Published in Pediatr Radiol on July 05, 2003
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Kirner deformity: a specific digital curvature abnormality. Pediatr Radiol (2004) 0.83
Kirner's deformity: progressiveness and classification. Surg Radiol Anat (2005) 0.75
Kirner's deformity of the fifth finger: a case report. BMC Musculoskelet Disord (2016) 0.75
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Multiple phenotypes in phosphoglucomutase 1 deficiency. N Engl J Med (2014) 2.62
Differentiation of malignant and benign cardiac tumors using 18F-FDG PET/CT. J Nucl Med (2012) 2.25
A gene encoding a putative FAD-dependent L-2-hydroxyglutarate dehydrogenase is mutated in L-2-hydroxyglutaric aciduria. Proc Natl Acad Sci U S A (2004) 2.19
Optimal systolic and diastolic reconstruction windows for coronary CT angiography using dual-source CT. AJR Am J Roentgenol (2007) 2.11
Methotrexate withdrawal at 6 vs 12 months in juvenile idiopathic arthritis in remission: a randomized clinical trial. JAMA (2010) 2.02
Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. J Pediatr (2004) 2.01
Phagocyte-specific calcium-binding S100 proteins as clinical laboratory markers of inflammation. Clin Chim Acta (2004) 1.87
Population dynamics of persistent Staphylococcus aureus isolated from the airways of cystic fibrosis patients during a 6-year prospective study. J Clin Microbiol (2003) 1.69
Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nat Genet (2009) 1.55
Diastolic isthmus length and 'vertical' isthmus angulation identify patients with difficult catheter ablation of typical atrial flutter: a pre-procedural MRI study. Europace (2008) 1.54
Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression. Hum Mutat (2010) 1.43
Giant cavernous haemangioma with Kasabach-Merritt syndrome: a case report and review. Eur J Pediatr (2002) 1.42
S100A12 is a novel molecular marker differentiating systemic-onset juvenile idiopathic arthritis from other causes of fever of unknown origin. Arthritis Rheum (2008) 1.33
Serial contrast-enhanced cardiac magnetic resonance imaging demonstrates regression of hyperenhancement within the coronary artery wall in patients after acute myocardial infarction. JACC Cardiovasc Imaging (2009) 1.32
MR imaging of thrombi using EP-2104R, a fibrin-specific contrast agent: initial results in patients. Eur Radiol (2008) 1.32
Multi-detector row CT of left ventricular function with dedicated analysis software versus MR imaging: initial experience. Radiology (2003) 1.32
Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation. Blood (2003) 1.31
Clinical features, treatment, and outcome of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a multinational, multicenter study of 362 patients. Arthritis Rheumatol (2014) 1.22
Proinflammatory role of proteinase-activated receptor-2 in humans and mice during cutaneous inflammation in vivo. FASEB J (2003) 1.22
Ultrasound studies on the time course of clavicular ossification. Int J Legal Med (2008) 1.22
A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS. Hum Mutat (2006) 1.20
Magnetic resonance 4D flow analysis of cerebrospinal fluid dynamics in Chiari I malformation with and without syringomyelia. Eur Radiol (2012) 1.19
A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy. Am J Hum Genet (2007) 1.17
Delayed-enhancement cardiovascular magnetic resonance coronary artery wall imaging: comparison with multislice computed tomography and quantitative coronary angiography. J Am Coll Cardiol (2007) 1.17
The Toll-like receptor 4 agonist MRP8/14 protein complex is a sensitive indicator for disease activity and predicts relapses in systemic-onset juvenile idiopathic arthritis. Ann Rheum Dis (2012) 1.16
Kocuria rhizophila adds to the emerging spectrum of micrococcal species involved in human infections. J Clin Microbiol (2008) 1.16
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I. Am J Hum Genet (2004) 1.14
Quantification of biventricular myocardial function using cardiac magnetic resonance feature tracking, endocardial border delineation and echocardiographic speckle tracking in patients with repaired tetralogy of Fallot and healthy controls. J Cardiovasc Magn Reson (2012) 1.13
Right ventricular-left ventricular interaction in adults with Tetralogy of Fallot: a combined cardiac magnetic resonance and echocardiographic speckle tracking study. Int J Cardiol (2010) 1.12
64- Versus 16-slice CT angiography for coronary artery stent assessment: in vitro experience. Invest Radiol (2006) 1.10
Monitoring neutrophil activation in juvenile rheumatoid arthritis by S100A12 serum concentrations. Arthritis Rheum (2004) 1.09
Farber disease: clinical presentation, pathogenesis and a new approach to treatment. Pediatr Rheumatol Online J (2007) 1.09
Comparison of 4D phase-contrast MRI flow measurements to computational fluid dynamics simulations of cerebrospinal fluid motion in the cervical spine. PLoS One (2012) 1.08
Evidence and consensus based GKJR guidelines for the treatment of juvenile idiopathic arthritis. Clin Immunol (2011) 1.06
Phagocyte-specific S100 proteins and high-sensitivity C reactive protein as biomarkers for a risk-adapted treatment to maintain remission in juvenile idiopathic arthritis: a comparative study. Ann Rheum Dis (2012) 1.05
Increased perivascular synovial membrane expression of myeloid-related proteins in psoriatic arthritis. Arthritis Rheum (2003) 1.05
Diagnostic value of [(18)F]-FDG PET/CT in children with fever of unknown origin or unexplained signs of inflammation. Eur J Nucl Med Mol Imaging (2010) 1.05
Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis (2013) 1.04
Magnetic resonance 4D flow characteristics of cerebrospinal fluid at the craniocervical junction and the cervical spinal canal. Eur Radiol (2011) 1.02
Cardiomyopathy in congenital disorders of glycosylation. Cardiol Young (2003) 1.01
Mutation analysis in patients with N-acetylglutamate synthase deficiency. Hum Mutat (2003) 0.99
Expression of toll-like receptors in neonatal sepsis. Pediatr Res (2005) 0.98
Granulocyte-colony stimulating factor (G-CSF) and G-CSF receptor expression in human ischemic stroke. Acta Neuropathol (2006) 0.98
Successful hematopoietic stem cell transplantation in Farber disease. J Pediatr (2004) 0.98
Effects of intra-articular corticosteroids and anti-TNF therapy on neutrophil activation in rheumatoid arthritis. Ann Rheum Dis (2007) 0.97
Autologous placental blood transfusion for the therapy of anaemic neonates. Biol Neonate (2002) 0.97
Severe transient myocardial ischaemia caused by hypertrophic cardiomyopathy in a patient with congenital disorder of glycosylation type Ia. Eur J Pediatr (2002) 0.96
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria. Ann Neurol (2005) 0.96
Analysis of the CTNS gene in patients of German and Swiss origin with nephropathic cystinosis. Hum Mutat (2002) 0.95
Sonographic assessment of the ossification of the medial clavicular epiphysis in 616 individuals. Forensic Sci Med Pathol (2013) 0.95
First NIH/Office of Rare Diseases Conference on Cystinosis: past, present, and future. Pediatr Nephrol (2005) 0.94
Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism. Hum Mutat (2004) 0.94
Efficacy, recovery, and safety of RBCs from autologous placental blood: clinical experience in 52 newborns. Transfusion (2003) 0.93
3.0 T vs. 1.5 T MR angiography: in vitro comparison of intravascular stent artifacts. J Magn Reson Imaging (2005) 0.92
Assessment of coronary artery stents using 16-slice MDCT angiography: evaluation of a dedicated reconstruction kernel and a noise reduction filter. Eur Radiol (2005) 0.92
Raine syndrome: report of a family with three affected sibs and further delineation of the syndrome. Clin Dysmorphol (2003) 0.90
Acute focal bacterial nephritis in 25 children. Pediatr Nephrol (2007) 0.90
Validation of relapse risk biomarkers for routine use in patients with juvenile idiopathic arthritis. Arthritis Care Res (Hoboken) (2014) 0.90
Introduction of an individually optimized protocol for the injection of contrast medium for coronary CT angiography. Eur Radiol (2009) 0.90
Comparison of 3D segmented gradient-echo and steady-state free precession coronary MRI sequences in patients with coronary artery disease. AJR Am J Roentgenol (2005) 0.90
Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now? Biochim Biophys Acta (2008) 0.89
Multi-detector row computed tomography of the heart: does a multi-segment reconstruction algorithm improve left ventricular volume measurements? Eur Radiol (2004) 0.89
Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction. Am J Hum Genet (2013) 0.88
Measurement of transcutaneous hemoglobin concentration by noninvasive white-light spectroscopy in infants. Pediatrics (2005) 0.88
Global left-ventricular function assessment using dual-source multidetector CT: effect of improved temporal resolution on ventricular volume measurement. Eur Radiol (2008) 0.87
Assessment of regional left ventricular function with multidetector-row computed tomography versus magnetic resonance imaging. Eur Radiol (2006) 0.87
Membrane-permeant derivatives of mannose-1-phosphate. Bioorg Med Chem (2002) 0.86
Leukocyte adhesion deficiency II patients with a dual defect of the GDP-fucose transporter. Blood (2006) 0.86
MR Angiography of Peripheral Arterial Stents: In Vitro Evaluation of 22 Different Stent Types. Radiol Res Pract (2010) 0.86
Prostate-Specific Membrane Antigen PET/CT in Splenic Sarcoidosis. Clin Nucl Med (2015) 0.86
Frequency of unexpected and important histopathological findings in routine intervertebral disc surgery. J Neurosurg Spine (2006) 0.84
Systemic juvenile rheumatoid arthritis: cognitive function and social adjustment. Ann Neurol (2005) 0.84
Glycoproteomics of N-glycosylation by in-gel deglycosylation and matrix-assisted laser desorption/ionisation-time of flight mass spectrometry mapping: application to congenital disorders of glycosylation. Proteomics (2005) 0.84
Next generation coronary CT angiography: in vitro evaluation of 27 coronary stents. Eur Radiol (2014) 0.83
T1-weighted MRI for the detection of coronary artery plaque haemorrhage. Eur Radiol (2010) 0.83
Long-term outcomes after liver transplantation for deoxyguanosine kinase deficiency: a single-center experience and a review of the literature. Liver Transpl (2014) 0.83
Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn. Eur J Hum Genet (2012) 0.83
High-pitch 128-slice dual-source CT for the assessment of coronary stents in a phantom model. Acad Radiol (2010) 0.82
Neurosonographical follow-up in patients with spontaneous cervical artery dissection. Neurol Res (2008) 0.82
Inhibition of Na(+)-dependent transporters in cystine-loaded human renal cells: electrophysiological studies on the Fanconi syndrome of cystinosis. J Am Soc Nephrol (2002) 0.82
A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation. Am J Pathol (2011) 0.82
Individual patient data meta-analysis for the clinical assessment of coronary computed tomography angiography: protocol of the Collaborative Meta-Analysis of Cardiac CT (CoMe-CCT). Syst Rev (2013) 0.82
Experimental evaluation of a portable indirect flat-panel detector for the pediatric chest: comparison with storage phosphor radiography at different exposures by using a chest phantom. Radiology (2005) 0.81
Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins. Pediatr Res (2005) 0.81
Palatal development of preterm and low birthweight infants compared to term infants - What do we know? Part 1: The palate of the term newborn. Head Face Med (2005) 0.81
Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS). Glycoconj J (2007) 0.81
Dual-Source CT Angiography of Peripheral Arterial Stents: In Vitro Evaluation of 22 Different Stent Types. Radiol Res Pract (2011) 0.81
Feasibility of functional cardiac MR imaging in mice using a clinical 3 Tesla whole body scanner. Invest Radiol (2009) 0.80
Thoracic type Ia endoleak: direct percutaneous coil embolization of the aortic arch at the blood entry site after TEVAR and double-chimney stent-grafts. Eur Radiol (2014) 0.79
Concomitant Ewing sarcoma and acute lymphoblastic leukemia in a 5-year-old girl. Pediatr Blood Cancer (2005) 0.79
Congenital ichthyosis in severe type II Gaucher disease with a homozygous null mutation. Neonatology (2011) 0.79
Portable flat-panel detector for low-dose imaging in a pediatric intensive care unit: comparison with an asymmetric film-screen system. Invest Radiol (2005) 0.79
Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih. Mol Genet Metab (2009) 0.79
Palatal development of preterm and low birthweight infants compared to term infants -- What do we know? Part 3: discussion and conclusion. Head Face Med (2005) 0.79
Cardiac magnetic resonance feature tracking: a novel method to assess myocardial strain. Comparison with echocardiographic speckle tracking in healthy volunteers and in patients with left ventricular hypertrophy. Kardiol Pol (2013) 0.79