Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hypoparathyroidism and HLA-B[original query] |
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AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype. The Journal of clinical endocrinology and metabolism 2002 Jun 87 (6): 2568-74. Halonen Maria, Eskelin Petra, Myhre Anne-Grethe, Perheentupa Jaakko, Husebye Eystein S, Kämpe Olle, Rorsman Fredrik, Peltonen Leena, Ulmanen Ismo, Partanen Juk |
Prevalence of calcium sensing receptor autoantibodies in patients with sporadic idiopathic hypoparathyroidism. European journal of endocrinology 2004 1 150 (1): 9-18. Goswami Ravinder, Brown Edward M, Kochupillai Narayana, Gupta Nandita, Rani Rajni, Kifor Olga, Chattopadhyay Naibed |
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED. Clinical endocrinology 2010 Nov 73 (5): 630-6. Cervato Sara, Morlin Luca, Albergoni Maria Paola, Masiero Stefano, Greggio Nella, Meossi Cristiano, Chen Shu, del Pilar Larosa Maria, Furmaniak Jadwiga, Rees Smith Bernard, Alimohammadi Mohammad, Kämpe Olle, Valenzise Mariella, Betterle Corra |
Presence of strong association of the major histocompatibility complex (MHC) class I allele HLA-A*26:01 with idiopathic hypoparathyroidism. The Journal of clinical endocrinology and metabolism 2012 Sep 97 (9): E1820-4. Goswami Ravinder, Singh Archana, Gupta Nandita, , Rani Raj |
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