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Latest Publications and Research on Creatine Supplementation


Sports (Basel)      

Effects of Creatine Supplementation on Lower-Limb Muscle Endurance Following an Acute Bout of Aerobic Exercise in Young Men.

Vieira IP, de Paula AG, Gentil P, Pichard C, Candow DG, Pimentel GD

We aimed to determine whether creatine supplementation influences lower-limb muscle endurance following an acute bout of aerobic exercise (AE) in youn ... Read More

Source: PubMed
Am. J. Nephrol.      

Calcium-Alkali Syndrome Associated with Hypoparathyroidism Following Total Thyroidectomy.

Kuroya S, Yazawa M, Shibagaki Y, Tominaga N

Patients with permanent postsurgical hypoparathyroidism, a complication of total thyroidectomy, often require high calcium supplementation with vitami ... Read More

Source: PubMed
Biomolecules      

Long-Term Effect of Combination of Creatine Monohydrate Plus ß-Hydroxy ß-Methylbutyrate (HMB) on Exercise-Induced Muscle Damage and Anabolic/Catabolic Hormones in Elite Male Endurance Athletes.

Fernández-Landa J, Fernández-Lázaro D, Calleja-González J, Caballero-García A, Córdova A, León-Guereño P, Mielgo-Ayuso J

Creatine monohydrate (CrM) and ß-hydroxy ß-methylbutyrate (HMB) are widely studied ergogenic aids. However, both supplements are usually studied in an ... Read More

Source: PubMed
Nutrients      

Effect of Ten Weeks of Creatine Monohydrate Plus HMB Supplementation on Athletic Performance Tests in Elite Male Endurance Athletes.

Fernández-Landa J, Fernández-Lázaro D, Calleja-González J, Caballero-García A, Córdova Martínez A, León-Guereño P, Mielgo-Ayuso J

Creatine monohydrate (CrM) and ß-hydroxy ß-methylbutyrate (HMB) are common ergogenic aids in the field of sports and are frequently used in an isolate ... Read More

Source: PubMed
Case Rep Crit Care      

Myogenic Disease and Metabolic Acidosis: Consider Multiple Acyl-Coenzyme A Dehydrogenase Deficiency.

Dernoncourt A, Bouchereau J, Acquaviva-Bourdain C, Wicker C, De Lonlay P, Gourguechon C, Sevestre H, Merle PE, Maizel J, Brault C

Multiple acyl-coA dehydrogenase deficiency (MADD) is a rare, inherited, autosomal-recessive disorder leading to the accumulation of acylcarnitine of a ... Read More

Source: PubMed
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