RARE TUMORS

Autor: C. Kiyotani, T. Uno, H. Ogiwara, N. Morota, A. Nakazawa, Y. Tsutsumi, H. Masaki, T. Mori, J. A. S. Sanz, M. Guibelalde, A. Tavera, I. Herandez, J. Ibanez, M. Brell, A. Mas, H. L. Muller, U. Gebhardt, M. Warmuth-Metz, T. Pietsch, N. Sorensen, R.-D. Kortmann, S. Stapleton, I. Gonzalez, S. Steinbrueck, L. Rodriguez, G. Tuite, M. Krzyzankova, S. Mertsch, A. Jeibmann, U. Kordes, J. Wolff, W. Paulus, M. Hasselblatt, Y. Nonaka, S. Hara, S. Fukazawa, K. Shimizu, M. Ben-Arush, S. Postovsky, H. Toledano, M. Peretz-Nahum, J. Fujimura, S. Sakaguchi, A. Kondo, Y. Saito, K. Shimoji, Y. Ohara, A. Arakawa, M. Saito, T. Shimizu, M. Benesch, A. O. von Bueren, T. Dantonello, K. von Hoff, I. Leuschner, A. Claviez, U. Bierbach, G. Kropshofer, R. Korinthenberg, N. Graf, M. Suttorp, R. D. Kortmann, C. Friedrich, T. Klingebiel, E. Koscielniak, S. Rutkowski, M. Mesa, M. Sanchez, J. Mejia, G. Pena, R. Dussan, M. Cabeza, A. Storino, F. Dincer, T. Roffidal, M. Powell, S. Berrak, J. E. Wolff, F. Fouyssac, C. Delaunay, J.-M. Vignaud, E. Schmitt, O. Klein, L. Mansuy, P. Chastagner, O. Cruz, A. Guillen, G. Garcia, M. Alamar, S. Candela, I. Roussos, M. Garzon, M. Sunol, J. Muchart, M. Rebollo, J. Mora, B. Diez, A. Muggeri, N. Arakaki, F. Meli, G. Sevlever, V. Tsitouras, B. Pettorini, G. Fellows, J. Blair, M. Didi, C. Daousi, C. Steele, M. Javadpour, A. Sinha, M. Hishii, H. Ishii, M. Miyajima, H. Arai, R. Dvir, D. Sayar, D. Levin, L. Ben-Sirah, S. Constantini, R. Elhasid, E. Gertsch, N. Foreman, E. T. Valera, M. S. Brassesco, H. R. Machado, R. S. Oliveira, A. C. Santos, V. C. Terra, M. V. Barros, C. A. Scrideli, L. G. Tone, D. Merino, M. Pienkowska, A. Shlien, U. Tabori, R. Gilbertson, D. Malkin, I. Jeeva, B. Chang, V. Long, S. Picton, D. Burton, S. Clark, C. Kwok, B. Mokete, O. Rafiq, I. Simmons, M. M. K. Shing, C. K. Li, G. C. F. Chan, S. Y. Ha, H. L. Yuen, C. W. Luk, S. C. Ling, R. C. H. Li, J. H. Yoon, H. J. Park, H. J. Shin, B.-K. Park, J.-Y. Kim, H. L. Jung, Y. S. Ra, T. T. Ghim, S. Hartung, M. Garami, H. Traunecker, P. Thall, A. Mahajan, D. Sumerauer, P. Grillner, A. Orrego, M. Mosskin, B. Gustavsson, S. Holm, N. Peters, M. Rogers, S. Chowdry, W. Selman, A. Mitchell, B. Bangert, S. Ahuja, K. Laschinger, D. Gold, D. Stearns, K. Wright, K. Gupta, P. Klimo, D. Ellison, G. Keating, L. Eckel, C. Giannini, N. Wetjen, A. Patton, W. Zaky, G. McComb, J. Finlay, J. Grimm, K. Wong, G. Dhall, F. Gilles, D. Ormandy, R. Alston, E. Estlin, R. Gattamaneni, J. Birch, I. Kamaly-Asl, M. Hemenway, S. Rush, Y. A. Reginald, G. Nicolin, U. Bartel, J. R. Buncic, D. Aguilera, R. Flamini, C. Mazewski, M. Schniederjan, L. Hayes, W. Boydston, T. MacDonald, A. Fleming, N. Jabado, C. Saint-Martin, S. Albrecht, D. A. Ramsay, J. P. Farmer, A. Bendel, M. Hansen, S. Dugan, N. Mendelsohn

Publikováno v: Neuro-Oncology. 14:i148-i156

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81d63bbcc3d5c1253fed5cb928aa1c5
https://doi.org/10.1093/neuonc/nos108

Keeping an Eye on Crohn’s Disease: Orbital Myositis as the Presenting Symptom

Autor: J R Buncic, Carol Durno, R Ehrlich, R Taylor, P Hughes, A M Griffiths

Publikováno v: Canadian Journal of Gastroenterology, Vol 11, Iss 6, Pp 497-500 (1997)

Episodic periorbital swelling due to presumed orbital inflammation and myositis caused intermittent apparent proptosis and was the presenting symptom of ileocecal Crohn's disease (CD) in a teenage female with a family history of autoimmune disorders

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a4501ca33049563c752d8709dd43de
https://doaj.org/article/5f33f65a19474a66b474ca160aece646

Cervical Spine Subluxation Associated with Congenital Muscular Torticollis and Craniofacial Asymmetry

Autor: J R Buncic, R K Slate, Derek Armstrong, Jeffrey C. Posnick

Publikováno v: Plastic and Reconstructive Surgery. 91:1187-1195

The relationship between craniofacial asymmetry, congenital muscular torticollis, and cervical spine subluxation was examined in a study of 30 children who presented to our Craniofacial Program from 1987 through 1990. Twenty-six of the 30 patients ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::657a25f34c976c580725b69e06fc431d
https://doi.org/10.1097/00006534-199306000-00001

Childhood Fibrous Dysplasia Presenting as Blindness: A Skull Base Approach for Resection and Immediate Reconstruction

Autor: M D Wells, Jeffrey C. Posnick, Derek Armstrong, J R Buncic, James M. Drake

Publikováno v: Pediatric Neurosurgery. 19:260-266

Fibrous dysplasia is an abnormal fibroosseous process of bone of unknown cause. The incidence of skull involvement varies, painless enlargement being the most common presenting symptom. Change in vision is a rare but recognized finding. We report a 3

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09510980cdf95083fcb929bcd1e32e86
https://doi.org/10.1159/000120742

Nonviability of cells with oxidative defects in galactose medium: A screening test for affected patient fibroblasts

Autor: Douglas C. Wallace, R. Petrova-Benedict, B. H. Robinson, J. R. Buncic

Publikováno v: Biochemical Medicine and Metabolic Biology. 48:122-126

Diagnosis of respiratory chain defects in cultured skin fibroblasts is a difficult diagnostic procedure. We investigated the feasibility of using survival of skin fibroblasts in culture medium with galactose as the major carbon source as a method of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4667576f1e83751979e03dbbd4286ec7
https://doi.org/10.1016/0885-4505(92)90056-5