arginine and Urination Disorders

arginine has been researched along with Urination Disorders in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adès, LC; Gilmour, E; Graf, N; Holme, SA; Maclean, K; Moss, C; Onikul, E; Scheffer, H; Smith, GH; Taylor, M; van Bokhoven, H	1
Burnett, AL; Calvin, DC; Chamness, SL; Dawson, TM; Dawson, VL; Klein, SL; Liu, JX; Nelson, RJ; Snyder, SH	1

Other Studies

2 other study(ies) available for arginine and Urination Disorders

Article	Year
EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation? American journal of medical genetics. Part A, 2007, May-15, Volume: 143A, Issue:10 Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders	2007
Urinary bladder-urethral sphincter dysfunction in mice with targeted disruption of neuronal nitric oxide synthase models idiopathic voiding disorders in humans. Nature medicine, 1997, Volume: 3, Issue:5 Topics: Animals; Arginine; Disease Models, Animal; Electric Stimulation; Endothelium, Vascular; Humans; Hypertrophy; Male; Mice; Mice, Inbred C57BL; Muscle Contraction; Neurons; Nitric Oxide; Nitric Oxide Synthase; Nitroprusside; Urethra; Urinary Bladder; Urination Disorders; Urothelium	1997

Article

Year

EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation?

American journal of medical genetics. Part A, 2007, May-15, Volume: 143A, Issue:10

Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders

2007

Urinary bladder-urethral sphincter dysfunction in mice with targeted disruption of neuronal nitric oxide synthase models idiopathic voiding disorders in humans.

Nature medicine, 1997, Volume: 3, Issue:5

Topics: Animals; Arginine; Disease Models, Animal; Electric Stimulation; Endothelium, Vascular; Humans; Hypertrophy; Male; Mice; Mice, Inbred C57BL; Muscle Contraction; Neurons; Nitric Oxide; Nitric Oxide Synthase; Nitroprusside; Urethra; Urinary Bladder; Urination Disorders; Urothelium

1997