Search Results - "BRAUNLIN, E"
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Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy
Published in Journal of inherited metabolic disease (01-03-2013)“…Characteristic cardiac valve abnormalities and left ventricular hypertrophy are present in untreated patients with mucopolysaccharidosis type VI (MPS VI)…”
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2
Increased longevity and metabolic correction following syngeneic BMT in a murine model of mucopolysaccharidosis type I
Published in Bone marrow transplantation (Basingstoke) (01-09-2012)“…Mucopolysaccharidosis type I (MPS I) is an autosomal recessive inherited disease caused by deficiency of the glycosidase α- L -iduronidase (IDUA). Deficiency…”
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3
Pre-transplant risk factors affecting outcome in Hurler syndrome
Published in Bone marrow transplantation (Basingstoke) (01-07-2010)“…Allogeneic transplantation remains the standard of care for patients with Hurler syndrome. As enzyme replacement therapy (ERT) has become available,…”
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4
Continued neurocognitive development and prevention of cardiopulmonary complications after successful BMT for I-cell disease: a long-term follow-up report
Published in Bone marrow transplantation (Basingstoke) (01-11-2003)“…I-cell disease or mucolipidosis type II, a rare inherited storage disorder of lysosomal enzyme localization, is characterized by dysostosis multiplex,…”
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5
Short-Course Total Lymphoid Irradiation in Management of Pediatric Heart Transplant Rejection
Published in International journal of radiation oncology, biology, physics (01-11-2022)Get full text
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99 Treatment of multiple sulfatase deficiency with recombinant human arylsulfatase B
Published in Molecular genetics and metabolism (01-12-2007)Get full text
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7
Cardiac Ultrasound Findings in Infants with Severe (Hurler Phenotype) Untreated Mucopolysaccharidosis (MPS) Type I
Published in JIMD Reports - Volume 10 (01-01-2013)“…Background: Serious cardiac valve disease and left ventricular hypertrophy occur in most untreated older children with severe mucopolysaccharidosis type I…”
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Book Chapter Journal Article -
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Antibody response of pediatric solid organ transplant recipients to immunization against influenza virus
Published in The Journal of pediatrics (01-12-1995)“…We studied the immunogenicity of the 1992-1993 trivalent split-virus influenza vaccine in pediatric solid organ transplant recipients (PSOTRs) and their…”
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9
Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the hurler syndrome
Published in The American journal of cardiology (01-11-2001)“…The coronary arteries in a patient with the Hurler Syndrome appear only minimally affected by the deposition of glycosaminoglycans 14 years after successful…”
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10
Association of coronary artery disease in cardiac transplant recipients with cytomegalovirus infection
Published in The American journal of cardiology (01-08-1989)“…Coronary artery disease (CAD) is now the major limitation to long-term survival after cardiac transplantation. Its etiology remains unclear. The possible role…”
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11
Enhancing efficacy of stem cell transplantation to the heart with a PEGylated fibrin biomatrix
Published in Tissue engineering. Part A (01-06-2008)“…Bone marrow-derived mononuclear cell (BMNC) transplantation provides the possibility of rescue or regeneration of myocardium lost during acute myocardial…”
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12
Usefulness of surveillance endomyocardial biopsy after pediatric cardiac transplantation
Published in Clinical transplantation (01-06-1998)“…Endomyocardial biopsy remains the 'gold standard' for the diagnosis of acute rejection after cardiac transplantation, but few guidelines exist to determine the…”
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13
Open-lung biopsy guides therapy in children
Published in The Annals of thoracic surgery (01-06-2001)“…Background. Open-lung biopsy is uncommon in children. Modern indications and outcomes are unknown. Methods. This is a retrospective review of 64 open-lung…”
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14
Evaluation of coronary artery disease in the Hurler syndrome by angiography
Published in The American journal of cardiology (01-06-1992)“…Hurler syndrome (mucopolysaccharidosis type I-H) is an inherited lysosomal storage disease characterized by the widespread accumulation of mucopolysaccharide…”
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15
A randomized, double-blind trial of lisinopril and losartan for the treatment of cardiomyopathy in duchenne muscular dystrophy
Published in PLoS currents (12-12-2013)“…This study sought to compare the effectiveness and safety of an angiotensin converting enzyme inhibitor (ACE-I) (lisinopril) vs. an angiotensin receptor…”
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16
Coronary artery disease in pediatric cardiac transplant recipients receiving triple-drug immunosuppression
Published in Circulation (New York, N.Y.) (01-11-1991)“…Although triple-drug immunosuppression (cyclosporine, azathioprine, and prednisone) has reduced the incidence of acute rejection after pediatric cardiac…”
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17
Outcome after referral for pediatric transplantation
Published in The Journal of heart and lung transplantation (01-09-1993)“…Although heart, heart-lung, or lung transplantation is performed in more than 200 children annually, the number of patients referred for such procedures is…”
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18
Cytomegalovirus colitis in a pediatric heart transplant patient
Published in Clinical transplantation (01-08-1994)“…Cytomegalovirus colitis is one of the sequelae of cytomegalovirus infection in transplant patients and can be associated with severe consequences. This case…”
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19
Resting Tl-201 scintigraphy in the evaluation of coronary artery disease in children with Hurler syndrome
Published in Clinical nuclear medicine (01-11-1994)“…Severe coronary artery disease may occur early in the course of mucopolysaccharidosis. The authors present radiologic, scintigraphic, and pathologic findings…”
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20
Electrocardiographic changes during long-term follow-up of pediatric heart transplant recipients
Published in The American journal of cardiology (15-05-1993)“…Although pediatric cardiac transplantation has become a viable treatment modality, long-term follow-up of potential cardiac and noncardiac complications is…”
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