1-year left ventricular assist device (LVAD) experience as bridge to heart transplantation in an infant with Bland-White-Garland syndrome.

PubWeight™: 0.87‹?›

🔗 View Article (PMID 20101533)

Published in Thorac Cardiovasc Surg on January 25, 2010

Authors

D Stege1, D Kiski, T Tjan, B Wolf, H H Scheld, H G Kehl

Author Affiliations

1: Department of Pediatric Cardiology, University Hospital Muenster, Albert-Schweitzer-Strasse 33, Muenster, Germany. Dirk.Stege@ukmuenster.de

Articles by these authors

(truncated to the top 100)

On the origin and direction of replication of the Escherichia coli K12 chromosome. J Mol Biol (1968) 3.46

Effect of receiving a heart transplant: analysis of a national cohort entered on to a waiting list, stratified by heart failure severity. Comparative Outcome and Clinical Profiles in Transplantation (COCPIT) Study Group. BMJ (2000) 2.69

Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency. Clin Chim Acta (1983) 2.17

Growth inhibition of human tumor cells in athymic mice by anti-epidermal growth factor receptor monoclonal antibodies. Cancer Res (1984) 2.17

[Anesthesia for minimal invasive coronary surgery without employing extracorporeal circulation]. Anasthesiol Intensivmed Notfallmed Schmerzther (1997) 2.01

[Efficacy of epidural steroid injections for chronic lumbar pain syndromes without neurological deficits. A randomized, double blind study as part of a multimodal treatment concept]. Schmerz (2015) 1.99

A qualitative study of physicians' own wellness-promotion practices. West J Med (2001) 1.88

Monitoring of cellular behaviour by impedance measurements on interdigitated electrode structures. Biosens Bioelectron (1997) 1.83

Phenotypic variation in biotinidase deficiency. J Pediatr (1983) 1.74

Comparative West Nile virus detection in organs of naturally infected American Crows (Corvus brachyrhynchos). Emerg Infect Dis (2001) 1.73

Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiency. Nat Genet (1995) 1.67

Biotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency. Biochem Mol Med (1995) 1.64

Expression of multiple functional chemokine receptors and monocyte chemoattractant protein-1 in human neurons. Neuroscience (2000) 1.61

Resistance to activated protein C (APCR) in children with venous or arterial thromboembolism. Br J Haematol (1996) 1.61

KRAS status and outcome of liver resection after neoadjuvant chemotherapy including bevacizumab. Br J Surg (2012) 1.60

The characteristics and genetic map location of a temperature sensitive DNA mutant of E. coli K12. Genetics (1972) 1.55

Immunoglobulin determinants on the lymphocytes of normal rabbits. 3. As4 and As6 determinants on individual lymphocytes and the concept of allelic exclusion. Immunology (1971) 1.54

Intraoperative radiofrequency ablation of chronic atrial fibrillation: a left atrial curative approach by elimination of anatomic "anchor" reentrant circuits. J Cardiovasc Electrophysiol (1999) 1.52

A screening method for biotinidase deficiency in newborns. Clin Chem (1984) 1.46

Relative abuse liability of different benzodiazepines in drug abusers. J Clin Psychopharmacol (1990) 1.45

Lack of prognostic significance of p53 and K-ras mutations in primary resected non-small-cell lung cancer on E4592: a Laboratory Ancillary Study on an Eastern Cooperative Oncology Group Prospective Randomized Trial of Postoperative Adjuvant Therapy. J Clin Oncol (2001) 1.45

Ex situ resection of primary cardiac tumors. Thorac Cardiovasc Surg (2003) 1.42

Structural transitions of deoxyribonucleic acid in aqueous electrolyte solutions. II. The role of hydration. Biochemistry (1975) 1.39

Ligament length patterns, strength, and rotational axes of the knee joint. Clin Orthop Relat Res (1976) 1.39

Patients with valvular heart disease presenting with sustained ventricular tachyarrhythmias or syncope: results of programmed ventricular stimulation and long-term follow-up. Circulation (1997) 1.39

Creation of a self-made total artificial heart using combined components of available ventricular assist devices. Thorac Cardiovasc Surg (2008) 1.39

Non-destructive evaluation of prosthetic heart valves by holographic interferometry. J Heart Valve Dis (1993) 1.38

Clinical relevance of intracranial microembolic signals in patients with left ventricular assist devices. A prospective study. Stroke (1996) 1.37

Diagnosis and treatment of nonocclusive mesenteric ischemia after open heart surgery. Ann Thorac Surg (2001) 1.32

Radical resection of cardiac sarcoma. Thorac Cardiovasc Surg (2004) 1.31

Impact of malignant hematological disorders on cardiac surgery. Cardiovasc Surg (2000) 1.30

Biotinidase deficiency: initial clinical features and rapid diagnosis. Ann Neurol (1985) 1.26

On the origin and direction of replication of the E. coli chromosome. Cold Spring Harb Symp Quant Biol (1968) 1.26

Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy. Ann Intern Med (1992) 1.25

Contralateral breast cancer: molecular differentiation between metastasis and second primary cancer. Breast Cancer Res Treat (2001) 1.25

Biochemical differences between mutant propionyl-CoA carboxylases from two complementation groups. Am J Hum Genet (1978) 1.25

Clinical heterogeneity in 80 home-reared children with cri du chat syndrome. J Pediatr (1983) 1.24

Structure of the human biotinidase gene. Mamm Genome (1998) 1.23

Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibship. Am J Med Genet (1981) 1.21

Mutations in the human biotinidase gene that cause profound biotinidase deficiency in symptomatic children: molecular, biochemical, and clinical analysis. Pediatr Res (1997) 1.20

Expression pattern of heme oxygenase isoenzymes 1 and 2 in normal and stress-exposed rat liver. Hepatology (1998) 1.20

The biotin-dependent carboxylase deficiencies. Am J Hum Genet (1982) 1.19

Impact of particle size distribution on rheological and textural properties of chocolate models with reduced fat content. J Food Sci (2007) 1.18

New low resolution model for 50S subunit of Escherichia coli ribosomes. Proc Natl Acad Sci U S A (1976) 1.18

Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups. J Clin Invest (1978) 1.18

Structural transitions of deoxyribonucleic acid in aqueous electrolyte solutions. I. Reference spectra of conformational limits. Biochemistry (1975) 1.17

Surgical management of extensive lipomatous hypertrophy of the right atrium. Cardiovasc Surg (2000) 1.16

Mutations in BTD causing biotinidase deficiency. Hum Mutat (2001) 1.16

Effect of a high loading dose of clopidogrel on platelet function in patients undergoing coronary stent placement. Heart (2001) 1.16

Leiomyosarcoma of the pulmonary artery--a diagnostic chameleon. Eur J Cardiothorac Surg (2001) 1.16

Expression of the c-erbB-2 gene product (p185) at different stages of neoplastic progression in the colon. Oncogene (1989) 1.15

Incidence and pathogenesis of late aneurysms after patch graft aortoplasty for coarctation. J Thorac Cardiovasc Surg (1986) 1.14

Human serum biotinidase. cDNA cloning, sequence, and characterization. J Biol Chem (1994) 1.12

Single-incision implantation of cardioverter defibrillators using nonthoracotomy lead systems. Ann Thorac Surg (1994) 1.12

Mixed conformations of deoxyribonucleic acid in chromatin: a preliminary report. Proc Natl Acad Sci U S A (1972) 1.12

Deficient biotinidase activity in late-onset multiple carboxylase deficiency. N Engl J Med (1983) 1.12

Biotinidase and its roles in biotin metabolism. Clin Chim Acta (1996) 1.12

Low-dose caffeine discrimination in humans. J Pharmacol Exp Ther (1990) 1.11

Implantable cardioverter defibrillator therapy in patients with arrhythmogenic right ventricular cardiomyopathy, long QT syndrome, or no structural heart disease. Am Heart J (1994) 1.09

Preparation of polymeric protein markers and an investigation of their behavior in sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Biochim Biophys Acta (1970) 1.09

Workshop on inborn errors of metabolism. Prog Clin Biol Res (1982) 1.09

Biphasic defibrillation using a single capacitor with large capacitance: reduction of peak voltages and ICD device size. Pacing Clin Electrophysiol (1996) 1.08

Phospholipid hydroperoxide glutathione peroxidase is a selenoenzyme distinct from the classical glutathione peroxidase as evident from cDNA and amino acid sequencing. Free Radic Res Commun (1991) 1.07

Biotinidase deficiency: accumulation of lactate in the brain and response to physiologic doses of biotin. Neurology (1986) 1.07

Impact of preoperative bimodality induction including twice-daily radiation on tumor regression and survival in stage III non-small-cell lung cancer. J Clin Oncol (1999) 1.06

The spectrum of neurologic disorder from vitamin E deficiency. Neurology (1986) 1.06

Psychomotor development in 65 home-reared children with cri-du-chat syndrome. J Pediatr (1980) 1.05

Adverse drug reactions. An epidemiological study at psychiatric hospitals. Acta Psychiatr Scand (1984) 1.05

Pulmonary manifestations in HIV seropositivity and malnutrition in Zimbabwe. Arch Dis Child (1997) 1.05

Neoplastic heart disease -- the Muenster experience with 108 patients. Thorac Cardiovasc Surg (2005) 1.04

Fetoscopic transesophageal electrocardiography and stimulation in fetal sheep: a minimally invasive approach aimed at diagnosis and termination of therapy-refractory supraventricular tachycardias in human fetuses. Circulation (1999) 1.04

Coexistence of non-Hodgkin's lymphoma and non-small cell lung carcinoma: diagnosis and treatment. Thorac Cardiovasc Surg (2002) 1.04

Low-dose caffeine physical dependence in humans. J Pharmacol Exp Ther (1990) 1.04

Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program. N Engl J Med (1985) 1.03

Neurologic symptoms of biotinidase deficiency: possible explanation. Neurology (1985) 1.03

Noncardiac surgery in patients with left ventricular assist devices. Surgery (2001) 1.01

Mutations causing profound biotinidase deficiency in children ascertained by newborn screening in the United States occur at different frequencies than in symptomatic children. Pediatr Res (1999) 1.01

Emergency coronary artery bypass grafting after failed coronary angioplasty: what has changed in a decade? Ann Thorac Surg (2000) 1.00

Diagnosis, treatment and outcome of patients with Askin-tumors. Thorac Cardiovasc Surg (2000) 0.99

Stain intensity of human nucleolus organizer region reflects incorporation of uridine into mature ribosomal RNA. Exp Cell Res (1983) 0.99

An unusual case of splenic abscess and sepsis in an immunocompromised host. Am J Clin Pathol (1987) 0.99

Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis (1992) 0.98

Nonketotic hyperglycinemia in two retarded adults: a mild form of infantile nonketotic hyperglycinemia. Neurology (1983) 0.97

Partial biotinidase deficiency is usually due to the D444H mutation in the biotinidase gene. Hum Genet (1998) 0.97

Left ventricular assist device infection is associated with increased mortality but is not a contraindication to transplantation. Circulation (1997) 0.97

EEG complexity and performance measures of creative thinking. Psychophysiology (1999) 0.97

Biotinidase deficiency: a novel vitamin recycling defect. J Inherit Metab Dis (1985) 0.96

Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts. Am J Hum Genet (1980) 0.95

Ophthalmologic findings in biotinidase deficiency. Ophthalmologica (1993) 0.95

Partial biotinidase deficiency: clinical and biochemical features. J Pediatr (1990) 0.95

Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States. Biochem Mol Med (1997) 0.95

Sex mismatch in heart transplantation is associated with increased number of severe rejection episodes and shorter long-term survival. Transplant Proc (2009) 0.95

A mechanism of the irreversible inactivation of bovine pancreatic ribonuclease by diethylpyrocarbonate. A general reaction of diethylpyrocarbonate . A general reaction of diethylpyrocarbonate with proteins. Eur J Biochem (1970) 0.95

Multimodal fetal transesophageal echocardiography for fetal cardiac intervention in sheep. Circulation (2001) 0.95

Helical CT of pulmonary nodules in patients with extrathoracic malignancy: CT-surgical correlation. AJR Am J Roentgenol (1999) 0.94

Deficient acetyl CoA carboxylase activity in multiple carboxylase deficiency. Clin Chim Acta (1981) 0.94

Identification of an abundant S-thiolated rat liver protein as carbonic anhydrase III; characterization of S-thiolation and dethiolation reactions. Arch Biochem Biophys (1991) 0.94

Minimally-invasive versus conventional aortic valve replacement--perioperative course and mid-term results. Eur J Cardiothorac Surg (1999) 0.94

Propionic acidemia: a clinical update. J Pediatr (1981) 0.94

Operative techniques and strategies for minimally invasive fetoscopic fetal cardiac interventions in sheep. Surg Endosc (2000) 0.93