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28. Oculo-cerebro-renal syndrome (Lowe's syndrome). Chen Y; Pang G Yan Ke Xue Bao; 1991 Mar; 7(1):40-2, 46. PubMed ID: 1843129 [TBL] [Abstract][Full Text] [Related]
29. Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases. Norden AG; Scheinman SJ; Deschodt-Lanckman MM; Lapsley M; Nortier JL; Thakker RV; Unwin RJ; Wrong O Kidney Int; 2000 Jan; 57(1):240-9. PubMed ID: 10620205 [TBL] [Abstract][Full Text] [Related]
30. Identification of OCRL1 mutations in two Taiwanese Lowe syndrome patients. Chou YY; Chao SC; Chiou YY; Lin SJ Acta Paediatr Taiwan; 2005; 46(4):226-9. PubMed ID: 16381338 [TBL] [Abstract][Full Text] [Related]
31. Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients. Lin T; Orrison BM; Suchy SF; Lewis RA; Nussbaum RL Mol Genet Metab; 1998 May; 64(1):58-61. PubMed ID: 9682219 [TBL] [Abstract][Full Text] [Related]
32. Second messengers and Lowe syndrome. Irvine R Nat Genet; 1992 Aug; 1(5):315-6. PubMed ID: 1338770 [No Abstract] [Full Text] [Related]
33. Bleeding disorders in Lowe syndrome patients: evidence for a link between OCRL mutations and primary haemostasis disorders. Lasne D; Baujat G; Mirault T; Lunardi J; Grelac F; Egot M; Salomon R; Bachelot-Loza C Br J Haematol; 2010 Sep; 150(6):685-8. PubMed ID: 20629659 [TBL] [Abstract][Full Text] [Related]
34. [Genetic transmission of Lowe's oculo-cerebro-renal syndrome in girl]. Bétend B; Scherrer M; Evrard A; Votan-Bonnamour B; Hermier M Arch Fr Pediatr; 1978 Mar; 35(3):269-79. PubMed ID: 666523 [TBL] [Abstract][Full Text] [Related]
36. Congenital diaphragmatic hernia in Lowe syndrome: a rare association? Race HJ; Elhadi N; Holder SE Clin Dysmorphol; 2010 Oct; 19(4):226. PubMed ID: 20823704 [No Abstract] [Full Text] [Related]
37. [Regulation of endocytosis by phosphoinositides]. Nakatsu F; De Camilli P Tanpakushitsu Kakusan Koso; 2008 Dec; 53(16 Suppl):2164-9. PubMed ID: 21038603 [No Abstract] [Full Text] [Related]
38. Prenatal diagnosis of Löwe's syndrome: a case report with evidence of de novo mutation. Gazit E; Brand N; Harel Y; Lotan D; Barkai G Prenat Diagn; 1990 Apr; 10(4):257-60. PubMed ID: 1973295 [No Abstract] [Full Text] [Related]
39. Delayed vitreous haemorrhage after paediatric cataract surgery in Lowe syndrome. Mikhail M; Modabber M; Koenekoop RK; Braverman N; Khan A Eye (Lond); 2016 Sep; 30(9):1272-3. PubMed ID: 27229703 [No Abstract] [Full Text] [Related]