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| 1 | Etiology and long-term outcome of extrahepatic portal vein obstruction in children显示文摘AIM:To study the management and outcome of children with extrahepatic portal vein obstruction(EHPVO) in a whole country population.METHODS:A nationwide multicenter retrospective case series of children with EHPVO was conducted.Data on demographics,radiographic studies,laboratory workup,endoscopic and surgical procedures,growth and development,were extracted from the patients' charts.Characteristics of clinical presentation,etiology of EHPVO,management and outcome were analyzed.RESULTS:Thirty patients,13 males and 17 females,19(63.3%) Israeli and 11(36.7%) Palestinians,were included in the analysis.Age at presentation was 4.8± 4.6 years,and mean follow-up was 4.9±4.3 years.Associated anomalies were found in 4 patients.The incidence of EHPVO in Israeli children aged 0-14 years was 0.72/million.Risk factors for EHPVO were detected in 13(43.3%)patients,including 9 patients(30%) with perinatal risk factors,and 4 patients(13.3%) with prothrombotic states:two had low levels of protein S and C,one had lupus anticoagulant,and one was homozygous for methyltetrahydrofolate reductase mutations.In 56.6% of patients,no predisposing factors were found.The most common presenting symptoms were an incidental finding of splenomegaly(43.3%),and upper gastrointestinal bleeding(40%).No differences were found between Israeli and Palestinian children with regard to age at presentation,etiology and clinical symptoms.Bleeding occurred in 18 patients(60%),at a median age of 3 years.Sclerotherapy or esophageal banding was performed in 20 patients.No sclerotherapy complications were reported.Portosystemic shunts were performed in 11 patients(36.6%),at a median age of 11(range 3-17)years:splenorenal in 9,mesocaval in 1,and a meso-Rex shunt in 1 patient.One patient underwent splenectomy due to severe pancytopenia.Patients were followed up for a median of 3(range 0.5-15)years.One patient died aged 3 years due to mucopolysaccharidase deficiency type Ⅲ.None of the patients died due to gastrointestinal bleeding.CONCLUSION:EHPVO is a rare disorder.The etiological factors are still mostly unknown,and the endoscopic and surgical treatment options ensure a good long-term prognosis. | Batia Weiss Eyal Shteyer Asaf Vivante Drora Berkowitz Shimon Reif Zvi Weizman Yoram Bujanover Rivka Shapiro | 2010 | World Journal of Gastroenterology2010，16，39： | 6 |
| 2 | Cleidocranial dysplasia: Part 1-General principles of the orthodontic and surgical treatment modality 显示文摘 | Becker A Lustmann J Shteyer A | 1997 | Am J Orthod Dentofacial Orthop1997，111，1： | 1 |
| 3 | Cleidocranial dysplasta: Part 2-Treatment protocol for the orthodontic and surgical modality 显示文摘 | Becket A Shteyer A Bimstein E | 1997 | Am J Orthod Dentofacial Orthop1997，111，2： | 1 |
| 4 | Surgical management of tem- poromandibular joint ankylosis Type III by retaining the displaced condyle and disc 显示文摘 | Nitzan DW Bar-Ziv J Shteyer A | 1998 | J Oral Maxillofac Surg1998，10，8： | 1 |
| 5 | The mural ameloblastoma:a review of the literature显示文摘 | Shteyer A Lustmann J Lewin-Epstein J | 1978 | J Oral Org1978，36，11： | 1 |
| 6 | Delayed hepatocellular mitotic progression and impaired liver regeneration in early growth response-1 deficient mice显示文摘 | Liao Y Shikapwasha O N Shteyer E | 2004 | J Biol Chem2004，279，43： | 1 |
| 7 | Attachment bonding to impacted teeth at the time of surgical exposure显示文摘 | Becker A Shpack N Shteyer A | 1996 | Eur J Orthod1996，18，5： | 1 |
| 8 | Outcome after portoenterostomy in biliary atresia:pivotal role of degree of liver fibrosis and intensity of stellate cell activation显示文摘 | Ramm GA Xu C | 2006 | J Pediatr Gastroenterol Nutr2006，42，： | 1 |
| 9 | Protein production by human gingival fibrnhlasts is enhanced by guanidine EDTA extracts of cementum 显示文摘 | Somerman MJ Archer SY Shteyer A | 1987 | J Periodont Res1987，22，1： | 1 |
| 10 | Assessment of 100 children in Jerusalem with supernumerary teeth 显示文摘 | Zilberman Y Malron M Shteyer A | 1992 | J Dent Child1992，59，1： | 1 |
| 11 | Outcome after portoenterostomy in biliary atresia:Pivotal role of degree of liver fibrosis and intensity of stellate cell activation显示文摘 | Shteyer E Ramm GA Xu C | 2006 | J Pediatr Gastroenterol Nutr2006，42，1： | 1 |
| 12 | Outcome after portoenterostomy in biliary atresia:pivotal role of degree of liver fibrosis and intensity of stellate cell activation显示文摘 | Shteyer E Ramm G A Xu C | 2006 | J Pediatr Gastroenterol Nutr2006，42，1： | 1 |
| 13 | Medical treatment of recurrent intussusception associated with intestinal lymph-oid hyperplasia显示文摘 | Shteyer E Koplewitz BZ Gross E | | 0，，03： | 1 |
| 14 | Assessment of 100 children in Jerusalen with supemumerary teeth显示文摘 | ZILBERMAN Y MALRON M SHTEYER A | 1992 | J Dent Child1992，59，1： | 1 |
| 15 | et al, Submandibular tuberculous lymphadenitis (scrofula) : report of two cases 显示文摘 | Bodner L Lewin-Epstein J Shteyer A | 1990 | J Oral Maxillofac Surg1990，48，2： | 1 |
| 16 | Reduced liver cell death using a bandage of alginate scaffold: A novel approach for liver reconstruction after extended partial hepatectomy显示文摘 | Eyal Shteyer Ami Ben Ya’acov Lidia Zolotaryova Avital Sinai Yoav Lichtenstein Orit Papoo Olga Kryukov Tsiona Elkayam Smadar Cohen Yaron Ilan | 2014 | Acta Biomaterialia2014，，： | 1 |
| 17 | Outcome after portoenterostomy in biliary atresia: pivotal role of degree of liver fihrosis and intensity of stellate cell activation 显示文摘 | Shteyer E Ramm GA Xu C | 2006 | J Pediatr Gastroenterol Nutr2006，，： | 1 |
| 18 | Medical treatment of recurrent intussusception associated with intestinal lymphoid hyperplasia显示文摘 | Shteyer E Koplewitz B Z Gross E | 2003 | Pediatrics2003，111，3： | 1 |
| 19 | Surgical management of temporomandibular joint ankylosis type Ⅲ by retaining the displaced condyle and disc显示文摘 | Bar-Ziv J Shteyer A | 1998 | J Oral Maxillofac Surg1998，56，11： | 1 |
| 20 | Bioactive pseudopeptidic analogues and cyclostereoisomers of osteogenic growth peptide Cterminal pentapeptide,OGP (10-14) 显示文摘 | Chen YC Muhlrad A Shteyer A | 2002 | J Med Chem2002，45，8： | 1 |
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