(Q33679228)

English

Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

cystic fibrosis

0 references

author name string

Gabolde M

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Guilloud-Bataille M

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Feingold J

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Besmond C

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 October 1999

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

319

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

7218

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1166-1167

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28266

21 June 2018

Molecular basis of opsonic defect in immunodeficient children

1 reference

https://pubmed.ncbi.nlm.nih.gov/10541506

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mannose binding protein gene mutations associated with unusual and severe infections in adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/10541506

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10541506

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased frequency of homozygosity of abnormal mannan-binding-protein alleles in patients with suspected immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/10541506

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/BMJ.319.7218.1166

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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