Publication list - Publika - Scientific publications from Oslo University Hospital

Publications by Anne Grethe Myhre

30 publications found

Original articles

Waehre A, Heggeli C, Hald K, Myhre AG, Diseth T (2022)
A 15-20-year follow-up of mental health, psychosocial functioning and quality of life in a single center sample of individuals with differences in sex development
Health Psychol Behav Med, 10 (1), 837-854
DOI 10.1080/21642850.2022.2116329, PubMed 36105256

Diab SG, Godang K, Müller LO, Almaas R, de Lange C, Brunvand L, Hansen KM, Myhre AG, Døhlen G, Thaulow E, Bollerslev J, Möller T (2019)
Progressive loss of bone mass in children with Fontan circulation
Congenit Heart Dis, 14 (6), 996-1004
DOI 10.1111/chd.12848, PubMed 31600039

Annexstad EJ, Bollerslev J, Westvik J, Myhre AG, Godang K, Holm I, Rasmussen M (2019)
The role of delayed bone age in the evaluation of stature and bone health in glucocorticoid treated patients with Duchenne muscular dystrophy
Int J Pediatr Endocrinol, 2019, 4
DOI 10.1186/s13633-019-0070-0, PubMed 31889957

Bruserud Ø, Oftedal BE, Landegren N, Erichsen MM, Bratland E, Lima K, Jørgensen AP, Myhre AG, Svartberg J, Fougner KJ, Bakke Å, Nedrebø BG, Mella B, Breivik L, Viken MK, Knappskog PM, Marthinussen MC, Løvås K, Kämpe O, Wolff AB, Husebye ES (2016)
A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1
J Clin Endocrinol Metab, 101 (8), 2975-83
DOI 10.1210/jc.2016-1821, PubMed 27253668

Astor MC, Løvås K, Debowska A, Eriksen EF, Evang JA, Fossum C, Fougner KJ, Holte SE, Lima K, Moe RB, Myhre AG, Kemp EH, Nedrebø BG, Svartberg J, Husebye ES (2016)
Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in Norway
J Clin Endocrinol Metab, 101 (8), 3045-53
DOI 10.1210/jc.2016-1477, PubMed 27186861

Overgaard KR, Aase H, Torgersen S, Reichborn-Kjennerud T, Oerbeck B, Myhre A, Zeiner P (2014)
Continuity in features of anxiety and attention deficit/hyperactivity disorder in young preschool children
Eur Child Adolesc Psychiatry, 23 (9), 743-52
DOI 10.1007/s00787-014-0538-7, PubMed 24687273

Wolff AS, Sarkadi AK, Maródi L, Kärner J, Orlova E, Oftedal BE, Kisand K, Oláh E, Meloni A, Myhre AG, Husebye ES, Motaghedi R, Perheentupa J, Peterson P, Willcox N, Meager A (2013)
Anti-cytokine autoantibodies preceding onset of autoimmune polyendocrine syndrome type I features in early childhood
J Clin Immunol, 33 (8), 1341-8
DOI 10.1007/s10875-013-9938-6, PubMed 24158785

Husebye ES, Erichsen MM, Myhre AG, Bratke H, Jørgensen AP, Dahlqvist P, Løvås K (2012)
[New steroid card for adrenal insufficiency]
Tidsskr Nor Laegeforen, 132 (18), 2043-4
DOI 10.4045/tidsskr.12.0946, PubMed 23038193

Barbaro M, Balsamo A, Anderlid BM, Myhre AG, Gennari M, Nicoletti A, Pittalis MC, Oscarson M, Wedell A (2009)
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA
Eur J Hum Genet, 17 (11), 1439-47
DOI 10.1038/ejhg.2009.70, PubMed 19417767

Oftedal BE, Wolff AS, Bratland E, Kämpe O, Perheentupa J, Myhre AG, Meager A, Purushothaman R, Ten S, Husebye ES (2008)
Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I
Clin Immunol, 129 (1), 163-9
DOI 10.1016/j.clim.2008.07.002, PubMed 18708298

Farooqi IS, Wangensteen T, Collins S, Kimber W, Matarese G, Keogh JM, Lank E, Bottomley B, Lopez-Fernandez J, Ferraz-Amaro I, Dattani MT, Ercan O, Myhre AG, Retterstol L, Stanhope R, Edge JA, McKenzie S, Lessan N, Ghodsi M, De Rosa V, Perna F, Fontana S, Barroso I, Undlien DE, O'Rahilly S (2007)
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor
N Engl J Med, 356 (3), 237-47
DOI 10.1056/NEJMoa063988, PubMed 17229951

Wolff AS, Erichsen MM, Meager A, Magitta NF, Myhre AG, Bollerslev J, Fougner KJ, Lima K, Knappskog PM, Husebye ES (2006)
Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene
J Clin Endocrinol Metab, 92 (2), 595-603
DOI 10.1210/jc.2006-1873, PubMed 17118990

Myhre AG, Stray-Pedersen A, Spangen S, Eide E, Veimo D, Knappskog PM, Abrahamsen TG, Husebye ES (2004)
Chronic mucocutaneous candidiasis and primary hypothyroidism in two families
Eur J Pediatr, 163 (10), 604-11
DOI 10.1007/s00431-004-1516-8, PubMed 15290270

Blomhoff A, Lie BA, Myhre AG, Kemp EH, Weetman AP, Akselsen HE, Huseby ES, Undlien DE (2004)
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease
J Clin Endocrinol Metab, 89 (7), 3474-6
DOI 10.1210/jc.2003-031854, PubMed 15240634

Söderbergh A, Myhre AG, Ekwall O, Gebre-Medhin G, Hedstrand H, Landgren E, Miettinen A, Eskelin P, Halonen M, Tuomi T, Gustafsson J, Husebye ES, Perheentupa J, Gylling M, Manns MP, Rorsman F, Kämpe O, Nilsson T (2004)
Prevalence and clinical associations of 10 defined autoantibodies in autoimmune polyendocrine syndrome type I
J Clin Endocrinol Metab, 89 (2), 557-62
DOI 10.1210/jc.2003-030279, PubMed 14764761

Myhre AG, Aarsetøy H, Undlien DE, Hovdenak N, Aksnes L, Husebye ES (2003)
High frequency of coeliac disease among patients with autoimmune adrenocortical failure
Scand J Gastroenterol, 38 (5), 511-5
DOI 10.1080/00365520310002544, PubMed 12795461

Halonen M, Eskelin P, Myhre AG, Perheentupa J, Husebye ES, Kämpe O, Rorsman F, Peltonen L, Ulmanen I, Partanen J (2002)
AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype
J Clin Endocrinol Metab, 87 (6), 2568-74
DOI 10.1210/jcem.87.6.8564, PubMed 12050215

Bøe AS, Knappskog PM, Myhre AG, Sørheim JI, Husebye ES (2002)
Mutational analysis of the autoimmune regulator (AIRE) gene in sporadic autoimmune Addison's disease can reveal patients with unidentified autoimmune polyendocrine syndrome type I
Eur J Endocrinol, 146 (4), 519-22
DOI 10.1530/eje.0.1460519, PubMed 11916620

Myhre AG, Undlien DE, Løvås K, Uhlving S, Nedrebø BG, Fougner KJ, Trovik T, Sørheim JI, Husebye ES (2002)
Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features
J Clin Endocrinol Metab, 87 (2), 618-23
DOI 10.1210/jcem.87.2.8192, PubMed 11836294

Grigelioniene G, Schoumans J, Neumeyer L, Ivarsson A, Eklöf O, Enkvist O, Tordai P, Fosdal I, Myhre AG, Westphal O, Nilsson NO, Elfving M, Ellis I, Anderlid BM, Fransson I, Tapia-Paez I, Nordenskjöld M, Hagenäs L, Dumanski JP (2001)
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
Hum Genet, 109 (5), 551-8
DOI 10.1007/s00439-001-0609-y, PubMed 11735031

Myhre AG, Halonen M, Eskelin P, Ekwall O, Hedstrand H, Rorsman F, Kämpe O, Husebye ES (2001)
Autoimmune polyendocrine syndrome type 1 (APS I) in Norway
Clin Endocrinol (Oxf), 54 (2), 211-7
DOI 10.1046/j.1365-2265.2001.01201.x, PubMed 11207636

Taillandier A, Lia-Baldini AS, Mouchard M, Robin B, Muller F, Simon-Bouy B, Serre JL, Bera-Louville A, Bonduelle M, Eckhardt J, Gaillard D, Myhre AG, Körtge-Jung S, Larget-Piet L, Malou E, Sillence D, Temple IK, Viot G, Mornet E (2001)
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia
Hum Mutat, 18 (1), 83-4
DOI 10.1002/humu.1154, PubMed 11438998

Myhre AG, Björses P, Dalen A, Husebye ES (1998)
Three sisters with Addison's disease
J Clin Endocrinol Metab, 83 (12), 4204-6
DOI 10.1210/jcem.83.12.5332, PubMed 9851752

Review articles

Løvås K, Erichsen MM, Husebye ES, Fougner KJ, Svartberg J, Mella B, Myhre AG, Berg JP, Aarskog D (2005)
[Primary adrenal failure--causes, diagnostics and therapy]
Tidsskr Nor Laegeforen, 125 (2), 155-8
PubMed 15665886