Crossref Citations
                  This article has been cited by the following publications. This list is generated based on data provided by Crossref.
                                
                                    
                                    Klomp, Leo W.J.
                                    
                                    de Koning, Tom J.
                                    
                                    Malingré, Helga E.M.
                                    
                                    van Beurden, Ellen A.C.M.
                                    
                                    Brink, Miny
                                    
                                    Opdam, Frans L.
                                    
                                    Duran, Marinus
                                    
                                    Jaeken, Jaak
                                    
                                    Pineda, Merce
                                    
                                    van Maldergem, Lionel
                                    
                                    Poll-The, Bwee Tien
                                    
                                    van den Berg, Inge E.T.
                                     and 
                                    Berger, Ruud
                                  2000.
                                  Molecular Characterization of 3-Phosphoglycerate Dehydrogenase Deficiency—a Neurometabolic Disorder Associated with Reduced L-Serine Biosynthesis.
                                  
                                  
                                  The American Journal of Human Genetics, 
                                  Vol. 67, 
                                  Issue. 6, 
                                
                                    p. 
                                    1389.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Pind, Steven
                                    
                                    Slominski, Elzbieta
                                    
                                    Mauthe, Jill
                                    
                                    Pearlman, Kayla
                                    
                                    Swoboda, Kathryn J.
                                    
                                    Wilkins, John A.
                                    
                                    Sauder, Patricia
                                     and 
                                    Natowicz, Marvin R.
                                  2002.
                                  V490M, a Common Mutation in 3-Phosphoglycerate Dehydrogenase Deficiency, Causes Enzyme Deficiency by Decreasing the Yield of Mature Enzyme.
                                  
                                  
                                  Journal of Biological Chemistry, 
                                  Vol. 277, 
                                  Issue. 9, 
                                
                                    p. 
                                    7136.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Jaeken, Jaak
                                    
                                    De Koning, Tom
                                     and 
                                    Van Hove, Johan
                                  2003.
                                  Physician’s Guide to the Laboratory Diagnosis of Metabolic Diseases.
                                  
                                  
                                  
                                  
                                  
                                
                                    p. 
                                    123.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    de Koning, Tom J
                                     and 
                                    Klomp, Leo WJ
                                  2004.
                                  Serine-deficiency syndromes.
                                  
                                  
                                  Current Opinion in Neurology, 
                                  Vol. 17, 
                                  Issue. 2, 
                                
                                    p. 
                                    197.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Veiga-da-Cunha, Maria
                                    
                                    Collet, Jean-François
                                    
                                    Prieur, Benoît
                                    
                                    Jaeken, Jaak
                                    
                                    Peeraer, Yves
                                    
                                    Rabbijns, Anja
                                     and 
                                    Van Schaftingen, Emile
                                  2004.
                                  Mutations responsible for 3-phosphoserine phosphatase deficiency.
                                  
                                  
                                  European Journal of Human Genetics, 
                                  Vol. 12, 
                                  Issue. 2, 
                                
                                    p. 
                                    163.
                                
                                
                        
                        
                        
                        
                                
                                  2005.
                                  Magnetic Resonance of Myelination and Myelin Disorders.
                                  
                                  
                                  
                                  
                                  
                                
                                    p. 
                                    369.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Jaeken, Jaak
                                     and 
                                    de Koning, Tom J.
                                  2006.
                                  Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases.
                                  
                                  
                                  
                                  
                                  
                                
                                    p. 
                                    43.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Scolari, M. J.
                                     and 
                                    Acosta, G. B.
                                  2007.
                                  D-serine: a new word in the glutamatergic neuro-glial language.
                                  
                                  
                                  Amino Acids, 
                                  Vol. 33, 
                                  Issue. 4, 
                                
                                    p. 
                                    563.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Hart, Claire E.
                                    
                                    Race, Valerie
                                    
                                    Achouri, Younes
                                    
                                    Wiame, Elsa
                                    
                                    Sharrard, Mark
                                    
                                    Olpin, Simon E.
                                    
                                    Watkinson, Jennifer
                                    
                                    Bonham, James R.
                                    
                                    Jaeken, Jaak
                                    
                                    Matthijs, Gert
                                     and 
                                    Van Schaftingen, Emile
                                  2007.
                                  Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway.
                                  
                                  
                                  The American Journal of Human Genetics, 
                                  Vol. 80, 
                                  Issue. 5, 
                                
                                    p. 
                                    931.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Tohyama, Jun
                                    
                                    Akasaka, Noriyuki
                                    
                                    Osaka, Hitoshi
                                    
                                    Maegaki, Yoshihiro
                                    
                                    Kato, Mitsuhiro
                                    
                                    Saito, Naka
                                    
                                    Yamashita, Sumimasa
                                     and 
                                    Ohno, Kousaku
                                  2008.
                                  Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter.
                                  
                                  
                                  Brain and Development, 
                                  Vol. 30, 
                                  Issue. 5, 
                                
                                    p. 
                                    349.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Tabatabaie, L.
                                    
                                    Klomp, L.W.
                                    
                                    Berger, R.
                                     and 
                                    de Koning, T.J.
                                  2010.
                                  l-Serine synthesis in the central nervous system: A review on serine deficiency disorders.
                                  
                                  
                                  Molecular Genetics and Metabolism, 
                                  Vol. 99, 
                                  Issue. 3, 
                                
                                    p. 
                                    256.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Chan, Derrick Wei Shih
                                    
                                    Tan, Ee Shien
                                     and 
                                    Cleary, Maureen Anne
                                  2010.
                                  Neonatal Seizures: When to Consider and How to Investigate for an Inborn Error of Metabolism.
                                  
                                  
                                  Proceedings of Singapore Healthcare, 
                                  Vol. 19, 
                                  Issue. 2, 
                                
                                    p. 
                                    112.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Ozeki, Yuji
                                    
                                    Pickard, Benjamin S.
                                    
                                    Kano, Shin-ichi
                                    
                                    Malloy, Mary P.
                                    
                                    Zeledon, Mariela
                                    
                                    Sun, Daniel Q.
                                    
                                    Fujii, Kumiko
                                    
                                    Wakui, Keiko
                                    
                                    Shirayama, Yukihiko
                                    
                                    Fukushima, Yoshimitsu
                                    
                                    Kunugi, Hiroshi
                                    
                                    Hashimoto, Kenji
                                    
                                    Muir, Walter J.
                                    
                                    Blackwood, Douglas H.
                                     and 
                                    Sawa, Akira
                                  2011.
                                  A novel balanced chromosomal translocation found in subjects with schizophrenia and schizotypal personality disorder: Altered l-serine level associated with disruption of PSAT1 gene expression.
                                  
                                  
                                  Neuroscience Research, 
                                  Vol. 69, 
                                  Issue. 2, 
                                
                                    p. 
                                    154.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Van Hove, Johan L.K.
                                     and 
                                    Lohr, Naomi J.
                                  2011.
                                  Metabolic and monogenic causes of seizures in neonates and young infants.
                                  
                                  
                                  Molecular Genetics and Metabolism, 
                                  Vol. 104, 
                                  Issue. 3, 
                                
                                    p. 
                                    214.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Wang, Raymond Y.
                                    
                                    Wilcox, William R.
                                     and 
                                    Cederbaum, Stephen D.
                                  2013.
                                  Emery and Rimoin's Principles and Practice of Medical Genetics.
                                  
                                  
                                  
                                  
                                  
                                
                                    p. 
                                    1.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Dulac, Olivier
                                    
                                    Plecko, Barbara
                                    
                                    Gataullina, Svetlana
                                     and 
                                    Wolf, Nicole I
                                  2014.
                                  Occasional seizures, epilepsy, and inborn errors of metabolism.
                                  
                                  
                                  The Lancet Neurology, 
                                  Vol. 13, 
                                  Issue. 7, 
                                
                                    p. 
                                    727.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    El-Hattab, Ayman W.
                                  2016.
                                  Serine biosynthesis and transport defects.
                                  
                                  
                                  Molecular Genetics and Metabolism, 
                                  Vol. 118, 
                                  Issue. 3, 
                                
                                    p. 
                                    153.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Benke, Paul J.
                                    
                                    Hidalgo, Ryan J.
                                    
                                    Braffman, Bruce H.
                                    
                                    Jans, Judith
                                    
                                    Gassen, Koen L.I. van
                                    
                                    Sunbul, Rawda
                                     and 
                                    El-Hattab, Ayman W.
                                  2017.
                                  Infantile Serine Biosynthesis Defect Due to Phosphoglycerate Dehydrogenase Deficiency: Variability in Phenotype and Treatment Response, Novel Mutations, and Diagnostic Challenges.
                                  
                                  
                                  Journal of Child Neurology, 
                                  Vol. 32, 
                                  Issue. 6, 
                                
                                    p. 
                                    543.
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Jia, Qiong
                                    
                                    Han, Yi
                                    
                                    Huang, Pin
                                    
                                    Woodward, Nicholas C.
                                    
                                    Gukasyan, Janet
                                    
                                    Kettunen, Johannes
                                    
                                    Ala‐Korpela, Mika
                                    
                                    Anufrieva, Olga
                                    
                                    Wang, Qin
                                    
                                    Perola, Markus
                                    
                                    Raitakari, Olli
                                    
                                    Lehtimäki, Terho
                                    
                                    Viikari, Jorma
                                    
                                    Järvelin, Marjo‐Riitta
                                    
                                    Boehnke, Michael
                                    
                                    Laakso, Markku
                                    
                                    Mohlke, Karen L.
                                    
                                    Fiehn, Oliver
                                    
                                    Wang, Zeneng
                                    
                                    Tang, W.H. Wilson
                                    
                                    Hazen, Stanley L.
                                    
                                    Hartiala, Jaana A.
                                     and 
                                    Allayee, Hooman
                                  2019.
                                  Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
                                  
                                  
                                  Journal of the American Heart Association, 
                                  Vol. 8, 
                                  Issue. 10, 
                                
                                
                                
                        
                        
                        
                        
                                
                                    
                                    Murtas, Giulia
                                    
                                    Marcone, Giorgia Letizia
                                    
                                    Sacchi, Silvia
                                     and 
                                    Pollegioni, Loredano
                                  2020.
                                  L-serine synthesis via the phosphorylated pathway in humans.
                                  
                                  
                                  Cellular and Molecular Life Sciences, 
                                  Vol. 77, 
                                  Issue. 24, 
                                
                                    p. 
                                    5131.
                                
                                
                        
                        
                        
                         
 