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Numrering	Referens	Omslagsbild	Hitta
1.	Berglund, Anna, 1949-, et al. (författare) Våldsutsatta kvinnor- samhällets ansvar 2014. - 3 Ingår i: Lärobok, tredje upplagan, framtagen av Nationellt centrum för kvinnofrid, Uppsala universitet. - Uppsala : Studentlitteratur AB. - 9789144094441 Bokkapitel (övrigt vetenskapligt/konstnärligt)
2.	Burman, Monica, et al. (författare) How to Integrate Sex/gender Perspectives into Legal Education 1999 Ingår i: 'Women’s Worlds 99: 7th International Interdisciplinary Congress on Women. Konferensbidrag (refereegranskat)
3.	Burman, Monica, et al. (författare) Regeringsprojektet. Jämställdhets- och genusperspektiv i juristutbildningen 2001 Ingår i: Lärares liv - vision och verklighet. Konferensbidrag (övrigt vetenskapligt/konstnärligt)
4.	Dahlin, Lars, et al. (författare) Glomus tumours in the long finger and in the thumb of a young patient with neurofibromatosis-1 (Nf-1) 2013 Ingår i: Journal of Plastic Surgery and Hand Surgery. - 2000-656X. ; 47:3, s. 238-240 Tidskriftsartikel (refereegranskat)abstract Glomus tumours are rare in adults, and such tumours may be associated with neurofibromatosis-1 (Nf-1). Here we describe successful treatment of two glomus tumours initially in the long finger and, one year later, in the thumb in a 17-year young girl with Nf-1.
5.	Gorcenco, Sorina, et al. (författare) Ataxia-pancytopenia syndrome with SAMD9L mutations 2017 Ingår i: Neurology: Genetics. - 2376-7839. ; 3:5 Tidskriftsartikel (refereegranskat)abstract OBJECTIVE: We describe the neurologic, neuroradiologic, and ophthalmologic phenotype of 1 Swedish and 1 Finnish family with autosomal dominant ataxia-pancytopenia (ATXPC) syndrome and SAMD9L mutations.METHODS: Members of these families with germline SAMD9L c.2956C>T, p.Arg986Cys, or c.2672T>C, p.Ile891Thr mutations underwent structured interviews and neurologic and ophthalmologic examinations. Neuroimaging was performed, and medical records were reviewed. Previous publications on SAMD9L-ATXPC were reviewed.RESULTS: Twelve individuals in both families were affected clinically. All mutation carriers examined had balance impairment, although severity was very variable. All but 1 had nystagmus, and all but 1 had pyramidal tract signs. Neurologic features were generally present from childhood on and progressed slowly. Two adult patients, who experienced increasing clumsiness, glare, and difficulties with gaze fixation, had paracentral retinal dysfunction verified by multifocal electroretinography. Brain MRI showed early, marked cerebellar atrophy in most carriers and variable cerebral periventricular white matter T2 hyperintensities. Two children were treated with hematopoietic stem cell transplantation for hematologic malignancies, and the neurologic symptoms of one of these worsened after treatment. Three affected individuals had attention deficit hyperactivity disorder or cognitive problems. Retinal dysfunction was not previously reported in individuals with ATXPC.CONCLUSIONS: The neurologic phenotype of this syndrome is defined by balance or gait impairment, nystagmus, hyperreflexia in the lower limbs and, frequently, marked cerebellar atrophy. Paracentral retinal dysfunction may contribute to glare, reading problems, and clumsiness. Timely diagnosis of ATXPC is important to address the risk for severe hemorrhage, infection, and hematologic malignancies inherent in this syndrome; regular hematologic follow-up might be beneficial.
6.	Król, Ladislav, et al. (författare) Astrovirus VA1/HMO encephalitis after allogeneic hematopoietic cell transplantation : Significant role of immune competence in virus control 2021 Ingår i: Pediatric Blood and Cancer. - : Wiley. - 1545-5009 .- 1545-5017. ; 68:12 Tidskriftsartikel (refereegranskat)
7.	Palmér, Lars, et al. (författare) Large-cell medulloblastoma in Aicardi syndrome. Case report and literature review. 2004 Ingår i: Neuropediatrics. - : Georg Thieme Verlag KG. - 0174-304X .- 1439-1899. ; 35:5, s. 307-11 Tidskriftsartikel (refereegranskat)abstract An eight-year-old girl with Aicardi syndrome (AIC) developed signs of increased intracranial pressure. A clinical and radiological investigation revealed a tumor in the posterior fossa, which was resected. The histopathological diagnosis was large-cell medulloblastoma. Eight months later, she died of a local recurrence, despite treatment with chemotherapy and radiotherapy according to a PNET protocol. In addition to the growth of a large-cell medulloblastoma at the location of the primary tumor and the meningeal spread of the tumor, the autopsy revealed major cortical and subcortical malformations of the brain. Various benign (e.g., plexus papillomas) and malignant tumors (angiosarcoma, embryonic carcinoma, and hepatoblastoma) have been reported in connection with Aicardi syndrome. A genetic analysis of AIC suggests that the mutation is localized on the distal part of the short arm of the X chromosome, an area that may be of importance for tumor development. This is the first report of a primary malignant brain tumor -- large-cell medulloblastoma -- in a patient with Aicardi syndrome.
8.	Strategier och kontrakt för ekonomi och kärlek : rapport från 10:e nordiska kvinnojuristmötet 2000 Proceedings (redaktörskap) (övrigt vetenskapligt/konstnärligt)
9.	Sveger, Tomas, et al. (författare) Apolipoprotein B as a marker of familial hyperlipoproteinemia. 2004 Ingår i: Journal of Atherosclerosis and Thrombosis. - 1880-3873. ; 11:5, s. 92-286 Tidskriftsartikel (refereegranskat)
10.	Watanabe, Kazuyuki, et al. (författare) Increase of sodium channels (nav 1.8 and nav 1.9) in rat dorsal root ganglion neurons exposed to autologous nucleus pulposus. 2014 Ingår i: The open orthopaedics journal. - : Bentham Science Publishers Ltd.. - 1874-3250. ; 8, s. 69-73 Tidskriftsartikel (refereegranskat)abstract It has been assumed that nucleus pulposus-induced activation of the dorsal root ganglion (DRG) may be related to an activation of sodium channels in the DRG neurons. In this study we assessed the expression of Nav 1.8 and Nav 1.9 following disc puncture.

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Resultat 1-10 av 10

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Typ av publikation: tidskriftsartikel (6); konferensbidrag (2); proceedings (redaktörskap) (1); bokkapitel (1)

Typ av innehåll: refereegranskat (7); övrigt vetenskapligt/konstnärligt (3)

Författare/redaktör: Nordborg, Karin (4); Nordborg, Gudrun (3); Ågren, Karin (2); Nordborg, Claes, 194 ... (2); Burman, Monica (2); Turkiewicz, Dominik (2); visa fler...; Nilsson, Lars (1); Kjellström, Ulrika (1); Andréasson, Sten (1); Nilsson, Christer (1); Englund, Elisabet (1); Tedgård, Ulf (1); Dahlin, Lars (1); Puschmann, Andreas (1); Anagnostaki, Lola (1); Pronk, Cornelis Jan (1); Karlberg, Mikael (1); Eriksson, Maria (1); Åman, Pierre, 1953 (1); Olmarker, Kjell, 195 ... (1); Davidsson, Josef (1); Larsson, Karin, 1955 ... (1); Cammenga, Jörg (1); Enander, Viveka (1); Kyllerman, Mårten, 1 ... (1); Karlsson Lindsjö, Os ... (1); Berglund, Anna, 1949 ... (1); Witkowski, Åsa, 1959 ... (1); Dahlgren, Petra (1); Gottzén, Lucas (1); Göransson, Birgitta (1); Johnsson-Latham, Ger ... (1); Nylén, Lars M (1); Sandell, Karin, 1965 ... (1); Sveger, Tomas (1); Uusimaa, Johanna (1); Rydevik, Björn, 1947 (1); Mannelqvist, Ruth (1); Steneryd, Karin (1); Gorcenco, Sorina (1); Müller, Gunilla (1); Stenberg, Lars (1); Ågren, Karin, 1949- (1); Komulainen-Ebrahim, ... (1); Suo-Palosaari, Maria (1); Krüger, Johanna (1); Rahikkala, Elisa (1); Nilsson, Eva, 1963- (1); Król, Ladislav (1); Lind Karlberg, Maria (1); visa färre...

Lärosäte: Umeå universitet (4); Lunds universitet (4); Göteborgs universitet (2); Uppsala universitet (1)

Språk: Engelska (7); Svenska (3)

Forskningsämne (UKÄ/SCB): Medicin och hälsovetenskap (5); Samhällsvetenskap (3)

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