Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Alexandra Jolley"'
Publikováno v:
Gynecologic Oncology Reports, Vol 48, Iss , Pp 101201- (2023)
We present the case of a 59-year-old woman who developed a right thigh pleomorphic sarcoma with rhabdomyoblastic differentiation 6 years following radiotherapy for a vaginal squamous cell carcinoma. The overall 5-year survival for a gynaecological ma
Externí odkaz:
https://doaj.org/article/666be3402ffe406badb916a3a4bc62f4
Molecular Characterization of Testicular Mesothelioma and the Role of Asbestos as a Causative Factor
Autor:
Ashleigh Jean Hocking, Elaine May Thomas, Sarita Prabhakaran, Alexandra Jolley, Susan Lesley Woods, Matthew J. Soeberg, Sonja Klebe
Publikováno v:
Archives of Pathology & Laboratory Medicine.
Context.— Mesothelioma of the tunica vaginalis testis (TVT) is an extremely rare form of mesothelioma. Objective.— To compare the clinical and molecular characteristics of mesothelioma of the TVT with those of mesothelioma at other more common si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::185823346f1e1ea2afe7d5e274e43b58
https://doi.org/10.5858/arpa.2022-0283-oa
https://doi.org/10.5858/arpa.2022-0283-oa
Autor:
Catherine Cord-Udy, Lynette Moore, Peter Muller, Elizabeth Jane Beare, Jeremy Granger, Alexandra Jolley
Publikováno v:
Pediatric and Developmental Pathology. 20:158-162
We present a severe case of vanishing gastroschisis resulting in intrauterine death with post mortem examination findings. Gastroschisis is defined as a full thickness paraumbilical abdominal wall defect associated with evisceration of fetal intestin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9663e0f4132c11b4f0bcff4b41098b
https://doi.org/10.1177/1093526616683872
https://doi.org/10.1177/1093526616683872
Autor:
David M. Ross, Alexandra Jolley, Magdalena Sobieraj-Teague, Alexander Gallus, Jir P. Boey, Catherine Nicholls, Nancy Lerda, Elizabeth M. Duncan
Publikováno v:
British Journal of Haematology. 172:811-813
Keywords: protein C deficiency; compound heterozygote; subcutaneous infusion; rivaroxaban; frameshift mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1df60e35ff4c8c61fa79b7d9240403f3
https://doi.org/10.1111/bjh.13538
https://doi.org/10.1111/bjh.13538
Autor:
Lesley M McGregor, Jillian Nicholl, Alexandra Jolley, Sue Brown, Wendy Waters, Mark A. Corbett, S. Yu
Publikováno v:
American Journal of Medical Genetics Part A. 161:1508-1512
Alexandra Jolley, Mark Corbett, Lesley McGregor, Wendy Waters, Susan Brown, Jillian Nicholl, and Sui Yu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59371a122fae4bc0ef14e695af664229
https://doi.org/10.1002/ajmg.a.35922
https://doi.org/10.1002/ajmg.a.35922
Autor:
Peter Muller, Jeremy Granger, Alexandra Jolley, Catherine Cord-Udy, Elizabeth Jane Beare, Lynette Moore
Publikováno v:
Pediatric and Developmental Pathology.
We present a severe case of vanishing gastroschisis resulting in intrauterine death with post mortem examination findings. Gastroschisis is defined as a full thickness paraumbilical abdominal wall defect associated with evisceration of fetal intestin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51bea1fa066ca3599f5f636773f47f5d
https://doi.org/10.2350/14-10-1558-cr.1
https://doi.org/10.2350/14-10-1558-cr.1
Publikováno v:
Pathology. 49:S75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28ae712c69fec78ccb10f5c2f94078fc
https://doi.org/10.1016/j.pathol.2016.12.194
https://doi.org/10.1016/j.pathol.2016.12.194
Autor:
Damian Clark, S. Yu, David R. Thorburn, Jillian Nicholl, Alexandra Jolley, Nicholas Manton, Drago Bratkovic, Dylan A. Mordaunt, Alison G. Compton, Hayley S. Mountford, Shanti Balasubramaniam, Kathryn Friend
Publikováno v:
American journal of medical genetics. Part A. 167(6)
Isolated mitochondrial respiratory chain complex III deficiency has been described in a heterogeneous group of clinical presentations in children and adults. It has been associated with mutations in MT-CYB, the only mitochondrial DNA encoded subunit,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8573c3338ce73fa6d24c03be9a196a68
https://pubmed.ncbi.nlm.nih.gov/25899669
https://pubmed.ncbi.nlm.nih.gov/25899669
Autor:
Catherine Nicholls, Hamish S. Scott, Alicia B. Byrne, Alexandra Jolley, Susan E. Rodgers, Simon McRae, Magdalena Sobieraj-Teague, David M. Ross, Nancy Lerda
Publikováno v:
Pathology. 45:S93
Background Protein C (PC) (OMIM 612283) is an inactive zymogen of a serine protease (activated protein C, APC) which is an important regulator of blood coagulation factor Va and factor VIIIa, with deficiency associated with thromboembolic disease. He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0593766710ca37cc6ca60354a00a1c83
https://doi.org/10.1097/01.pat.0000426978.41928.42
https://doi.org/10.1097/01.pat.0000426978.41928.42
Publikováno v:
Pathology. 45:S29
Backgound Array comparative genome hybridisation (CGH) was requested on a 9-year-old boy with mild developmental delay, mild learning difficulties, short stature and dysmorphic features. Methods Array CGH used the BlueGnome Cytochip oligo ISCA 8 × 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed408b95afeb2de5abfbbe91edbac67f
https://doi.org/10.1097/01.pat.0000426794.94880.2c
https://doi.org/10.1097/01.pat.0000426794.94880.2c