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Hartmut Neumann

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Jan-Helge Klingler; Marie T Krüger; Johannes R Lemke; Hartmut P H Neumann; Vera van Velthoven; Josef Zentner; Cordula Jilg; Sven Gläsker
Sequence variations in the von hippel-lindau tumor suppressor gene in patients with intracranial aneurysms.
Elena Panizza; Elena Rapizzi; Maurizio Castellano; Tonino Ercolino; Ileana Ferrero; Massimo Mannelli; Luigi Mori; Hartmut P H Neumann; Giuseppe Opocher; Paola Goffrini
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome.
Hannes Philipp Neeff; Hartmut P H Neumann; Przemyslaw Pisarski; Dietlind Tittelbach-Helmrich; Ulrich Theodor Hopt; Konstantin Karajanev; Oliver Drognitz
One hundred consecutive kidney transplantations with simultaneous ipsilateral nephrectomy in patients with autosomal dominant polycystic kidney disease.

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2013: Jan-Helge Klingler; Marie T Krüger; Johannes R Lemke; Hartmut P H Neumann; Vera van Velthoven; Josef Zentner; Cordula Jilg; Sven Gläsker
Sequence variations in the von hippel-lindau tumor suppressor gene in patients with intracranial aneurysms.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2013;22(4):437-43.
2013: Elena Panizza; Elena Rapizzi; Maurizio Castellano; Tonino Ercolino; Ileana Ferrero; Massimo Mannelli; Luigi Mori; Hartmut P H Neumann; Giuseppe Opocher; Paola Goffrini
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome.
Human molecular genetics 2013;22(4):804-15.
2013: Hannes Philipp Neeff; Hartmut P H Neumann; Przemyslaw Pisarski; Dietlind Tittelbach-Helmrich; Ulrich Theodor Hopt; Konstantin Karajanev; Oliver Drognitz
One hundred consecutive kidney transplantations with simultaneous ipsilateral nephrectomy in patients with autosomal dominant polycystic kidney disease.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2013;28(2):466-71.
2012: Hartmut P H Neumann; Mercedes Nunez; Jens Nürnberger; Nadine Ortiz Brüchle; Peter Riegler; Elke Schaeffner; Jochen Wilpert; Klaus Zerres; Pablo Azurmendi; Janina Bacher; R Corradini; Markus Cybulla; Sven Gläsker; Michael M Hoffmann; Annette Kraemer-Guth; Zinaida Nabulsi; Cordula Jilg
Adult patients with sporadic polycystic kidney disease: the importance of screening for mutations in the PKD1 and PKD2 genes.
International urology and nephrology 2012;44(6):1753-62.
2012: H Christian Rischke; Jochen Rössler; Jochen Seufert; Wolfgang A Weber; Thorsten Wiech; Damian Wild; Matthias R Benz; Dean Campbell; Rebecca A Dumont; Michael Mix; Hartmut P H Neumann
Correlation of the genotype of paragangliomas and pheochromocytomas with their metabolic phenotype on 3,4-dihydroxy-6-18F-fluoro-L-phenylalanin PET.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2012;53(9):1352-8.
2012: C A Jilg; Christian Leiber; Hartmut P H Neumann; Oliver Schäfer; P U Ardelt; Sven Gläsker; M Schwardt; Wolfgang Schultze-Seemann
Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-up.
Familial cancer 2012;11(3):387-94.
2012: Alexander Weber; Michael M Hoffmann; Hartmut P H Neumann; Zoran Erlic
Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.
Hormones & cancer 2012;3(4):187-92.
2012: Angelica Malinoc; Alexander Bosse; Serdar Deger; Charis Eng; Michael M Hoffmann; Cordula Jilg; Schmid Kurt Werner; Gerd Rasp; Joern Straeter; Maren Sullivan; Thorsten Wiech; Hartmut P H Neumann
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3.
Endocrine-related cancer 2012;19(3):283-90.
2012: Francesca Schiavi; Elisa Taschin; Franco Trabalzini; Stefania Zovato; Theodoros Savvoukidis; Pietro Amistà; Mattia Barbareschi; Susi Barollo; Sara Bobisse; Fabio Branz; Maria Enrica Cecchini; Antonella Del Piano; Serena Demattè; Davide Donner; Zoran Erlic; Cesare Grandi; Franco Grego; Vittorio Manera; Fabio Marroni; Hartmut P H Neumann; Giuseppe Opocher
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
The Journal of clinical endocrinology and metabolism 2012;97(4):E637-41.
2012: Piero F Alesina; Jakob Hinrichs; Beate Meier; Hartmut P H Neumann; Kurt W Schmid; Martin Walz
Minimally invasive cortical-sparing surgery for bilateral pheochromocytomas.
Langenbeck's archives of surgery / Deutsche Gesellschaft für Chirurgie 2012;397(2):233-8.
2012: Hartmut P H Neumann; Peter Riegler; Elke Schaeffner; Klaus Zerres; Pablo J Azurmendi; Janina Bacher; Nadine Ortiz Bruechle; Christian Burchardi; Charis Eng; Michael M Hoffmann; Vera Ivanovas; Cordula Jilg; Annette Kraemer-Guth; Irina Mader; Angelica Malinoc; Rodolfo S Martin; Zinaida Nabulsi; Sven Gläsker
Characteristics of intracranial aneurysms in the else kröner-fresenius registry of autosomal dominant polycystic kidney disease.
Cerebrovascular diseases extra 2012;2(1):71-9.
2012: C A Jilg; Hartmut P H Neumann; Oliver Schäfer; P U Ardelt; Sven Gläsker; M Schwardt; Wolfgang Schultze-Seemann
Growth kinetics in von Hippel-Lindau-associated renal cell carcinoma.
Urologia internationalis 2012;88(1):71-8.
2011: Maren Sullivan; Thorsten Wiech; Aurelia Winter; Magdalena Woznowski; Martin Zeier; Ludwig Patzer; Stefanie Reiermann; Lisa A Rybicki; Klaus Arbeiter; Gani Berisha; Andreas Bock; Klemens Budde; Charis Eng; Thomas Fehr; Ariana Gaspert; Oemer-Necmi Goek; Michael M Hoffmann; Bernd Hoppe; Karl Lhotta; Hannah Linke; Angelica Malinoc; Hartmut P H Neumann
Age-related penetrance of hereditary atypical hemolytic uremic syndrome.
Annals of human genetics 2011;75(6):639-47.
2011: Hartmut P H Neumann; Kurt W Schmid; Maren Sullivan; Martin K Walz; Aurelia Winter; Hartmut Bertz; Carsten Christof Boedeker; Michael M Hoffmann; Angelica Malinoc; Lars C Moeller; Charis Eng
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites.
The Journal of clinical endocrinology and metabolism 2011;96(8):E1279-82.
2011: Kristi L Bennett; Rebecca Campbell; Ram Ganapathi; Shireen Ganapathi; Hartmut P H Neumann; Brian Rini; Ming Zhou; Charis Eng
Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma.
Genes, chromosomes & cancer 2011;50(8):654-61.
2011: Sven Gläsker; Beate Hippchen; Hartmut P H Neumann; Mukesch J Shah; Vera van Velthoven
Doppler-sonographically guided resection of central nervous system hemangioblastomas.
Neurosurgery 2011;68(2 Suppl Operative):267-75; discussion 274-5.
2011: Claudia Papewalis; Christiane Kouatchoua; Margret Ehlers; Benedikt Jacobs; Dominika Porwol; Sven Schinner; Holger S Willenberg; Martin Anlauf; Andreas Raffel; Graeme Eisenhofer; Hartmut P H Neumann; Stefan R Bornstein; Werner A Scherbaum; Matthias Schott
Chromogranin A as potential target for immunotherapy of malignant pheochromocytoma.
Molecular and cellular endocrinology 2011;335(1):69-77.
2011: Laura von Dücker; Martin K Walz; Christian Voss; Georg Arnold; Charis Eng; Hartmut P H Neumann
Laparoscopic organ-sparing resection of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors.
World journal of surgery 2011;35(3):563-7.
2011: Nazli Gonc; Ozlem Engiz; Hartmut P H Neumann; Huseyin Demirbilek; Alev Ozon; Ayfer Alikasifoglu; Nurgun Kandemir
Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient.
Journal of pediatric endocrinology & metabolism : JPEM 2011;24(1-2):109-12.
2010: Heiko Schweizer; Joachim Boehm; Jan Thorsten Winterer; Damian Wild; Hartmut P H Neumann; Thorsten Wiech; Mike Stubanus; E Wolfgang Kuehn
Phaeochromocytoma and thrombotic microangiopathy: favourable outcome despite advanced renal failure.
Journal of clinical pathology 2010;63(8):754-6.
2010: Nelson Wohllk; Heiko Schweizer; Zoran Erlic; Kurt Werner Schmid; Martin K Walz; Friedhelm Raue; Hartmut P H Neumann
Multiple endocrine neoplasia type 2.
Best practice & research. Clinical endocrinology & metabolism 2010;24(3):371-87.
2010: Maren Sullivan; Zoran Erlic; Michael M Hoffmann; Klaus Arbeiter; Ludwig Patzer; Klemens Budde; Bernd Hoppe; Martin Zeier; Karl Lhotta; Lisa A Rybicki; Andreas Bock; Gani Berisha; Hartmut P H Neumann
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.
Annals of human genetics 2010;74(1):17-26.
2010: Zoran Erlic; Michael M Hoffmann; Maren Sullivan; Gerlind Franke; Mariola Peczkowska; Igor Harsch; Matthias Schott; Helmut E Gabbert; Matti Valimäki; Simon F Preuss; Kornelia Hasse-Lazar; Dariusz Waligorski; Mercedes Robledo; Andrzej Januszewicz; Charis Eng; Hartmut P H Neumann
Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.
The Journal of clinical endocrinology and metabolism 2010;95(1):308-13.
2009: José Gaal; Francien H van Nederveen; Zoran Erlic; Esther Korpershoek; Rogier Oldenburg; Carsten C Boedeker; Udo Kontny; Hartmut P H Neumann; Winand N M Dinjens; Ronald R de Krijger
Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.
The Journal of clinical endocrinology and metabolism 2009;94(11):4367-71.
2009: Zoran Erlic; Lisa Rybicki; Mariola Peczkowska; Henriette Golcher; Peter H Kann; Michael Brauckhoff; Karsten Müssig; Michaela Muresan; Andreas Schäffler; Nicole Reisch; Matthias Schott; Martin Fassnacht; Giuseppe Opocher; Silke Klose; Christian Fottner; Flavio Forrer; Ursula Plöckinger; Stephan Petersenn; Dimitry Zabolotny; Oleg Kollukch; Svetlana Yaremchuk; Andrzej Januszewicz; Martin Walz; Charis Eng; Hartmut P H Neumann
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009;15(20):6378-85.
2009: Hartmut P H Neumann; Charis Eng
The approach to the patient with paraganglioma.
The Journal of clinical endocrinology and metabolism 2009;94(8):2677-83.
2009: Zoran Erlic; Hartmut P H Neumann
Diagnosing patients with hereditary paraganglial tumours.
The lancet oncology 2009;10(8):741.
2009: Carsten Christof Boedeker; Zoran Erlic; Stéphane Richard; Udo Kontny; Anne-Paule Gimenez-Roqueplo; Alberto Cascon; Mercedes Robledo; José M de Campos; Francien H van Nederveen; Ronald R de Krijger; Nelly Burnichon; José Gaal; Martin A Walter; Kirsten Reschke; Thorsten Wiech; Johannes Weber; Klaus Dieter Rückauer; Pierre Francois Plouin; Vincent Darrouzet; Sophie Giraud; Charis Eng; Hartmut P H Neumann
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
The Journal of clinical endocrinology and metabolism 2009;94(6):1938-44.
2009: Gerlind Franke; Birke Bausch; Michael M Hoffmann; Markus Cybulla; Christian Wilhelm; Juergen Kohlhase; Gerd Scherer; Hartmut P H Neumann
Alu-Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype-phenotype correlations in VHL patients.
Human mutation 2009;30(5):776-86.
2009: Zoran Erlic; Hartmut P H Neumann
When should genetic testing be obtained in a patient with phaeochromocytoma or paraganglioma?
Clinical endocrinology 2009;70(3):354-7.
2009: Joerg Schipper; Uwe Spetzger; Marcos Tatagiba; Steffen K Rosahl; Hartmut P H Neumann; Carsten Christof Boedeker; Wolfgang Maier
Juxtacondylar approach in temporal paraganglioma surgery: when and why?
Skull base : official journal of North American Skull Base Society ... [et al.] 2009;19(1):43-7.
2009: Carsten Christof Boedeker; Hartmut P H Neumann; Christian Offergeld; Wolfgang Maier; Maurizio Falcioni; Ansgar Berlis; Joerg Schipper
Clinical features of paraganglioma syndromes.
Skull base : official journal of North American Skull Base Society ... [et al.] 2009;19(1):17-25.
2009: Zoran Erlic; Hartmut P H Neumann
Familial pheochromocytoma.
Hormones (Athens, Greece) 2009;8(1):29-38.
2009: Daniel Romaker; Michael Puetz; Sven Teschner; Johannes Donauer; Marcel Geyer; Peter Gerke; Brigitta Rumberger; Bernd Dworniczak; Petra Pennekamp; Björn Buchholz; Hartmut P H Neumann; Rajiv Kumar; Joachim Gloy; Kai-Uwe Eckardt; Gerd Walz
Increased expression of secreted frizzled-related protein 4 in polycystic kidneys.
Journal of the American Society of Nephrology : JASN 2009;20(1):48-56.
2008: Mariola Peczkowska; Zoran Erlic; Michael M Hoffmann; Mariusz Furmanek; Jaroslaw Cwikla; Agata Kubaszek; Aleksander Prejbisz; Zbigniew Szutkowski; Andrzej Kawecki; Krzysztof Chojnowski; Anna Lewczuk; Mieczyslaw Litwin; Witold Szyfter; Martin A Walter; Maren Sullivan; Charis Eng; Andrzej Januszewicz; Hartmut P H Neumann
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.
The Journal of clinical endocrinology and metabolism 2008;93(12):4818-25.
2008: Ioana N Milos; Karin Frank-Raue; Nelson Wohllk; Ana Luiza Maia; Eduardo Pusiol; Attila Patocs; Mercedes Robledo; Josefina Biarnes; Marta Barontini; Thera P Links; Jan Willem de Groot; Sarka Dvorakova; Mariola Peczkowska; Lisa A Rybicki; Maren Sullivan; Friedhelm Raue; Ioana Zosin; Charis Eng; Hartmut P H Neumann
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation.
Endocrine-related cancer 2008;15(4):1035-41.
2008: Caroline D E Margetts; Mark Morris; Dewi Astuti; Dean Gentle; Alberto Cascon; Fiona E McRonald; Daniel Catchpoole; Mercedes Robledo; Hartmut P H Neumann; Farida Latif; Eamonn R Maher
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma.
Endocrine-related cancer 2008;15(3):777-86.
2008: Hartmut P H Neumann; Zoran Erlic
Maternal transmission of symptomatic disease with SDHD mutation: fact or fiction?
The Journal of clinical endocrinology and metabolism 2008;93(5):1573-5.
2008: Mariola Peczkowska; Alberto Cascon; Aleksander Prejbisz; Agata Kubaszek; B Jarosław Cwikła; Mariusz Furmanek; Zoran Erlic; Charis Eng; Andrzej Januszewicz; Hartmut P H Neumann
Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation.
Nature clinical practice. Endocrinology & metabolism 2008;4(2):111-5.
2007: Markus Cybulla; Hartmut P H Neumann
[Fabry disease. An interdisciplinary challenge].
Deutsche medizinische Wochenschrift (1946) 2007;132(43):2271-7.
2007: Hartmut P H Neumann; Alexander O Vortmeyer; Dieter Schmidt; Martin Werner; Zoran Erlic; Alberto Cascon; Birke Bausch; Andrzej Januszewicz; Charis Eng
Evidence of MEN-2 in the original description of classic pheochromocytoma.
The New England journal of medicine 2007;357(13):1311-5.
2007: Sebastian Chakrit Bhakdi; Panudda Sratongno; Pattamawan Chimma; Thanaporn Rungruang; Aporn Chuncharunee; Hartmut P H Neumann; Prida Malasit; Kovit Pattanapanyasat
Re-evaluating acridine orange for rapid flow cytometric enumeration of parasitemia in malaria-infected rodents.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 2007;71(9):662-7.
2007: Markus Cybulla; K Walter; Hartmut P H Neumann; U Widmer; M Schärer; G Sunder-Plassmann; T Jansen; A Rolfs; M Beck
[Fabry disease: demographic data since introduction of enzyme replacement therapy].
Deutsche medizinische Wochenschrift (1946) 2007;132(28-29):1505-9.
2007: Jan M Langrehr; Marcus Bahra; Glen Kristiansen; Hartmut P H Neumann; Luitgard M Neumann; Ursula Plöckinger; Enrique Lopez-Hänninen
Neuroendocrine tumor of the pancreas and bilateral adrenal pheochromocytomas. A rare manifestation of von Hippel-Lindau disease in childhood.
Journal of pediatric surgery 2007;42(7):1291-4.
2007: Carsten Christof Boedeker; Hartmut P H Neumann; Wolfgang Maier; Birke Bausch; Jörg Schipper; Gerd Jürgen Ridder
Malignant head and neck paragangliomas in SDHB mutation carriers.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2007;137(1):126-9.
2007: Klaus-Martin Kreusel; Nikolaos E Bechrakis; Hartmut P H Neumann; Dieter Schmidt; Michael H Foerster
Solitary juxtapapillary capillary retinal angioma and von Hippel-Lindau disease.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2007;42(2):251-5.
2007: Klaus-Martin Kreusel; Nikolaos E Bechrakis; Hartmut P H Neumann; Michael H Foerster
[Juxtapapillary capillary retinal angioma with epiretinal membrane of the macula in familial Von-Hippel-Lindau-Syndrome].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2007;104(4):317-20.
2007: Hartmut P H Neumann; Markus Cybulla; Sven Gläsker; C Coulin; Vera van Velthoven; Ansgar Berlis; C Hader; Oliver Schäfer; M Treier; Ingo Brink; Wolfgang Schultze-Seemann; Christian Leiber; Klaus Dieter Rückauer; Bernd Junker; F J Agostini; Andreas Hetzel; C C Boedeker
[Von Hippel-Lindau disease. Interdisciplinary patient care].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2007;104(2):119-26.
2007: Bernhard U Bender; Thomas Quaschning; Hartmut P H Neumann; Dieter Schmidt; Annette Kraemer-Guth
A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2007;45(4):483-6.
2007: Detlef Boehm; Janina Bacher; Hartmut P H Neumann
Gross genomic rearrangement involving the TSC2-PKD1 contiguous deletion syndrome: characterization of the deletion event by quantitative polymerase chain reaction deletion assay.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2007;49(1):e11-21.
2006: Martin Walz; Piero F Alesina; Frank A Wenger; Anastasios Deligiannis; Eduard Szuczik; Stephan Petersenn; Andreas Ommer; Harald Groeben; Klaus Peitgen; Onno Eilard Janssen; Thomas Philipp; Hartmut P H Neumann; Kurt W Schmid; Klaus Mann
Posterior retroperitoneoscopic adrenalectomy--results of 560 procedures in 520 patients.
Surgery 2006;140(6):943-8; discussion 948-50.
2006: Nicole Reisch; Mariola Peczkowska; Andrzej Januszewicz; Hartmut P H Neumann
Pheochromocytoma: presentation, diagnosis and treatment.
Journal of hypertension 2006;24(12):2331-9.
2006: Markus Cybulla; M Kleber; K N Walter; S M Kroeber; Hartmut P H Neumann; Monika Engelhardt
Is Fabry disease associated with leukaemia?
British journal of haematology 2006;135(2):264-5.
2006: Manfred Fliegauf; Judit Horvath; Christian von Schnakenburg; Heike Olbrich; Dominik Müller; Julia Thumfart; Bernhard Schermer; Gregory Pazour; Hartmut P H Neumann; Hanswalter Zentgraf; Thomas Benzing; Heymut Omran
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia.
Journal of the American Society of Nephrology : JASN 2006;17(9):2424-33.
2006: Birke Bausch; Ann-Cathrin Koschker; Martin Fassnacht; Johanna Stoevesandt; Michael M Hoffmann; Charis Eng; Bruno Allolio; Hartmut P H Neumann
Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma.
The Journal of clinical endocrinology and metabolism 2006;91(9):3478-81.
2006: Vassilios I Vougioukas; Sven Gläsker; Ulrich Hubbe; Ansgar Berlis; Heymut Omran; Hartmut P H Neumann; Vera van Velthoven
Surgical treatment of hemangioblastomas of the central nervous system in pediatric patients.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2006;22(9):1149-53.
2006: Birke Bausch; Carsten Christof Boedeker; Ansgar Berlis; Ingo Brink; Markus Cybulla; Martin Walz; Andrzej Januszewicz; Claudio Letizia; Giuseppe Opocher; Charis Eng; Hartmut P H Neumann
Genetic and clinical investigation of pheochromocytoma: a 22-year experience, from Freiburg, Germany to international effort.
Annals of the New York Academy of Sciences 2006;1073():122-37.
2006: Klaus-Martin Kreusel; Nikolaos E Bechrakis; Lothar Krause; Hartmut P H Neumann; Michael H Foerster
Retinal angiomatosis in von Hippel-Lindau disease: a longitudinal ophthalmologic study.
Ophthalmology 2006;113(8):1418-24.
2006: Albrecht M Müller; Annette Geibel; Hartmut P H Neumann; Alexander Kühnemund; Annette Schmitt-Gräff; Joachim Böhm; Monika Engelhardt
Primary (AL) amyloidosis in plasma cell disorders.
The oncologist 2006;11(7):824-30.
2006: Birke Bausch; Wiktor Borozdin; Hartmut P H Neumann
Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma.
The New England journal of medicine 2006;354(25):2729-31.
2006: Martin Walz; Piero F Alesina; Frank A Wenger; J Albrecht Koch; Hartmut P H Neumann; Stephan Petersenn; Kurt W Schmid; Klaus Mann
Laparoscopic and retroperitoneoscopic treatment of pheochromocytomas and retroperitoneal paragangliomas: results of 161 tumors in 126 patients.
World journal of surgery 2006;30(5):899-908.
2006: Klaus-Martin Kreusel; Nikolaos E Bechrakis; Hartmut P H Neumann; Michael H Foerster
Pars plana vitrectomy for juxtapapillary capillary retinal angioma.
American journal of ophthalmology 2006;141(3):587-9.
2006: Christian A Koch; Frederieke M Brouwers; Alexander O Vortmeyer; Andrea Tannapfel; Steven Libutti; Zhengping Zhuang; Karel Pacak; Hartmut P H Neumann; Ralf Paschke
Somatic VHL gene alterations in MEN2-associated medullary thyroid carcinoma.
BMC cancer 2006;6():131.
2006: Ingo Brink; Oliver Schaefer; Martin Walz; Hartmut P H Neumann
Fluorine-18 DOPA PET imaging of paraganglioma syndrome.
Clinical nuclear medicine 2006;31(1):39-41.
2005: Dieter Schmidt; Hartmut P H Neumann
Spontaneous regression of retinal angiomatous lesions in v. Hippel-Lindau disease (VHL).
European journal of medical research 2005;10(12):532-4.
2005: Francesca Schiavi; Carsten Christof Boedeker; Birke Bausch; Mariola Peçzkowska; Clara Fuentes Gomez; Thomas Strassburg; Christian Pawlu; Mary Buchta; Maren Salzmann; Michael M Hoffmann; Ansgar Berlis; Ingo Brink; Markus Cybulla; Mihaela Muresan; Martin A Walter; Flavio Forrer; Matti Välimäki; Andrzej Kawecki; Zbigniew Szutkowski; Jörg Schipper; Martin Walz; Pascal Pigny; Catherine Bauters; Joan E Willet-Brozick; Bora E Baysal; Andrzej Januszewicz; Charis Eng; Giuseppe Opocher; Hartmut P H Neumann
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.
JAMA : the journal of the American Medical Association 2005;294(16):2057-63.
2005: Christian Pawlu; Birke Bausch; N Reisch; Hartmut P H Neumann
Genetic testing for pheochromocytoma-associated syndromes.
Annales d'endocrinologie 2005;66(3):178-85.
2005: Markus Cybulla; Ellen Schaefer; Susanne Wendt; hao LING; Stefan Kröber; Ulrich Hövelborn; Stefan Schandelmaier; Rolf Rohrbach; Hartmut P H Neumann
Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneys.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2005;45(5):e82-9.
2005: Thiagarajan Nambirajan; Karl Leeb; Hartmut P H Neumann; Ulrike B Graubner; Günter Janetschek
Laparoscopic adrenal surgery for recurrent tumours in patients with hereditary phaeochromocytoma.
European urology 2005;47(5):622-6.
2005: Ellen Schäfer; Karin Baron; Urs Widmer; Patrick Deegan; Hartmut P H Neumann; Gere Sunder-Plassmann; Jan-Ove Johansson; Catharina Whybra; Markus Ries; Gregory M Pastores; Atul Mehta; Michael Beck; Andreas Gal
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry disease.
Human mutation 2005;25(4):412.
2005: Hartmut P H Neumann; Markus Cybulla; Hirotaka Shibata; Mototsugu Oya; Mitsuhide Naruse; Eiji Higashihara; Toshiro Terachi; hao LING; Hiroshi Takami; Taro Shuin; Masaru Murai
New genetic causes of pheochromocytoma: current concepts and the clinical relevance.
The Keio journal of medicine 2005;54(1):15-21.
2005: C D E Margetts; Dewi Astuti; Dean Gentle; Wendy N Cooper; Alberto Cascon; Daniel Catchpoole; Mercedes Robledo; Hartmut P H Neumann; Farida Latif; Eamonn R Maher
Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas.
Endocrine-related cancer 2005;12(1):161-72.
2005: Markus Joerger; Dieter Koeberle; Hartmut P H Neumann; Silke Gillessen
Von Hippel-Lindau disease--a rare disease important to recognize.
Onkologie 2005;28(3):159-63.
2005: Carsten Christof Boedeker; Hartmut P H Neumann; Gerd Jürgen Ridder; Wolfgang Maier; Jörg Schipper
Paragangliomas in patients with mutations of the SDHD gene.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2005;132(3):467-70.
2005: Christian Pawlu; Birke Bausch; Hartmut P H Neumann
Mutations of the SDHB and SDHD genes.
Familial cancer 2005;4(1):49-54.
2004: Martin Walz; Klaus Peitgen; Daniela Diesing; Stephan Petersenn; Onno Eilard Janssen; Thomas Philipp; Klaus A Metz; Klaus Mann; Kurt W Schmid; Hartmut P H Neumann
Partial versus total adrenalectomy by the posterior retroperitoneoscopic approach: early and long-term results of 325 consecutive procedures in primary adrenal neoplasias.
World journal of surgery 2004;28(12):1323-9.
2004: Dewi Astuti; Mark Morris; Cecilia Krona; Frida Abel; Dean Gentle; Tommy Martinsson; Per Kogner; Hartmut P H Neumann; R Voutilainen; Charis Eng; P Rustin; Farida Latif; Eamonn R Maher
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma.
British journal of cancer 2004;91(10):1835-41.
2004: Zishan Allibhai; George Rodrigues; Ed Brecevic; Hartmut P H Neumann; Eric Winquist
Malignant pheochromocytoma associated with germline mutation of the SDHB gene.
The Journal of urology 2004;172(4 Pt 1):1409-10.
2004: Graeme Eisenhofer; Stefan R Bornstein; Frederieke M Brouwers; Nai-Kong V Cheung; Patricia Dahia; Ronald R de Krijger; Thomas J Giordano; Lloyd A Greene; David S Goldstein; Hendrik Lehnert; William M Manger; John M Maris; Hartmut P H Neumann; Karel Pacak; Barry L Shulkin; David I Smith; Arthur S Tischler; William F Young
Malignant pheochromocytoma: current status and initiatives for future progress.
Endocrine-related cancer 2004;11(3):423-36.
2004: Hartmut P H Neumann; Christian Pawlu; Mariola Peczkowska; Birke Bausch; Sarah R McWhinney; Mihaela Muresan; Mary Buchta; Gerlind Franke; Joachim Klisch; Thorsten A Bley; Stefan Hoegerle; Carsten Christof Boedeker; Giuseppe Opocher; Jörg Schipper; Andrzej Januszewicz; Charis Eng
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
JAMA : the journal of the American Medical Association 2004;292(8):943-51.
2004: Jörg Schipper; Carsten Christof Boedeker; Wolfgang Maier; Hartmut P H Neumann
[Paragangliomas of the head and neck. Part 2: Therapy and follow-up].
HNO 2004;52(7):651-60; quiz 661.
2004: Jörg Schipper; Carsten Christof Boedeker; Wolfgang Maier; Hartmut P H Neumann
[Paragangliomas in the head-/neck region. I: Classification and diagnosis].
HNO 2004;52(6):569-74; quiz 575.
2004: Julia Hoefele; Edgar Otto; Helmut Felten; Karlwilhelm Kühn; Thorsten A Bley; Ingeborg Zäuner; Friedhelm Hildebrandt; Hartmut P H Neumann
Clinical and histological presentation of 3 siblings with mutations in the NPHP4 gene.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2004;43(2):358-64.
2004: hao LING; Markus Cybulla; Oliver Schaefer; Christian Arnold; Marcus Schories; Hartmut P H Neumann
When to look for Von Hippel-Lindau disease in gastroenteropancreatic neuroendocrine tumors?
Neuroendocrinology 2004;80 Suppl 1():39-46.
2004: Sakari Vanharanta; Mary Buchta; Sarah R McWhinney; Sanna K Virta; Mariola Peçzkowska; Carl D Morrison; Rainer Lehtonen; Andrzej Januszewicz; Heikki Järvinen; Matti Juhola; Jukka-Pekka Mecklin; Eero Pukkala; Riitta Herva; Maija Kiuru; Nina N Nupponen; Lauri A Aaltonen; Hartmut P H Neumann; Charis Eng
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma.
American journal of human genetics 2004;74(1):153-9.
2003: Martin Leverkus; Hartmut P H Neumann; Eva-Bettina Brocker; Henning Hamm; Johannes Mayer
Soft nodules at the tip of the tongue of a 26-year-old man.
Archives of dermatology 2003;139(12):1647-52.
2003: Vera van Velthoven; Peter C Reinacher; Joachim Klisch; Hartmut P H Neumann; Sven Gläsker
Treatment of intramedullary hemangioblastomas, with special attention to von Hippel-Lindau disease.
Neurosurgery 2003;53(6):1306-13; discussion 1313-4.
2003: Ansgar Berlis; Martin Schumacher; Joachim Spreer; Hartmut P H Neumann; Vera van Velthoven
Subarachnoid haemorrhage due to cervical spinal cord haemangioblastomas in a patient with von Hippel-Lindau disease.
Acta neurochirurgica 2003;145(11):1009-13; discussion 1013.
2003: Peter F Zipfel; Hartmut P H Neumann; Mihály Józsi
Genetic screening in haemolytic uraemic syndrome.
Current opinion in nephrology and hypertension 2003;12(6):653-7.
2003: Matthias T F Wolf; Bettina Mucha; Massimo Attanasio; Isabella Zalewski; Stephanie M Karle; Hartmut P H Neumann; Nazneen Rahman; Birgit Bader; Conrad A Baldamus; Edgar Otto; Ralph Witzgall; Arno Fuchshuber; Friedhelm Hildebrandt
Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains.
Kidney international 2003;64(5):1580-7.
2003: Sarah R McWhinney; Getachew Boru; Philip K Binkley; Mariola Peczkowska; Andrzej Januszewicz; Hartmut P H Neumann; Charis Eng
Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset.
The Journal of clinical endocrinology and metabolism 2003;88(10):4911-6.
2003: Hartmut P H Neumann; M Salzmann; B Bohnert-Iwan; T Mannuelian; C Skerka; D Lenk; Bernhard U Bender; Markus Cybulla; Peter Riegler; A Königsrainer; Ulrich Neyer; A Bock; U Widmer; D A Male; Gerlind Franke; P F Zipfel
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
Journal of medical genetics 2003;40(9):676-81.
2003: Sebastian M Arnold; Ralph Strecker; Klaus Scheffler; Joachim Spreer; Jörg Schipper; Hartmut P H Neumann; Joachim Klisch
Dynamic contrast enhancement of paragangliomas of the head and neck: evaluation with time-resolved 2D MR projection angiography.
European radiology 2003;13(7):1608-11.
2003: Klaus-Martin Kreusel; Nikolaos E Bechrakis; Hartmut P H Neumann; Michael H Foerster
A sporadic case of von Hippel-Lindau disease with a secondary maculopathy as the presenting sign.
Acta ophthalmologica Scandinavica 2003;81(3):309-10.
2003: Stefan Hoegerle; Nadir Ghanem; Carsten Altehoefer; Jörg Schipper; Ingo Brink; Ernst Moser; Hartmut P H Neumann
18F-DOPA positron emission tomography for the detection of glomus tumours.
European journal of nuclear medicine and molecular imaging 2003;30(5):689-94.
2003: Tamara Manuelian; Jens Hellwage; Seppo Meri; Jessica Caprioli; Marina Noris; Stefan Heinen; Mihaly Jozsi; Hartmut P H Neumann; Giuseppe Remuzzi; Peter F Zipfel
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.
The Journal of clinical investigation 2003;111(8):1181-90.
2002: Martin Walz; Klaus Peitgen; Hartmut P H Neumann; Onno Eilard Janssen; Thomas Philipp; Klaus Mann
Endoscopic treatment of solitary, bilateral, multiple, and recurrent pheochromocytomas and paragangliomas.
World journal of surgery 2002;26(8):1005-12.
2002: Hartmut P H Neumann
Imaging vs biochemical testing for pheochromocytoma.
JAMA : the journal of the American Medical Association 2002;288(3):314-5; author reply 315.
2002: Hartmut P H Neumann; Birke Bausch; Sarah R McWhinney; Bernhard U Bender; Oliver Gimm; Gerlind Franke; Jörg Schipper; Joachim Klisch; Carsten Altehoefer; Klaus Zerres; Andrzej Januszewicz; Charis Eng; Wendy M Smith; Robin Munk; Tanja Manz; Sven Glaesker; Thomas W Apel; Markus Treier; Martin Reineke; Martin Walz; Cuong Hoang-Vu; Michael Brauckhoff; Andreas Klein-Franke; Peter Klose; Heinrich Schmidt; Margarete Maier-Woelfle; Mariola Peçzkowska; Cezary Szmigielski; Charis Eng
Germ-line mutations in nonsyndromic pheochromocytoma.
The New England journal of medicine 2002;346(19):1459-66.
2002: Hartmut P H Neumann; Stefan Hoegerle; Tanja Manz; Keith Brenner; Othon Iliopoulos
How many pathways to pheochromocytoma?
Seminars in nephrology 2002;22(2):89-99.
2002: Weng-Onn Lui; Jindong Chen; Sven Gläsker; Bernhard U Bender; Casey Madura; Sok Kean Khoo; Eric Kort; Catharina Larsson; Hartmut P H Neumann; Bin Tean Teh
Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome.
Oncogene 2002;21(7):1117-22.
2002: Peter Reichardt; Thomas W Apel; Manfred Domula; Ralf-Bodo Tröbs; Ingrid Krause; Uta Bierbach; Hartmut P H Neumann; Wieland Kiess
Recurrent polytopic chromaffin paragangliomas in a 9-year-old boy resulting from a novel germline mutation in the von Hippel-Lindau gene.
Journal of pediatric hematology/oncology 2002;24(2):145-8.
2002: Stefan Hoegerle; Egbert Nitzsche; Carsten Altehoefer; Nadir Ghanem; Tanja Manz; Ingo Brink; Martin Reincke; Ernst Moser; Hartmut P H Neumann
Pheochromocytomas: detection with 18F DOPA whole body PET--initial results..
Radiology 2002;222(2):507-12.
2002: Mariola Peczkowska; Jacek Gessek; Andrzej Januszewicz; Hartmut P H Neumann; Magdalena Januszewicz; Hanna Janaszek-Sitkowska; Aleksander Prejbisz; Marek Kabat; Janusz S Skierski; Witold Cieśla; Mieczyslaw Szostek
Pheochromocytoma of the urinary bladder coexisting with another extra-adrenal tumour--case report of a 19-year-old male patient.
Blood pressure 2002;11(2):101-5.
2001: Dewi Astuti; Angelo Agathanggelou; Sofia Honorio; Ashraf Dallol; Tommy Martinsson; Per Kogner; Carole Cummins; Hartmut P H Neumann; R Voutilainen; Patricia Dahia; Charis Eng; Eamonn R Maher; Farida Latif
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours.
Oncogene 2001;20(51):7573-7.
2001: Bernhard U Bender; Charis Eng; M Olschewski; Dietmar P Berger; Jörg Laubenberger; C Altehöfer; Günter Kirste; M Orszagh; Vera van Velthoven; H Miosczka; Dieter Schmidt; Hartmut P H Neumann
VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality.
Journal of medical genetics 2001;38(8):508-14.
2001: Sven Gläsker; Bernhard U Bender; Thomas W Apel; Vera van Velthoven; L M Mulligan; Josef Zentner; Hartmut P H Neumann
Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system.
Journal of neurology, neurosurgery, and psychiatry 2001;70(5):644-8.
2001: Tanja Manz; Wolfgang Grotz; M Orszagh; Benedikt Volk; Günter Kirste; Hartmut P H Neumann
A patient with neurological deficits and seizures after renal transplantation.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2001;16(3):631-3.
2001: Hartmut P H Neumann; Peter Riegler; W Huber; R Corradini; A Sessa; D Fontana; Ulrich Wetterauer; G Janetschek
The challenge of kidney lesions in von Hippel-Lindau disease.
Contributions to nephrology 2001;(136):193-207.
2000: Oliver Gimm; Mary Armanios; Heather Dziema; Hartmut P H Neumann; Charis Eng
Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.
Cancer research 2000;60(24):6822-5.
2000: Bernhard U Bender; M Gutsche; Sven Gläsker; B Müller; Günter Kirste; Charis Eng; Hartmut P H Neumann
Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas.
The Journal of clinical endocrinology and metabolism 2000;85(12):4568-74.
2000: Andrzej Januszewicz; Hartmut P H Neumann; I Loń; Cezary Szmigielski; Bartosz Symonides; Marek Kabat; Thomas W Apel; Bozenna Wocial; M Lapiński; Wlodzimierz Januszewicz
Incidence and clinical relevance of RET proto-oncogene germline mutations in pheochromocytoma patients.
Journal of hypertension 2000;18(8):1019-23.
2000: Dieter Schmidt; E Natt; Hartmut P H Neumann
Long-term results of laser treatment for retinal angiomatosis in von Hippel-Lindau disease.
European journal of medical research 2000;5(2):47-58.
2000: Peter Riegler; W Huber; R Corradini; Hartmut P H Neumann; S Glaesker; A Sessa
Von Hippel-Lindau disease: the role of gene analysis in affected families.
Nephron 2000;84(1):95-7.
1999: Sven Gläsker; Bernhard U Bender; Thomas W Apel; E Natt; Vera van Velthoven; R Scheremet; Josef Zentner; Hartmut P H Neumann
The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system.
Journal of neurology, neurosurgery, and psychiatry 1999;67(6):758-62.
1999: Hartmut P H Neumann
The spectrum of renal cysts in adulthood--discussion of eight cases.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1999;14(9):2234-44.
1999: Hartmut P H Neumann; Martin Reincke; Bernhard U Bender; R Elsner; G Janetschek
Preserved adrenocortical function after laparoscopic bilateral adrenal sparing surgery for hereditary pheochromocytoma.
The Journal of clinical endocrinology and metabolism 1999;84(8):2608-10.
1999: Hartmut P H Neumann; B Krumme; Vera van Velthoven; M Orszagh; Klaus Zerres
Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney disease.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1999;14(4):936-9.
1999: Klaus-Martin Kreusel; Norbert Bornfeld; Bernhard U Bender; L Neumann; Michael H Foerster; Hartmut P H Neumann
[Retinal capillary angioma. Clinical and molecular genetic studies].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 1999;96(2):71-6.
1999: Myriam Hemberger; Heinz Himmelbauer; Hartmut P H Neumann; Karl H Plate; Georg Schwarzkopf; Reinald Fundele
Expression of the von Hippel-Lindau-binding protein-1 (Vbp1) in fetal and adult mouse tissues.
Human molecular genetics 1999;8(2):229-36.
1999: Hartmut P H Neumann; Bernhard U Bender; Martin Reincke; Stefan Eggstein; Jörg Laubenberger; Günter Kirste
Adrenal-sparing surgery for phaeochromocytoma.
The British journal of surgery 1999;86(1):94-7.
1998: Hartmut P H Neumann; Georg Schwarzkopf; E P Henske
Renal angiomyolipomas, cysts, and cancer in tuberous sclerosis complex.
Seminars in pediatric neurology 1998;5(4):269-75.
1998: Hartmut P H Neumann; Bernhard U Bender; Dietmar P Berger; Jörg Laubenberger; Wolfgang Schultze-Seemann; Ulrich Wetterauer; F J Ferstl; E W Herbst; Georg Schwarzkopf; Frederik J Hes; Cornelis J M Lips; J M Lamiell; O Masek; Peter Riegler; B Mueller; Damjan Glavac; Hiltrud Brauch
Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma.
The Journal of urology 1998;160(4):1248-54.
1998: G Kempermann; Hartmut P H Neumann; Benedikt Volk
Endolymphatic sac tumours.
Histopathology 1998;33(1):2-10.
1998: Hartmut P H Neumann; Bernhard U Bender
Genotype-phenotype correlations in von Hippel-Lindau disease.
Journal of internal medicine 1998;243(6):541-5.
1998: B Bender; C Altehöfer; Joachim Hasse; Hartmut P H Neumann
The hypertensive lady with elevated plasma norepinephrine concentration and no demonstrable tumour--the search for pheochromocytoma.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1998;13(5):1295-6.
1997: Bernhard U Bender; C Altehöfer; Andrzej Januszewicz; R Gärtner; H Schmidt; Michael M Hoffmann; P H Heidemann; Hartmut P H Neumann
Functioning thoracic paraganglioma: association with Von Hippel-Lindau syndrome.
The Journal of clinical endocrinology and metabolism 1997;82(10):3356-60.
1997: Hartmut P H Neumann; Ingeborg Zäuner; Brigitte Strahm; Bernhard U Bender; Peter Schollmeyer; U Blum; Rolf Rohrbach; Friedhelm Hildebrandt
Late occurrence of cysts in autosomal dominant medullary cystic kidney disease.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1997;12(6):1242-6.
1997: Bernhard U Bender; Ulrich Wetterauer; Peter Schollmeyer; Hartmut P H Neumann
An incidental finding--bilateral multifocal renal oncocytoma.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1997;12(5):1034-6.
1997: Hartmut P H Neumann; Bernhard U Bender; Andrzej Januszewicz; G Janetschek; Charis Eng
Inherited pheochromocytoma.
Advances in nephrology from the Necker Hospital 1997;27():361-76.
1997: Hartmut P H Neumann; Bernhard U Bender; Wolfgang Schultze-Seemann; T Krause; Carsten Altehoefer; R Scheremet; M Orszagh; Georg Schwarzkopf; Andrzej Januszewicz; G Janetschek; Peter Riegler
The kidney and von Hippel-Lindau disease: impact of molecular genetic analysis of the VHL gene for clinical management.
Contributions to nephrology 1997;122():102-8.
1996: K Anding; G Köhler; N Böhm; KG Petersen; Peter Schollmeyer; Hartmut P H Neumann
[Primary pigmented nodular adrenocortical dysplasia. A rare cause of Cushing's syndrome].
Deutsche medizinische Wochenschrift (1946) 1996;121(43):1321-4.
1996: Hartmut P H Neumann; B Bender; Ingeborg Zäuner; Dietmar P Berger; Charis Eng; H Brauch; B Zbar
Monogenetic hypertension and pheochromocytoma.
American journal of kidney diseases : the official journal of the National Kidney Foundation 1996;28(3):329-33.
1996: G Kempermann; Hartmut P H Neumann; R Scheremet; Benedikt Volk; W Mann; J Gilsbach; R Laszig
Deafness due to bilateral endolymphatic sac tumours in a case of von Hippel-Lindau syndrome.
Journal of neurology, neurosurgery, and psychiatry 1996;61(3):318-20.
1996: D Glavac; Hartmut P H Neumann; C Wittke; H Jaenig; O Masek; T Streicher; F Pausch; D Engelhardt; K H Plate; Heinz Höfler; F Chen; B Zbar; H Brauch
Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central Europe.
Human genetics 1996;98(3):271-80.
1996: Hartmut P H Neumann
[The Hippel-Lindau syndrome is often misdiagnosed and its frequency underestimated].
Orvosi hetilap 1996;137(22):1191-5.
1996: B Zbar; T Kishida; F Chen; L Schmidt; Eamonn R Maher; Frances M Richards; P A Crossey; AR Webster; Nabeel A Affara; Malcolm A Ferguson-Smith; H Brauch; D Glavac; Hartmut P H Neumann; S Tisherman; J J Mulvihill; D J Gross; T Shuin; J Whaley; BR Seizinger; N Kley; Sylviane Olschwang; Cécile Boisson; Stéphane Richard; C H Lips; M Lerman
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
Human mutation 1996;8(4):348-57.
1995: Hartmut P H Neumann; Charis Eng; Lois M Mulligan; D Glavac; Ingeborg Zäuner; B A Ponder; P A Crossey; Eamonn R Maher; H Brauch
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.
JAMA : the journal of the American Medical Association 1995;274(14):1149-51.
1995: Elizabeth Petri Henske; Hartmut P H Neumann; B W Scheithauer; E W Herbst; M P Short; David J Kwiatkowski
Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomas.
Genes, chromosomes & cancer 1995;13(4):295-8.
1995: H Brauch; T Kishida; D Glavac; F Chen; F Pausch; Heinz Höfler; F Latif; M I Lerman; B Zbar; Hartmut P H Neumann
Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.
Human genetics 1995;95(5):551-6.
1995: Hartmut P H Neumann; C J Lips; Y E Hsia; B Zbar
Von Hippel-Lindau syndrome.
Brain pathology (Zurich, Switzerland) 1995;5(2):181-93.
1995: Hartmut P H Neumann; V Brüggen; Dietmar P Berger; E Herbst; U Blum; A Morgenroth; Peter Schollmeyer; Ulrich Wetterauer
Tuberous sclerosis complex with end-stage renal failure.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1995;10(3):349-53.
1994: J M Whaley; J Naglich; L Gelbert; Y E Hsia; J M Lamiell; J S Green; D Collins; Hartmut P H Neumann; J Laidlaw; Frederick P Li
Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma.
American journal of human genetics 1994;55(6):1092-102.
1994: Hartmut P H Neumann
[Risk of rupture of kidney cysts].
Deutsche medizinische Wochenschrift (1946) 1994;119(43):1486.
1994: Hartmut P H Neumann
Genetics of hypertension: the pheochromocytoma model.
The Clinical investigator 1994;72(9):729-30.
1994: Hartmut P H Neumann
Von Hippel-Lindau syndrome.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1994;9(3):313-5.
1994: Hartmut P H Neumann
Postoperative flank pain after surgery of pheochromocytoma.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1994;9(6):721-2.
1994: Hartmut P H Neumann; O D Wiestler
Von Hippel-Lindau disease: a syndrome providing insights into growth control and tumorigenesis.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1994;9(12):1832-3.
1993: Hartmut P H Neumann; Dietmar P Berger; G Sigmund; U Blum; D Schmidt; R J Parmer; Benedikt Volk; Günter Kirste
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
The New England journal of medicine 1993;329(21):1531-8.
1993: Hartmut P H Neumann
[Arvid Lindau on his 100th birthday].
Der Pathologe 1993;14(3):178-80.
1993: Hartmut P H Neumann
[Von Hippel-Lindau syndrome].
Der Pathologe 1993;14(3):150-7.
1993: Hartmut P H Neumann; Ingeborg Zäuner
[The complex of aftercare for C-cell carcinoma of the thyroid gland].
Deutsche medizinische Wochenschrift (1946) 1993;118(1-2):25-9.
1993: Hartmut P H Neumann; A Coester; Ingeborg Zäuner; L Kanz; G Würtemberger; Peter Schollmeyer; U Blum; Carl Schümichen; Ulrich Wetterauer
Echinococcosis of the kidney.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1993;8(8):757-60.
1992: Hartmut P H Neumann; V Hofmann; Ingeborg Zäuner; G Sigmund; U Blum; Carl Schümichen; D Schmidt; Günter Kirste
[Pheochromocytoma as dominant manifestation of v. Hippel-Lindau syndrome].
Deutsche medizinische Wochenschrift (1946) 1992;117(45):1709-16.
1992: Hartmut P H Neumann; H R Eggert; R Scheremet; Martin Schumacher; M Mohadjer; Ajay K Wakhloo; Benedikt Volk; U Hettmannsperger; Peter Riegler; P Schollmeyer
Central nervous system lesions in von Hippel-Lindau syndrome.
Journal of neurology, neurosurgery, and psychiatry 1992;55(10):898-901.
1991: Hartmut P H Neumann; E Dinkel; H Brambs; B Wimmer; H Friedburg; Benedikt Volk; G Sigmund; Peter Riegler; Klaus Haag; P Schollmeyer
Pancreatic lesions in the von Hippel-Lindau syndrome.
Gastroenterology 1991;101(2):465-71.
1991: Hartmut P H Neumann; O D Wiestler
Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus.
Lancet 1991;337(8749):1052-4.
1991: Hartmut P H Neumann
[The von Hippel-Lindau syndrome].
Deutsche medizinische Wochenschrift (1946) 1991;116(1):28-34.
1990: Hartmut P H Neumann; O A Müller; B A Ponder; C G Mathew; H Telenius; Werner Schempp; C Schuemichen; N Freudenberg; Peter Schollmeyer
[Diagnosis of multiple endocrine neoplasms type IIa using DNA analysis].
Verhandlungen der Deutschen Gesellschaft für Pathologie 1990;74():429-31.
1989: Hartmut P H Neumann; O A Müller; B A Ponder; C G Mathew; H Telenius; Werner Schempp; C Schuemichen; N Freudenberg; Peter Schollmeyer
Early diagnosis of multiple endocrine neoplasia type IIa.
Klinische Wochenschrift 1989;67(18):951-6.
1989: H J Decker; Robert M Gemmill; Hartmut P H Neumann; T A Walter; Avery A Sandberg
Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndrome.
Cancer genetics and cytogenetics 1989;39(2):289-93.
1989: M Kiechle-Schwarz; Hartmut P H Neumann; H J Decker; C Dietrich; B Wullich; Werner Schempp
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome.
Human genetics 1989;82(2):127-30.
1989: Hartmut P H Neumann; H R Eggert; K Weigel; H Friedburg; O D Wiestler; P Schollmeyer
Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome.
Journal of neurosurgery 1989;70(1):24-30.
1988: H J Decker; Hartmut P H Neumann; T A Walter; Avery A Sandberg
3p involvement in a renal cell carcinoma in von Hippel-Lindau syndrome. Region of tumor breakpoint clustering on 3p?
Cancer genetics and cytogenetics 1988;33(1):59-65.
1988: Hartmut P H Neumann; K Zerres; C L Fischer; G Wolff; H E Schaefer; A Gal; Brunhilde Wirth; T Kröpelin; Klaus Haag; Peter Schollmeyer
Late manifestation of autosomal-recessive polycystic kidney disease in two sisters.
American journal of nephrology 1988;8(3):194-7.
1988: D Schmidt; Hartmut P H Neumann; H R Eggert; H Friedburg
[Neuro-ophthalmologic findings in hemangioblastoma of the cerebellum and brain stem--downbeat nystagmus as the first symptom of hemangioblastoma in Hippel-Lindau disease].
Fortschritte der Ophthalmologie : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 1988;85(4):427-33.