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  2. Carnitine - Wikipedia

    en.wikipedia.org/wiki/Carnitine

    Carnitine has no effect on most parameters in end-stage kidney disease, although it may lower C-reactive protein, a biomarker for systemic inflammation. [26] Carnitine blood levels and muscle stores can become low, which may contribute to anemia , muscle weakness, fatigue, altered levels of blood fats, and heart disorders. [ 1 ]

  3. Gamma-butyrobetaine dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Gamma-butyrobetaine_di...

    Gamma-butyrobetaine dioxygenase (also known as BBOX, GBBH or γ-butyrobetaine hydroxylase) is an enzyme that in humans is encoded by the BBOX1 gene. [5] [6] Gamma-butyrobetaine dioxygenase catalyses the formation of L-carnitine from gamma-butyrobetaine, the last step in the L-carnitine biosynthesis pathway. [7]

  4. Oculocerebrorenal syndrome - Wikipedia

    en.wikipedia.org/wiki/Oculocerebrorenal_syndrome

    While not present at birth, kidney problems develop in many affected boys at about one year of age. [1] Renal pathology is characterized by an abnormal loss of certain substances into the urine, including bicarbonate, sodium, potassium, amino acids, organic acids, albumin, calcium and L-carnitine. This problem is known as Fanconi-type renal ...

  5. Glycine propionyl-L-carnitine - Wikipedia

    en.wikipedia.org/wiki/Glycine_propionyl-l-carnitine

    In other studies, GPLC has been shown to have no effect on aerobic and anaerobic exercise performance, with results showing that up to 3 grams per day for 8 weeks in conjunction with aerobic-exercise training is ineffective for increasing muscle carnitine content and has no significant effects on aerobic- or anaerobic-exercise performance. [7]

  6. Systemic primary carnitine deficiency - Wikipedia

    en.wikipedia.org/wiki/Systemic_primary_carnitine...

    The presentation of patient with SPCD can be incredibly varied, from asymptomatic to lethal cardiac manifestations. [5] Early cases were reported with liver dysfunction, muscular findings (weakness and underdevelopment), hypoketotic hypoglycemia, cardiomegaly, cardiomyopathy and marked carnitine deficiency in plasma and tissues, combined with increased excretion in urine. [5]

  7. Propionic acidemia - Wikipedia

    en.wikipedia.org/wiki/Propionic_acidemia

    Patients with propionic acidemia should be started as early as possible on a low protein diet. In addition to a protein mixture that is devoid of methionine, threonine, valine, and isoleucine, the patient should also receive L-carnitine treatment and should be given antibiotics 10 days per month in order to remove the intestinal propiogenic ...

  8. Carnitine dehydratase - Wikipedia

    en.wikipedia.org/wiki/Carnitine_dehydratase

    In enzymology, a carnitine dehydratase (EC 4.2.1.89) is an enzyme that catalyzes the chemical reaction L-carnitine ⇌ {\displaystyle \rightleftharpoons } 4-(trimethylammonio)but-2-enoate + H 2 O Hence, this enzyme has one substrate , L-carnitine , and two products , 4-(trimethylammonio)but-2-enoate and H 2 O .

  9. Renal physiology - Wikipedia

    en.wikipedia.org/wiki/Renal_physiology

    This illustration demonstrates the normal kidney physiology, including the Proximal Convoluted Tubule (PCT), Loop of Henle, and Distal Convoluted Tubule (DCT). It also includes illustrations showing where some types of diuretics act, and what they do. Renal physiology (Latin renes, "kidneys") is the study of the physiology of the kidney.

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