Lennart Hulthén (Former)
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- 2009
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Mark
The metabolic syndrome and risk of myocardial infarction in familial hypertension (Hypertension Heredity in Malmö Evaluation study).
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- Contribution to journal › Article
- 2008
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Mark
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
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- Contribution to journal › Article
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Mark
Determinants of kidney function in Swedish families: role of heritable factors.
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- Contribution to journal › Article
- 2007
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Mark
Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes
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- Contribution to journal › Article
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Mark
Moderate salt restriction effectively lowers blood pressure and degree of salt sensitivity is related to baseline concentration of renin and N-terminal atrial natriuretic peptide in plasma.
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- Contribution to journal › Article
- 2005
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Mark
Dipping and variability of blood pressure and heart rate at night are heritable traits.
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
- 2004
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Mark
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
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- Contribution to journal › Article
- 2003
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Mark
No evidence of a relation between 11beta-hydroxysteroid dehydrogenasetype 2 activity and salt sensitivity.
(
- Contribution to journal › Article
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Mark
Nephrin: a pivotal molecule in proteinuria influenced by angiotensin II
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- Contribution to journal › Debate/Note/Editorial
- 2002
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Mark
Plasma ProANP(1-30) reflects salt sensitivity in subjects with heredity for hypertension
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- Contribution to journal › Article
- 2001
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Mark
Metaiodobenzylguanidine (MIBG) scintigraphy and computed tomography (CT) in clinical practice. Primary and secondary evaluation for localization of phaeochromocytomas
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- Contribution to journal › Article
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Mark
Hormone replacement therapy in healthy postmenopausal women: a randomized, placebo-controlled study of effects on coagulation and fibrinolytic factors
(
- Contribution to journal › Article
- 2000
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Mark
Association between a variant in the 11 beta-hydroxysteroid dehydrogenase type 2 gene and primary hypertension
(
- Contribution to journal › Article
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Mark
Role of the Gly460Trp polymorphism of the alpha-adducin gene in primary hypertension in Scandinavians
(
- Contribution to journal › Article
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Mark
Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension
(
- Contribution to journal › Article
- 1999
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Mark
Reduced transcapillary fluid absorption from skeletal muscle and skin during hypovolaemia in insulin-dependent diabetes mellitus
(
- Contribution to journal › Article
- 1993
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Mark
Determination of urinary N-acetyl-beta-glucosaminidase in patients with hypertension and renal artery stenosis
(
- Contribution to journal › Article