Ngā hua rapu kaituhi :: APM

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AIRE Mutations and Human Leukocyte Antigen Genotypes as Determinants of the Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Phenotype mā Maria Halonen, Petra Eskelin, Anne-Grethe Myhre, Jaakko Perheentupa, Eystein S. Husebye, Olle Kämpe, Fredrik Rorsman, Leena Peltonen, Ismo Ulmanen, Jukka Partanen

I whakaputaina 2002

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Artigo

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2

Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA mā Michela Barbaro, Antonio Balsamo, Britt Marie Anderlid, Anne Grethe Myhre, Monia Gennari, Annalisa Nicoletti, Maria Carla Pittalis, Mikael Oscarson, Anna Wedell

I whakaputaina 2009

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Artigo

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3

Polymorphisms in the Cytotoxic T Lymphocyte Antigen-4 Gene Region Confer Susceptibility to Addison’s Disease mā Anne Blomhoff, Benedicte A. Lie, Anne Grethe Myhre, E. Helen Kemp, Anthony P. Weetman, Hanne E. Akselsen, Eystein S. Huseby, Dag E. Undlien

I whakaputaina 2004

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Artigo

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4

Autoimmune Polyendocrine Syndrome Type 1 in Norway: Phenotypic Variation, Autoantibodies, and Novel Mutations in the Autoimmune Regulator Gene mā 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

I whakaputaina 2006

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Artigo

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5

Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in Norway mā 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

I whakaputaina 2016

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Artigo

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A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1 mā 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

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor mā 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

I whakaputaina 2007

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Artigo

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