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	题名	作者	年代	出处	被引量
1	Pancreatic fistula after a pancreaticoduodenectomy for ductal adenocarcinoma and its association with morbidity: a multicentre study of the F rench S urgical A ssociation显示文摘	Pietro Addeo Jean Robert Delpero Francois Paye Elie Oussoultzoglou Pascal R Fuchshuber Alain Sauvanet Antonio Sa Cunha Yves Patrice Le Treut Mustapha Adham Jean‐Yves Mabrut Laurence Chiche Philippe Bachellier	2014	HPB2014，，1：	2
2	Prediction of core saturation instability at an HVDC converter显示文摘	Burton R S Fuchshuber C Woodford DA	1996	IEEE Trans on Power Delivery1996，11，4：	1
3	Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2:two facets of the same disease?显示文摘	Dahan K Fuchshuber A Adamis S	2001	J Am Soc Nephrol2001，12，：	1
4	Prediction of core saturation instability at an HVDC converter 显示文摘	BURTON R S FUCHSHUBER C WOODFORD D A	1996	IEEETransonPower Delivery1996，11，4：	1
5	Medullary carcinoma of the thyroid:prognostic factors and treatment recommendation显示文摘	Fuchshuber PR Loree TR Hicks WL	1998	Ann Surg Oncol1998，5，1：	1
6	Reoperative surgery after repair of postcholecystectomy bile duct injuries: is it worthwhile? 显示文摘	Addeo P Oussoultzoglou E Fuchshuber P	2013	World J Surg2013，37，：	1
7	Clinical andgenetic evaluation of familial steroid-responsive nephroticsyndrome in childhood显示文摘	Fuchshuber A Gribouval O Ronner V	2001	J Am Soc Nephrol2001，12，2：	1
8	Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood显示文摘	Fuchshuber A Gribouval O Ronner V	2001	J Am Soc Nephrol2001，12，2：	1
9	Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitro 显示文摘	Suormala T Fowler B Duran M Burtscher A Fuchshuber A Tratzmuller R	1997	Pediatr Res1997，41，5：	1
10	Mapping gene(SRN1)to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis显示文摘	Fuchshuber A Jean G Gribouval O	1995	Hum Mol Genet1995，4，11：	1
11	Fh3 ligand promotes the generation of a distinct CD34( + )human natural killer cell progenitor that responds to interleukin - 15 显示文摘	Yu H Fehniger TA Fuchshuber P	1998	Blood1998，，92：	1
12	What is a safe future liver remnant size in patients undergoing major hepatectomy for colorectal liver metastases and treated by intensive preoperative chemotherapy? 显示文摘	Narita M Oussouhzoglou E Fuchshuber P	2012	Anu Surg Oncol2012，19，8：	1
13	Prediction of core saturation instability at an HVDCconverter 显示文摘	Burton R S Fuchshuber C F Woodford D A	1996	IEEE Transactions on Power Delivery1996，11，4：	1
14	What Is a Safe Future Liver Remnant Size in Patients Undergoing Major Hepatectomy for Colorectal Liver Metastases and Treated by Intensive Preoperative Chemotherapy?显示文摘	Masato Narita Elie Oussoultzoglou Pascal Fuchshuber Patrick Pessaux Marie-Pierre Chenard Edoardo Rosso Cinzia Nobili Daniel Jaeck Philippe Bachellier	2012	Annals of Surgical Oncology2012，，8：	1
15	Medullary carcinoma of the thyroid:prognostic factors and treatment recommendation显示文摘	Fuchshuber P R Loree T R Hicks W L Jr	1998	Ann Surg Oncol1998，5，：	1
16	Mapping a gene(SRNl)to chromosome 1q25-q3l inidiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis显示文摘	Fuchshuber A Jean G Gribouval O et a1	1995	Hum Mol Genet1995，4，11：	1
17	S680N substitution of the follicle-stimulating hormone receptor is a common polymorphism not associated with spontaneous human twinning显示文摘	Hasbargen U Ruebsamen H Fuchshuber S	2001	Eur J Med Res2001，6，7：	1
18	NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome 显示文摘	Bounte N Gribouval O Roselli S Benessy F Lee H Fuchshuber A	2000	Nat Genet2000，24，4：	1
19	Reoperative Surgery After Repair of Postcholecystectomy Bile Duct Injuries: Is it Worthwhile?显示文摘	Pietro Addeo Elie Oussoultzoglou Pascal Fuchshuber Edoardo Rosso Cinzia Nobili Regis Souche Daniel Jaeck Philippe Bachellier	2013	World Journal of Surgery2013，，3：	1
20	mut0methylmalonic acidemia: eleven novel mutations of themethylmalonyl CoA mutase including a deletion-insertionmutation 显示文摘	Fuchshuber A Mucha B Baumgartner ER	2000	Hum Mutat2000，16，2：	1

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