acidosis/phosphatase

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Noninferiority Trial of Liquid Human Milk Fortifier (HMF) Hydrolyzed Protein Versus Liquid HMF With Supplemental Liquid Protein

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All infants admitted to the Neonatal Intensive Care Unit (NICU) at Cardinal Glennon at gestational age <32 weeks and birthweight <1500g, and whose mothers intend to use breast milk (maternal or donor) will be approached for study participation. Infants can be enrolled at any point up until their

Exercise in Type 1 Diabetes Mellitus

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1.1. Pathophysiology of type 1 diabetes mellitus Type 1 diabetes mellitus (T1DM) is an metabolic disease with insulin deficiency and a dysfunctional release of counter regulatory hormone glucagon. In the pathogenesis of T1DM autoantibodies to insulin (IAA), Glutamic Acid Decarboxylase Antibody

Correction of Metabolic Acidosis in End Stage Renal Disease (ESRD)

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Rationale: Chronic Kidney Disease (CKD) is associated with a high incidence of morbility and mortality. In this regard, the National Health and Nutrition Examination Survey (NANHES) shows that 19% of the uremic population presents metabolic acidosis (CKD stage 4). This high prevalence and the low

Randomized Multicenter Cross-over Study to Compare the Effect of Physioneal 35 to 40 on the Protein Metabolism

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- Fat oxidation (13C-enrichment in expiration breath samples for U-C13-algae turnover) - Growth markers (plasma levels of IgF-1, IgF-BP3, leptin) - Biochemical markers of anabolism (plasma levels of total protein, albumin, transferrin) - Serum thyroid function (fT3, fT4, TSH) - Serum lipid status -

The Effects of Potassium Citrate on Bone Metabolism

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Participants were recruited from a single academic center. Subjects underwent screening at the Clinical Translational Science Center (CTSC) at Weill Cornell Medical College (WCMC). Study visits occurred at the CTSC where investigators administered and monitored questionnaires, compliance, adverse

Quetiapine Treatment for Symptoms Associated With Borderline Personality Disorder

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Study Design: A six week, open-label, flexible dosing study using quetiapine. Subjects who qualify at Screening will then proceed to the baseline visit. If all inclusion and exclusion criteria are met, subjects will be administered quetiapine at the baseline visit. Enrollment will be 15 subjects.

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