Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency-x-linked recessive ichthyosis: a case report and review of literature (Q37993800)

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scientific article published on 15 March 2012

Language	Label	Description	Also known as
English	Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency-x-linked recessive ichthyosis: a case report and review of literature	scientific article published on 15 March 2012

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency-x-linked recessive ichthyosis: a case report and review of literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

nephrotic syndrome

1 reference

based on heuristic

inferred from title

author name string

Kirtisudha Mishra

1

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Vineeta Vijay Batra

2

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Srikanta Basu

3

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Bimbadhar Rath

4

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Renu Saxena

5

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

15 March 2012

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

171

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

847-850

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1712-X

21 January 2018

X-linked recessive ichthyosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid sulfatase: molecular biology, regulation, and inhibition.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked ichthyosis: an update

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The glomerular slit diaphragm is a modified adherens junction

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in childhood.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localisation of a pseudoautosomal growth gene(s)

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessive X-linked ichthyosis associated with hypertrophic pyloric stenosis: a chance occurrence?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional assignment of the steroid sulfatase—X-linked ichthyosis locus: Implications for a noninactivated region on the short arm of human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transglutaminase type 1 and its cross-linking activity are concentrated at adherens junctions in simple epithelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

End-stage renal failure in a child with X-linked ichthyosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome with X-linked ichthyosis, Kallmann Syndrome and unilateral renal agenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22419362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-012-1712-X

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

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