(Q40542360)

21 September 2017

The burden of genetic disease on inpatient care in a children's hospital (English)

1 reference

21 September 2017

1 reference

Shawn E McCandless

1

1 reference

21 September 2017

Jeanne W Brunger

series ordinal

2

1 reference

21 September 2017

Suzanne B Cassidy

series ordinal

3

1 reference

21 September 2017

language of work or name

English

0 references

publication date

12 December 2003

1 reference

American Journal of Human Genetics

21 September 2017

1 reference

21 September 2017

74

1 reference

21 September 2017

1

1 reference

21 September 2017

121-127

1 reference

Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic [...]

21 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Human complement factor H deficiency associated with hemolytic uremic syndrome.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Contribution of heritable disorders to mortality in the pediatric intensive care unit

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

The frequency of genetic disease and congenital malformation among patients in a pediatric hospital

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

The incidence of genetic disease in a University hospital population

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Congenital anomalies: an increasingly important cause of mortality and workload in a neonatal intensive care unit.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

The frequency and economic burden of genetic disease in a pediatric hospital in Mexico City.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Genetic aspects of admissions to a paediatric intensive care unit

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Frequency and load of congenital anomalies in a neonatal intensive care unit, prenatal diagnosis, and perinatal management

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

The frequency and financial burden of genetic disease in a pediatric hospital

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

Annual summary of vital statistics: 2000.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181899

The Impact of Birth Defects and Genetic Diseases

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14681831

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital anomalies: mortality and morbidity, burden and classification

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14681831

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/381053

1 reference

21 September 2017

1 reference

21 September 2017

PubMed publication ID

14681831

1 reference