Article Information
PubMed
Published By
Print ISSN
Online ISSN
History
- Received for publication July 9, 1999
- Accepted for publication September 10, 1999
- Published online April 1, 2000.
Copyright & Usage
© 2000 American Society of Nephrology
Author Information
- JEAN PHILIPPE JAIS*,
- BERTRAND KNEBELMANN†,
- IANNIS GIATRAS†,
- MARIO DE MARCHI‡,
- GIANFRANCO RIZZONI‡,
- ALESSANDRA RENIERI‡,
- MANFRED WEBER§,
- OLIVER GROSS§,
- KAI-OLAF NETZER§,
- FRANCES FLINTER∥,
- YVES PIRSON¶,
- CHRISTINE VERELLEN¶,
- JÖRGEN WIESLANDER#,
- ULF PERSSON#,
- KARL TRYGGVASON**,
- PAULA MARTIN**,
- JENS MICHAEL HERTZ††,
- CORNELIS SCHRÖDER‡‡,
- MAREK SANAK∥∥,
- SARKA KREJCOVA¶¶,
- MARIA FERNANDA CARVALHO##,
- JUAN SAUS***,
- CORINNE ANTIGNAC†,
- HUBERT SMEETS§§ and
- MARIE CLAIRE GUBLER†
- * Biostatistique et Informatique Médicale, U423, Hôpital Necker Enfants Malades, Université René Descartes, Paris, France
- † Institut Nationale de la Santé et de la Recherche Médicale U423, Hôpital Necker Enfants Malades, Université René Descartes, Paris, France
- ‡ The Italian Multicenter Study on Alport Syndrome, Italy
- § Hospital Köln Merheim, Cologne, Germany
- ∥ Guy's Hospital, University of London, United Kingdom
- ¶ Université Catholique de Louvain, Belgium
- # University Hospital, Lund, Sweden
- ** Karolinska Institute, Stockholm, Sweden
- †† Aarhus University Hospital, Denmark
- ‡‡ University Hospital of Nijmegen, The Netherlands
- §§ University of Maastricht, The Netherlands
- ∥∥ Jagiellonian University Medical School, Krakow, Poland
- ¶¶ Charles University, Prague, Czech Republic
- ## Curry Cabral Hospital, Lisbonne, Portugal
- *** Fundación Valenciana de Investigaciones Biomédicas, Instituto de Investigaciones Citológicas, Valencia, Spain.
- Correspondence to Dr. Marie Claire Gubler, Institut National de la Santé et de la Recherche Médicale, U 423, Hôpital Necker Enfants Malades, 149 rue de Sèvres, 75743 Paris Cedex 15, France. Phone: +33 1 47 83 90 16; Fax: +33 1 44 49 02 90; E-mail: gubler{at}necker.fr
Statistics from Altmetric.com
Article usage
Cited By...
X-linked Alport Syndrome
Jump to section
More in this TOC Section
Cited By...
- Heterozygous Urinary Abnormality-Causing Variants of COL4A3 and COL4A4 Affect Severity of Autosomal Recessive Alport Syndrome
- Approach to Persistent Microscopic Hematuria in Children
- Pilot Study of Return of Genetic Results to Patients in Adult Nephrology
- Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome
- Genetic diagnosis of polycystic kidney disease, Alport syndrome, and thalassemia minor in a large Chinese family
- Alport Syndrome in Women and Girls
- Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome
- HANAC Syndrome Col4a1 Mutation Causes Neonate Glomerular Hyperpermeability and Adult Glomerulocystic Kidney Disease
- Isolated microscopic haematuria of glomerular origin: clinical significance and diagnosis in the 21st century
- Crescentic and necrotising glomerulonephritis: a rare histological manifestation of Alport syndrome
- Ocular Features in Alport Syndrome: Pathogenesis and Clinical Significance
- Evidence of digenic inheritance in Alport syndrome
- Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing
- X-Linked Alport Syndrome Caused by Splicing Mutations in COL4A5
- Familial haematuria: when to consider genetic testing
- COL4A3/COL4A4 Mutations and Features in Individuals with Autosomal Recessive Alport Syndrome
- Prognostic Value of Glomerular Collagen IV Immunofluorescence Studies in Male Patients with X-Linked Alport Syndrome
- Expert Guidelines for the Management of Alport Syndrome and Thin Basement Membrane Nephropathy
- Outcomes of Male Patients with Alport Syndrome Undergoing Renal Replacement Therapy
- Retinal Abnormalities Characteristic of Inherited Renal Disease
- The Value of Clinical Criteria in Identifying Patients with X-Linked Alport Syndrome
- Identification of the NC1 Domain of {alpha}3 Chain as Critical for {alpha}3{alpha}4{alpha}5 Type IV Collagen Network Assembly
- Genotype-Phenotype Correlation in X-Linked Alport Syndrome
- Retinal Basement Membrane Abnormalities and the Retinopathy of Alport Syndrome
- Alport Retinopathy Results from "Severe" COL4A5 Mutations and Predicts Early Renal Failure
- The Renal Lesions of Alport Syndrome
- The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failure
- The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms
- Type IV Procollagen Missense Mutations Associated With Defects of the Eye, Vascular Stability, the Brain, Kidney Function and Embryonic or Postnatal Viability in the Mouse, Mus musculus: An Extension of the Col4a1 Allelic Series and the Identification of the First Two Col4a2 Mutant Alleles
- Loss of {alpha}3/{alpha}4(IV) Collagen from the Glomerular Basement Membrane Induces a Strain-Dependent Isoform Switch to {alpha}5{alpha}6(IV) Collagen Associated with Longer Renal Survival in Col4a3-/- Alport Mice
- The Molecular Basis of Goodpasture and Alport Syndromes: Beacons for the Discovery of the Collagen IV Family
- Mouse Model of X-Linked Alport Syndrome
- X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study
- Cyclosporine A Slows the Progressive Renal Disease of Alport Syndrome (X-Linked Hereditary Nephritis): Results from a Canine Model
- The Position of the Polycystic Kidney Disease 1 (PKD1) Gene Mutation Correlates with the Severity of Renal Disease
- Type IV Collagen of the Glomerular Basement Membrane: EVIDENCE THAT THE CHAIN SPECIFICITY OF NETWORK ASSEMBLY IS ENCODED BY THE NONCOLLAGENOUS NC1 DOMAINS
- Type IV Collagen of the Glomerular Basement Membrane: EVIDENCE THAT THE CHAIN SPECIFICITY OF NETWORK ASSEMBLY IS ENCODED BY THE NONCOLLAGENOUS NC1 DOMAINS