Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
- Author
- SELLIER-LEDERC, Anne-Laure1 ; FREMEAUX-BACCHI, Veronique2 ; TSIMARATOS, Michel8 ; FISCHBACH, Michel9 ; MORIN, Denis10 ; NIVET, Hubert11 ; ALBERTI, Corinne12 ; LOIRAT, Chantal1 ; DRAGON-DUREY, Marie-Agnès2 ; MACHER, Marie-Alice1 ; NIAUDET, Patrick3 ; GUEST, Geneviève3 ; BOUDAILLIEZ, Bernard4 ; BOUISSOU, Frangois5 ; DESCHENES, Georges6 ; GIE, Sophie7
[1] Assistance Publique-Hôpitaux de Paris, Service de Néphrologie Pédiatrique, Hôpital Robert Debré, Université Paris VII, Faculté de Médecine Denis Diderot, Paris, France
[2] Assistance Publique-Hôpitaux de Paris, Laboratoire d'Immunologie Biologique, Hôpital Européen Georges Pompidou, Paris, France
[3] Assistance Publique-Hôpitaux de Paris, Service de Néphrologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, France
[4] Département de Pédiatrie, Hôpital Nord, Amiens, France
[5] Service de Néphrologie Pédiatrique, Hôpital des Enfants, Toulouse, France
[6] Assistance Publique-Hôpitaux de Paris, Service de Néphrologie Pédiatrique, Hôpital Trousseau, Paris, France
[7] Service de Néphrologie, Hôpital de Pontchaillou, Rennes, France
[8] Service de Néphrologie, Hôpital de la Timone, Marseille, France
[9] Service de Pédiatrie, Hôpital Hautepierre, Strasbourg, France
[10] Service de Pédiatrie 1, Hôpital Arnault de Villeneuve, Montpellier, France
[11] Service de Néphrologie, Hôpital de Clocheville, Tours, France
[12] Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré, Unité d'Epidémiologie Clinique, Paris, France
French Society of Pediatric Nephrology, France - Source
Journal of the American Society of Nephrology. 2007, Vol 18, Num 8, pp 2392-2400, 9 p ; ref : 36 ref
- CODEN
- JASNEU
- ISSN
- 1046-6673
- Scientific domain
- Urology, nephrology
- Publisher
- Lippincott Williams & Wilkins, Hagerstown, MD
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aigu Atypique Complément Génétique Hémolyse urémie Microangiopathie thrombohémolytique Mutation Symptomatologie Thrombocyte Thrombopénie Urologie Néphrologie Anémie hémolytique Appareil circulatoire pathologie Appareil urinaire pathologie Hémopathie Insuffisance rénale Rein pathologie Vaisseau sanguin pathologie
- Keyword (en)
- Acute Atypical Complement Genetics Hemolytic uremic syndrome Thrombohemolytic microangiopathy Mutation Symptomatology Platelet Thrombocytopenia Urology Nephrology Hemolytic anemia Cardiovascular disease Urinary system disease Hemopathy Renal failure Kidney disease Vascular disease
- Keyword (es)
- Agudo Atípico Complemento Genética Hemólisis urémica Microangiopatía trombohemolítica Mutación Sintomatología Trombocito Trombopenia Urología Nefrología Anemia hemolítica Aparato circulatorio patología Aparato urinario patología Hemopatía Insuficiencia renal Riñón patología Vaso sanguíneo patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B14 Nephrology. Urinary tract diseases / 002B14A Nephropathies. Renovascular diseases. Renal failure / 002B14A05 Renal failure
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19C Platelet diseases and coagulopathies
- Discipline
- Blood diseases Nephrology. Urinary tract diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18973235
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1681/ASN.2006080811 
https://dx.doi.org/10.1681/ASN.2006080811
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