(Q67902840)

English

Omenn's syndrome and related combined immunodeficiency syndromes: Diagnostic considerations in infants with persistent erythroderma and failure to thrive

scientific article published on 01 August 1991

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scholarly article

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19 September 2019

Omenn's syndrome and related combined immunodeficiency syndromes: diagnostic considerations in infants with persistent erythroderma and failure to thrive (English)

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1832695%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Omenn's syndrome and related combined immunodeficiency syndromes: Diagnostic considerations in infants with persistent erythroderma and failure to thrive (English)

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10.1016/0190-9622(91)70225-Q

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5 December 2022

combined immunodeficiency

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based on heuristic

inferred from title

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based on heuristic

inferred from title

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5 December 2022

author name string

R. A. Pupo

1

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5 December 2022

S. K. Tyring

2

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5 December 2022

S. S. Raimer

3

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5 December 2022

D. P. Wirt

4

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5 December 2022

E. G. Brooks

5

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5 December 2022

R. M. Goldblum

6

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publication date

1 August 1991

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19 September 2019

full work available at URL

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https://api.elsevier.com/content/article/PII:019096229170225Q?httpAccept=text/plain

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10.1016/0190-9622(91)70225-Q

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5 December 2022

Journal of the American Academy of Dermatology

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19 September 2019

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19 September 2019

2 Pt 2

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19 September 2019

442-446

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19 September 2019

Erythrodermic psoriasis in childhood. A young Negro child treated with methotrexate

2

1 reference

10.1016/0190-9622(91)70225-Q

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5 December 2022

Cutaneous Manifestations of Defective Host Defenses

4

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5 December 2022

Novel T-lymphocyte population in combined immunodeficiency with features of graft-versus-host disease

6

1 reference

10.1016/0190-9622(91)70225-Q

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5 December 2022

Combined immunodeficiency and reticuloendotheliosis with eosinophilia

8

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10.1016/0190-9622(91)70225-Q

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5 December 2022

Defective opsonization. A common immunity deficiency

11

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5 December 2022

Yeast opsonization defect and immunoglobulin deficiency in severe infantile dermatitis (Leiner's disease)

13

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10.1016/0190-9622(91)70225-Q

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5 December 2022

Familial Reticuloendotheliosis with Eosinophilia

14

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10.1016/0190-9622(91)70225-Q

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5 December 2022

Clinical and immunological findings in four infants with Omenn's syndrome: a form of severe combined immunodeficiency with phenotypically normal T cells, elevated IgE, and eosinophilia

15

1 reference

10.1016/0190-9622(91)70225-Q

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5 December 2022

The Omenn's syndrome: histological, immunohistochemical and ultrastructural evidence for a partial T cell deficiency evolving in an abnormal proliferation of T lymphocytes and S-100 +/T-6 + Langerhans-like cells

16

1 reference

10.1016/0190-9622(91)70225-Q

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5 December 2022

Rapidly fatal familial histiocytosis associated with eosinophilia and primary immunological deficiency

17

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5 December 2022

Omenn's syndrome--pathologic arguments in favor of a graft versus host pathogenesis: a report of nine cases

18

1 reference

10.1016/0190-9622(91)70225-Q

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5 December 2022

Imbalances in subsets of T lymphocytes in an inbred pedigree with Omenn's syndrome

19

1 reference

10.1016/0190-9622(91)70225-Q

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5 December 2022

A lymphoproliferative syndrome, "cutaneous dystrophy" and combined immune deficiency with lack of helper T-cell factor

20

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10.1016/0190-9622(91)70225-Q

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5 December 2022

Identifiers

10.1016/0190-9622(91)70225-Q

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Europe PubMed Central

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19 September 2019

1 reference

Europe PubMed Central

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19 September 2019

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