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Endocrine
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September 16, 2025
Prevalence of pendrin defects in sudanese families with congenital hypothyroidism
Mohammad S Islam, Alexandra M Dumitrescu, Amna Ahmed, et al.
Endocrinology
|
May 20, 2006
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice
Alexandra M Dumitrescu, Xiao-Hui Liao, Roy E Weiss, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 24, 2007
Intractable early childhood obesity as the initial sign of insulin resistant hyperinsulinism and precursor of polycystic ovary syndrome
Elizabeth E Littlejohn, Roy E Weiss, Dianne Deplewski, et al.
Endocrinology
|
August 11, 2007
Effects of maternal levels of thyroid hormone (TH) on the hypothalamus-pituitary-thyroid set point: studies in TH receptor beta knockout mice
Manuela Alonso, Charles Goodwin, XiaoHui Liao, et al.
Antioxidants & Redox Signaling
|
September 23, 2009
The syndrome of inherited partial SBP2 deficiency in humans
Alexandra M Dumitrescu, Caterina Di Cosmo, Xiao-Hui Liao, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 10, 2012
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature
Alfonso Massimiliano Ferrara, Kazumichi Onigata, Oya Ercan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 23, 2017
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications
Theodora Pappa, João Anselmo, Sunnee Mamanasiri, et al.
Endocrinology
|
June 6, 2009
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport
Caterina Di Cosmo, Xiao-Hui Liao, Alexandra M Dumitrescu, et al.
Thyroid : Official Journal of the American Thyroid Association
|
June 15, 2021
Novel <i>DIO1</i> Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous <i>TPO</i> Gene Mutations Causing Congenital Hypothyroidism
Aryel Furman, Zeina Hannoush, Francisco Barrera Echegoyen, et al.
AACE Clinical Case Reports
|
May 30, 2017
A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE
Hara Rosen Berger, Matthew K Creech, Zeina Hannoush, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 111) with videos related to
Sort By:
Page
of 12
Endocrine
|
September 16, 2025
Prevalence of pendrin defects in sudanese families with congenital hypothyroidism
Mohammad S Islam, Alexandra M Dumitrescu, Amna Ahmed, et al.
Endocrinology
|
May 20, 2006
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice
Alexandra M Dumitrescu, Xiao-Hui Liao, Roy E Weiss, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 24, 2007
Intractable early childhood obesity as the initial sign of insulin resistant hyperinsulinism and precursor of polycystic ovary syndrome
Elizabeth E Littlejohn, Roy E Weiss, Dianne Deplewski, et al.
Endocrinology
|
August 11, 2007
Effects of maternal levels of thyroid hormone (TH) on the hypothalamus-pituitary-thyroid set point: studies in TH receptor beta knockout mice
Manuela Alonso, Charles Goodwin, XiaoHui Liao, et al.
Antioxidants & Redox Signaling
|
September 23, 2009
The syndrome of inherited partial SBP2 deficiency in humans
Alexandra M Dumitrescu, Caterina Di Cosmo, Xiao-Hui Liao, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 10, 2012
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature
Alfonso Massimiliano Ferrara, Kazumichi Onigata, Oya Ercan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 23, 2017
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications
Theodora Pappa, João Anselmo, Sunnee Mamanasiri, et al.
Endocrinology
|
June 6, 2009
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport
Caterina Di Cosmo, Xiao-Hui Liao, Alexandra M Dumitrescu, et al.
Thyroid : Official Journal of the American Thyroid Association
|
June 15, 2021
Novel <i>DIO1</i> Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous <i>TPO</i> Gene Mutations Causing Congenital Hypothyroidism
Aryel Furman, Zeina Hannoush, Francisco Barrera Echegoyen, et al.
AACE Clinical Case Reports
|
May 30, 2017
A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE
Hara Rosen Berger, Matthew K Creech, Zeina Hannoush, et al.
Page
of 12