(Q35615894)

9 August 2017

0 references

Prolonged pancytopenia in a gene therapy patient with ADA-deficient SCID and trisomy 8 mosaicism: a case report (English)

1 reference

9 August 2017

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1 reference

1 reference

18

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9 August 2017

11

Gay M Crooks

1 reference

9 August 2017

Barbara C Engel

1

1 reference

9 August 2017

Greg M Podsakoff

2

1 reference

9 August 2017

Joanna L Ireland

3

1 reference

9 August 2017

E Monika Smogorzewska

4

1 reference

9 August 2017

Denise A Carbonaro

5

1 reference

9 August 2017

Kathy Wilson

6

1 reference

9 August 2017

Ami Shah

7

1 reference

9 August 2017

Neena Kapoor

8

1 reference

9 August 2017

Mirna Sweeney

9

1 reference

9 August 2017

Mark Borchert

10

1 reference

9 August 2017

Kenneth I Weinberg

12

1 reference

9 August 2017

Robertson Parkman

13

1 reference

9 August 2017

Howard M Rosenblatt

14

1 reference

9 August 2017

Shi-Qi Wu

15

1 reference

9 August 2017

Michael S Hershfield

16

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9 August 2017

Fabio Candotti

17

1 reference

9 August 2017

language of work or name

English

0 references

publication date

14 September 2006

1 reference

9 August 2017

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9 August 2017

volume

109

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9 August 2017

issue

2

1 reference

9 August 2017

page(s)

503-506

1 reference

Successful reconstitution of immunity in ADA-SCID by stem cell gene therapy following cessation of PEG-ADA and use of mild preconditioning

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Characterization of bone marrow stromal abnormalities in a patient with constitutional trisomy 8 mosaicism and myelodysplastic syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Genotype is an important determinant of phenotype in adenosine deaminase deficiency

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Cognitive and behavioral abnormalities in adenosine deaminase deficient severe combined immunodeficiency

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Dapsone-mediated agranulocytosis: risks, possible mechanisms and prevention

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Consistent, persistent expression from modified retroviral vectors in murine hematopoietic stem cells

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Development of improved adenosine deaminase retroviral vectors

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Dapsone-induced optic atrophy and motor neuropathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

A case of partial trisomy of chromosome 8p associated with autism.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Purine nucleoside phosphorylase deficiency associated with a dysplastic marrow morphology

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785101

Prognostic significance of single chromosome abnormalities in preleukemic states

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16973956

12 December 2020

inferred from PubMed ID database lookup

Constitutional and acquired trisomy 8

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16973956

12 December 2020

inferred from PubMed ID database lookup

Ophthalmic manifestations of trisomy 8 mosaic syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16973956

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1182/BLOOD-2006-06-031476

1 reference

release_k2q7ossx4rdxvajcdyjanlwsrm

9 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/k2q7ossx4rdxvajcdyjanlwsrm

24 November 2022

mapped directly with Wikidata item

PMC publication ID

1785101

1 reference

9 August 2017

1 reference