Rittig S - Search Results

1

A novel splicing mutation in the V2 vasopressin receptor.

Kamperis K, Siggaard C, Herlin T, Nathan E, Hertz JM, Rittig S. Kamperis K, et al. Among authors: rittig s. Pediatr Nephrol. 2000 Nov;15(1-2):43-9. doi: 10.1007/s004670000431. Pediatr Nephrol. 2000. PMID: 11095010

2

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

Rittig S, Robertson GL, Siggaard C, Kovács L, Gregersen N, Nyborg J, Pedersen EB. Rittig S, et al. Am J Hum Genet. 1996 Jan;58(1):107-17. Am J Hum Genet. 1996. PMID: 8554046 Free PMC article.

3

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.

Siggaard C, Rittig S, Corydon TJ, Andreasen PH, Jensen TG, Andresen BS, Robertson GL, Gregersen N, Bolund L, Pedersen EB. Siggaard C, et al. Among authors: rittig s. J Clin Endocrinol Metab. 1999 Aug;84(8):2933-41. doi: 10.1210/jcem.84.8.5869. J Clin Endocrinol Metab. 1999. PMID: 10443701

4

IERC strategy for characterising nocturnal enuresis. International Enuresis Research Center.

Schaumburg HL, Schmidt F, Siggaard C, Rittig S, Jørgensen TM, Djurhuus JC. Schaumburg HL, et al. Among authors: rittig s. Scand J Urol Nephrol Suppl. 1999;202:12-3. doi: 10.1080/00365599950510102-1. Scand J Urol Nephrol Suppl. 1999. PMID: 10573783 No abstract available.

5

Intra-individual variability in nighttime urine production and functional bladder capacity estimated by home recordings in patients with nocturnal enuresis.

Hansen MN, Rittig S, Siggaard C, Kamperis K, Hvistendahl G, Schaumburg HL, Schmidt F, Rawashdeh Y, Djurhuus JC. Hansen MN, et al. Among authors: rittig s. J Urol. 2001 Dec;166(6):2452-5. J Urol. 2001. PMID: 11696810

6

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

Mundschenk J, Rittig S, Siggaard C, Hensen J, Lehnert H. Mundschenk J, et al. Among authors: rittig s. Exp Clin Endocrinol Diabetes. 2001;109(8):406-9. doi: 10.1055/s-2001-18994. Exp Clin Endocrinol Diabetes. 2001. PMID: 11748489

7

The relationship between desmopressin treatment and voiding pattern in children.

Hvistendahl GM, Rawashdeh YF, Kamperis K, Hansen MN, Rittig S, Djurhuus JC. Hvistendahl GM, et al. Among authors: rittig s. BJU Int. 2002 Jun;89(9):917-22. doi: 10.1046/j.1464-410x.2002.02788.x. BJU Int. 2002. PMID: 12010240 Clinical Trial.

8

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

Rittig S, Siggaard C, Ozata M, Yetkin I, Gregersen N, Pedersen EB, Robertson GL. Rittig S, et al. J Clin Endocrinol Metab. 2002 Jul;87(7):3351-5. doi: 10.1210/jcem.87.7.8677. J Clin Endocrinol Metab. 2002. PMID: 12107248

9

Autosomal dominant familial neurohypophyseal diabetes insipidus.

Christensen JH, Siggaard C, Rittig S. Christensen JH, et al. Among authors: rittig s. APMIS Suppl. 2003;(109):92-5. APMIS Suppl. 2003. PMID: 12874957 Review.

10

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

Christensen JH, Siggaard C, Corydon TJ, deSanctis L, Kovacs L, Robertson GL, Gregersen N, Rittig S. Christensen JH, et al. Among authors: rittig s. Eur J Hum Genet. 2004 Jan;12(1):44-51. doi: 10.1038/sj.ejhg.5201086. Eur J Hum Genet. 2004. PMID: 14673472

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