Adaptation of the hypothalamic-pituitary hormones during intensive endurance training.

Stress and the neuroendocrine system: the role of exercise as a stressor and modifier of stress. Expert Rev Endocrinol Metab (2006) 0.94

Intense physical exercise increases systemic 11beta-hydroxysteroid dehydrogenase type 1 activity in healthy adult subjects. Eur J Appl Physiol (2009) 0.88

Plasma ghrelin responses to acute sculling exercises in elite male rowers. Eur J Appl Physiol (2006) 0.81

Glucocorticoid antagonism limits adiposity rebound and glucose intolerance in young male rats following the cessation of daily exercise and caloric restriction. Am J Physiol Endocrinol Metab (2016) 0.77

Comparison of low and high dose corticotropin stimulation tests in patients with pituitary disease. J Clin Endocrinol Metab (1998) 3.78

Function of DNA polymerase 3 in DNA replication. Nat New Biol (1971) 3.10

Deoxyribonucleic acid replication in vitro. J Mol Biol (1972) 2.64

Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study. Diabetologia (2011) 2.43

Isolation and characterization of thermosensitive Escherichia coli mutants defective in deoxyribonucleic acid replication. J Bacteriol (1973) 2.38

Metaphyseal chondrodysplasia, Schmid type. Clinical and radiographic delineation with a review of the literature. Pediatr Radiol (1988) 2.06

Errors of morphogenesis: concepts and terms. Recommendations of an international working group. J Pediatr (1982) 2.04

Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritis. Eur J Pediatr (1983) 1.98

The Nicotiana tabacum plasma membrane aquaporin NtAQP1 is mercury-insensitive and permeable for glycerol. Plant J (1999) 1.86

Diagnosis and therapy surveillance in Addison's disease: rapid adrenocorticotropin (ACTH) test and measurement of plasma ACTH, renin activity, and aldosterone. J Clin Endocrinol Metab (1992) 1.82

A dietary pattern protective against type 2 diabetes in the European Prospective Investigation into Cancer and Nutrition (EPIC)--Potsdam Study cohort. Diabetologia (2005) 1.79

Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998). Arch Gynecol Obstet (2002) 1.79

Signalling mechanisms linking hepatic glucose and lipid metabolism. Diabetologia (2006) 1.78

Bone mineral density is not significantly reduced in adult patients on low-dose glucocorticoid replacement therapy. J Clin Endocrinol Metab (2011) 1.75

Cyclic temperature treatments of dark-grown pea seedlings induce a rise in specific transcript levels of light-regulated genes related to photomorphogenesis. Mol Gen Genet (1991) 1.63

Spondyloepiphyseal dysplasia. Birth Defects Orig Artic Ser (1974) 1.60

Glucose inhibits the insulin-induced activation of the insulin-degrading enzyme in HepG2 cells. Diabetologia (2009) 1.55

The comparison of venous plasma glucose and whole blood capillary glucose in diagnoses of Type 2 diabetes: a population-based screening study. Diabet Med (2005) 1.53

Pandemic H1N1 Influenza Infection and Vaccination in Humans Induces Cross-Protective Antibodies that Target the Hemagglutinin Stem. Front Immunol (2012) 1.50

"New" dwarfing syndromes. Birth Defects Orig Artic Ser (1977) 1.49

Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature. Eur J Pediatr (2000) 1.48

Short rib-polydactyly (SRP) syndromes, types Majewski and Saldino-Noonan. Z Kinderheilkd (1974) 1.48

Duplicate publication and related problems. Pediatrics (1990) 1.46

[Irritable bowel syndrome: German consensus guidelines on definition, pathophysiology and management]. Z Gastroenterol (2011) 1.46

Further delineation of the 3-M syndrome with review of the literature. Am J Med Genet (1987) 1.43

Osteogenesis imperfecta: a clinical study of the first ten years of life. Calcif Tissue Int (1992) 1.43

Xenon anesthesia impairs hepatic oxygenation and perfusion in healthy pigs. Minerva Anestesiol (2008) 1.40

Mental retardation syndrome with renal concentration deficiency and intracerebral calcification. Eur J Pediatr (1990) 1.40

Replication of polyoma DNA in isolated nuclei. V. Complementation of in vitro DNA replication. J Virol (1975) 1.39

[Lipomucopolysaccharidosis, A new storage disease]. Z Kinderheilkd (1968) 1.38

[68-year-old female patient with dyspnea and hypokalemic hypertension]. Internist (Berl) (2007) 1.38

DNA polymerase alpha is associated with replicating SV40 nucleoprotein complexes. Nucleic Acids Res (1978) 1.36

Hypochondroplasia: clinical and radiological aspects in 39 cases. Radiology (1979) 1.34

Maturation of newly replicated chromatin of simian virus 40 and its host cell. J Mol Biol (1980) 1.31

Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect. Nat Genet (1993) 1.31

Cardiovascular and cerebrovascular comorbidities of hypokalemic and normokalemic primary aldosteronism: results of the German Conn's Registry. J Clin Endocrinol Metab (2009) 1.30

Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutation. J Med Genet (1999) 1.29

Mucopolysaccharidosis. VII. Beta-glucuronidase deficiency. Humangenetik (1974) 1.26

Campylobacter jejuni infection of infant mice: acute enterocolitis is followed by asymptomatic intestinal and extra-intestinal immune responses. Eur J Microbiol Immunol (Bp) (2012) 1.24

A new familial intrauterine growth retardation syndrome the "3-M syndrome". Eur J Pediatr (1976) 1.24

[Dysosteosclerosis--a special form of generalized osteosclerosis]. Fortschr Geb Rontgenstr Nuklearmed (1968) 1.22

Wormian bones in osteogenesis imperfecta and other disorders. Skeletal Radiol (1982) 1.21

A new mass-spectrometric C-terminal sequencing technique finds a similarity between gamma-interferon and alpha 2-interferon and identifies a proteolytically clipped gamma-interferon that retains full antiviral activity. Biochem J (1983) 1.21

[Metatrophic dwarfism]. Arch Kinderheilkd (1966) 1.21

[The campomelic syndrome]. Presse Med (1971) 1.21

Role of duodenal lipid and cholecystokinin A receptors in the pathophysiology of functional dyspepsia. Gut (2001) 1.20

Mucolipidosis I: increased sialic acid content and deficiency of an alpha-N-acetylneuraminidase in cultured fibroblasts. Biochem Biophys Res Commun (1977) 1.18

Continuous glucose monitoring in people with diabetes: the randomized controlled Glucose Level Awareness in Diabetes Study (GLADIS). Diabet Med (2015) 1.18

Impairment of fat oxidation under high- vs. low-glycemic index diet occurs before the development of an obese phenotype. Am J Physiol Endocrinol Metab (2009) 1.18

Euglycemic hyperinsulinemia, but not lipid infusion, decreases circulating ghrelin levels in humans. J Endocrinol Invest (2002) 1.17

Maroteaux-Lamy disease (mucopolysaccharidosis VI), subtype A: deficiency of a N-acetylgalactosamine-4-sulfatase. Biochem Biophys Res Commun (1974) 1.17

Endogenous and exogenous glucocorticoids decrease plasma ghrelin in humans. Eur J Endocrinol (2004) 1.16

Chronic sputum production: correlations between clinical features and findings on high resolution computed tomographic scanning of the chest. Thorax (1996) 1.15

Impact of cereal fibre on glucose-regulating factors. Diabetologia (2005) 1.15

[Prevention, diagnosis, therapy, and follow-up of lung cancer]. Pneumologie (2010) 1.14

Effect of human body weight changes on circulating levels of peptide YY and peptide YY3-36. J Clin Endocrinol Metab (2006) 1.13

The Dyggve-Melchior-Clausen syndrome. Radiology (1975) 1.13

The pallister mosaic syndrome. Birth Defects Orig Artic Ser (1977) 1.12

Wolcott-Rallison syndrome: diabetes mellitus and spondyloepiphyseal dysplasia. Eur J Pediatr (1982) 1.12

Congenital anomalies in children of epileptic mothers and fathers. Neuropediatrics (1980) 1.09

Microalbuminuria is a major determinant of elevated plasma retinol-binding protein 4 in type 2 diabetic patients. Kidney Int (2007) 1.09

Diagnostic performance of a commercially available computer-aided diagnosis system for automatic detection of pulmonary nodules: comparison with single and double reading. Rofo (2004) 1.09

Therapeutic strategies in adrenal insufficiency. Ann Endocrinol (Paris) (2001) 1.09

The clinical spectrum of alpha-L-iduronidase deficiency. Am J Med Genet (1985) 1.08

Effects of marked weight loss on plasma levels of adiponectin, markers of chronic subclinical inflammation and insulin resistance in morbidly obese women. Int J Obes (Lond) (2005) 1.08

The role of the adrenal gland in hypertensive transgenic rat TGR(mREN2)27. Endocrinology (1992) 1.08

A single-strand-specific DNA-binding protein from mouse cells that stimulates DNA polymerase. Eur J Biochem (1977) 1.08

Pyle's disease (familial metaphyseal dysplasia). A presentation of two cases and argument for its separation from craniometaphyseal dysplasia. J Bone Joint Surg Am (1970) 1.08

Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W. J Med Genet (2003) 1.07

The effect of moderate alcohol consumption on adiponectin oligomers and muscle oxidative capacity: a human intervention study. Diabetologia (2007) 1.07

Environmental aspects in pediatrics. New item in the European Journal of Pediatrics. Eur J Pediatr (1995) 1.06

Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome). Am J Med Genet (1998) 1.06

Prevention, diagnosis, therapy, and follow-up of lung cancer: interdisciplinary guideline of the German Respiratory Society and the German Cancer Society. Pneumologie (2010) 1.06

Isoflavonoid compounds extracted from Pueraria lobata suppress alcohol preference in a pharmacogenetic rat model of alcoholism. Alcohol Clin Exp Res (1996) 1.06

Heterogeneity of Morquio disease. Clin Genet (1986) 1.05

Clinical and ultrastructural findings in three patients with geleophysic dysplasia. Am J Med Genet (1996) 1.05

Fat digestion modulates gastrointestinal sensations induced by gastric distention and duodenal lipid in humans. Gastroenterology (2001) 1.05

Duplicate publication and related problems. Arch Dis Child (1990) 1.05

Insulin decreases human adiponectin plasma levels. Horm Metab Res (2003) 1.05

Purification and properties of DNA polymerase 3. Eur J Biochem (1973) 1.05

Atelosteogenesis. Am J Med Genet (1982) 1.04

Arabinoxylan consumption decreases postprandial serum glucose, serum insulin and plasma total ghrelin response in subjects with impaired glucose tolerance. Eur J Clin Nutr (2006) 1.03

Heterogeneity in Schwartz-Jampel chondrodystrophic myotonia. Eur J Pediatr (1997) 1.03

The systemic mucopolysaccharidoses. Ergeb Inn Med Kinderheilkd (1972) 1.03

A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia. Am J Med Genet (1996) 1.03

The spondylometaphyseal dysplasias. A tentative classification. Pediatr Radiol (1991) 1.03

A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasia. Physiol Genomics (2000) 1.03

Two peculiar types of enchondromatosis. Pediatr Radiol (1978) 1.02

Neuroendocrinological effects of acupuncture treatment in patients with irritable bowel syndrome. Complement Ther Med (2007) 1.01

Iron-regulatory protein hepcidin is increased in female athletes after a marathon. Eur J Appl Physiol (2005) 1.01