Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Henning Laursen"'
Autor:
Grethe Badsberg Samuelsen, Nenad Bogdanović, Henning Laursen, Niels Graem, Jørgen Falck Larsen, Bente Pakkenberg
Publikováno v:
Image Analysis and Stereology, Vol 19, Iss 1, Pp 35-38 (2011)
In this study the material comprises brains from three aborted fetuses and two fullterm infants who died at birth.The gestational ages ranged from the 22nd week to term. All cases were without malformations, known chromosomal abnormality, hydrops, an
Externí odkaz:
https://doaj.org/article/de49b3cedc5c4a3c8d3e6817bb0804c1
Autor:
Jesús de Pedro-Cuesta, Ignacio Mahillo-Fernandez, Miguel Calero, Alberto Rábano, Mabel Cruz, Åke Siden, Pablo Martínez-Martín, Henning Laursen, María Ruiz-Tovar, Kåre Mølbak, EUROSURGYCJD Research Group
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e109412 (2014)
Sporadic Creutzfeldt-Jakob disease (sCJD) might be transmitted by surgery. The purpose of this study was to investigate potential susceptibility to sCJD from surgery at juvenile age and in early adulthood.From Danish and Swedish national registries w
Externí odkaz:
https://doaj.org/article/f665ddd954854fe8b75aacf090c369f5
Autor:
Linea Melchior, Jørgen E Nielsen, Eva Løbner Lund, Suzanne G. Lindquist, Lars-Henrik Krarup, Henning Laursen, Ausrine Areskeviciute, Peter Johansen, Neil McKenzie, Helle Broholm, Alison Green
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 77:673-684
This is the first report of presumed sporadic Creutzfeldt-Jakob disease (sCJD) and Gerstmann-Straussler-Scheinker disease (GSS) with the prion protein gene c.305C>T mutation (p.P102L) occurring in one family. The father and son were affected with GSS
Publikováno v:
Acta Neurochirurgica. 155:1763-1772
We hypothesized that shunt dysfunction in the ventricular catheter and the shunt valve is caused by different cellular responses. We also hypothesized that the cellular responses depend on different pathophysiological mechanisms. Removed shunt materi
Publikováno v:
Neuropathology and Applied Neurobiology. 39:179-191
A. D. Skjolding, A. V. Holst, H. Broholm, H. Laursen and M. Juhler (2013) Neuropathology and Applied Neurobiology39, 179–191 Differences in distribution and regulation of astrocytic aquaporin-4 in human and rat hydrocephalic brain Aims: Aquaporin-4
Autor:
Henrik Dyrbye, Henning Laursen, Marianne Juhler, Helle Broholm, Damoun Nassehi, Lars Peter Sørensen
Publikováno v:
Clinical neuropathology. 35(1)
For decades, the preferred and almost sole method for measurement of gene expression has been RT-qPCR. The method is robust, inexpensive, and well-studied; however, PCR is also quite laborious and vulnerable to contamination. As part of an investigat
Autor:
Helle Broholm, Carsten Thomsen, Henrik Dyrbye, Marianne Juhler, Damoun Nassehi, Henning Laursen, Morten Andresen
Publikováno v:
APMIS. 119:831-843
Nassehi D, Dyrbye H, Andresen M, Thomsen C, Juhler M, Laursen H, Broholm H. Vascular endothelial growth factor A protein level and gene expression in intracranial meningiomas with brain edema. APMIS 2011; 119: 831–43. Meningiomas are the second mos
Autor:
Troels Edsen, Jacob Bertram Springborg, Henning Laursen, Pernille Koefoed, Niels Vidiendal Olsen, Finn Borgbjerg Moltke, Henning B. Nielsen, Morten Nielsen, Jonatan Myrup Staalsø
Publikováno v:
Journal of Neurosurgical Anesthesiology. 23:304-309
Objective The intron 16 insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene has been associated with rupture of intracranial aneurysms, but the effect of haplotypes within ACE has not been studied. This study investi
Autor:
Morten Møller, Henning Laursen, Kjeld Møllgård, Melissa C. Lutterodt, Bente Pakkenberg, Karen B. Larsen, Niels Graem
Publikováno v:
Developmental Neuroscience. 32:149-162
The development of the human neocortex is a complex and highly regulated process involving a time-related expression of many transcription factors including the homeobox genes Pax6 and Meis2. During early development, Pax6 is expressed in nuclei of r
Autor:
Henning Laursen, Susanne Holck
Publikováno v:
Acta Pathologica Microbiologica Scandinavica Series A :Pathology. :13-20
Thirty cases of silent pituitary adenomas were studied clinico-morphologically and classified into 4 groups according to their fine structural characteristics. Tumors poor in organelles (7 cases) and typical oncocytomas (6 cases) produced pituitary i