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Akademický článek
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Autor:
I. Scheimberg, M.C. Cohen
This chapter describes the placenta in ideal conditions, which may not always be possible in forensic cases. It presents a standardized macroscopic description and an approach to the histological sampling. The chapter addresses the features of the pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2390fb033286320bd1930b3c821f9b8
https://doi.org/10.1016/b978-0-12-800034-2.00122-1
https://doi.org/10.1016/b978-0-12-800034-2.00122-1
Autor:
Robert C. Tasker, I. Scheimberg, H. L. Whitwell, J. F. Geddes, C. D. Nickols, A. K. Hackshaw, Gillian G.W. Adams
Publikováno v:
Neuropathology and Applied Neurobiology. 29:14-22
A histological review of dura mater taken from a post-mortem series of 50 paediatric cases aged up to 5 months revealed fresh bleeding in the dura in 36/50, the bleeding ranging from small perivascular haemorrhages to extensive haemorrhage which had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06f1e065972770d6a6bbc1342c25f3dd
https://doi.org/10.1046/j.1365-2990.2003.00434.x
https://doi.org/10.1046/j.1365-2990.2003.00434.x
Autor:
Cgd Brook, Richard Stanhope, Fergus J. Cameron, P. C. Hindmarsh, Martin O. Savage, John W. Honour, I Scheimberg, O.D. Wolthers
Publikováno v:
Archives of Disease in Childhood. 80:46-50
Background—Androgensecretingadrenocortical tumours are rare in children and the determination of their malignant potential can be diYcult. Objectives—To assess the presentation, histology, and clinical behaviour of these tumours. Setting—Two te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14ca646b0a5e472fcabaa3c94b052399
https://doi.org/10.1136/adc.80.1.46
https://doi.org/10.1136/adc.80.1.46
Publikováno v:
The British Journal of Radiology. 70:852-855
Small adrenocortical tumours in children are rarely associated with hepatic pathology. We present two case reports of children with hepatic pathology associated with small adrenal tumours on computed tomography. One child had multiple granulomatous l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b1eb3649202f7be8faf966bc18a0b3b
https://doi.org/10.1259/bjr.70.836.9486055
https://doi.org/10.1259/bjr.70.836.9486055
Publikováno v:
Forensic science international. 212(1-3)
This preliminary communication describes seven babies with β-amyloid precursor protein (βAPP) positive axonal swellings in nerve roots at multiple levels of the spinal cord. All seven babies died of natural causes. Two died in utero providing evide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7490250b6c60de028408eeacfa0a86
https://pubmed.ncbi.nlm.nih.gov/21620594
https://pubmed.ncbi.nlm.nih.gov/21620594
Publikováno v:
Acta Paediatrica. 86:1016-1018
We describe a juvenile granulosa cell tumour resulting in pseudopuberty in an infant female. The progression of the clinical signs of puberty were non-consonant and the diagnosis was complicated by marginally elevated serum alpha-fetoprotein levels.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eba3e9f0c7f9ca1eb8ccb07547c46a68
https://doi.org/10.1111/j.1651-2227.1997.tb15193.x
https://doi.org/10.1111/j.1651-2227.1997.tb15193.x
Publikováno v:
Journal of perinatal medicine. 32(4)
Polysplenia syndrome is a condition that persists as a defect of lateralisation, the embryonic process by which the site of body organs is determined. The most frequent manifestations of this syndrome, in addition to polysplenia are complex cardiac m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d4ee931f8722f19db65b4ce0851502
https://pubmed.ncbi.nlm.nih.gov/15346829
https://pubmed.ncbi.nlm.nih.gov/15346829
Autor:
K. Banerjee, I. Scheimberg, Li F. Chan, Cecilia Camacho-Hübner, Farideh Miraki-Moud, M.O. Savage, Les Perry, Helen L Storr
Publikováno v:
Europe PubMed Central
We report a female child who presented at age 3.92 years with a 2-year history of consonant pubertal development caused by a large right-sided ovarian juvenile granulosa cell tumour (JGCT). Although JGCTs causing pseudo-precocious puberty have been p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ac68273ad2598fc1ab656d964e729b1
https://pubmed.ncbi.nlm.nih.gov/15198302
https://pubmed.ncbi.nlm.nih.gov/15198302