PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Žigman, T.* et al. ATP synthase deficiency due to m.8528T>C mutation - A novel cause of severe neonatal hyperammonemia requiring hemodialysis. J. Pediatr. Endocrinol. Metab. 34, 389-393 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60606&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60606&la=de Mon, 30 Nov 2020 00:00:00 +0000 <![CDATA[Steichen-Gersdorf, E.* ; Lorenz-Depiereux, B. ; Strom, T.M. & Shaw, N.J.* Early onset hearing loss in autosomal recessive hypophosphatemic rickets caused by loss of function mutation in ENPP1. J. Pediatr. Endocrinol. Metab. 28, 967-970 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44450&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44450&la=de Wed, 22 Apr 2015 00:00:00 +0000 <![CDATA[Hinney, A.* et al. No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children. J. Pediatr. Endocrinol. Metab. 26, 1209-1213 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28106&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28106&la=de Wed, 06 Nov 2013 00:00:00 +0000 <![CDATA[Lombardo, F.* et al. Clinical picture, evolution and peculiar molecular findings in a very large pedigree with Wolfram syndrome. J. Pediatr. Endocrinol. Metab. 18, 1391-1397 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2175&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2175&la=de Wed, 05 Jul 2006 00:00:00 +0000