(Q46665037)

24 December 2017

title

Congenital hypothyroidism with gland in situ: diagnostic re-evaluation (English)

1 reference

24 December 2017

congenital hypothyroidism

main subject

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G Weber

1

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24 December 2017

M C Vigone

2

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24 December 2017

A Passoni

3

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24 December 2017

M Odoni

4

1 reference

24 December 2017

P L Paesano

5

1 reference

24 December 2017

F Dosio

6

1 reference

24 December 2017

M C Proverbio

7

1 reference

24 December 2017

C Corbetta

8

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24 December 2017

L Persani

9

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24 December 2017

G Chiumello

10

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24 December 2017

publication date

1 June 2005

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24 December 2017

Journal of Endocrinological Investigation

published in

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24 December 2017

volume

28

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24 December 2017

issue

6

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24 December 2017

page(s)

516-522

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24 December 2017

https://scigraph.springernature.com/pub.10.1007/bf03347239

exact match

0 references

cites work

Three-year follow-up of borderline congenital hypothyroidism.

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Molecular pathogenesis of neonatal hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Neonatal screening for congenital hypothyroidism: results and perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Primary congenital hypothyroidism: defects in iodine pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Neonatal hypothyroidism: treatment and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Congenital hypothyroidism: etiologies, diagnosis, and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Subclinical thyroid disease: scientific review and guidelines for diagnosis and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Subclinical hypothyroidism in early childhood: a frequent outcome of transient neonatal hyperthyrotropinemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Determination of thyroid volume by ultrasound from the neonatal period to late adolescence

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347239

Neonatal thyroid disorders

21 January 2018

1 reference

12 December 2020

Inborn errors of thyroid hormone biosynthesis.

1 reference

12 December 2020

Alterations of neonatal thyroid function.

1 reference

12 December 2020

Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene

1 reference

12 December 2020

Significance of iodide-perchlorate discharge test for detection of iodine organification defect of the thyroid

1 reference

12 December 2020

Pertechnetate scintigraphy in primary congenital hypothyroidism

1 reference

12 December 2020

Perspective: genetic defects in the etiology of congenital hypothyroidism

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03347239

1 reference

24 December 2017

1 reference

24 December 2017