Medullary Cystic Disease and Juvenile Nephronophthisis in Separate Members of the Same Family

Author:

Sworn M. J.,Eisinger A. J.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference11 articles.

1. Congenital cystic kidney and liver with family tendency;Bunting, C.H.;Journal of Experimental Medicine,1906

2. Familial visual defects associated with polycystic kidney and medullary sponge kidney;Fairley, K.F.; Leighton, P.W.; Kincaid-Smith, P.;British Medical Journal,1963

3. Die familiare juvenile Nephronophthise (die idiopathische parenchymatose Schrumpfniere);Fanconi, G.; Hanart, E.; Albertini, A.V.; thlinger, E.; Dolivo, G.; Prader, A.;Helvetica Paediatrica Acta,1951

4. Hereditary occurrence of cystic disease of the renal medulla;Goldman, S.H.; Walker, S.R.; Merigan, Jr., T.C.; Gardner, Jr., K.D.; Bull, J.M.C.;New England Journal of Medicine,1966

5. Medullary cystic disease in two siblings;Herdman, R.C.; Good, R.A.; Vernier, R.L.;American Journal of Medicine,1967

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3. Ciliopathies;Cold Spring Harbor Perspectives in Biology;2016-10-28

4. Nephronophthisis and Medullary Cystic Kidney Disease in Children;Pediatric Nephrology;2015-11-12

5. Nephronophthisis–Medullary Cystic Kidney Disease in Children;Pediatric Nephrology;2015

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