Authors: DEMEIRLEIR L LISSENS W BENELLI C MARSAC C DEKLERK J SCHOLTE J VANDIGGELEN O KLEIJER W SENECA S LIEBAERS I

Citation: L. Demeirleir et al., PYRUVATE-DEHYDROGENASE COMPLEX DEFICIENCY AND ABSENCE OF SUBUNIT-X, Journal of inherited metabolic disease, 21(1), 1998, pp. 9-16

Authors: LISSENS W DEMEIRLEIR L SENECA S BENELLI C MARSAC C POLLTHE BT BRIONES P RUITENBEEK W VANDIGGELEN O CHAIGNE D RAMAEKERS V LIEBAERS I

Citation: W. Lissens et al., MUTATION ANALYSIS OF THE PYRUVATE-DEHYDROGENASE E(1)ALPHA GENE IN 8 PATIENTS WITH A PYRUVATE-DEHYDROGENASE COMPLEX DEFICIENCY, Human mutation, 7(1), 1996, pp. 46-51

Authors: WOKKE JHJ AUSEMS MGEM VANDENBOOGAARD MJH IPPEL EF VANDIGGELEN O KROOS MA BOER M JENNEKENS FGI REUSER AJJ VANAMSTEL HKP

Citation: Jhj. Wokke et al., GENOTYPE-PHENOTYPE CORRELATION IN ADULT-ONSET ACID MALTASE DEFICIENCY, Annals of neurology, 38(3), 1995, pp. 450-454

Authors: DEJONG J VANDENBERG C WIJBURG H WILLEMSEN R VANDIGGELEN O SCHINDLER D HOEVENAARS F WEVERS R

Citation: J. Dejong et al., ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY WITH MILD CLINICAL MANIFESTATIONS AND DIFFICULT BIOCHEMICAL-DIAGNOSIS, The Journal of pediatrics, 125(3), 1994, pp. 385-391