Results 281 to 290 of about 911,999 (359)

American Agriculture, 1899-1939: A Study of Output, Employment and Productivity [PDF]

Hans H. Landsberg, Harold Barger
core  

Carnitine Deficiency Caused by Salcaprozic Acid Sodium Contained in Oral Semaglutide in a Patient with Multiple Acyl-CoA Dehydrogenase Deficiency. [PDF]

Int J Mol Sci
Mikami-Saito Y, Maekawa M, Watanabe M, Hosaka S, Takahashi K, Totsune E, Arai-Ichinoi N, Kikuchi A, Kure S, Katagiri H, Wada Y.   +10 more
europepmc   +1 more source

Practical supplements for prevention and management of migraine attacks: a narrative review. [PDF]

Front Nutr
Hajhashemy Z, Golpour-Hamedani S, Eshaghian N, Sadeghi O, Khorvash F, Askari G.   +5 more
europepmc   +1 more source

Metabolic Profile of Histomonas meleagridis in Dwyer's Media with and Without Rice Starch. [PDF]

Metabolites
Ammar S, Christopher CJ, Szafranski N, Jones R, Rajeev S, Castro HF, Campagna SR, Gerhold R.   +7 more
europepmc   +1 more source

Dihydrolipoamide dehydrogenase deficiency in five siblings with variable phenotypes, including fulminant fatal liver failure despite good engraftment of transplanted liver. [PDF]

JIMD Rep
Mihaljević M, Petković Ramadža D, Žigman T, Rako I, Galić S, Matić T, Rubić F, Čulo Čagalj I, Mayer D, Gojević A, Ćavar S, Ćorić M, Achleitner MT, Mayr JA, Fumić K, Vuković J, Barić I.   +16 more
europepmc   +1 more source

ETFDH mutation involves excessive apoptosis and neurite outgrowth defect via Bcl2 pathway. [PDF]

Sci Rep
Lin CY, Liang WC, Yu YC, Chang SC, Lai MC, Jong YJ.   +5 more
europepmc   +1 more source

MADD-like pattern of acylcarnitines associated with sertraline use. [PDF]

Mol Genet Metab Rep
Ingoglia F, Tanfous M, Ellezam B, Anderson KJ, Pasquali M, Botto LD.   +5 more
europepmc   +1 more source

The Nutrient-Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs. [PDF]

Nutrients
Rallis E, Lotsaris K, Grech VS, Tertipi N, Sfyri E, Kefala V.   +5 more
europepmc   +1 more source

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Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2

IUBMB Life - A Journal of the International Union of Biochemistry and Molecular Biology, 2021
Riboflavin transporter deficiency 2 (RTD2) is a rare neurological disorder caused by mutations in the Solute carrier family 52 member 2 (Slc52a2) gene encoding human riboflavin transporter 2 (RFVT2).
Lara Console, M. Tolomeo, J. Cosco, K. Massey, M. Barile, C. Indiveri   +5 more
semanticscholar   +1 more source