Žigman, T.* ; Šikić, K.* ; Petković Ramadža, D.* ; Mayr, J.* ; Wortmann, S.* ; Prokisch, H. ; Ninković, D.* ; Dilber, D.* ; Šarić, D.* ; Rubić, F.* ; Galić, S.* ; Slaviček, J.* ; Belina, D.* ; Fumić, K.* ; Barić, I.*
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)
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)
Hinney, A.* ; Wolters, B.* ; Pütter, C.* ; Grallert, H. ; Illig, T. ; Hebebrand, J.* ; Reinehr, T.*
No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children.
J. Pediatr. Endocrinol. Metab. 26, 1209-1213 (2013)
Nitsche, H.* ; Nitsche, M.* ; Sudi, K.* ; Tschöp, M.H. ; Zotter, H.* ; Weinhand, G.* ; Froehlich-Reiterer, E.E.* ; Gallistl, S.* ; Pirker, M.* ; Borkenstein, M.*
Ghrelin--an indicator for fat oxidation in obese children and adolescents during a weight reduction program.
J. Pediatr. Endocrinol. Metab. 20, 719-723 (2007)
Lombardo, F.* ; Chiurazzi, P.* ; Hörtnagel, K. ; Arrigo, T.* ; Valenzise, M.* ; Meitinger, T. ; Messina, M.F.* ; Salzano, G.* ; Barberi, I.* ; de Luca, F.*
Clinical picture, evolution and peculiar molecular findings in a very large pedigree with Wolfram syndrome.
J. Pediatr. Endocrinol. Metab. 18, 1391-1397 (2005)