Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Maud Eriksson"'
Autor:
Emmelie Widmark-Jensen, Susanne Bernhardsson, Maud Eriksson, Håkan Hallberg, Christian Jepsen, Lennart Jivegård, Ann Liljegren, Max Petzold, Mikael Svensson, Fredrik Wärnberg, Emma Hansson
Publikováno v:
BMC Surgery, Vol 21, Iss 1, Pp 1-23 (2021)
Abstract Background There is no consensus for when publicly funded breast reduction is indicated and recommendations in guidelines vary greatly, indicating a lack of evidence and unequal access. The primary aim of this review was to examine risks and
Externí odkaz:
https://doaj.org/article/afe43e3054e04c4a98c706123d1831b6
Autor:
Ann Liljegren, Fredrik Wärnberg, Lennart Jivegård, Maud Eriksson, Christian Jepsen, Håkan Hallberg, Emma Hansson, Emmelie Widmark-Jensen, Mikael Svensson, Max Petzold, Susanne Bernhardsson
Publikováno v:
BMC Surgery, Vol 21, Iss 1, Pp 1-23 (2021)
BMC Surgery
BMC Surgery
Background There is no consensus for when publicly funded breast reduction is indicated and recommendations in guidelines vary greatly, indicating a lack of evidence and unequal access. The primary aim of this review was to examine risks and benefits
Autor:
Margareta Albåge, Malin Rohdin, Hugo Lagercrantz, Karolina Wallenborg, Ola Hermanson, Maud Eriksson, Karin Björkman, Tobias Lilja
Publikováno v:
Epigenetics
Rett syndrome (RTT) is a neurodevelopmental disorder with neurological symptoms, such as motor disorders and mental retardation. In most cases, RTT is caused by mutations in the DNA binding protein MeCP2. In mice, MeCP2 gene deletion has been reporte
Autor:
Jacqueline Schoumans, Helena Malmgren, Anna Lindstrand, Ann Nordgren, Britt-Marie Anderlid, Elisa Benetti, Irina Golovleva, Elisabeth Blennow, Maud Eriksson, Annapia Verri
Publikováno v:
American Journal of Medical Genetics Part A. :1233-1243
Chromosome 10p terminal deletions have been associated with DiGeorge phenotype, and within the same genomic region haploinsufficiency of GATA3 causes the HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia). We have performed de
Publikováno v:
Molecular Genetics and Metabolism. 110:342-344
A 4-month old boy presented with multiple epileptic seizure types including West syndrome. Screening for infectious and structural etiologies showed normal results. A metabolic investigation was undertaken to investigate the cause of his neurological
Publikováno v:
British Journal of Audiology. 29:309-314
Eighteen patients judged the sound quality of the new Classic 300 and the existing HC 100 or HC 200 on 4 five-stage sound quality scales. Two of the scales relate to the perceptual dimensions softness and clarity, one relates to interference or noise
Autor:
Maud Eriksson, Pawel Alster, Kerstin Uvnäs-Moberg, Eva Björkstrand, A.-S. Matthiesen, Ulrika Smedh
Publikováno v:
Acta Physiologica Scandinavica. 151:453-459
The aim of this study was to investigate the role of vagal nerve activity for the release of oxytocin, prolactin and gastrointestinal (GI) hormones during suckling as well as for the secretion of milk in lactating rats. We have therefore performed ex
Publikováno v:
Acta Physiologica Scandinavica. 144:355-359
Oxytocin has been shown to influence insulin, glucagon and blood glucose levels in various experimental situations. The present study was performed in order to obtain support for a possible interaction of glucose and oxytocin under physiological cond
Publikováno v:
Scandinavian Audiology. 21:201-206
The hearing measurement scale (HMS), targeting the experience of being hearing impaired, was translated into Swedish and answered by 122 patients with slight to moderate hearing losses. According to the item analysis the test construction of the HMS
Publikováno v:
Acta Oto-Laryngologica. 109:70-75
A basic problem in hearing-aid fitting is the difficulty in finding one setting optimal to all listening situations that might occur. The objective was to develop a behind-the-ear hearing-aid with a very flexible analog signal processor which is digi