Torthaí cuardaigh - Anne-Grethe Myhre
- 1 - 7 toradh as 7 á dtaispeáint
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1
AIRE Mutations and Human Leukocyte Antigen Genotypes as Determinants of the Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Phenotype de réir Maria Halonen, Petra Eskelin, Anne-Grethe Myhre, Jaakko Perheentupa, Eystein S. Husebye, Olle Kämpe, Fredrik Rorsman, Leena Peltonen, Ismo Ulmanen, Jukka Partanen
Foilsithe / Cruthaithe 2002Artigo -
2
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA de réir Michela Barbaro, Antonio Balsamo, Britt Marie Anderlid, Anne Grethe Myhre, Monia Gennari, Annalisa Nicoletti, Maria Carla Pittalis, Mikael Oscarson, Anna Wedell
Foilsithe / Cruthaithe 2009Artigo -
3
Polymorphisms in the Cytotoxic T Lymphocyte Antigen-4 Gene Region Confer Susceptibility to Addison’s Disease de réir Anne Blomhoff, Benedicte A. Lie, Anne Grethe Myhre, E. Helen Kemp, Anthony P. Weetman, Hanne E. Akselsen, Eystein S. Huseby, Dag E. Undlien
Foilsithe / Cruthaithe 2004Artigo -
4
Autoimmune Polyendocrine Syndrome Type 1 in Norway: Phenotypic Variation, Autoantibodies, and Novel Mutations in the Autoimmune Regulator Gene de réir 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
Foilsithe / Cruthaithe 2006Artigo -
5
Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in Norway de réir 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
Foilsithe / Cruthaithe 2016Artigo -
6
A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1 de réir 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
Foilsithe / Cruthaithe 2016Artigo -
7
Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor de réir 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
Foilsithe / Cruthaithe 2007Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
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