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The Journal of Pediatrics, ISSN 0022-3476, 06/2019, Volume 209, pp. 252 - 252
Journal Article
by Liu, W and Xuan, Y and Xu, GZ and Zhang, YJ
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, ISSN 0275-004X, 01/2019, Volume 39, Issue 1, pp. E6 - E7
Journal Article
Neurosurgery, ISSN 0148-396X, 12/2017, Volume 81, Issue 6, pp. 886 - 892
Journal Article
03/2011
We report on a family with von Hippel-Lindau (VHL) disease and atypically aggressive renal cell carcinoma. A woman and her brother had progressive VHL disease... 
treatment | Renal cell carcinoma | von Hippel-Lindau disease
Web Resource
Scandinavian Journal of Immunology, ISSN 0300-9475, 09/2017, Volume 86, Issue 3, p. 179
Journal Article
2013, Frontiers of hormone research, ISBN 3318023302, Volume 41., xi, 187
In these times, a book should aspire to present the most significant advances in the field, reflect the themes of the moment, and provide a useful compendium... 
genetics | Peutz-Jeghers Syndrome | Endocrine glands | Endocrine Gland Neoplasms | Neurofibromatosis 1 | von Hippel-Lindau Disease | Multiple Endocrine Neoplasia | Tumors | Genetic aspects | Cancer | Diseases
Book
Journal Article
WORLD NEUROSURGERY, ISSN 1878-8750, 12/2017, Volume 108, pp. 981 - 982
Journal Article
Pancreatology, ISSN 1424-3903, 06/2018, Volume 18, Issue 4, pp. S135 - S136
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 12/2017, Volume 8
Inactivation of the VHL (Von Hippel Lindau) tumour suppressor has long been recognised as necessary for the pathogenesis of clear cell renal cancer (ccRCC);... 
REPAIR | ACTIVATION | COMPLEX | HIPPEL-LINDAU DISEASE | MULTIDISCIPLINARY SCIENCES | TUMOR-SUPPRESSOR GENE | MICE | IDENTIFICATION | CANCER | CELL CARCINOMA | DNA-REPLICATION
Journal Article
Gastroenterology, ISSN 0016-5085, 03/2018, Volume 154, Issue 4, pp. 814 - 815
Journal Article
Retina (Philadelphia, Pa.), ISSN 0275-004X, 06/2019, Volume 39, Issue 6, pp. 1230 - 1232
Journal Article
Journal of Neurosurgery, ISSN 0022-3085, 2014, Volume 120, Issue 5, pp. 1055 - 1062
Object. The tumors most frequently associated with von Hippel-Lindau (VHL) disease are hemangioblastomas. While they are associated with significant... 
Oncology | von Hippel-Lindau disease | Hemangioblastoma | Natural history | Central nervous system | SURGERY | PROTEIN | MANAGEMENT | hemangioblastoma | natural history | CANCER | oncology | CLINICAL NEUROLOGY | central nervous system | FEATURES | FAMILIES | MUTATIONS | ENDOLYMPHATIC SAC TUMORS | MORBID HEARING-LOSS | PROGRESSION | MANIFESTATIONS
Journal Article
JOURNAL OF NEUROSURGERY, ISSN 0022-3085, 02/2018, Volume 128, Issue 2, pp. 645 - 648
Journal Article
Journal Article
by Krauss, Tobias and Ferrara, Alfonso Massimiliano and Links, Thera P and Wellner, Ulrich and Bancos, Irina and Kvachenyuk, Andrey and Villar Gómez de Las Heras, Karina and Yukina, Marina Y and Petrov, Roman and Bullivant, Garrett and von Duecker, Laura and Jadhav, Swati and Ploeckinger, Ursula and Welin, Staffan and Schalin-Jäntti, Camilla and Gimm, Oliver and Pfeifer, Marija and Ngeow, Joanne and Hasse-Lazar, Kornelia and Sansó, Gabriela and Qi, Xiaoping and Ugurlu, M Umit and Diaz, Rene E and Wohllk, Nelson and Peczkowska, Mariola and Aberle, Jens and Lourenço, Delmar M and Pereira, Maria A A and Fragoso, Maria C B V and Hoff, Ana O and Almeida, Madson Q and Violante, Alice H D and Quidute, Ana R P and Zhang, Zhewei and Recasens, Mònica and Díaz, Luis Robles and Kunavisarut, Tada and Wannachalee, Taweesak and Sirinvaravong, Sirinart and Jonasch, Eric and Grozinsky-Glasberg, Simona and Fraenkel, Merav and Beltsevich, Dmitry and Egorov, Viacheslav I and Bausch, Dirk and Schott, Matthias and Tiling, Nikolaus and Pennelli, Gianmaria and Zschiedrich, Stefan and Därr, Roland and Ruf, Juri and Denecke, Timm and Link, Karl-Heinrich and Zovato, Stefania and von Dobschuetz, Ernst and Yaremchuk, Svetlana and Amthauer, Holger and Makay, Özer and Patocs, Attila and Walz, Martin K and Huber, Tobias B and Seufert, Jochen and Hellman, Per and Kim, Raymond H and Kuchinskaya, Ekaterina and Schiavi, Francesca and Malinoc, Angelica and Reisch, Nicole and Jarzab, Barbara and Barontini, Marta and Januszewicz, Andrzej and Shah, Nalini and Young, William F and Opocher, Giuseppe and Eng, Charis and Neumann, Hartmut P H and Bausch, Birke and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Endokrinkirurgi and Institutionen för kirurgiska vetenskaper
Endocrine-Related Cancer, ISSN 1351-0088, 2018, Volume 25, Issue 9, p. 783
Pancreatic neuroendocrine tumors (PanNETs) are rare in von Hippel-Lindau disease (VHL) but cause serious morbidity and mortality. Management guidelines for... 
management recommendations | Medical and Health Sciences | Medicin och hälsovetenskap | survival | von Hippel–Lindau disease | PanNET
Journal Article
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