Access to innovative medicines for metastatic melanoma worldwide: Melanoma World Society and European Association of Dermato-oncology survey in 34 countries
Kandolf Sekulovic, L., Guo, J., Agarwala, S., Hauschild, A., McArthur, G., Cinat, G., Wainstein, A., Caglevic, C., Lorigan, P., Gogas, H., Alvarez, M., Duncombe, R., Lebbe, C., Peris, K., Rutkowski, P., Stratigos, A., Forsea, A.-M., De La Cruz Merino, L., Kukushkina, M., Dummer, R., Hoeller, C., Gorry, C., Bastholt, L., Herceg, D., Neyns, B., Vieira, R., Arenberger, P., Bylaite-Bucinskiene, M., Babovic, N., Banjin, M., Putnik, K., Todorovic, V., Kirov, K., Ocvirk, J., Zhukavets, A., Ymeri, A., Stojkovski, I., Garbe, C.
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Published in European journal of cancer (1990) (01.11.2018)
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Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy
Hart, T C, Gorry, M C, Hart, P S, Woodard, A S, Shihabi, Z, Sandhu, J, Shirts, B, Xu, L, Zhu, H, Barmada, M M, Bleyer, A J
Published in Journal of medical genetics (01.12.2002)
Published in Journal of medical genetics (01.12.2002)
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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
Whitcomb, David C, Gorry, Michael C, Preston, Robert A, Furey, William, Sossenheimer, Michael J, Ulrich, Charles D, Martin, Stephen P, Gates, Lawrence K, Amann, Stephen T, Toskes, Phillip P, Liddle, Roger, McGrath, Kevin, Uomo, G, Post, J. C, Ehrlich, Garth D
Published in Nature genetics (01.10.1996)
Published in Nature genetics (01.10.1996)
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A Rationally Designed A34R Mutant Oncolytic Poxvirus: Improved Efficacy in Peritoneal Carcinomatosis
Thirunavukarasu, Pragatheeshwar, Sathaiah, Magesh, Gorry, Michael C, O'Malley, Mark E, Ravindranathan, Roshni, Austin, Frances, Thorne, Steven H, Guo, Zong Sheng, Bartlett, David L
Published in Molecular therapy (01.05.2013)
Published in Molecular therapy (01.05.2013)
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A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1
Hart, Thomas C., Zhang, Yingze, Gorry, Michael C., Hart, P. Suzanne, Cooper, Margaret, Marazita, Mary L., Marks, Jared M., Cortelli, Jose R., Pallos, Debora
Published in American journal of human genetics (01.04.2002)
Published in American journal of human genetics (01.04.2002)
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Evidence of Bacterial Metabolic Activity in Culture-Negative Otitis Media With Effusion
Rayner, Mark G, Zhang, Yingze, Gorry, Michael C, Chen, Yiping, Post, J. Christopher, Ehrlich, Garth D
Published in JAMA : the journal of the American Medical Association (28.01.1998)
Published in JAMA : the journal of the American Medical Association (28.01.1998)
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Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis
Gorry, M C, Gabbaizedeh, D, Furey, W, Gates, Jr, L K, Preston, R A, Aston, C E, Zhang, Y, Ulrich, C, Ehrlich, G D, Whitcomb, D C
Published in Gastroenterology (New York, N.Y. 1943) (01.10.1997)
Published in Gastroenterology (New York, N.Y. 1943) (01.10.1997)
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Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
Hart, T C, Hart, P S, Gorry, M C, Michalec, M D, Ryu, O H, Uygur, C, Ozdemir, D, Firatli, S, Aren, G, Firatli, E
Published in Journal of medical genetics (01.12.2003)
Published in Journal of medical genetics (01.12.2003)
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Oncolytic virotherapy for ovarian carcinomatosis using a replication-selective vaccinia virus armed with a yeast cytosine deaminase gene
Chalikonda, S, Kivlen, M H, O'Malley, M E, (Eric) Dong, X D, McCart, J A, Gorry, M C, Yin, X-Y, Brown, C K, Zeh, H J, Guo, Z S, Bartlett, D L
Published in Cancer gene therapy (01.02.2008)
Published in Cancer gene therapy (01.02.2008)
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Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients
ZHANG, Y, SYED, R, HART, T. C, UYGAR, C, PALLOS, D, GORRY, M. C, FIRATLI, E, CORTELLI, J. R, VANDYKE, T. E, HART, P. S, FEINGOLD, E
Published in Genes and immunity (01.01.2003)
Published in Genes and immunity (01.01.2003)
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Clinico-pathologic findings in medullary cystic kidney disease type 2
Bleyer, Anthony J, Hart, Thomas C, Willingham, Mark C, Iskandar, Samy S, Gorry, Michael C, Trachtman, Howard
Published in Pediatric nephrology (Berlin, West) (01.06.2005)
Published in Pediatric nephrology (Berlin, West) (01.06.2005)
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Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene
Bleyer, Anthony J., Woodard, Arch S., Shihabi, Zak, Sandhu, Jaspreet, Zhu, Honping, Satko, Scott G., Weller, Nelson, Deterding, Elizabeth, Mcbride, Debra, Gorry, Michael C., Xu, Linda, Ganier, Deann, Hart, Thomas C.
Published in Kidney international (01.07.2003)
Published in Kidney international (01.07.2003)
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18 The outcomes we choose in cardiology: a literature review and analysis of core outcome sets in PCI
Duncan, A, Gorry, C, Shiely, F, Casserly, I
Published in Heart (British Cardiac Society) (01.10.2023)
Published in Heart (British Cardiac Society) (01.10.2023)
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