Familial dysalbuminemic hyperthyroxinemia coexisting with a Grave’s disease: a Belgian case report
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| Veröffentlicht in: | Clinical chemistry and laboratory medicine 2024-08, Vol.62 (9), p.197-199 |
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| container_end_page | 199 |
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| container_issue | 9 |
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| container_title | Clinical chemistry and laboratory medicine |
| container_volume | 62 |
| creator | Wolff, Fleur Fery, Françoise Désir, Julie Gadisseur, Romy Cavalier, Etienne Cotton, Frédéric |
| description | |
| doi_str_mv | 10.1515/cclm-2024-0204 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1434-6621 |
| ispartof | Clinical chemistry and laboratory medicine, 2024-08, Vol.62 (9), p.197-199 |
| issn | 1434-6621 1437-4331 1437-4331 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_3031137654 |
| source | MEDLINE; De Gruyter journals |
| subjects | Adult Belgium Case reports Endocrinology Female Graves Disease - blood Graves Disease - complications Graves Disease - diagnosis Grave’s disease high affinity HSA variants Humans hyperthyroxinemia Hyperthyroxinemia, Familial Dysalbuminemic - blood Hyperthyroxinemia, Familial Dysalbuminemic - diagnosis Immunoassay Male Mutation Patients Population Proteins Thyroid gland Tumors White people |
| title | Familial dysalbuminemic hyperthyroxinemia coexisting with a Grave’s disease: a Belgian case report |
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