H H Seydewitz
Overview
Explore the profile of H H Seydewitz including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
28
Citations
328
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ramalho A, Beck S, Penque D, Gonska T, Seydewitz H, Mall M, et al.
J Med Genet
. 2003 Jul;
40(7):e88.
PMID: 12843337
No abstract available.
2.
Seydewitz H, Gram J, Bruhn H, Witt I
Hamostaseologie
. 2002 Aug;
22(2):7-10.
PMID: 12193970
No abstract available.
3.
Seydewitz H, Henschen M, KUHNEL W, Brandis M
Clin Chem Lab Med
. 2002 Jan;
39(10):980-2.
PMID: 11758615
Pediatric reference ranges for osteocalcin measured by a new, fully automated, chemiluminescent immunometric assay on the Immulite immunoanalyzer are presented. Samples from 627 children, ranging from newborns to 18 years...
4.
Seydewitz H, Gonska T, Mall M, Kueh J
Hum Mutat
. 2000 Sep;
16(3):277.
PMID: 10980550
No abstract available.
5.
Mall M, Wissner A, Schreiber R, Kuehr J, Seydewitz H, Brandis M, et al.
Am J Respir Cell Mol Biol
. 2000 Sep;
23(3):283-9.
PMID: 10970817
Ion transport defects underlying cystic fibrosis (CF) lung disease are characterized by impaired cyclic adenosine monophosphate (cAMP)-dependent Cl(-) conductance. Activation of Cl(-) secretion in airways depends on simultaneous activation of...
6.
Weston B, Lin J, Muenzer J, Cameron H, Arnold R, Seydewitz H, et al.
Pediatr Res
. 2000 Aug;
48(3):329-34.
PMID: 10960498
Glycogen storage disease type 1a (GSD 1a) is caused by a deficiency in microsomal glucose-6-phosphatase (G6Pase). A variant (GSD 1b) is caused by a defect in the transport of glucose-6-phosphate...
7.
Mall M, Wissner A, Seydewitz H, Hubner M, Kuehr J, Brandis M, et al.
Br J Pharmacol
. 2000 Aug;
130(8):1884-92.
PMID: 10952679
The flavonoid genistein has been shown to activate a Cl(-) conductance in various cell types expressing CFTR. We examined if similar effects can be observed when genistein is applied to...
8.
Dork T, Macek Jr M, Mekus F, Tummler B, Tzountzouris J, Casals T, et al.
Hum Genet
. 2000 May;
106(3):259-68.
PMID: 10798353
We report a large genomic deletion of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, viz., a deletion that is frequently observed in Central and Eastern Europe. The mutation, termed...
9.
Mall M, Wissner A, Seydewitz H, Kuehr J, Brandis M, Greger R, et al.
Am J Physiol Gastrointest Liver Physiol
. 2000 Apr;
278(4):G617-24.
PMID: 10762616
Rectal biopsies from cystic fibrosis (CF) patients show defective cAMP-activated Cl(-) secretion and an inverse response of the short-circuit current (I(sc)) toward stimulation with carbachol (CCh). Alternative Cl(-) channels are...
10.