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Translational Research for Pediatric Lower Urinary Tract Dysfunction
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scholarly article
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PubMed
review article
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Europe PubMed Central
title
Translational Research for Pediatric Lower Urinary Tract Dysfunction
(English)
1 reference
stated in
PubMed
author
Akihiro Kanematsu
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
author name string
Akihiro Kanematsu
series ordinal
1
1 reference
stated in
Crossref
language of work or name
English
1 reference
stated in
PubMed
publication date
November 2016
1 reference
stated in
PubMed
published in
International neurourology journal
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
volume
20
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
issue
Suppl 2
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
page(s)
S105-111
2 references
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PubMed
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
copyright license
Creative Commons Attribution-NonCommercial 3.0 Unported
start time
22 November 2016
1 reference
stated in
April 2022 Public Data File from Crossref
copyright status
copyrighted
0 references
cites work
Urinary proteomics and metabolomics studies to monitor bladder health and urological diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
20 March 2017
Mutations in HPSE2 cause urofacial syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
20 March 2017
Prevalence of Enuresis and Its Association With Attention-Deficit/Hyperactivity Disorder Among U.S. Children: Results From a Nationally Representative Study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
20 March 2017
Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
20 March 2017
LRIG2 mutations cause urofacial syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
20 March 2017
Copy-number variation and association studies of human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
20 March 2017
CNV analysis in 169 patients with bladder exstrophy-epispadias complex
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
The Urinary Bladder Transcriptome and Proteome Defined by Transcriptomics and Antibody-Based Profiling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Can urinary nerve growth factor and bladder wall thickness correlation in children have a potential role to predict the outcome of non-monosymptomatic nocturnal enuresis?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Regenerative medicine
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Expression of parathyroid hormone/parathyroid hormone-related peptide receptor 1 in normal and diseased bladder detrusor muscles: a clinico-pathological study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Clinical and genetic characteristics for the Urofacial Syndrome (UFS).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
DNA copy number variations in patients with persistent cloaca
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Phenotypic characteristics of early Wolfram syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Chronobiology of micturition: putative role of the circadian clock.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
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.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Urinary proteomics for early diagnosis in diabetic nephropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Involvement of urinary bladder Connexin43 and the circadian clock in coordination of diurnal micturition rhythm.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Clinical practice. Evaluation and management of enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Diagnosis and management of nocturnal enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
The molecular pathways behind bladder stretch injury
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Changing concepts of bladder regeneration
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Relief of nocturnal enuresis by desmopressin is kidney and vasopressin type 2 receptor independent
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Accurate and reliable high-throughput detection of copy number variation in the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
The genetics of enuresis: a review
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Cognitive and behavioral profile of fragile X boys: correlations to molecular data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
An epidemiological study of enuresis in Korean children
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
29 September 2017
Incontinence in persons with Noonan Syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
2 June 2018
Effect of DDAVP on nocturnal enuresis in a patient with nephrogenic diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
2 June 2018
Abnormal diurnal rhythm of plasma vasopressin and urinary output in patients with enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
2 June 2018
Rare copy number variants implicated in posterior urethral valves.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Assessment of lower urinary tract function in children with Down syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
PTHrP is endogenous relaxant for spontaneous smooth muscle contraction in urinary bladder of female rat.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Urinary nerve growth factor in children with overactive bladder: a promising, noninvasive and objective biomarker
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Rs 6313 polymorphism in 5-hydroxytryptamine receptor 2A gene association with polysymptomatic primary nocturnal enuresis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
A higher level of prostaglandin E2 in the urinary bladder in young boys and boys with lower urinary tract obstruction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Hereditary phenotypes in nocturnal enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Nocturnal enuresis and overactive bladder in children: an epidemiological study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Familial central diabetes insipidus detected by nocturnal enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Reduction in nocturnal functional bladder capacity is a common factor in the pathogenesis of refractory nocturnal enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Desmopressin for nocturnal enuresis in nephrogenic diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Linkage study of a large Danish 4-generation family with urge incontinence and nocturnal enuresis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
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.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5169095
retrieved
27 November 2018
Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27915476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27915476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27915476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Nitric oxide synthase gene polymorphisms in children with primary nocturnal enuresis: a preliminary study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27915476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Draining the edema: a new role for aquaretics?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27915476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Urofacial (ochoa) syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27915476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.5213/INJ.1632726.363
1 reference
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
PMC publication ID
5169095
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
PubMed publication ID
27915476
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
5169095
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27915476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 June 2020
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