid, Sana Karoui, Mouna Zribi, Thouraya Ben Younes, Louis Januel, Estelle Lafont, Audrey Labalme, Meriem Ben Hafsa, Go Hun Seo, Safa Khatrouch, Hela Boudabous, Amel Ben Chehida, Damien Sanlaville, Houweyda Jilani, Lamia Benjemaa, Ichraf Kraoua, Gaetan Lesca, Nicolas Chatron   +17 more
wiley   +1 more source

Conditional Overexpression of Net1 Enhances the Trans‐Differentiation of Lgr5+ Progenitors into Hair Cells in the Neonatal Mouse Cochlea

Cell Proliferation, Volume 58, Issue 4, April 2025.
This work investigated the in vivo role of Net1 in cochlear hair cell (HC) regeneration. Conditional overexpression of Net1 in Lgr5+ progenitors of neonatal mouse cochlea enhance HC regeneration by inducing direct trans‐differentiation of Lgr5+ progenitors into HCs probably via activation of Atoh1, Gfi1, and Pou4f3 transcription factors.
Yanqin Lin, Qiuyue Zhang, Wei Tong, Yintao Wang, Leilei Wu, Hairong Xiao, Xujun Tang, Mingchen Dai, Zixuan Ye, Renjie Chai, Shasha Zhang   +10 more
wiley   +1 more source

Inactivation of beef brain alpha-ketoglutarate dehydrogenase complex by valproic acid and valproic acid metabolites. Possible mechanism of anticonvulsant and toxic actions. [PDF]

, 1990
Anthony Luder, Janice K. Parks, Frank E. Frerman, W. Davis Parker   +3 more
openalex   +1 more source

Safety and effectiveness of stiripentol in patients with Dravet syndrome: A prospective, 3‐year, postmarketing surveillance study

Developmental Medicine &Child Neurology, EarlyView.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16285 Abstract Aim To conduct a postmarketing surveillance study of patients with Dravet syndrome in Japan to investigate the safety and effectiveness of long‐term, real‐world, clinical use of stiripentol (STP).
Yuki Kitamura, Hiroaki Ohyabu, Tatsuo Miura, Naomi Takei‐Masuda, Daisuke Matsui, Yushi Inoue, Yoko Ohtsuka   +6 more
wiley   +1 more source