Results 111 to 120 of about 1,698 (148)
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Hyperthyroxinemia in patients with acute psychiatric disorders

The American Journal of Medicine, 1982
Thyroid function tests were measured in 645 patients admitted to an acute psychiatric disorders unit. Thirty-three percent had elevated serum thyroxine (T4), and 18 percent had an elevated free T4 index (FTI). Serum triiodothyronine (T3) was low, normal, or minimally elevated in 77 patients, with a high initial free T4 index.
D I, Spratt   +5 more
openaire   +2 more sources

Prevalence of Familial Dysalbuminemic Hyperthyroxinemia in Hispanics

Annals of Internal Medicine, 1987
Excerpt To the editor: Familial dysalbuminemic hyperthyroxinemia is a recently recognized autosomal dominant syndrome often confused with thyrotoxicosis in laboratory tests (1-3).
D R, DeCosimo, S L, Fang, L E, Braverman
openaire   +2 more sources

Familial Dysalbuminemic Hyperthyroxinemia in a Hispanic Family

Annals of Internal Medicine, 1988
Excerpt To the editor: We read with interest the letter by DeCosimo and associates (1) about the increased prevalence of familial dysalbuminemic hyperthyroxinemia in Hispanics.
J M, Kunitake   +2 more
openaire   +2 more sources

Hyperthyroxinemia after surgery for primary hyperparathyroidism

Langenbecks Archiv f�r Chirurgie, 1994
Episodes of transient thyrotoxicosis after surgery for primary hyperparathyroidism have previously been described, and surgical trauma to the thyroid gland has been suggested as an etiologic factor. However, there are several links between the thyroid and parathyroid hormonal systems, and therefore other explanations are possible as well. In this study
A, Bergenfelz, B, Ahrén
openaire   +2 more sources

[Hyperthyroxinemia without hyperthyroidism].

Tijdschrift voor kindergeneeskunde, 1986
The various causes of persisting hyperthyroxinemia without hyperthyroidism are discussed after short case histories of an infant with hyperthyroxinemia due to TBG excess, discovered by newborn screening for congenital hypothyroidism and a girl with peripheral resistance to thyroid hormones disclosed by investigation of a small goiter.
C, Rongen-Westerlaken   +2 more
openaire   +1 more source

[Prealbumin-associated hyperthyroxinemia].

Acta medica Austriaca, 1986
Prealbumin associated hyperthyroxinaemia represents a rare but important protein binding anomaly, causing difficulties in differential diagnostics. This anomaly is based on a variant prealbumin showing an increased affinity to T4 and rT3 and in some cases also when using T4 analogue tracers. The condition of the patient is clinically euthyroid which is
P, Lind   +4 more
openaire   +1 more source

Transient hyperthyroxinemia in symptomatic hyponatremic patients.

Archives of internal medicine, 1986
Twenty-two patients with severe hyponatremia were divided into 12 patients with and ten without associated neurologic manifestations (groups 1 and 2, respectively). Marked hyperthyroxinemia was demonstrated in seven patients in group 1 but in none in group 2. The triiodothyronine concentration was also higher than normal in two patients in group 1. All
Cogan, Elie, Abramow, Maurice
openaire   +2 more sources

Hyperthyroxinemia and hypotriiodothyroninemia with clinical euthyroidism.

The American journal of the medical sciences, 1981
A clinically euthyroid woman had substernal goiter and thrombocytopenia. There was a striking elevation in serum thyroxine (T4) level when the level of triiodothyronine (T3) ws low, reverse T3 (rT3) was normal I131 uptake was suppressed, and thyroid stimulating hormone (TSH) response to thyrotropin-releasing hormone (TRH) was blunted.
J A, Amico, F R, Derubertis
openaire   +1 more source

[Post-traumatic hyperthyroxinemia or hyperthyroidism].

Annales francaises d'anesthesie et de reanimation, 1985
A fifteen year-old girl presented with several fractures after a road traffic accident. Five days later, fat embolism occurred, complicated by adult respiratory distress syndrome (ARDS) and disseminated coagulation (DIC). She was successfully managed in the intensive therapy unit, and was transferred to a general surgery after five weeks.
J F, Doussin, J, Dubost, V, Banssillon
openaire   +1 more source

Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia

Journal of Pediatric Endocrinology and Metabolism, 2021
Saygin Abalı   +2 more
exaly  

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