High prevalence of associated birth defects in congenital hypothyroidism (Q33829317)

29 July 2017

High prevalence of associated birth defects in congenital hypothyroidism (English)

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29 July 2017

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P Amaresh Reddy

1

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29 July 2017

G Rajagopal

2

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29 July 2017

C V Harinarayan

3

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29 July 2017

V Vanaja

4

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29 July 2017

D Rajasekhar

5

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29 July 2017

V Suresh

6

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29 July 2017

Alok Sachan

7

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29 July 2017

4 May 2010

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International journal of pediatric endocrinology

29 July 2017

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29 July 2017

2010

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29 July 2017

940980

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https://scigraph.springernature.com/pub.10.1186/1687-9856-2010-940980

29 July 2017

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cites work

Increased incidence of extrathyroidal congenital malformations in Japanese patients with congenital hypothyroidism and their relationship with Down syndrome and other factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Prevalence of minor musculoskeletal anomalies in children with congenital hypothyroidism.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991-1998).

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

A genetic blueprint for cardiac development

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Disorders of thyroid gland in India

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Recent advances in understanding the molecular basis of primary congenital hypothyroidism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Molecular genetics of congenital hypothyroidism

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Expression of the homebox gene Hex during early stages of chick embryo development

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864451

Congenital heart disease caused by mutations in the transcription factor NKX2-5

4 July 2018

1 reference

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Inborn errors of thyroid hormone biosynthesis.

4 July 2018

1 reference

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Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors.

4 July 2018

1 reference

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Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992.

4 July 2018

1 reference

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Persistent truncus arteriosus in the Splotch mutant mouse

4 July 2018

1 reference

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Role of neural crest in congenital heart disease

4 July 2018

1 reference

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Congenital heart disease in India: a status report.

4 July 2018

1 reference

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Characteristics of infantile hypothyroidism discovered on neonatal screening

29 October 2018

1 reference

12 December 2020

Congenital anomalies in infants with congenital hypothyroidism: is it a coincidental or an associated finding?

1 reference

12 December 2020

Intellectual development in children with congenital hypothyroidism in relation to recommended thyroxine treatment

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12 December 2020

Prevalence of congenital heart disease, Kanpur, India

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12 December 2020

Congenital abnormalities and congenital hypothyroidism

1 reference

12 December 2020

High prevalence of extrathyroid malformations in a cohort of Brazilian patients with permanent primary congenital hypothyroidism

1 reference

12 December 2020

Malformations in offspring of diabetic rats: morphometric analysis of neural crest-derived organs and effects of maternal vitamin E treatment

1 reference

12 December 2020

Congenital anomalies concomitant with persistent primary congenital hypothyroidism

1 reference

12 December 2020

Improved prognosis in congenital bypothyroidism treated before age three months

1 reference

12 December 2020

Cellular and molecular contributions of the cardiac neural crest to cardiovascular development

1 reference

12 December 2020

[The association between hypothyroidism and other congenital defects. The experience of the National Registry in 1987-1992]

1 reference

12 December 2020

Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factors

1 reference

12 December 2020

Dependence of thymus development on derivatives of the neural crest

1 reference

12 December 2020

Intellectual outcome in children with fetal hypothyroidism

1 reference

12 December 2020

Incidence of congenital heart disease among hospital live births in India

1 reference

12 December 2020

10.1186/1687-9856-2010-940980

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29 July 2017

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29 July 2017

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