1 to 8 of 8 literature results

• Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene.

  Steatorrhea and malabsorption of lipid-soluble vitamins due to exocrine pancreatic insufficiency are common in patients with cystic fibrosis and are p…

  Authors: Eyal Shteyer, Ann Saada, Avraham Shaag, Fida' Aziz Al-Hijawi, Rojette Kidess, Shoshanah Revel-Vilk, Orly Elpeleg

  Source: American journal of human genetics. 2009 Mar

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• Medical treatment of recurrent intussusception associated with intestinal lymphoid hyperplasia.

  Intestinal lymphoid hyperplasia (ILH) is an uncommon cause of recurrent intussusception in infants and young children. Surgical treatment has been sug…

  Authors: Eyal Shteyer, Benjamin Z Koplewitz, Eitan Gross, Esther Granot

  Source: Pediatrics. 2003 Mar

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• Outcome after portoenterostomy in biliary atresia: pivotal role of degree of liver fibrosis and intensity of stellate cell activation.

  OBJECTIVES: Biliary atresia (BA), a congenital idiopathic obliterative cholangiopathy, rapidly leads to liver cirrhosis and liver failure if untreated…

  Authors: Eyal Shteyer, Grant A Ramm, Chunxia Xu, Frances V White, Ross W Shepherd

  Source: Journal of pediatric gastroenterology and nutrition. 2006 Jan

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• Novel therapeutic modalities in pediatric inflammatory bowel disease.

  Management of inflammatory bowel disease in childhood poses great challenges. Apart from the disease complications, the drugs' adverse affects, especi…

  Authors: Eyal Shteyer, Michael Wilschanski

  Source: The Israel Medical Association journal : IMAJ. 2008 Nov

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• Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis.

  GOALS: To understand the relationship between acute recurrent pancreatitis and cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction.…

  Authors: Idit Segal, Yasmin Yaakov, Samuel N Adler, Hannah Blau, Efrat Broide, Moshe Santo, Yaakov Yahav, Aharon Klar, Aaron Lerner, Micha Aviram,…

  Source: Journal of clinical gastroenterology. 2008 Aug

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• Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndrome.

  Congenital cardiac defects such as peripheral pulmonary stenosis are well described in Alagille syndrome (AGS), which is transmitted in an autosomal d…

  Authors: Annick Raas-Rothschild, Eyal Shteyer, Israela Lerer, Amiram Nir, Esther Granot, Azaria J J T Rein

  Source: American journal of medical genetics. 2002 Sep 15

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• Disruption of hepatic adipogenesis is associated with impaired liver regeneration in mice.

  The liver responds to injury with regulated tissue regeneration. During early regeneration, the liver accumulates fat. Neither the mechanisms responsi…

  Authors: Eyal Shteyer, Yunjun Liao, Louis J Muglia, Paul W Hruz, David A Rudnick

  Source: Hepatology (Baltimore, Md.). 2004 Dec

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• Delayed hepatocellular mitotic progression and impaired liver regeneration in early growth response-1-deficient mice.

  The early growth response-1 transcription factor (Egr-1) is induced as part of the immediate-early gene expression response during early liver regener…

  Authors: Yunjun Liao, Olga N Shikapwashya, Eyal Shteyer, Brian K Dieckgraefe, Paul W Hruz, David A Rudnick

  Source: The Journal of biological chemistry. 2004 Oct 8

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