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Literature DB >> 14497974

Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness.

Abstract

Entities: Disease

Keywords: BRAIN/diseases; KIDNEY DISEASES/genetics

Source DB: PubMed Journal: N Engl J Med ISSN： 0028-4793 Impact factor: 91.245

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22 in total

Authors: H K VISSER; H W VEENSTRA; C PIK
Journal: Arch Dis Child Date: 1964-08 Impact factor: 3.791

Authors: T HARGREAVES
Journal: J Clin Pathol Date: 1963-07 Impact factor: 3.411

Authors: N A CARSON; D C CUSWORTH; C E DENT; C M FIELD; D W NEILL; R G WESTALL
Journal: Arch Dis Child Date: 1963-10 Impact factor: 3.791

Authors: C R SCRIVER; M L EFRON; I A SCHAFER
Journal: J Clin Invest Date: 1964-03 Impact factor: 14.808

Authors: R L Blake
Journal: Biochem J Date: 1972-10 Impact factor: 3.857

Authors: D Dotchev; H Hungerland; N Liappis
Journal: Klin Wochenschr Date: 1972-06-15

Authors: P S Dhatt; H L Gupta; A S Saini
Journal: Indian J Pediatr Date: 1968-10 Impact factor: 1.967

Authors: J T Harries; A T Piesowicz; J W Seakins; D E Francis; O H Wolff
Journal: Arch Dis Child Date: 1971-02 Impact factor: 3.791

Authors: H Völkl; S Silbernagl
Journal: Pflugers Arch Date: 1980-09 Impact factor: 3.657

Authors: Wei Liu; James M Phang
Journal: Biofactors Date: 2012-08-08 Impact factor: 6.113