» Authors » G Hoeffken

G Hoeffken

Explore the profile of G Hoeffken including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 13
Citations 449
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Korfel A, Kreuser E, Hoeffken G, Baumgart J, Sass G, Thiel E, et al.
Int J Oncol . 2011 May; 7(1):65-8. PMID: 21552807
5-methyltetrahydrofolate (MTHF) is a main serum metabolite of 5-formyltetrahydrofolate (folinic acid, FA), a standard agent for potentiation of the cytotoxic activity of 5-fluorouracil (5-FU). The clinical application of MTHF instead...
2.
Ewig S, Birkner N, Strauss R, Schaefer E, Pauletzki J, Bischoff H, et al.
Thorax . 2009 May; 64(12):1062-9. PMID: 19454409
Background: The database of the German programme for quality in healthcare including data of every hospitalised patient with community-acquired pneumonia (CAP) during a 2-year period (n = 388 406 patients...
3.
Beyer J, Kolditz M, Ewert R, Rubens C, Opitz C, Schellong S, et al.
Vasa . 2008 Jun; 37(1):61-7. PMID: 18512543
Background: Idiopathic pulmonary arterial hypertension (iPAH) is a rare disease of unknown aetiology characterized by a poor prognosis. Impairment of nitric oxide (NO) synthesis or NO-induced vasorelaxation has been suspected...
4.
Hoeper M, Seyfarth H, Hoeffken G, Wirtz H, Spiekerkoetter E, Pletz M, et al.
Eur Respir J . 2007 Jul; 30(6):1096-102. PMID: 17652314
Novel treatments, such as prostanoids or endothelin receptor antagonists, have been introduced for various forms of pulmonary arterial hypertension, but the long-term effects of these treatments on portopulmonary hypertension (PPHT)...
5.
Hoeper M, Leuchte H, Halank M, Wilkens H, Meyer F, Seyfarth H, et al.
Eur Respir J . 2006 Oct; 28(4):691-4. PMID: 17012628
Addition of inhaled iloprost to bosentan may have beneficial effects in patients with idiopathic pulmonary arterial hypertension (IPAH). A multicentre, open, randomised, controlled trial was performed to assess the safety...
6.
Halank M, Miehlke S, Kolditz M, Hoeffken G
Z Gastroenterol . 2005 Jul; 43(7):677-85. PMID: 16001350
Patients with portal hypertension may develop pulmonary complications such as hepatopulmonary syndrome (HPS) or portopulmonary hypertension (PPHT). PPHT is defined as elevated pulmonary pressure, elevated pulmonary vascular resistance, a normal...
7.
Hoeper M, Halank M, Marx C, Hoeffken G, Seyfarth H, Schauer J, et al.
Eur Respir J . 2005 Mar; 25(3):502-8. PMID: 15738295
The dual endothelin receptor antagonist bosentan has been approved in several countries for pulmonary arterial hypertension, and patients with portopulmonary hypertension (PPHTN) have not specifically been excluded. However, no data...
8.
Hoeffken G, Talan D, Larsen L, Peloquin S, Choudhri S, Haverstock D, et al.
Eur J Clin Microbiol Infect Dis . 2004 Dec; 23(10):772-5. PMID: 15605184
In two prospective, randomized studies intravenous (IV)/oral (PO) moxifloxacin (400 mg q.i.d.) was compared to IV/PO antimicrobial comparator agents for the treatment of hospitalized patients with community-acquired pneumonia. Reported here...
9.
Halank M, Marx C, Hoeffken G
Heart . 2004 Jun; 90(7):e40. PMID: 15201266
The mean survival of patients with severe primary pulmonary hypertension (PPH) is < 3 years without appropriate treatment. There are no long term reports on the spontaneous course of mild...
10.
Finch R, Schurmann D, Collins O, KUBIN R, McGivern J, Bobbaers H, et al.
Antimicrob Agents Chemother . 2002 May; 46(6):1746-54. PMID: 12019085
The objective of the present trial was to compare the efficacy, safety, and tolerability of moxifloxacin (400 mg) given intravenously (i.v.) once daily followed by oral moxifloxacin (400 mg) for...