Results 51 to 60 of about 1,020 (91)

Mitochondrial DNA release and inflammation in mitochondrial disease pathogenesis. [PDF]

Brain
Szabo M, Lagos D, Cross E, Collier JJ, Horvath R.   +4 more
europepmc   +1 more source

Carnitine-acylcarnitine translocase deficiency: a case report with autopsy. [PDF]

Autops Case Rep
Thunga C, Mitra S, Dayal D, Lal S.
europepmc   +1 more source

Editorial: Inborn errors of carbohydrate metabolism. [PDF]

Front Genet
Martínez-Duncker I, Doederlein-Schwartz IV, Abreu-González M, García-Ortiz JE.   +3 more
europepmc   +1 more source

Cellular and organismal function of choline metabolism. [PDF]

Nat Metab
Kenny TC, Scharenberg S, Abu-Remaileh M, Birsoy K.   +3 more
europepmc   +1 more source

Kidney lipid metabolism: impact on pediatric kidney diseases and modulation by early-life nutrition. [PDF]

Pediatr Nephrol
Nüsken E, Voggel J, Saschin L, Weber LT, Dötsch J, Alcazar MAA, Nüsken KD.   +6 more
europepmc   +1 more source

Quo vadis ureagenesis disorders? A journey from 90 years ago into the future. [PDF]

J Inherit Metab Dis
Häberle J, Siri B, Dionisi-Vici C.
europepmc   +1 more source

L-carnitine for valproic acid-induced toxicity. [PDF]

Br J Clin Pharmacol
Gziut T, Thanacoody R.
europepmc   +1 more source

Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose-galactose transporter SLC5A1. [PDF]

Front Pediatr
López-Mejía L, Guillén-Lopez S, Vela-Amieva M, Santillán-Martínez R, Abreu M, González-Herrra MD, Díaz-Martínez R, Reyes-Magaña JG.   +7 more
europepmc   +1 more source

Hyperoxaluria: Diagnosis and Treatment. [PDF]

Urol Clin North Am
Cunneely OP, Camargo Maluf F, Fargue S, Knight J, Assimos DG, Wood KD.   +5 more
europepmc   +1 more source

Recent research advances in the biological function and molecular mechanism of methylmalonic acid. [PDF]

J Zhejiang Univ Sci B
Wang Z, Cheng W, Wang T, Zhang Y, Shi X, Lv Y, Jin J.   +6 more
europepmc   +1 more source