Citation Impact
Citing Papers
Complement Factor H Polymorphism and Age-Related Macular Degeneration
2005 StandoutScience
Clinical Significance of Primary Vesicoureteral Reflux and Urinary Antibiotic Prophylaxis After Acute Pyelonephritis: A Multicenter, Randomized, Controlled Study
2006
An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels.
1990 Standout
Pathophysiology of uric acid nephrolithiasis
2002
Mechanisms of Thrombus Formation
2008 Standout
Kidney stones: pathophysiology and medical management
2006 Standout
Pathophysiology of Progressive Nephropathies
1998 Standout
Hypocomplementemia Discloses Genetic Predisposition to Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura
1999
The FGF family: biology, pathophysiology and therapy
2009 Standout
Intravenous Immunoglobulin G Therapy in Streptococcal Toxic Shock Syndrome: A European Randomized, Double-Blind, Placebo-Controlled Trial
2003
Expert Committee Recommendations Regarding the Prevention, Assessment, and Treatment of Child and Adolescent Overweight and Obesity: Summary Report
2007 Standout
Antithrombotic Therapy for VTE Disease
2016 Standout
A germline mutation abolishing the original stop codon of the human adenine phosphoribosyltransferase (APRT) gene leads to complete loss of the enzyme protein
1998
Purine and pyrimidine metabolites in children's urine
2003
Vitamin D Deficiency
2007 Standout
Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents
2017 Standout
Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome
2005 Standout
Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction
1992 StandoutNature
Extracellular Proteins Organize the Mechanosensory Channel Complex in C. elegans Touch Receptor Neurons
2004 StandoutNobel
Timing of Thyroid Hormone Action in the Developing Brain: Clinical Observations and Experimental Findings
2004
UK Prospective Diabetes Study (UKPDS) 14: association of angiotensin-converting enzyme insertion/deletion polymorphism with myocardial infarction in NIDDM
1995 StandoutNobel
Lymphangiogenesis in development and human disease
2005 StandoutNature
Antithrombotic Therapy for VTE Disease
2012 Standout
Developmental consequences of the renin-angiotensin system
1995
Fibroblast growth factor signalling: from development to cancer
2010 Standout
Prevalence and aetiology of hypothyroidism in the young
2000
Familial Hemolytic-Uremic Syndrome and Homozygous Factor H Deficiency
1994
Hyperoxaluric calcium nephrolithiasis
2002
ACE I/D-corrected Z-scores to identify normal and elevated ACE activity in sarcoidosis
2006
Urinary Tract Infection: Clinical Practice Guideline for the Diagnosis and Management of the Initial UTI in Febrile Infants and Children 2 to 24 Months
2011 Standout
Oral Water Intoxication in Infants
1991
The Molecular Basis of Familial Hemolytic Uremic Syndrome
2001
A rapid bedside test for B-type peptide predicts treatment outcomes in patients admitted for decompensated heart failure: a pilot study
2001 Standout
Measured Haplotype Analysis of the Angiotensin-I Converting Enzyme Gene
1998 StandoutNobel
LADD syndrome is caused byFGF10mutations
2006
Purine and Pyrimidine Metabolism Between Millennia: What has been Accomplished, What has to be Done?
2002
Complement
2001 Standout
Hypertension in infancy: diagnosis, management and outcome
2011
Antithrombotic Therapy in Neonates and Children
2008
Imaging Studies after a First Febrile Urinary Tract Infection in Young Children
2003
Antithrombotic Therapy in Neonates and Children
2012
Chylous ascites complicating neonatal peritoneal dialysis
1995
Iodine-deficiency disorders
2008 Standout
The Effect of Spironolactone on Morbidity and Mortality in Patients with Severe Heart Failure
1999 Standout
Renin Cells Are Precursors for Multiple Cell Types that Switch to the Renin Phenotype When Homeostasis Is Threatened
2004 StandoutNobel
Sarcoidosis
2007 Standout
Regulation of thyroid hormone metabolism during fetal development
1999
Chylous ascites: A collective review
2000 Standout
Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association
2017 Standout
Heterozygous and Homozygous Factor H Deficiencies Associated with Hemolytic Uremic Syndrome or Membranoproliferative Glomerulonephritis
2004
Biomarkers in Heart Failure
2008 Standout
Incorporation of Pseudouridine Into mRNA Yields Superior Nonimmunogenic Vector With Increased Translational Capacity and Biological Stability
2008 StandoutNobel
Tricine–SDS-PAGE
2006 Standout
Relative in Vitro Efficacy of the Phosphate Binders Lanthanum Carbonate and Sevelamer Hydrochloride
2007 StandoutNobel
Molecular Characterization of a Functional cDNA Encoding the Serotonin 1c Receptor
1988 StandoutScienceNobel
Blood Pressures and Cardiovascular Homeostasis in Mice Having Reduced or Absent Angiotensin-Converting Enzyme Gene Function
1997 StandoutNobel
Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update by the Infectious Diseases Society of America
2014 Standout
Immunoblotting and dot immunobinding — Current status and outlook
1984 Standout
Iodine supplementation for the prevention of mortality and adverse neurodevelopmental outcomes in preterm infants
2006
EDC-2: The Endocrine Society's Second Scientific Statement on Endocrine-Disrupting Chemicals
2015 Standout
Aberrant Renal Vascular Morphology and Renin Expression in Mutant Mice Lacking Angiotensin-Converting Enzyme
1997 StandoutNobel
Endocrine-Disrupting Chemicals: An Endocrine Society Scientific Statement
2009 Standout
Purification of Adenine Phosphoribosyltransferase by Affinity Chromatography
1978
Gene Polymorphism but not Catalytic Activity of Angiotensin I–Converting Enzyme Is Associated With Coronary Artery Disease and Myocardial Infarction in Low-Risk Patients
1995
Guidelines for the Management of Pediatric and Adult Tumor Lysis Syndrome: An Evidence-Based Review
2008 Standout
Familial resemblance of plasma angiotensin-converting enzyme level: the Nancy Study.
1988
Angiotensin-Converting Enzyme Gene and Atherosclerosis
1997 StandoutNobel
Comparative Study of In Vivo Lymphatic Sealing Capability of the Porcine Thoracic Duct Using Laparoscopic Dissection Devices
2008 StandoutNobel
Protein blotting
1986
Physiological and Molecular Basis of Thyroid Hormone Action
2001 Standout
Management of Massive and Submassive Pulmonary Embolism, Iliofemoral Deep Vein Thrombosis, and Chronic Thromboembolic Pulmonary Hypertension
2011 Standout
Transient pseudohypoaldosteronism secondary to obstructive uropathy in infancy
1983
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
Hormones and Endocrine-Disrupting Chemicals: Low-Dose Effects and Nonmonotonic Dose Responses
2012 Standout
Hormones regulating cardiovascular function in patients with severe congestive heart failure and their relation to mortality. CONSENSUS Trial Study Group.
1990
Expression of size-selected mRNA encoding the intestinal Na/glucose cotransporter in Xenopus laevis oocytes.
1987
Trends in the biochemical pharmacology of 5′-deoxy-5′-methylthioadenosine
1982
Renal protective effect of enalapril in diabetic nephropathy.
1992
Angiotensin-Converting Enzyme Gene Mutations, Blood Pressures, and Cardiovascular Homeostasis
1997 StandoutNobel
Functional Significance of Cell Volume Regulatory Mechanisms
1998 Standout
Technical Report: Urinary Tract Infections in Febrile Infants and Young Children
1999
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
1996 StandoutScience
Bone metabolism and disease in chronic kidney disease
2003
Factor H and the pathogenesis of renal diseases
2000
Isolation of transforming DNA: Cloning the hamster aprt gene
1980 StandoutNobel
Recent advances in the biochemistry of polyamines in eukaryotes
1986 Standout
Works of K. J. Van Acker being referenced
Low thyroxinaemia occurs in the majority of very preterm newborns
1996
Idiopathic arterial calcification of infancy
1991
Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria
1996
Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement
1990
Involvement of the renal parenchyma in acute urinary tract infection: The contribution of99mTc dimercaptosuccinic acid scan
1992
Congenital streptococcal toxic shock syndrome with absence of antibodies against streptococcal pyrogenic exotoxins
1995
Lacrimo‐auriculo‐dento‐digital (LADD) syndrome with renal and foot anomalies
1990
Chylous Peritonitis: An Infrequent Complication of Peritoneal Dialysis
1987
Primary glucose-galactose malabsorption.
1980
2, 8-Dihydroxyadeninuria: Or When is a Uric Acid Stone not a Uric Acid Stone?
1981
Complete Deficiency of Adenine Phosphoribosyltransferase
1977
Intracardiac thrombus formation with rapidly progressive heart failure in the neonate: treatment with tissue type plasminogen activator.
1992
Renin-angiotensin-aldosterone system in the healthy infant and child
1979
Improved micromethod for assay of serum angiotensin converting enzyme.
1982
The identification of 2,8-dihydroxyadenine, a new component of urinary stones
1976
Human adenine phosphoribosyltransferase. Immunochemical quantitation and protein blot analysis of mutant forms of the enzyme.
1982
Protein restriction in chronic renal failure.
1993