scholarly journals Basal serum thyroxine level should guide initial thyroxine replacement dose in neonates with congenital hypothyroidism

2020 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Ceren Günbey ◽  
Alev Özön ◽  
E. Nazlı Gönç ◽  
Ayfer Alikaşifoğlu ◽  
Sevilay Karahan ◽  
...  
Keyword(s):  
Congenital Hypothyroidism ◽  
Serum Thyroxine ◽  
Thyroxine Level ◽  
Basal Serum ◽  
Thyroxine Replacement

DECREASE IN SERUM THYROXINE LEVEL BY PHENOBARBITAL IN RATS IS NOT NECESSARILY DEPENDENT ON INCREASE IN HEPATIC UDP-GLUCURONOSYLTRANSFERASE

2005 ◽  
Vol 33 (11) ◽  
pp. 1608-1612 ◽  
Author(s):  
Yoshihisa Kato ◽  
Hiroshi Suzuki ◽  
Shinichi Ikushiro ◽  
Shizuo Yamada ◽  
Masakuni Degawa
Keyword(s):  
Serum Thyroxine ◽  
Thyroxine Level ◽  
Udp Glucuronosyltransferase

4-Hydroxy-2,2′,3,4′,5,5′,6-heptachlorobiphenyl-Mediated Decrease in Serum Thyroxine Level in Mice Occurs through Increase in Accumulation of Thyroxine in the Liver

2009 ◽  
Vol 37 (10) ◽  
pp. 2095-2102 ◽  
Author(s):  
Yoshihisa Kato ◽  
Koichi Haraguchi ◽  
Makiko Kubota ◽  
Yoshiki Seto ◽  
Shin-ichi Ikushiro ◽  
...  
Keyword(s):  
Serum Thyroxine ◽  
Thyroxine Level

Serum thyroxine level and cognitive decline in euthyroid older women

Neurology ◽  
2002 ◽  
Vol 58 (7) ◽  
pp. 1055-1061 ◽  
Author(s):  
S. Volpato ◽  
J. M. Guralnik ◽  
L. P. Fried ◽  
A. T. Remaley ◽  
A. R. Cappola ◽  
...  
Keyword(s):  
Cognitive Decline ◽  
Older Women ◽  
Serum Thyroxine ◽  
Thyroxine Level

scholarly journals Effect of Prolonged Discontinuation of L-Thyroxine Replacement in a Child with Congenital Hypothyroidism

2012 ◽  
Vol 2012 ◽  
pp. 1-5
Author(s):  
Rita Ann Kubicky ◽  
Evan Weiner ◽  
Bronwyn Carlson ◽  
Francesco De Luca
Keyword(s):  
Early Childhood ◽  
Developmental Delay ◽  
Congenital Hypothyroidism ◽  
Neonatal Screening ◽  
Growth Failure ◽  
Physical Growth ◽  
Neurological Development ◽  
Adherence To Treatment ◽  
Thyroxine Replacement ◽  
Infancy And Early Childhood

When diagnosed through neonatal screening and treated promptly and adequately, infants with congenital hypothyroidism (CH) experience normal physical growth and neurological development. Here we present a 3-year-old boy diagnosed with CH as a newborn, who was subsequently left untreated and experienced significant growth failure and developmental delay. This case emphasizes the importance of a consistent adherence to treatment in preventing such complications, especially in infancy and early childhood.

Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during l -thyroxine replacement

2003 ◽  
Vol 59 (2) ◽  
pp. 230-236 ◽  
Author(s):  
Laura Fugazzola ◽  
Luca Persani ◽  
Deborah Mannavola ◽  
Eugenio Reschini ◽  
Guia Vannucchi ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Congenital Hypothyroidism ◽  
Recombinant Human Tsh ◽  
Thyroxine Replacement

A Novel Mechanism for Polychlorinated Biphenyl-Induced Decrease in Serum Thyroxine Level in Rats

2007 ◽  
Vol 35 (10) ◽  
pp. 1949-1955 ◽  
Author(s):  
Yoshihisa Kato ◽  
Shin-ichi Ikushiro ◽  
Rie Takiguchi ◽  
Koichi Haraguchi ◽  
Nobuyuki Koga ◽  
...  
Keyword(s):  
Polychlorinated Biphenyl ◽  
Serum Thyroxine ◽  
Thyroxine Level

A possible mechanism for the decrease in serum thyroxine level by phenobarbital in rodents

2010 ◽  
Vol 249 (3) ◽  
pp. 238-246 ◽  
Author(s):  
Yoshihisa Kato ◽  
Hiroshi Suzuki ◽  
Koichi Haraguchi ◽  
Shinichi Ikushiro ◽  
Yoshihiko Ito ◽  
...  
Keyword(s):  
Serum Thyroxine ◽  
Thyroxine Level
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