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Transcutaneous Electrical Nerve Stimulation Combined with Oxybutynin is Superior to Monotherapy in Children with Urge Incontinence: A Randomized, Placebo Controlled Study

The Journal of urology, 2017-08, Vol.198 (2), p.430-435

2017

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International children's continence society's recommendations for therapeutic intervention in congenital neuropathic bladder and bowel dysfunction in children

Neurourology and urodynamics, 2012-06, Vol.31 (5), p.615-620

2012

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Age Related Nocturnal Urine Volume and Maximum Voided Volume in Healthy Children: Reappraisal of International Children's Continence Society Definitions

The Journal of urology, 2010-04, Vol.183 (4), p.1561-1567

2010

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The macrophage activation marker, soluble CD163 is associated with hepatic inflammation and fibrosis in chronic viral hepatitis C and declines during effective direct-acting antiviral therapy

Journal of hepatology, 2017, Vol.66 (1), p.S742-S742

2017

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FUNCTIONAL CONSTIPATION IN CHILDREN

The Journal of urology, 2004-06, Vol.171 (6), p.2641-2643

2004

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Vitamin D insufficiency in Greenlanders on a westernized fare: ethnic differences in calcitropic hormones between Greenlanders and Danes

Calcified tissue international, 2004-03, Vol.74 (3), p.255-263

2004

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Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus

American journal of human genetics, 1996, Vol.58 (1), p.107-117

1996

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INTRA-INDIVIDUAL VARIABILITY IN NIGHTTIME URINE PRODUCTION AND FUNCTIONAL BLADDER CAPACITY ESTIMATED BY HOME RECORDINGS IN PATIENTS WITH NOCTURNAL ENURESIS

The Journal of urology, 2001-12, Vol.166 (6), p.2452-2455

2001

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Clinical and molecular evidence of abnormal processing and trafficking of the vasopressin preprohormone in a large kindred with familial neurohypophyseal diabetes insipidus due to a signal peptide mutation

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2933-2941

1999

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SAT-282 - The macrophage activation marker, soluble CD163 is associated with hepatic inflammation and fibrosis in chronic viral hepatitis C and declines during effective direct-acting antiviral therapy

Journal of hepatology, 2017, Vol.66 (1), p.S742-S742

2017

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A novel splicing mutation in the V 2 vasopressin receptor

Pediatric nephrology (Berlin, West), 2000-11, Vol.15 (1-2), p.43-49

2000

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A new mutation of the arginine vasopressin-neurophysin II gene in a family with autosomal dominant neurohypophyseal diabetes insipidus

Experimental and clinical endocrinology & diabetes, 2001, Vol.109 (8), p.406

2001

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A novel splicing mutation in the V2 vasopressin receptor

Pediatric nephrology (Berlin, West), 2000-11, Vol.15 (1-2), p.43-49

2000

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Age Related Nocturnal Urine Volume and Maximum Voided Volume in Healthy Children: Reappraisal of International Children's Continence Society Definitions. Editorial comment

The Journal of urology, 2010, Vol.183 (4), p.1561-1567

2010

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Twenty-four-hour blood pressure among Greenlanders and Danes: relationship to diet and lifestyle

Scandinavian journal of clinical and laboratory investigation, 2002, Vol.62 (6), p.413-422

2002

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Differential Cellular Handling of Defective Arginine Vasopressin (AVP) Prohormones in Cells Expressing Mutations of the AVP Gene Associated with Autosomal Dominant and Recessive Familial Neurohypophyseal Diabetes Insipidus

The journal of clinical endocrinology and metabolism, 2004-09, Vol.89 (9), p.4521-4531

2004

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Relationship Between Mercury in Blood and 24-h Ambulatory Blood Pressure in Greenlanders and Danes

American journal of hypertension, 2005-05, Vol.18 (5), p.612-618

2005

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Autosomal dominant neurohypophyseal diabetes insipidus due to substitution of histidine for tyrosine(2) in the vasopressin moiety of the hormone precursor

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3351-3355

2002

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Expression of three different mutations in the arginine vasopressin gene suggests genotype-phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds

Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.207-216

2005

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Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis

European journal of human genetics : EJHG, 2004-01, Vol.12 (1), p.44-51

2004

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Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

Clinical endocrinology (Oxford), 2004-01, Vol.60 (1), p.125-136

2004

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Plasma amino acids in Greenlanders and Danes. influence of seasons, residence, ethnicity, and diet

American journal of human biology, 2006-01, Vol.18 (1), p.99-111

2006

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Combined urinary and fecal incontinence--a neglected problem. Danish Society of Pediatrics

Ugeskrift for læger, 2005-03, Vol.167 (12-13), p.1403

2005

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Autosomal dominant familial neurohypophyseal diabetes insipidus

APMIS. Acta pathologica, microbiologica et immunologica Scandinavica. Supplementum, 2003 (109), p.92

2003

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INTRA-INDIVIDUAL VARIABILITY IN NIGHTTIME URINE PRODUCTION AND FUNCTIONAL BLADDER CAPACITY ESTIMATED BY HOME RECORDINGS IN PATIENTS WITH NOCTURNAL ENURESIS

The Journal of urology, 2001-12, p.2452-2455

2001

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Transcutaneous Electrical Nerve Stimulation Combined with Oxybutynin is Superior to Monotherapy in Children with Urge Incontinence: A Randomized, Placebo Controlled Study

International children's continence society's recommendations for therapeutic intervention in congenital neuropathic bladder and bowel dysfunction in children

Age Related Nocturnal Urine Volume and Maximum Voided Volume in Healthy Children: Reappraisal of International Children's Continence Society Definitions

The macrophage activation marker, soluble CD163 is associated with hepatic inflammation and fibrosis in chronic viral hepatitis C and declines during effective direct-acting antiviral therapy

FUNCTIONAL CONSTIPATION IN CHILDREN

Vitamin D insufficiency in Greenlanders on a westernized fare: ethnic differences in calcitropic hormones between Greenlanders and Danes

Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus

INTRA-INDIVIDUAL VARIABILITY IN NIGHTTIME URINE PRODUCTION AND FUNCTIONAL BLADDER CAPACITY ESTIMATED BY HOME RECORDINGS IN PATIENTS WITH NOCTURNAL ENURESIS

Clinical and molecular evidence of abnormal processing and trafficking of the vasopressin preprohormone in a large kindred with familial neurohypophyseal diabetes insipidus due to a signal peptide mutation

SAT-282 - The macrophage activation marker, soluble CD163 is associated with hepatic inflammation and fibrosis in chronic viral hepatitis C and declines during effective direct-acting antiviral therapy

A novel splicing mutation in the V 2 vasopressin receptor

A new mutation of the arginine vasopressin-neurophysin II gene in a family with autosomal dominant neurohypophyseal diabetes insipidus

A novel splicing mutation in the V2 vasopressin receptor

Age Related Nocturnal Urine Volume and Maximum Voided Volume in Healthy Children: Reappraisal of International Children's Continence Society Definitions. Editorial comment

Twenty-four-hour blood pressure among Greenlanders and Danes: relationship to diet and lifestyle

Differential Cellular Handling of Defective Arginine Vasopressin (AVP) Prohormones in Cells Expressing Mutations of the AVP Gene Associated with Autosomal Dominant and Recessive Familial Neurohypophyseal Diabetes Insipidus

Relationship Between Mercury in Blood and 24-h Ambulatory Blood Pressure in Greenlanders and Danes

Autosomal dominant neurohypophyseal diabetes insipidus due to substitution of histidine for tyrosine(2) in the vasopressin moiety of the hormone precursor

Expression of three different mutations in the arginine vasopressin gene suggests genotype-phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds

Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis

Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

Plasma amino acids in Greenlanders and Danes. influence of seasons, residence, ethnicity, and diet

Combined urinary and fecal incontinence--a neglected problem. Danish Society of Pediatrics

Autosomal dominant familial neurohypophyseal diabetes insipidus

INTRA-INDIVIDUAL VARIABILITY IN NIGHTTIME URINE PRODUCTION AND FUNCTIONAL BLADDER CAPACITY ESTIMATED BY HOME RECORDINGS IN PATIENTS WITH NOCTURNAL ENURESIS

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