Argininemia and vitamin K-dependent coagulation factors deficiency: A case report and a brief review of the literature.
Hadj TB, Te VLT, Le Guyader M, Voyer A, Durand-Maugard C, Galmiche A, Garçon L, Demagny J.
Thromb Res. 2023 Sep;229:42-45. doi: 10.1016/j.thromres.2023.06.029. Epub 2023 Jun 30.
Genetic mimics of cerebral palsy.
Pearson TS, Pons R, Ghaoui R, Sue CM.
Mov Disord. 2019 May;34(5):625-636. doi: 10.1002/mds.27655. Epub 2019 Mar 26.
Neurophysiological characteristics in argininemia: a case report.
Cui B, Wei L, Zhu ZJ, Sun LY.
Transl Pediatr. 2021 Jul;10(7):1947-1951. doi: 10.21037/tp-21-112.
Argininemia.
Snyderman SE, Sansaricq C, Chen WJ, Norton PM, Phansalkar SV.
J Pediatr. 1977 Apr;90(4):563-8. doi: 10.1016/s0022-3476(77)80367-3.
[Argininemia].
Matsuura T.
Ryoikibetsu Shokogun Shirizu. 2001;(33):219-20.
Argininemia, Hyperornithinemia, and 3-Hydroxyisovaleric Aciduria.
Tal G, Dar DE, Idin A, Korman SH, Dumin E.
Clin Chem. 2018 Jun;64(6):978-980. doi: 10.1373/clinchem.2018.286617.
[Advances in clinical and molecular genetics studies on argininemia].
Wu TF, Yang YL.
Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):954-9.
Argininemia presenting with progressive spastic diplegia.
Lee BH, Jin HY, Kim GH, Choi JH, Yoo HW.
Pediatr Neurol. 2011 Mar;44(3):218-20. doi: 10.1016/j.pediatrneurol.2010.11.003.
Coagulation Disturbances in Patients with Argininemia.
Kiykim E, Zubarioglu T, Cansever MS, Celkan T, Häberle J, Aktuglu Zeybek AC.
Acta Haematol. 2018;140(4):221-225. doi: 10.1159/000493678. Epub 2018 Oct 24.
Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review.
Prasad AN, Breen JC, Ampola MG, Rosman NP.
J Child Neurol. 1997 Aug;12(5):301-9. doi: 10.1177/088307389701200502.
