(Q74430826)

English

Gonadoblastoma and dysgerminoma associated with XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome

scientific article published on 01 June 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Gonadoblastoma and dysgerminoma associated with XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Frasier syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Tapio Visakorpi

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

Minna M Joki-Erkkilä

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Riitta Karikoski

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Immo Rantala

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Hanna-Liisa Lenko

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Pentti K Heinonen

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 June 2002

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Journal of Pediatric and Adolescent Gynecology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

15

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

145-149

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A syndrome of chronic renal failure and XY gonadal dysgenesis in young phenotypic females without genital ambiguity

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

XY gonadal dysgenesis with gonadoblastoma discovered after kidney transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

WT-1 is required for early kidney development

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Male pseudohermaphroditism: a hitherto undescribed form.

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A frame shift mutation in the DNA-binding domain of the androgen receptor gene associated with complete androgen insensitivity, persistent müllerian structures, and germ cell tumors in dysgenetic gonads

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Immunohistochemical localization of inhibin and activin subunits in human epithelial ovarian tumors

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Serum lactic dehydrogenase and its isoenzymes in patients with ovarian dysgerminoma

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pregnancy in a 46, XY patient

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pregnancies following ovum donation in gonadal dysgenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronic renal disease, myotonic dystrophy, and gonadoblastoma in XY gonadal dysgenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular analysis of the sex-determining region from the Y chromosome in two patients with Frasier syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The same mutation affecting the splicing ofWT1 gene is present on Frasier syndrome patients with or without Wilms' tumor

1 reference

https://api.crossref.org/works/10.1016%2FS1083-3188%2802%2900147-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1083-3188(02)00147-X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12106750%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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