(Q34266067)

1 August 2017

Follow-up of newborns with elevated screening T4 concentrations (English)

1 reference

1 August 2017

Nalini Singh

5

1 reference

1 August 2017

Stephen H. Lafranchi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14517508

15 March 2024

David B. Snyder

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14517508

15 March 2024

David E. Sesser

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14517508

15 March 2024

Michael R. Skeels

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14517508

15 March 2024

Gregory A. Brent

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14517508

15 March 2024

Jerald C. Nelson

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14517508

15 March 2024

language of work or name

English

0 references

publication date

1 September 2003

1 reference

full work available at URL

1 August 2017

https://api.elsevier.com/content/article/PII:S0022347603001847?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

https://api.elsevier.com/content/article/PII:S0022347603001847?httpAccept=text/plain

15 March 2024

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

The Journal of Pediatrics

15 March 2024

published in

1 reference

1 August 2017

143

1 reference

1 August 2017

3

1 reference

1 August 2017

296-301

1 reference

Neonatal thyrotoxicosis: intellectual impairment and craniosynostosis in later years

1 August 2017

2

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Inherited thyroxine-binding globulin abnormalities in man.

15 March 2024

3

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

15 March 2024

4

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Reference ranges for newer thyroid function tests in premature infants

15 March 2024

5

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Reference intervals from birth to adulthood for serum thyroxine (T4), triiodothyronine (T3), free T3, free T4, thyroxine binding globulin (TBG) and thyrotropin (TSH).

15 March 2024

6

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Prediction and therapy of intrauterine and late-onset neonatal hyperthyroidism

15 March 2024

7

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Thyrotoxicosis detected in a mass-screening program for neonatal hypothyroidism: demonstration of placental transfer of an immunoglobulin with marked lipolytic activity

15 March 2024

8

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene

15 March 2024

9

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism

15 March 2024

10

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor gene

15 March 2024

11

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism

15 March 2024

12

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Thyroid abnormalities in the McCune-Albright syndrome: ultrasonography and hormonal studies.

15 March 2024

13

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

McCune-Albright syndrome. Long-term follow-up.

15 March 2024

14

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Hyperthyroidism in McCune-Albright syndrome with a review of thyroid abnormalities sixty years after the first report

15 March 2024

15

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

A case of neonatal McCune-Albright syndrome with Cushing syndrome and hyperthyroidism.

15 March 2024

16

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Prenatal diagnosis of thyroid hormone resistance.

15 March 2024

17

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Neonatal detection of generalized resistance to thyroid hormone.

15 March 2024

18

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Detection of resistance to thyroid hormone by cord blood screening

15 March 2024

19

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Resistance to thyroid hormone caused by a new mutation (V336M) in the thyroid hormone receptor beta gene

15 March 2024

20

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Attention deficit-hyperactivity disorder in people with generalized resistance to thyroid hormone

15 March 2024

21

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene

15 March 2024

24

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Inherited thyroxine-binding globulin abnormalities in man.

15 March 2024

25

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

Familial occurrence of dysalbuminaemic hyperthyroxinaemia, lipomatosis and ankylosing spondylitis

15 March 2024

27

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families

15 March 2024

28

1 reference

https://api.crossref.org/works/10.1067/S0022-3476(03)00184-7

15 March 2024

Identifiers

1 reference

release_ml5zqqgipbborhjp6szyoom7dm

1 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ml5zqqgipbborhjp6szyoom7dm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference