(Q51936029)

English

Brain-Thyroid-Lung syndrome: a patient with a severe multi-system disorder due to a de novo mutation in the thyroid transcription factor 1 gene.

scientific article published on 23 October 2004

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Brain-Thyroid-Lung syndrome: a patient with a severe multi-system disorder due to a de novo mutation in the thyroid transcription factor 1 gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

1 reference

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object named as

Martin Lammens

6

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author name string

Michel A A P Willemsen

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Guido J Breedveld

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Siep Wouda

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Barto J Otten

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Jan L Yntema

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Bert B A de Vries

7

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

publication date

23 October 2004

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

European Journal of Pediatrics

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

164

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

1

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

28-30

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

Mutations in TITF-1 are associated with benign hereditary chorea

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The transcription factor TTF-1 is expressed at the onset of thyroid and lung morphogenesis and in restricted regions of the foetal brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nkx2.1 transcription factor in lung cells and a transforming growth factor-beta1 heterozygous mouse model of lung carcinogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary alveolar proteinosis: progress in the first 44 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional regulation of lung development: emergence of specificity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary alveolar proteinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intramolecular control of transcriptional activity by the NK2-specific domain in NK-2 homeodomain proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign hereditary chorea: clinical, genetic, and pathological findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary alveolar proteinosis: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-004-1559-X

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15517377

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