Resultats de la cerca - Anne-Grethe Myhre
- Mostrar 1 - 7 resultats de 7
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1
AIRE Mutations and Human Leukocyte Antigen Genotypes as Determinants of the Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Phenotype per Maria Halonen, Petra Eskelin, Anne-Grethe Myhre, Jaakko Perheentupa, Eystein S. Husebye, Olle Kämpe, Fredrik Rorsman, Leena Peltonen, Ismo Ulmanen, Jukka Partanen
Publicat 2002Artigo -
2
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA per Michela Barbaro, Antonio Balsamo, Britt Marie Anderlid, Anne Grethe Myhre, Monia Gennari, Annalisa Nicoletti, Maria Carla Pittalis, Mikael Oscarson, Anna Wedell
Publicat 2009Artigo -
3
Polymorphisms in the Cytotoxic T Lymphocyte Antigen-4 Gene Region Confer Susceptibility to Addison’s Disease per Anne Blomhoff, Benedicte A. Lie, Anne Grethe Myhre, E. Helen Kemp, Anthony P. Weetman, Hanne E. Akselsen, Eystein S. Huseby, Dag E. Undlien
Publicat 2004Artigo -
4
Autoimmune Polyendocrine Syndrome Type 1 in Norway: Phenotypic Variation, Autoantibodies, and Novel Mutations in the Autoimmune Regulator Gene per Anette S. B. Wolff, Martina M. Erichsen, Anthony Meager, Ngweina Francis Magitta, Anne Grethe Myhre, Jens Bollerslev, Kristian J. Fougner, Kari Lima, Per M. Knappskog, Eystein S. Husebye
Publicat 2006Artigo -
5
Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in Norway per Marianne C. Astor, Kristian Løvås, Aleksandra Dębowska, Erik Fink Eriksen, Johan Arild Evang, Caroline Fossum, Kristian J. Fougner, Synnøve Emblem Holte, Kari Lima, Ragnar Bekkhus Moe, Anne Grethe Myhre, E. Helen Kemp, Bjørn Gunnar Nedrebø, Johan Svartberg, Eystein S. Husebye
Publicat 2016Artigo -
6
A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1 per Øyvind Bruserud, Bergithe E Oftedal, Nils Landegren, Martina M. Erichsen, Eirik Bratland, Kari Lima, Anders Palmstrøm Jørgensen, Anne Grethe Myhre, Johan Svartberg, Kristian J. Fougner, A Bakke, Bjørn Gunnar Nedrebø, Bjarne Mella, Lars Breivik, Marte K. Viken, Per M. Knappskog, Mihaela Cuida Marthinussen, Kristian Løvås, Olle Kämpe, Anette S. B. Wolff, Eystein S. Husebye
Publicat 2016Artigo -
7
Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor per I. Sadaf Farooqi, Teresia Wangensteen, Stephan C. Collins, Wendy L. Kimber, Giuseppe Matarese, Julia M. Keogh, Emma Lank, Bill Bottomley, Judith López‐Fernández, Iván Ferraz‐Amaro, Mehul Dattani, Oya Ercan, Anne Grethe Myhre, Lars Retterstøl, R Stanhope, Julie Edge, S A McKenzie, Nader Lessan, Maryam Ghodsi, Veronica De Rosa, Francesco Perna, Silvia Fontana, Inês Barroso, Dag E. Undlien, Stephen O’Rahilly
Publicat 2007Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Internal medicine
Medicine
Antibody
Autoimmune disease
Immunology
Autoimmune regulator
Autoimmunity
Disease
Hypoparathyroidism
Phenotype
Antigen
Autoantibody
Chronic mucocutaneous candidiasis
Endocrinology
Immune system
Mutation
Pediatrics
Adrenal insufficiency
Anxiety
Breakpoint
Candidate gene
Chromosome
Cytotoxic T cell
Depression (economics)
DiGeorge syndrome
Disorders of sex development
Economics