(Q41939401)

English

Unusual case of XXY Klinefelter's syndrome with pancreatic insufficiency, hypothyroidism, deafness, chronic lung disease, dwarfism and microcephaly

scientific article published on September 1966

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Unusual case of XXY Klinefelter's syndrome with pancreatic insufficiency, hypothyroidism, deafness, chronic lung disease, dwarfism and microcephaly (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

0 references

1 reference

based on heuristic

inferred from title

Klinefelter's syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

chromosome abnormality

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5914119

13 July 2023

author name string

Di Sant'Agnese PA

3

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

R. J. Grand

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5914119

13 July 2023

S. W. Rosen

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5914119

13 July 2023

P. A. Di Sant'Agnese

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5914119

13 July 2023

W. R. Kirkham

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5914119

13 July 2023

language of work or name

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publication date

1 September 1966

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Europe PubMed Central

PubMed publication ID

14 October 2017

full work available at URL

https://api.elsevier.com/content/article/PII:0002934366900945?httpAccept=text/xml

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

https://api.elsevier.com/content/article/PII:0002934366900945?httpAccept=text/plain

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

American Journal of Medicine

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

41

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Europe PubMed Central

PubMed publication ID

14 October 2017

3

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Europe PubMed Central

PubMed publication ID

14 October 2017

478-485

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Relationship between relapsing pancreatitis and essential hyperlipemia

2

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.

4

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

ELEVATION OF THE SERUM PROTEIN-BOUND IODINE IN ACUTE INTERMITTENT PORPHYRIA.

7

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism, and Increased Excretion of Follicle-Stimulating Hormone1

8

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

CHROMATIN-POSITIVE KLINEFELTER'S SYNDROME: CLINICAL AND CYTOGENETIC STUDIES

10

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Klinefelter's syndrome: report of an autopsy, with particular reference to the histology and histochemistry of the endocrine glands

13

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

An XXXY sex chromosome complex in Klinefelter subjects with duplicated sex chromatin

16

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Thyroid Function in Patients with Aspermiogenesis and Testicular Tubular Sclerosis

17

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Hashimoto's disease in Turner's syndrome with isochromosome X

20

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Goitre in Klinefelter's syndrome

21

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

A genetical study of goitre

22

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

COEXISTING CRETINISM AND KLINEFELTER'S SYNDROME.

24

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Congenital hypothyroidism with goitre. Absence of an iodide-concentrating mechanism

25

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

CONGENITAL GOITROUS CRETINISM DUE TO THE ABSENCE OF IODIDE-CONCENTRATING ABILITY

26

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Struma lymphomatosa: primary thyroid failure with compensatory thyroid enlargement

28

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10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

An unusual iodinated protein of the serum in Hashimoto's thyroiditis

29

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Hydriodic acid-induced myxedema followed by recovery and thyroidal failure

30

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10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

THE ELECTROENCEPHALOGRAM IN THE KLINEFELTER SYNDROME

33

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10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

POSITIVE SEX CHROMATIN IN MEN WITH EPILEPSY

35

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

KLINEFELTER'S SYNDROME AND BEHAVIOUR

36

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Hereditary nephropathy, deafness and renal foam cells.

37

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

The association of deafness with thyroid dysfunction.

38

1 reference

10.1016/0002-9343(66)90094-5

https://api.crossref.org/works/10.1016/0002-9343(66)90094-5

13 July 2023

Identifiers

10.1016/0002-9343(66)90094-5

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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