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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 | Inactivation of Mitochondrial Complex Ⅰ Induces the Expression of a Twin Cysteine Protein that Targets and Affects Cytosolic, Chloroplastidic and Mitochondrial Function显示文摘At12Cys-1 (At5g64400 ) 和 At12Cys-2 (At5g09570 ) 是二密切相关的 isogenes 编码小、成双的半胱氨酸蛋白质,典型地在线粒体定位了。At12Cys-2 抄本与破坏 mitochondrial 蛋白质,而是 At12Cys 的增加在许多异种被导致蛋白质仅仅与减少的 mitochondrial 在异种被检测复杂我丰富。在缺乏 mitochondrial 建筑群的异种的 At12Cys 蛋白质感应我被位于线粒体,叶绿体,和 cytosol 的 At12Cys 蛋白质伴随。生物化学的分析揭示了那甚至单个的基因删除,即, At12cys-1 或 At12cys-2,在 mitochondrial 和叶绿体功能上有效果。然而,仅仅加倍异种,即, At12cys-1 : At12cys-2,影响许多蛋白质和 mRNA 抄本编码翻译延伸因素以及 rRNA 丰富。蓝本国的页证明 At12Cys 与 mitochondrial supercomplex 共同移居我 + III。同样, At12cys-1 和 At12cys-2 基因的删除,然而并非单个基因删除,导致提高的忍耐到干旱和轻应力和增加的抗氧化剂能力。正式就职和在在建筑群的减小之上的 At12Cys 的多重本地化我丰富提供机制明确地表明 mitochondrial 机能障碍到 cytosol 然后在以外到在房间的另外的细胞器。 | Yan Wang Wenhui Lyu Oliver Berkowitz Jordan D. Radomiljac Simon R. Law Monika W. Murcha Chris Carrie Pedro F. Teixeira Beata Kmiec Owen Duncan Olivier Van Aken Reena Narsai Elzbieta Glaser Shaobai Huang Ute Roessner A. Harvey Millar James Whelan | 2016 | Molecular Plant2016，9，5： | 5 |
| 3 | Economic development, legality, and the transplant effect显示文摘 | Daniel Berkowitz Katharina Pistor Jean-Francois Richard | 2001 | European Economic Review2001，，1： | 4 |
| 4 | 食物是良药:将食物和营养融入医疗保健服务的行动显示文摘Sarah Downer及其同事探讨在医疗保健服务体系中将食品和营养纳入膳食相关疾病的预防、管理和治疗的新举措。与膳食相关的慢性病的全球流行,促使人们尝试将改善饮食作为患者医疗和护理的正规举措。 | Sarah Downer Seth A Berkowitz Timothy S Harlan Dana Lee Olstad Dariush Mozaffarian 冯琳(译) 武阳丰(校) | 2021 | 英国医学杂志中文版2021，24，4： | 2 |
| 5 | Hepatosplenic cat-scratch disease and abdominal pain显示文摘 | MICHAEL W. DUNN FRANK E. BERKOWITZ JUDSON J. MILLER JOSEPH A. SNITZER | 1997 | The Pediatric Infectious Disease Journal1997，，3： | 2 |
| 6 | Antibiotic resistance in bacteria 显示文摘 | Berkowitz F E | 1995 | South Med J1995，88，： | 2 |
| 7 | A comparison of treatment results in complete bilateral cleft lip and palate using a conservative approach versus Millard/Latham PSOT procedure显示文摘 | Berkowitz S | 1996 | Semin Orthod1996，2，1： | 2 |
| 8 | Repeat Gamma Knife Radiosurgery for Trigeminal Neuralgia显示文摘 | Kyung-Jae Park Douglas Kondziolka Oren Berkowitz Hideyuki Kano Josef Novotny Ajay Niranjan John C. Flickinger L. Dade Lunsford | 2012 | Neurosurgery2012，，2： | 2 |
| 9 | Prenatal Diagnosis and Multiple Pregnancy显示文摘 | Jane Cleary-Goldman Mary E. D'Alton Richard L. Berkowitz | 2005 | Seminars in Perinatology2005，，5： | 2 |
| 10 | A Randomized Controlled Comparison of Epidural Analgesia and Combined Spinal-Epidural Analgesia in a Private Practice Setting: Pain Scores During First and Second Stages of Labor and at Delivery显示文摘 | David Gambling Jonathan Berkowitz Thomas R. Farrell Alex Pue Dennis Shay | 2013 | Anesthesia & Analgesia2013，，3： | 2 |
| 11 | 国际卒中遗传学联盟的推荐意见(第2部分):生物样本的采集和储存显示文摘在2003年人类基因组测序以及全基因组基因分型技术发展的共同促进下,人类遗传学的进步已使我们识别出2000多个与性状相关的基因突变。由于这些突变大多数对疾病风险仅有微小的独立影响,因此成功的遗传学研究需要很大的样本量(包含数以千计、万计或者十万计的病例和对照)才能达到足够的研究效能。如此大的样本量积累需要依赖在人类遗传学研究乃至在临床研究中史无前例的大规模国际协作。现在已有许多常见疾病的专病联盟将大量独立机构和合作者联合起来。每个联盟均面临至少2个基本问题:如何整合具有足够数量、同质性和表型质量高的研究样本以及如何储存和分析来自入组受试者的生物样本,有时可能需要在数年间反复进行。 | Thomas W.K.Battey Valerie Valant Sylvia Baedorf Kassis Christina Kourkoulis Chaeyoung Lee Christopher D. Anderson Guido J. Falcone Jordi Jimenez-Conde Israel Fernandez-Cadenas Guillaume Pare Tatjana Rundek Michael L. James Robin Lemmens Tsong-Hai Lee Turgut Tatlisumak Steven J. Kittner Arne Lindgren Farrah J. Mateen Aaron L. Berkowitz Elizabeth G. Holliday Jennifer Majersik 李海峰 姜平 岳耀先 | 2015 | 国际脑血管病杂志2015，23，9： | 2 |
| 12 | Characteristics and outcomes of patients hospitalized for heart failure in the United States: Rationale, design, and preliminary observations from the first 100,000 cases in the Acute Decompensated Heart Failure National Registry (ADHERE)显示文摘 | Kirkwood F. Adams Gregg C. Fonarow Charles L. Emerman Thierry H. LeJemtel Maria Rosa Costanzo William T. Abraham Robert L. Berkowitz Marie Galvao Darlene P. Horton | 2005 | American Heart Journal2005，，2： | 2 |
| 13 | A further look at household portfolio choice and health status显示文摘 | Michael K. Berkowitz Jiaping Qiu | 2005 | Journal of Banking and Finance2005，，4： | 2 |
| 14 | NOD2/CARD15 mutation analysis and genotype-phenotype correlation in Jewish pediatric patients compared with adults with Crohn’s disease显示文摘 | Batia Weiss Raanan Shamir Yoram Bujanover Mati Waterman Corina Hartman Akiva Fradkin Drora Berkowitz Ilana Weintraub Ram Eliakim Amir Karban | 2004 | The Journal of Pediatrics2004，，2： | 2 |
| 15 | In-Hospital Mortality in Patients With Acute Decompensated Heart Failure Requiring Intravenous Vasoactive Medications显示文摘 | William T. Abraham Kirkwood F. Adams Gregg C. Fonarow Maria Rosa Costanzo Robert L. Berkowitz Thierry H. LeJemtel Mei L. Cheng Janet Wynne | 2005 | Journal of the American College of Cardiology2005，，： | 2 |
| 16 | How Accurate are Value-at-Risk Models at Commercial Banks?显示文摘 | BERKOWITZ J O'BRIEN J | 2002 | Journal of Finance2002，57，3： | 1 |
| 17 | Relationship of pentazocine plasma levels to pharmacological activity in man显示文摘 | BERKOWITZ B A ASLING J H SHNIDER S M | 1969 | Clin Pharm Ther1969，10，3： | 1 |
| 18 | Cough in the pediatric population显示文摘 | Chang AB Berkowitz RG | 2010 | Otolaryngol Clin North Am2010，43，1： | 1 |
| 19 | Accurate charac- terization of extravascular lung water in acute respiratory dis- tress syndrome 显示文摘 | Berkowitz DM Danai PA Eaton S | 2008 | Crit Care Med2008，36，6： | 1 |
| 20 | Educating Relatives of Schizophrenic Patients显示文摘 | Berkowitz R Shavit N Leff J P | 1990 | Social Psychiatry and Psychiatric Epidemiology1990，25，： | 1 |
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