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324 related items for PubMed ID: 19762333
1. Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease. Kishnani PS, Chuang TP, Bali D, Koeberl D, Austin S, Weinstein DA, Murphy E, Chen YT, Boyette K, Liu CH, Chen YT, Li LH. Hum Mol Genet; 2009 Dec 15; 18(24):4781-90. PubMed ID: 19762333 [Abstract] [Full Text] [Related]
2. Molecular characterization of hepatocellular adenomas developed in patients with glycogen storage disease type I. Calderaro J, Labrune P, Morcrette G, Rebouissou S, Franco D, Prévot S, Quaglia A, Bedossa P, Libbrecht L, Terracciano L, Smit GP, Bioulac-Sage P, Zucman-Rossi J. J Hepatol; 2013 Feb 15; 58(2):350-7. PubMed ID: 23046672 [Abstract] [Full Text] [Related]
3. Resection of hepatocellular adenoma in patients with glycogen storage disease type Ia. Reddy SK, Kishnani PS, Sullivan JA, Koeberl DD, Desai DM, Skinner MA, Rice HE, Clary BM. J Hepatol; 2007 Nov 15; 47(5):658-63. PubMed ID: 17637480 [Abstract] [Full Text] [Related]
5. Glycogen storage disease type Ia and VI associated with hepatocellular carcinoma: two case reports. Manzia TM, Angelico R, Toti L, Cillis A, Ciano P, Orlando G, Anselmo A, Angelico M, Tisone G. Transplant Proc; 2011 May 15; 43(4):1181-3. PubMed ID: 21620082 [Abstract] [Full Text] [Related]
12. A case study of a liver transplant-treated patient with glycogen storage disease type Ia presenting with multiple inflammatory hepatic adenomas: an analysis of clinicopathologic and genetic data. Wang A, Wu J, Yuan X, Liu J, Lu C. BMC Med Genomics; 2024 May 06; 17(1):124. PubMed ID: 38711024 [Abstract] [Full Text] [Related]
13. Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutations. Seydewitz HH, Matern D. Hum Mutat; 2000 Jan 06; 15(1):115-6. PubMed ID: 10612834 [Abstract] [Full Text] [Related]
14. An adult male patient with multiple adenomas and a hepatocellular carcinoma: mild glycogen storage disease type Ia. Cassiman D, Libbrecht L, Verslype C, Meersseman W, Troisi R, Zucman-Rossi J, Van Vlierberghe H. J Hepatol; 2010 Jul 06; 53(1):213-7. PubMed ID: 20447711 [Abstract] [Full Text] [Related]
15. Loss of hepatocyte nuclear factor 1alpha function in human hepatocellular adenomas leads to aberrant activation of signaling pathways involved in tumorigenesis. Pelletier L, Rebouissou S, Paris A, Rathahao-Paris E, Perdu E, Bioulac-Sage P, Imbeaud S, Zucman-Rossi J. Hepatology; 2010 Feb 06; 51(2):557-66. PubMed ID: 20041408 [Abstract] [Full Text] [Related]
16. [Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis]. Qiu WJ, Zhang YF, Pan J, Ye J, Liu XQ, Han LS, Gu XF. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 06; 22(1):44-8. PubMed ID: 15696478 [Abstract] [Full Text] [Related]
17. Glycogen storage disease type Ia: molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells. Akanuma J, Nishigaki T, Fujii K, Matsubara Y, Inui K, Takahashi K, Kure S, Suzuki Y, Ohura T, Miyabayashi S, Ogawa E, Iinuma K, Okada S, Narisawa K. Am J Med Genet; 2000 Mar 13; 91(2):107-12. PubMed ID: 10748407 [Abstract] [Full Text] [Related]
18. A copy number gain of the 6p arm is linked with advanced hepatocellular carcinoma: an array-based comparative genomic hybridization study. Chochi Y, Kawauchi S, Nakao M, Furuya T, Hashimoto K, Oga A, Oka M, Sasaki K. J Pathol; 2009 Apr 13; 217(5):677-84. PubMed ID: 19097070 [Abstract] [Full Text] [Related]
19. Glycogen storage disease type I: diagnosis and phenotype/genotype correlation. Matern D, Seydewitz HH, Bali D, Lang C, Chen YT. Eur J Pediatr; 2002 Oct 13; 161 Suppl 1():S10-9. PubMed ID: 12373566 [Abstract] [Full Text] [Related]
20. Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type ia, including novel mutations K76N, V166A and 540del5. Kozák L, Francová H, Hrabincová E, Stastná S, Pesková K, Elleder M. Hum Mutat; 2000 Jul 13; 16(1):89. PubMed ID: 10874313 [Abstract] [Full Text] [Related] Page: [Next] [New Search]