Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bo Y Ngan"'
Publikováno v:
Journal of Pediatric Hematology/Oncology. 34:552-555
Mucosa-associated lymphoid tissue (MALT) lymphoma is very rare in children. We report the first case of pediatric thymic MALT lymphoma in an adolescent Asian girl. She presented with chest pain, dyspnea, and low-grade fever. A large anterior mediasti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9336141333d24fa16bb587b77cb051b2
https://doi.org/10.1097/mph.0b013e3182459f0a
https://doi.org/10.1097/mph.0b013e3182459f0a
Autor:
Richard J. Mount, Sharon L. Cushing, Daniel Martin‐Munoz, Susan Blaser, Robert V. Harrison, Bo Y. Ngan, Blake C. Papsin, Evan J. Propst
Publikováno v:
The Laryngoscope. 123:528-532
Auriculo-condylar syndrome (ACS) is a rare condition affecting first branchial arch structures. The types of hearing loss and temporal bone findings in ACS have not been reported. We describe a 14-year-old male with constricted pinnae, mandibular dys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fd612ba42d1ba96617980ef74f51899
https://doi.org/10.1002/lary.23492
https://doi.org/10.1002/lary.23492
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 45:222-227
De novo autoimmune hepatitis (AIH) recently was recognized as an important cause of late graft dysfunction after pediatric liver transplantation (LT). However, the significance of isolated elevation of autoantibodies in children after LT without hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f067665e4a00d9833e96d9866ab56c0
https://doi.org/10.1097/mpg.0b013e31805ce219
https://doi.org/10.1097/mpg.0b013e31805ce219
Publikováno v:
Pediatric and Developmental Pathology. 7:538-545
Primitive neuroectodermal tumor/Ewing sarcoma (PNET/ES) rarely occurs in the skin and subcutaneous tissues. We present a case of a 16-year-old girl with primary cutaneous and subcutaneous PNET/ES of the abdominal wall. Despite wide local excision and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::874d2ec47512aba8c02f9c0db9ec61e0
https://doi.org/10.1007/s10024-004-2024-6
https://doi.org/10.1007/s10024-004-2024-6
Autor:
Rosanna Weksberg, Patricia C. Parkin, Ernest Cutz, Elyanne M. Ratcliffe, Justin T. Gerstle, Alain E. Lagarde, Bo Y. Ngan, Aaron Pollett, Marina E. Croitoru, Melyssa Aronson, Steven Gallinger, Ewa Baumann, Heidi Rothenmund, Katayoon Shayan, Helen S. L. Chan, Robert H. Riddell, Peter R. Durie
Publikováno v:
Gastroenterology. 126:576-585
Heterozygous germline DNA mismatch repair gene mutations are typically associated with hereditary nonpolyposis colorectal cancer. The molecular hallmark of this syndrome is high-frequency microsatellite instability in the tumors. Rare childhood cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a77e2b4a0569beba962093cdd75fc370
https://doi.org/10.1053/j.gastro.2003.11.008
https://doi.org/10.1053/j.gastro.2003.11.008
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 62:159-164
Congenital germ cell tumors are uncommon. The most common site of origin is in the saccrococygeal region. Teratomas arising from the head and neck comprise a small proportion of this entity, and of these, nasopharyngeal lesions are rare. Also known b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca8d5cede328cfaf6a0bcedf51f4af06
https://doi.org/10.1016/s0165-5876(01)00575-4
https://doi.org/10.1016/s0165-5876(01)00575-4
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 18:379-385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d64c8daa8ae06e7c503dace3b05b245f
https://doi.org/10.1097/00005176-199404000-00022
https://doi.org/10.1097/00005176-199404000-00022
Publikováno v:
Blood. 83:191-198
Diffuse large cell lymphomas are aggressive tumors of B-cell origin. In some cases they arise from low-grade follicular lymphomas carrying the t(14;18) translocation, an event that leads to the overexpression of the BCL-2 gene product. More frequentl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5fa5d73393719f980e6bc69fc5fe8d2
https://doi.org/10.1182/blood.v83.1.191.191
https://doi.org/10.1182/blood.v83.1.191.191
Autor:
Daniel Brody, Stan Moroz, Vicky L. Ng, Ralph Wong, Bo Y Ngan, Oscar M. Navarro, Chee Y. Ooi, David M. Grant, Annie Fecteau
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 52(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d7a1d695871ea971e01dce5c0f34f6
https://pubmed.ncbi.nlm.nih.gov/21150654
https://pubmed.ncbi.nlm.nih.gov/21150654
Publikováno v:
International journal of pediatric otorhinolaryngology. 68(10)
Summary Objective: A paucity of data exists in the literature regarding the pediatric bony myxoma. Controversy exists regarding both its histopathologic origins and surgical management. The purpose of this study was to report on our experience in man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c27159968af5277f1931a8212775ea6a
https://pubmed.ncbi.nlm.nih.gov/15364495
https://pubmed.ncbi.nlm.nih.gov/15364495