| scholarly article | Q13442814 |
| P356 | DOI | 10.1515/JPEM.2005.18.2.155 |
| P698 | PubMed publication ID | 15751604 |
| P2093 | author name string | Roberto Perniola | |
| Maria Cristina Rosatelli | |||
| Giambattista Lobreglio | |||
| Corrado De Rinaldis | |||
| Elena Pitotti | |||
| Elisa Accogli | |||
| P2860 | cites work | An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains | Q24313206 |
| Chronic mucocutaneous candidiasis | Q34165812 | ||
| Human CD4(+)CD25(+) cells: a naturally occurring population of regulatory T cells. | Q34518941 | ||
| The Vogt-Koyanagi-Harada syndrome: association with autoimmune polyglandular syndrome type 1 | Q36680908 | ||
| Autoimmune Thyroid Disease: Developments in Our Understanding | Q40142954 | ||
| Chronic idiopathic hypoparathyroidism with superimposed Addison's disease in a child | Q41088685 | ||
| Premature ovarian failure and ovarian autoimmunity | Q41349658 | ||
| Severe malabsorption in autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy syndrome successfully treated with immunosuppression | Q42063894 | ||
| Restricted expression of p55 interleukin 2 receptor (CD25) on normal T cells | Q43585573 | ||
| Lymphocyte subset reference ranges in adult caucasians | Q43887664 | ||
| Immunological findings in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and their family members: are heterozygotes subclinically affected? | Q50761662 | ||
| Organ-specific and non-organ-specific autoantibodies in children and young adults with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). | Q51553283 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 155-164 | |
| P577 | publication date | 2005-02-01 | |
| P1433 | published in | Journal of Pediatric Endocrinology and Metabolism | Q6295720 |
| P1476 | title | Immunophenotypic characterisation of peripheral blood lymphocytes in autoimmune polyglandular syndrome type 1: clinical study and review of the literature | |
| P478 | volume | 18 |
| Q37974985 | Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy: known and novel aspects of the syndrome |
| Q51770590 | Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in the Irish population. |
| Q34977002 | Clinical manifestations and management of patients with autoimmune polyendocrine syndrome type I. |
| Q39709707 | Expanded CD4(+) Effector/Memory T Cell Subset in APECED Produces Predominantly Interferon Gamma. |
| Q55052934 | Flow cytometry study of blood cell subtypes reflects autoimmune and inflammatory processes in autoimmune polyendocrine syndrome type I. |
| Q37217551 | Human APECED; a Sick Thymus Syndrome? |
| Q38160483 | Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia |
| Q36886212 | Impact of methimazole treatment on magnesium concentration and lymphocytes activation in adolescents with Graves' disease. |
| Q44994544 | Innate and adaptive immunity in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy |
| Q27333247 | Redefined clinical features and diagnostic criteria in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy |
| Q26740115 | Type 1 Diabetes in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome (APECED): A "Rare" Manifestation in a "Rare" Disease |
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