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5. Renal involvement in type I glycogen storage disease. Chen YT; Van Hove JL Adv Nephrol Necker Hosp; 1995; 24():357-65. PubMed ID: 7572419 [No Abstract] [Full Text] [Related]
6. Leprechaunism--an unusual case with cardiac anomaly. Chandra M; Tayal JP Indian Pediatr; 1979 Jan; 16(1):83-5. PubMed ID: 437889 [No Abstract] [Full Text] [Related]
7. Renal disease in type 1 glycogen storage disease. N Engl J Med; 1988 Jun; 318(26):1759-60. PubMed ID: 3163776 [No Abstract] [Full Text] [Related]
8. Hyperammonemia associated with glycogen storage disease type I. Tunçer M; Yalçin H; Ozalp I; Cağlar M Turk J Pediatr; 1982; 24(1):53-7. PubMed ID: 6956070 [No Abstract] [Full Text] [Related]
9. Glycogen Storage Disease Type I Presenting with Hypertension During Infancy. Bhowmik E; Ghosh M; Sabui TK; Mondal R Indian J Pediatr; 2015 Aug; 82(8):767. PubMed ID: 25735438 [No Abstract] [Full Text] [Related]
10. More about renal disease in type Ia glycogen storage disease. Tomé Martínez de Rituerto S; Sanchez-Guisande D; Forteza J; Novoa D; Romero R; Rodriguez MI; Barrio E Nephron; 1992; 62(4):477-8. PubMed ID: 1300450 [No Abstract] [Full Text] [Related]
11. [On the clinical picture of progressive lipodystrophy]. Oppermann J; Pester F Kinderarztl Prax; 1966 Nov; 34(11):511-6. PubMed ID: 5955374 [No Abstract] [Full Text] [Related]
12. [Exomphalos-makroglossy-gigantism-syndrome, gneralized muscular hypertrophy, progressive lipodystrophy and Miescher's syndrome--congenital diencephalic syndromes?]. Wiedemann HR; Spranger J; Mogharei M; Kübler W; Tolksdorf M; Bontemps M; Drescher J; Gunschera H Z Kinderheilkd; 1968; 102(1):1-36. PubMed ID: 5723220 [No Abstract] [Full Text] [Related]
13. The nephromegaly of chronic alcoholics with liver disease. Laube H; Norris HT; Robbins SL Arch Pathol; 1967 Sep; 84(3):290-4. PubMed ID: 6030969 [No Abstract] [Full Text] [Related]
14. Late sepsis in a G-6-PD deficient newborn. D'Souza NA; Krishnan L; Baliga M Indian Pediatr; 1994 Oct; 31(10):1273-5. PubMed ID: 7875793 [No Abstract] [Full Text] [Related]
15. [Glycogen storage disease type I in a child with coexistent Cryptococcus histolyticus meningitis]. Han QH; Song YZ; Liu GS Zhongguo Dang Dai Er Ke Za Zhi; 2006 Oct; 8(5):439-40. PubMed ID: 17052413 [No Abstract] [Full Text] [Related]
16. Severe lactic acidosis and nephrolithiasis in an infant--etiology?: type 1 glycogen storage disease (GSD). Güven AG; Koyun M; Artan R; Dursun O; Baysal YE; Akman S Pediatr Nephrol; 2006 Jun; 21(6):761-5. PubMed ID: 16703371 [No Abstract] [Full Text] [Related]
17. [Congenital myopathy with lipid and glycogen overload of muscle fiber and partial deficit of carnitine]. Gilly R; Carrier H; Lamit J Ann Pediatr (Paris); 1980 May; 27(5):319-24. PubMed ID: 6940512 [No Abstract] [Full Text] [Related]
18. A case of congenital glycogen storage disease type IV with a novel GBE1 mutation. Raju GP; Li HC; Bali DS; Chen YT; Urion DK; Lidov HG; Kang PB J Child Neurol; 2008 Mar; 23(3):349-52. PubMed ID: 18230843 [TBL] [Abstract][Full Text] [Related]
19. Type I glycogen storage disease with focal nodular hyperplasia of the liver and vasoconstrictive pulmonary hypertension. Pizzo CJ Pediatrics; 1980 Feb; 65(2):341-3. PubMed ID: 6928317 [No Abstract] [Full Text] [Related]
20. A monocentric pilot study of an antioxidative defense and hsCRP in pediatric patients with glycogen storage disease type IA and III. Kalkan Ucar S; Coker M; Sözmen E; Goksen Simsek D; Darcan S Nutr Metab Cardiovasc Dis; 2009 Jul; 19(6):383-90. PubMed ID: 19073362 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]