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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

Autor: Kazuaki Chayama, Holger Jon Møller, Jacob George, T.L. Laursen, C. Siggaard, Henning Grønbæk, Mark W. Douglas, K. Kazankov, T. Nakahara, Thomas Damgaard Sandahl, Peter Derek Christian Leutscher, Andrew T.L. Ong, Alex Lund Laursen, A. Hiramatsu

Publikováno v: Laursen, T L, Siggaard, C, Kazankov, K, Sandahl, T, Møller, H J, George, J, Ong, A, Douglas, M W, Laursen, A L, Leutscher, P, Hiramatsu, A, Nakahara, T, Chayama, K & Gronbaek, H 2017, ' 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, vol. 66, no. 1, SAT-282, pp. S742 . < http://www.sciencedirect.com/science/journal/01688278/66/1/supp/S?sdc=1 >

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9f92e3debc49f97ef59cd1c1bb73153
https://vbn.aau.dk/da/publications/74c35138-5887-471b-80b3-68b6f261d3a6

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International Children's Continence Society's recommendations for therapeutic intervention in congenital neuropathic bladder and bowel dysfunction in children

Autor: Y F, Rawashdeh, P, Austin, C, Siggaard, S B, Bauer, I, Franco, T P, de Jong, T M, Jorgensen

Publikováno v: Neurourology and urodynamics. 31(5)

We present a consensus view of members of the International Children's Continence Society on the therapeutic intervention in congenital neuropatic bladder and bowel dysfunction in children.Discussions were held by a group of pediatric urologists and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3de9e4cf2e2ed951739f654622b1263e
https://pubmed.ncbi.nlm.nih.gov/22532368

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Functional constipation in children

Autor: Y. Homsy, W.F. Bower, C. Siggaard, F.K.Y. Sit, J. W. Chase

Publikováno v: Chase, J W, Homsy, Y, Siggaard, C, Sit, F & Bower, W F 2004, ' Functional constipation in children ' J. Urol., vol. 171, pp. 2641-2643 .

Purpose: Constipation in children increases the likelihood of urinary incontinence, bladder overactivity, dyscoordinated voiding, a large capacity, poorly emptying bladder, recurrent urinary tract infection and deterioration of vesicoureteral reflux.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c58cf25c146d2cdc4b66277e5cc5c865
https://pure.au.dk/portal/da/publications/functional-constipation-in-children(52102c70-af7f-11da-bee9-02004c4f4f50).html

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

Autor: M N, Hansen, S, Rittig, C, Siggaard, K, Kamperis, G, Hvistendahl, H L, Schaumburg, F, Schmidt, Y, Rawashdeh, J C, Djurhuus

Publikováno v: The Journal of urology. 166(6)

We evaluated the intra-individual variability and reproducibility of nighttime urine production on wet nights and functional bladder capacity estimated by long-term home recordings of monosymptomatic nocturnal enuresis. In particular, the intention w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cfbee6c4e5934b71f014764224c77abc
https://pubmed.ncbi.nlm.nih.gov/11696810

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A Novel AVP-Neurophysin Gene Mutation in Familial Neurohypophyseal Diabetes Insipidus Presenting with Nocturnal Enuresis

Autor: E.B. Pedersen, Gary L. Robertson, C. Siggaard, S. Rittig, B.S. Chertow, N.Q. Goking

Publikováno v: Goking, N Q, Cherton, B S, Robertson, G L, Rittig, S, Siggaard, C & Pedersen, E B 2001, ' A novel AVP-neurophysin gene mutation in familial neurohypophyseal diabetes insipidus presenting with nocturnal enuresis ', Journal Endocrine Genetics, vol. 2, pp. 105-113 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff01b100592cb0d9d3af6fedf56ab0a0
https://doi.org/10.1515/ijdhd.2001.2.2.105

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

Autor: J Hensen, J Mundschenk, Hendrik Lehnert, C Siggaard, S Rittig

Publikováno v: Mundschenk, J, Rittig, S, Siggaard, C, Hensen, J & Lehnert, H 2001, ' A new mutation of the arginine vasopressin-neurophysin II gene in a family with autosomal dominant neurohypophyseal diabetes insipidus ' Exp Clin Endocrinol Diabetes, vol. 109, pp. 406-409 .

Familial neurohypophyseal diabetes insipidus (FNDI) is an autosomally dominant inherited disorder with a typical onset at one to six years of age. The genetic locus of FNDI is the arginine vasopressin-neurophysin II (AVP-NPII) gene. The gene encoding

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7ef6c0544bb90bfd6b69c1f75a3e74b
https://pure.au.dk/portal/da/publications/a-new-mutation-of-the-arginine-vasopressinneurophysin-ii-gene-in-a-family-with-autosomal-dominant-neurohypophyseal-diabetes-insipidus(b5622220-b2d0-11da-bee9-02004c4f4f50).html

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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

Autor: C, Siggaard, S, Rittig, T J, Corydon, P H, Andreasen, T G, Jensen, B S, Andresen, G L, Robertson, N, Gregersen, L, Bolund, E B, Pedersen

Publikováno v: The Journal of clinical endocrinology and metabolism. 84(8)

The autosomal dominant form of familial neurohypophyseal diabetes insipidus (adFNDI) is a rare disease characterized by postnatal onset of polyuria and a deficient neurosecretion of the antidiuretic hormone, arginine vasopressin (AVP). Since 1991, ad

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0b3056ad338f2d49bbf6898556e40435
https://pubmed.ncbi.nlm.nih.gov/10443701

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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

Autor: S, Rittig, G L, Robertson, C, Siggaard, L, Kovács, N, Gregersen, J, Nyborg, E B, Pedersen

Publikováno v: American journal of human genetics. 58(1)

Familial neurohypophyseal diabetes insipidus (FNDI) is an autosomal dominant disorder characterized by progressive postnatal deficiency of arginine vasopressin as a result of mutation in the gene that encodes the hormone. To determine the extent of m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::da72f1aa1eed34b12c1f0e19ffb08f96
https://pubmed.ncbi.nlm.nih.gov/8554046

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Danish/Greenlandic Society for Circumpolar Health. 24-hour blood pressure among Greenlanders. Influence of diet and life-style

Autor: Michael Pedersen, M.E. Jørgensen, M. Pedersen, C. Siggaard, T.B. Sørensen, G. Mulvad, J.C. Hansen, H. Skjoldborg, E.B. Pedersen

Publikováno v: International Journal of Circumpolar Health; Vol 62, No 4 (2003)

Introduction. Greenlanders have a lower cardiovascular mortality than Danes, possibly due to a lower blood pressure (BP). However, 24-hour BP has never been measured in Greenlanders. Objective. to compare 24-hour BP between Greenlanders and Danes, an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5cc0b3c63b3a1865cc28dd6a53ff96b
https://doi.org/10.3402/ijch.v62i4.17591

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