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Journal Abstract Search
98 related items for PubMed ID: 2507251
1. [The blood galactokinase activity in Chinese with reference to congenital cataract]. Xu GT. Zhonghua Yan Ke Za Zhi; 1989 Mar; 25(2):100-3. PubMed ID: 2507251 [Abstract] [Full Text] [Related]
2. [Studies on blood galactokinase of patients with presenile and senile cataracts]. Xu G. Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1990 Apr; 12(2):101-4. PubMed ID: 2143108 [Abstract] [Full Text] [Related]
3. Cataracts in patients heterozygous for galactokinase deficiency. Stambolian D, Scarpino-Myers V, Eagle RC, Hodes B, Harris H. Invest Ophthalmol Vis Sci; 1986 Mar; 27(3):429-33. PubMed ID: 3949470 [Abstract] [Full Text] [Related]
4. Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts. Stambolian D, Ai Y, Sidjanin D, Nesburn K, Sathe G, Rosenberg M, Bergsma DJ. Nat Genet; 1995 Jul; 10(3):307-12. PubMed ID: 7670469 [Abstract] [Full Text] [Related]
5. Galactokinase activity in patients with idiopathic cataracts. Elman MJ, Miller MT, Matalon R. Ophthalmology; 1986 Feb; 93(2):210-5. PubMed ID: 3951827 [Abstract] [Full Text] [Related]
6. Congenital cataract etiology. El Fkih L, Hmaied W, El Hif S, Moalla S, Marakchi S, Tabib N, Azzouz H. Tunis Med; 2007 Dec; 85(12):1025-9. PubMed ID: 19170381 [Abstract] [Full Text] [Related]
7. Strain difference in galactokinase level and susceptibility to the teratogenic effect of dietary galactose in mice: I. Teratogenic and embryopathic effect. Shih LY, Kuerer HM, Chen TH, Desposito F. Teratology; 1988 Aug; 38(2):175-9. PubMed ID: 3175951 [Abstract] [Full Text] [Related]
9. Have we stopped looking for a red reflex in newborn screening? Sotomi O, Ryan CA, O'Connor G, Murphy BP. Ir Med J; 2007 Mar; 100(3):398-400. PubMed ID: 17491540 [Abstract] [Full Text] [Related]
10. A nationwide Danish study of 1027 cases of congenital/infantile cataracts: etiological and clinical classifications. Haargaard B, Wohlfahrt J, Fledelius HC, Rosenberg T, Melbye M. Ophthalmology; 2004 Dec; 111(12):2292-8. PubMed ID: 15582089 [Abstract] [Full Text] [Related]
11. Descriptive epidemiology of infantile cataracts in metropolitan Atlanta, GA, 1968-1998. Bhatti TR, Dott M, Yoon PW, Moore CA, Gambrell D, Rasmussen SA. Arch Pediatr Adolesc Med; 2003 Apr; 157(4):341-7. PubMed ID: 12695229 [Abstract] [Full Text] [Related]
12. [Measurement of the erythrocyte galactokinase activity in patients with presenile and senile idiopathic cataract. Preliminary study]. Simonelli F, Frunzio S, Rinaldi M, Balestrieri P, Giovane A, Cotticelli L, Rinaldi E. Boll Soc Ital Biol Sper; 1990 Sep; 66(9):887-92. PubMed ID: 2073390 [Abstract] [Full Text] [Related]
13. [Activity of enzymes of galactose metabolism in so-called congenital cataract (author's transl)]. Kaloud H, Sitzmann FC, Schenker H, Prestele H. Dtsch Med Wochenschr; 1975 Apr 18; 100(16):873-6. PubMed ID: 164335 [Abstract] [Full Text] [Related]
14. Red blood cell galactokinase activity and presenile cataracts. Magnani M, Cucchiarini L, Stocchi V, Dachà M. Enzyme; 1983 Apr 18; 29(1):58-60. PubMed ID: 6840050 [Abstract] [Full Text] [Related]
15. Persistent fetal vasculature and minimal fetal vascular remnants: a frequent cause of unilateral congenital cataracts. Müllner-Eidenböck A, Amon M, Moser E, Klebermass N. Ophthalmology; 2004 May 18; 111(5):906-13. PubMed ID: 15121367 [Abstract] [Full Text] [Related]
16. Nationwide trends in hospitalization and surgical treatment of congenital and infantile cataract among italian children 4 years and younger. Ricci B, Volpe M, Coppola G, Ziccardi L. J Pediatr Ophthalmol Strabismus; 2009 May 18; 46(4):210-4. PubMed ID: 19645398 [Abstract] [Full Text] [Related]
17. Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studies. Benson PF, Brown SP, Cree J, Fensom AH, Grant AR. Birth Defects Orig Artic Ser; 1976 May 18; 12(3):305-12. PubMed ID: 182297 [Abstract] [Full Text] [Related]
18. Galactokinase activity in patients with cataracts. Stambolian D. Ophthalmology; 1987 Jan 18; 94(1):91-2. PubMed ID: 3561966 [No Abstract] [Full Text] [Related]
19. Genetic Blood Disorders Survey in the Sultanate of Oman. Al-Riyami A, Ebrahim GJ. J Trop Pediatr; 2003 Jul 18; 49 Suppl 1():i1-20. PubMed ID: 12934793 [Abstract] [Full Text] [Related]