Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Karin Hult"'
Autor:
Cecilia Rohdin, Chao Wang, Gustaf Brander, Veronica Rondahl, Åsa Karlsson, Lisa Friling, Anthony Fischetti, Jennifer Meadows, Jens Häggström, Karin Hultin Jäderlund, Ingrid Ljungvall, Kerstin Lindblad‐Toh
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 37, Iss 4, Pp 1507-1513 (2023)
Abstract Rickets is a disorder of bone development and can be the result of either dietary or genetic causes. Here, related pugs from 2 litters were included. Three pugs had clinical signs including, lameness, bone deformities, and dyspnea. One other
Externí odkaz:
https://doaj.org/article/65907c8dd5204c1abeae34e96a2b91a2
Publikováno v:
International Emergency Nursing. 22:75-80
Background Ambulance nurses work daily in both emergency and non-emergency situations that can be demanding. One emotionally demanding situation for ambulance nurses is to nurse children who are ill. Aim The aim of this study was to describe ambulanc
Autor:
Josefin Hultman, Marco Rosati, Tone Kristensen Grøn, Kaspar Matiasek, Cathrine Trangerud, Karin Hultin Jäderlund
Publikováno v:
Acta Veterinaria Scandinavica, Vol 63, Iss 1, Pp 1-7 (2021)
Abstract Background Granulomatous myositis is a rare condition in both humans and dogs. In humans it is most frequently related to sarcoidosis, where a concurrent granulomatous neuritis has been reported occasionally. Simultaneous granulomatous myosi
Externí odkaz:
https://doaj.org/article/f1e27b7ada2c497497fc1e290762a193
Autor:
Cecilia Rohdin, Ingrid Ljungvall, Jens Häggström, Alexandra Leijon, Kerstin Lindblad‐Toh, Kaspar Matiasek, Marco Rosati, Peter Wohlsein, Karin Hultin Jäderlund
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 34, Iss 2, Pp 797-807 (2020)
Abstract Background Thoracolumbar myelopathies associated with spinal cord and vertebral column lesions, with a similar clinical phenotype, but different underlying etiologies, occur in pugs. Objectives To further characterize the clinical and neurop
Externí odkaz:
https://doaj.org/article/f9d69aec5646433f9ea27058021fe278
Autor:
Kim K. L. Bellamy, Fredrik S. Skedsmo, Josefin Hultman, Ellen F. Arnet, Ole Albert Guttersrud, Hege Kippenes Skogmo, Stein Istre Thoresen, Arild Espenes, Karin Hultin Jäderlund, Frode Lingaas
Publikováno v:
PLoS ONE, Vol 17, Iss 1 (2022)
A number of inherited ataxias is known in humans, with more than 250 loci implicated, most of which are included in human ataxia screening panels. Anecdotally, cases of ataxia in the Norwegian elkhound black have been known for the last 40 years. Aff
Externí odkaz:
https://doaj.org/article/bed343755c994577b5b10d192a242b13
Autor:
Henriette Frikke-Schmidt, Karin Hultman, Joseph W. Galaske, Sebastian B. Jørgensen, Martin G. Myers, Jr., Randy J. Seeley
Publikováno v:
Molecular Metabolism, Vol 21, Iss , Pp 13-21 (2019)
Objective: Analogues of GDF15 (Growth Differentiation Factor 15) are promising new anti-obesity therapies as pharmacological treatment with GDF15 results in dramatic reductions of food intake and body weight. GDF15 exerts its central anorexic effects
Externí odkaz:
https://doaj.org/article/6ed104bf859d4f83bfdbc8d15725ef9c
Autor:
Leif Thorning, Pla Kihle, Timo Tervo, Karin Hult, Tapio Ruotoistenmäk, Atle Sindre, Nisse Gustavsson, Jan Reidar Skilbrei, Seppo Elo, Sven Aaro
Publikováno v:
Journal of Applied Geophysics. 34:163-164
Autor:
Eva Bengtsson, Karin Hultman, Pontus Dunér, Giuseppe Asciutto, Peter Almgren, Marju Orho-Melander, Olle Melander, Jan Nilsson, Anna Hultgårdh-Nilsson, Isabel Gonçalves
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Several large-scale genome-wide association studies have identified single-nucleotide polymorphisms in the genomic region of A Disintegrin And Metalloproteinase with ThromboSpondin type 1 repeats (ADAMTS)-7 and associations to coronary arter
Externí odkaz:
https://doaj.org/article/7ee6747cf6c04da9988e3b3a763f33a5
Autor:
Karin Hultin Jäderlund, Cecilia Rohdin, Mette Berendt, Øyvind Stigen, Merete Fredholm, Arild Espenes, Inge Bjerkås, Lars Moe
Publikováno v:
Acta Veterinaria Scandinavica, Vol 59, Iss 1, Pp 1-4 (2017)
Abstract A homozygous mutation has been identified in the N-myc downstream-regulated gene 1 (NDRG1) in recent cases of polyneuropathy in Alaskan malamute dogs from the Nordic countries and USA. The objective of the present study was to determine if c
Externí odkaz:
https://doaj.org/article/667be6f659bd455e9836fe5cc86b3be0
Autor:
Kerstin Hahn, Cecilia Rohdin, Vidhya Jagannathan, Peter Wohlsein, Wolfgang Baumgärtner, Frauke Seehusen, Ingo Spitzbarth, Rodrigo Grandon, Cord Drögemüller, Karin Hultin Jäderlund
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0141824 (2015)
Clinical, pathological and genetic examination revealed an as yet uncharacterized juvenile-onset neuroaxonal dystrophy (NAD) in Spanish water dogs. Affected dogs presented with various neurological deficits including gait abnormalities and behavioral
Externí odkaz:
https://doaj.org/article/fc02c43e5be44bf6aeff833dd44c45fb