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Results of search for 'su:"Hyperthyroxinemia"', page 11 of 11
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Authors
Agostini, Maura
Ahrén, B
Almeida, M R
Altland, K
Alves, I L
Angkeow, P
Arevalo, G
Benson, M D
Bergenfelz, A
Bhagavan, N V
Braverman, L E
Chatterjee, V Krishna
Eber, O
Faber, J
Jensen, I W
Költringer, P
Langsteger, W
Refetoff, S
Refetoff, Samuel
Weiss, R E
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Topics
Adult
Aged
Diagnosis, Differential
Female
Humans
Hyperthyroxinemia
Male
Middle Aged
Serum Albumin
Thyroid Function Tests
Thyrotropin
Thyroxine
Thyroxine-Binding Proteins
Triiodothyronine
analysis
blood
complications
diagnosis
genetics
metabolism
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Results
201.
Rising serum thyroxine levels and chorea in graves' disease.
[electronic resource]
by
Leblicq, Coralie
Duval, Michel
Carmant, Lionel
Van Vliet, Guy
Alos, Nathalie
Producer:
20130411
In:
Pediatrics
vol. 131
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202.
A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.
[electronic resource]
by
Wada, N
Chiba, H
Shimizu, C
Kijima, H
Kubo, M
Koike, T
Producer:
19971117
In:
The Journal of clinical endocrinology and metabolism
vol. 82
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203.
Induction of hyperthyroxinemia in BALB/C but not in several other strains of mice.
[electronic resource]
by
Wagle, N M
Dallas, J S
Seetharamaiah, G S
Fan, J L
Desai, R K
Memar, O
Rajaraman, S
Prabhakar, B S
Producer:
19950615
In:
Autoimmunity
vol. 18
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204.
Hyperthyroxinemia is positively associated with prevalent and incident type 2 diabetes mellitus in two population-based samples from Northeast Germany and Denmark.
[electronic resource]
by
Ittermann, T
Schipf, S
Dörr, M
Thuesen, B H
Jørgensen, T
Völzke, H
Markus, M R P
Producer:
20190314
In:
Nutrition, metabolism, and cardiovascular diseases : NMCD
vol. 28
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205.
Excessive thyroid hormone replacement therapy.
[electronic resource]
by
Nuovo, J
Ellsworth, A
Christensen, D B
Reynolds, R
Producer:
19960320
In:
The Journal of the American Board of Family Practice
vol. 8
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206.
Thrombin-activatable fibrinolysis inhibitor in hypothyroidism and hyperthyroxinaemia.
[electronic resource]
by
Verkleij, Chantal J N
Stuijver, Danka J F
van Zaane, Bregje
Squizzato, Alessandro
Brandjes, Dees P M
Büller, Harry R
Meijers, Joost C M
Gerdes, Victor E A
Producer:
20130827
In:
Thrombosis and haemostasis
vol. 109
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207.
Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome.
[electronic resource]
by
Schneider, Tomasz
Skitt, Zara
Liu, Yiwen
Deacon, Robert M J
Flint, Jonathan
Karmiloff-Smith, Annette
Rawlins, J Nick P
Tassabehji, May
Producer:
20121210
In:
Behavioural brain research
vol. 233
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