Translational Research for Pediatric Lower Urinary Tract Dysfunction (Q28069958)

title

Translational Research for Pediatric Lower Urinary Tract Dysfunction (English)

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

author name string

Akihiro Kanematsu

series ordinal

1

1 reference

Crossref

language of work or name

1 reference

November 2016

1 reference

International neurourology journal

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

volume

20

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

issue

Suppl 2

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

page(s)

S105-111

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution-NonCommercial 3.0 Unported

6 June 2020

copyright license

start time

22 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Integrated next-generation sequencing of 16S rDNA and metaproteomics differentiate the healthy urine microbiome from asymptomatic bacteriuria in neuropathic bladder associated with spinal cord injury.

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.

29 September 2017

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2 June 2018

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27 November 2018

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De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.

27 November 2018

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PTHrP is endogenous relaxant for spontaneous smooth muscle contraction in urinary bladder of female rat.

27 November 2018

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Urinary nerve growth factor in children with overactive bladder: a promising, noninvasive and objective biomarker

27 November 2018

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Rs 6313 polymorphism in 5-hydroxytryptamine receptor 2A gene association with polysymptomatic primary nocturnal enuresis.

27 November 2018

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A higher level of prostaglandin E2 in the urinary bladder in young boys and boys with lower urinary tract obstruction

27 November 2018

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Hereditary phenotypes in nocturnal enuresis

27 November 2018

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Nocturnal enuresis and overactive bladder in children: an epidemiological study.

27 November 2018

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Familial central diabetes insipidus detected by nocturnal enuresis

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095

Reduction in nocturnal functional bladder capacity is a common factor in the pathogenesis of refractory nocturnal enuresis

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095

Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095

Desmopressin for nocturnal enuresis in nephrogenic diabetes insipidus

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095

Linkage study of a large Danish 4-generation family with urge incontinence and nocturnal enuresis

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095

Total genome scan analysis in a single extended family for primary nocturnal enuresis: evidence for a new locus (ENUR3) for primary nocturnal enuresis on chromosome 22q11.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095

Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus

27 November 2018

1 reference

12 December 2020

Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q

1 reference

12 December 2020

Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family

1 reference

12 December 2020

Nitric oxide synthase gene polymorphisms in children with primary nocturnal enuresis: a preliminary study

1 reference

12 December 2020

Draining the edema: a new role for aquaretics?

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12 December 2020

Urofacial (ochoa) syndrome

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12 December 2020

Identifiers

DOI

10.5213/INJ.1632726.363

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

PubMed publication ID

2 references