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17 in total

Review 1. Major malformations with valproic acid.

Authors: Gideon Koren; Alejandro A Nava-Ocampo; Myla E Moretti; Reuven Sussman; Irena Nulman
Journal: Can Fam Physician Date: 2006-04 Impact factor: 3.275

2. Pharmacokinetic aspects of drug effects in vitro: effects of serum protein binding on concentration and teratogenicity of valproic acid and 2-en-valproic acid in whole embryos in culture.

Authors: C Lewandowski; S Klug; H Nau; D Neubert
Journal: Arch Toxicol Date: 1986-04 Impact factor: 5.153

Review 3. Principles and problems in assessing prenatal toxicity.

Authors: D Neubert; I Chahoud; T Platzek; R Meister
Journal: Arch Toxicol Date: 1987 Impact factor: 5.153

4. Interferon regulatory factor-1 binds c-Cbl, enhances mitogen activated protein kinase signaling and promotes retinoic acid-induced differentiation of HL-60 human myelo-monoblastic leukemia cells.

Authors: Miaoqing Shen; Rodica P Bunaciu; Johanna Congleton; Holly A Jensen; Lavanya G Sayam; Jeffrey D Varner; Andrew Yen
Journal: Leuk Lymphoma Date: 2011-08-24

8. Effects of valproic acid derivatives on inositol trisphosphate depletion, teratogenicity, glycogen synthase kinase-3beta inhibition, and viral replication: a screening approach for new bipolar disorder drugs derived from the valproic acid core structure.

Authors: B J Eickholt; G J Towers; W J Ryves; D Eikel; K Adley; L M J Ylinen; N H Chadborn; A J Harwood; H Nau; R S B Williams
Journal: Mol Pharmacol Date: 2005-02-01 Impact factor: 4.436

9. Abnormal metabolism of valproic acid in fatal hepatic failure.

Authors: W Kochen; A Schneider; A Ritz
Journal: Eur J Pediatr Date: 1983-10 Impact factor: 3.183

10. The enantiomers of the valproic acid analogue 2-n-propyl-4-pentynoic acid (4-yn-VPA): asymmetric synthesis and highly stereoselective teratogenicity in mice.

Authors: R S Hauck; H Nau
Journal: Pharm Res Date: 1992-07 Impact factor: 4.200

A new model for embryotoxicity testing: teratogenicity and pharmacokinetics of valproic acid following constant-rate administration in the mouse using human therapeutic drug and metabolite concentrations.