(Q37875658)

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16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn (English)

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

arterial hypertension

0 references

persistent fetal circulation syndrome

1 reference

based on heuristic

inferred from title

object named as

Eric Giannoni

5

0 references

Jacques S Beckmann

object named as

Jacques S Beckmann

8

0 references

Pawel Stankiewicz

10

object named as

Pawel Stankiewicz

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

author name string

Flore Zufferey

1

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Danielle Martinet

2

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Maria-Chiara Osterheld

3

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Florence Niel-Bütschi

4

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Nathalie Besuchet Schmutz

6

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Zhilian Xia

7

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Charles Shaw-Smith

9

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Claire Langston

11

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Florence Fellmann

12

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

publication date

1 November 2011

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Pediatric Critical Care Medicine

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

12

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

e427-32

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

Interstitial lung diseases in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Recent advances in the pathogenesis and treatment of persistent pulmonary hypertension of the newborn

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Congenital alveolar capillary dysplasia and associated gastrointestinal anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Alveolar capillary dysplasia: a logical approach to a fatal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Histopathological features of open lung biopsies in children treated with extracorporeal membrane oxygenation (ECMO).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Expanding the phenotype of alveolar capillary dysplasia (ACD).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Open lung biopsy in neonatal and paediatric patients referred for extracorporeal membrane oxygenation (ECMO).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Incidence of alveolar capillary dysplasia in severe idiopathic persistent pulmonary hypertension of the newborn

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Alveolar capillary dysplasia: a cause of persistent pulmonary hypertension of the newborn

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Open-lung biopsy guides therapy in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Congenital alveolar capillary dysplasia with misalignment of pulmonary veins associated with hypoplastic left heart syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Alveolar capillary dysplasia. Report of a case of prolonged life without extracorporeal membrane oxygenation (ECMO) and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

Pulmonary hypertension of the newborn and urogenital anomalies in two male siblings: a new family with misalignment of pulmonary vessels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

6 September 2017

A second course of extracorporeal membrane oxygenation in the neonate--is there a benefit?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

14 September 2017

Alveolar capillary dysplasia--a cause of persistent pulmonary hypertension unresponsive to a second course of extracorporeal membrane oxygenation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

14 September 2017

Congenital Alveolar Capillary Dysplasia—An Unusual Cause of Respiratory Distress in the Newborn

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

23 June 2018

Profound hypoxemia and pulmonary hypertension in a 7-month-old infant: late presentation of alveolar capillary dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

1 September 2018

Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

1 September 2018

Late presentation of alveolar capillary dysplasia in an infant.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

1 September 2018

Alveolar capillary dysplasia: a six-year single center experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

1 September 2018

The incidence and characteristics of neonatal irreversible lung dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3655521

1 September 2018

Persistent pulmonary hypertension of the newborn. Trends in incidence, diagnosis, and management

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Misalignment of pulmonary veins and alveolar capillary dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late presentation of misalignment of lung vessels with alveolar capillary dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Open lung biopsy in pediatric patients on extracorporeal membrane oxygenation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Open lung biopsies in neonates on ECMO: additional cases. Extracorporeal membrane oxygenation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploinsufficiencies of FOXF1 and FOXC2 genes associated with lethal alveolar capillary dysplasia and congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital misalignment of pulmonary veins with alveolar capillary dysplasia causing persistent neonatal pulmonary hypertension: report of two affected siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/21572369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/PCC.0B013E3182192C96

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

24 August 2017

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