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9,429 Possible Causes for Enzyme, Replacement, Therapies

  • Congenital Sucrase-Isomaltase Deficiency

    Six cases of congenital SI deficiency treated with Sucraid (sacrosidase, a yeast-derived enzyme that facilitates sucrose digestion) are described.[] Therapy relies on dietary adjustments and enzyme replacement.[] BACKGROUND & AIMS: Congenital sucrase-isomaltase deficiency (CSID) is an autosomal recessive human disorder characterized by reduced activities of the brush border enzyme[]

  • Influenza

    BACKGROUND: Natalizumab (NTZ) is an effective therapy for multiple sclerosis (MS).[] IgG1, IgG2, IgG3, and IgG4 anti-influenza titers were also evaluated by enzyme-linked immunosorbent assay (ELISA).[] In this commentary, we discuss some important aspects that policymakers in LMICs might wish to take into account when considering replacing TIV by QIV.[]

  • Gaucher Disease Type 1

    BACKGROUND: Gaucher disease type 1 (GD1) was the first lysosomal storage disorder for which an effective enzyme replacement therapy was developed.[] Within 8 years of enzyme replacement therapy, most clinical parameters studied became normal or nearly normal.[] […] and for potential alternative future therapies for Gaucher disease.[]

  • Acute Gastroenteritis

    […] for observation during therapy, and which ones should immediately receive more intensive therapy.[] Stool was tested for presence of rotavirus using an enzyme immunoassay kit.[] The patient had experienced two episodes of quadriparesis within a short interval and responded dramatically to potassium replacement therapy.[]

  • Pneumonia

    […] as well as respiratory support with extracorporeal membrane oxygenation therapy.[] Age of onset, liver enzymes, pulmonary inflammation, and pneumonia absorption were not different between groups.[] It is not intended to replace the advice of your own physician. Contact your physician if you believe you have a health problem.[]

  • Osteoporosis

    […] the important role of autophagy in the pathogenesis of GIOP, here we review the potential mechanisms about the impacts of autophagy in GIOP and its association with GIOP therapy[] Her hepatic enzyme levels returned to nearly normal range 9 days post-infusion.[] Fluticasone was suspended and oral corticosteroid replacement initiated, with a favourable outcome. 2015 BMJ Publishing Group Ltd.[]

  • Adrenal Insufficiency

    We review the management of current standard MC replacement therapy in PAI and its plausible impact on outcome.[] Patients with partial deficiencies of steroidogenic enzymes are at risk to be misdiagnosed if adrenal function is not assessed.[] […] spectrum of genetic defects has increased in recent years with the use of next-generation sequencing methods and now has reached far beyond genetic defects in all known enzymes[]

  • Gaucher Disease Type 3

    KEYWORDS: Enzyme replacement therapy; Gaucher disease type 3; intraocular lesions; neuronopathic; optical coherence tomography; retina[] A Caucasian male with Gaucher disease type 3, treated with continuous enzyme therapy (ET) for 11 years, experienced progressive mesenteric and retroperitoneal lymphadenopathy[] Abstract Exogenous enzyme replacement therapy achieves satisfactory biomedical correction in Gaucher type 1 disease and may halt or reverse neurological progression in type[]

  • Salmonella Infection

    Although antimicrobial therapy is usually not indicated for uncomplicated Salmonella gastroenteritis, recent studies indicated that a short-course ceftriaxone therapy (3-5[] With initiation of enzyme replacement therapy (ERT) in addition to specific antibiotic treatment, defervescence and gradual healing occurred.[] We present an interesting case report of an infected revision total knee replacement following foreign travel to a region with an increased prevalence of Salmonella.[]

  • Urinary Tract Infection

    This study highlights the importance of monitoring local resistance rates and its risk factors in order to improve empiric therapy in a local environment.[] The productions of these enzymes cause bacterial resistance to a wide range of antibiotics.[] It is not intended to replace clinical judgment or to establish an exclusive protocol for the care of all children with this condition.[]