Clinical practice recommendations for the treatment of Alport syndrome: A statement of the Alport Syndrome Research Collaborative

Pediatric Nephrology

Volumn 28, Issue 1, 2013, Pages 5-11

  Kashtan, Clifford E ^a   Ding, Jie ^b   Gregory, Martin ^c   Gross, Oliver ^d   Heidet, Laurence ^e   Knebelmann, Bertrand ^e   Rheault, Michelle ^a   Licht, Christoph ^f  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b PEKING UNIVERSITY FIRST HOSPITAL   (China)

^c UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^d UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

^f HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Aldosterone inhibitor; Alport syndrome; Angiotensin receptor blocker; Angiotensin converting enzyme inhibitor; Proteinuria

Indexed keywords

ALDOSTERONE ANTAGONIST; ANGIOTENSIN RECEPTOR ANTAGONIST; BENAZEPRIL; CANDESARTAN; CILAZAPRIL; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; ENALAPRIL; EPROSARTAN; FOSINOPRIL; IRBESARTAN; LISINOPRIL; LOSARTAN; PERINDOPRIL; QUINAPRIL; RAMIPRIL; SPIRONOLACTONE; TELMISARTAN; TRANDOLAPRIL; VALSARTAN;

ACUTE KIDNEY FAILURE; ALPORT SYNDROME; CLINICAL EFFECTIVENESS; CLINICAL PRACTICE; CLINICAL PROTOCOL; CLINICAL TRIAL (TOPIC); CREATININE BLOOD LEVEL; FAINTNESS; FETUS DISEASE; GLOMERULUS FILTRATION RATE; GYNECOMASTIA; HUMAN; HYPERKALEMIA; HYPOTENSION; KIDNEY FIBROSIS; NONHUMAN; ORTHOSTATIC HYPOTENSION; PATIENT SAFETY; PRIORITY JOURNAL; PROTEINURIA; REVIEW; SIDE EFFECT; STANDARD; SURGICAL APPROACH;

CHILD; FEMALE; HUMANS; MALE; NEPHRITIS, HEREDITARY;

EID: 84870405692     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-012-2138-4     Document Type: Review

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