Results 121 to 130 of about 76,676 (194)

Methylmalonic Aciduria Due to Methylmalonyl-CoA Mutase Deficiency [PDF]

, 2020
openaire   +1 more source

A Methylmalonyl-CoA mutase in Escherichia coli?

, 1997
Roy, I., Leadlay, P.F.
core  

Inherited disorders of cobalamin metabolism in childhood: biochemical and clinical perspectives. [PDF]

Front Nutr
Saini AG, Gunasekaran PK, Prasad AN.
europepmc   +1 more source

Correction: Untargeted metabolomics reveals distinct metabolic profiles in MUT-type methylmalonic acidemia. [PDF]

Mol Cell Pediatr
Alsuhaymi S, AlMalki RH, Al Mogren M, Alodaib A, Emwas AH, Dasouki M, Alfares A, Jaremko M, Abdel Rahman AM.   +8 more
europepmc   +1 more source

The Dynamic Coenzyme Network of B Vitamins in Nutritional Neuropathy and Neuropsychiatric Vulnerability: A Mechanistic Narrative Review. [PDF]

Nutrients
Yoon Y, Hwang J, Park R, Shim J, Lam KHS, de Castro JC, Suryadi T, Suhaimi A, Yang CM.   +8 more
europepmc   +1 more source

Untargeted metabolomics reveals distinct metabolic profiles in MUT-type methylmalonic acidemia. [PDF]

Mol Cell Pediatr
Alsuhaymi S, AlMalki RH, Al Mogren M, Alodaib A, Emwas AH, Dasouki M, Alfares A, Jaremko M, Abdel Rahman AM.   +8 more
europepmc   +1 more source

Mutation analysis of methylmalonyl CoA mutase gene exon 2 in Egyptian families: Identification of 25 novel allelic variants. [PDF]

Meta Gene, 2015
Ghoraba DA, Mohammed MM, Zaki OK.
europepmc   +1 more source

Clinical, magnetic resonance imaging, and neuropathological features of suspected inborn methylmalonic aciduria in a domestic shorthair kitten. [PDF]

J Vet Intern Med
Fisher C, Degl'Innocenti S, Ortiz A, Major A, Rawson F, Scarin G, Fadda A.   +6 more
europepmc   +1 more source

Clinical and Genetic Characterization of Isolated Methylmalonic Acidemia in Malaysian Children: Identification of Two Novel <i>MMUT</i> Variants. [PDF]

Diagnostics (Basel)
Masri M, Khalid N, Salleh N, Lua SH, Abdul Azize NA, Yakob Y, Ali EZ, Munusamy VA, Ngu LH, Lee JS, Toh TH, Habib A.   +11 more
europepmc   +1 more source

Personalized Genome-Scale Modeling Reveals Metabolic Perturbations in Fibroblasts of Methylmalonic Aciduria Patients. [PDF]

J Inherit Metab Dis
Heinken A, Awada H, Zanotelli VRT, Froese DS, Guéant-Rodriguez RM, Guéant JL.   +5 more
europepmc   +1 more source