8 research outputs found
Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease
- Author
- Aaltonen M
- Abdur Rahman M
- Abell T
- Abide W. Jr
- Acheatel R
- Achiri P
- Acon J
- Adams T
- Affinito S
- Agarwal S
- Aggarwal K
- Aggarwal R
- Ahlström P
- Ahmad A
- Ahmed M
- Aillon C
- Airaksinen A
- Ait-sadi R
- Akers J
- Al-jumaily J
- Albers C
- Albert M
- Alberti A
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- Alford C
- Algotsson L
- Allen T
- Allworth M
- Almond E
- Aloisi A
- Alternburg C
- Alton M
- Amin J
- Amundson A
- Andersen K
- Andersen M
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- Andresen D
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- Zulauf N
- Ă…gĂĄrdh A
- Ă–ner A
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND:
Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes.
METHODS:
We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization.
RESULTS:
During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events.
CONCLUSIONS:
Among patients with atherosclerotic vascular disease who were receiving intensive statin therapy, the use of anacetrapib resulted in a lower incidence of major coronary events than the use of placebo. (Funded by Merck and others; Current Controlled Trials number, ISRCTN48678192 ; ClinicalTrials.gov number, NCT01252953 ; and EudraCT number, 2010-023467-18 .)
In vivo measurements of radiosensitivity of different cell populations within sarcoma-180 in mice. Abstr.
- Publication venue
- The Mouseion at the JAXlibrary
- Publication date
- 01/01/1974
- Field of study
Computerprogram for the Determination of Minimal Cardiac Transit Times
- Publication venue
- Kernforschungsanlage JĂĽlich GmbH Zentralbibliothek, Verlag
- Publication date
- 01/01/1982
- Field of study
Blood flow is an important parameter of cardiac performance and can be determined by measuring circulation times (1). For that purpose, usually an Anger-Type gamma-camera is used to register the first pass of a radioactive tracer of blood flow through the heart. The acquired data are processed by a suitable computer program yielding time-activity curves for sequential heart segments, which are selected by the region of interest technique. Appropriate smoothing of the curves facilitates theevaluation of data and also the automatic detection of activityarrival (2,3,4). Sequential activity arrivals describe thefastest flow or minimal transit time
External Measuring of Myocardial Structure and Function
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1983
- Field of study
Evolocumab and clinical outcomes in patients with cardiovascular disease
- Author
- Abelson M.
- Aboufakher R.
- Abrahamsen T. E.
- Accini Mendoza J. L.
- Acheatel R.
- Ackermann D.
- Adamkova V.
- Adams M.
- Adlam D.
- Aggarwal R.
- Aggarwal S.
- Ahsan A.
- Ainsworth P.
- Airody Govinda R.
- Akai A.
- Ako J.
- Al-Bahrani A.
- Al-Joundi T.
- Aldegather J.
- Aldrete Velasco J. A.
- Alfieri A.
- Alt I.
- Alzohaili O.
- Amerena J.
- Amin J.
- Amoedo R.
- Amuchastegui M.
- Anderson T.
- Andreka P.
- Andreotti F.
- Angoulvant D.
- Ansell B.
- Antalik L.
- Antkowiak-Piatyszek K.
- Appel K.
- Arakawa T.
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- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
peer reviewedBACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets. © 2017 Massachusetts Medical Society
Evolocumab and clinical outcomes in patients with cardiovascular disease
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- Potthoff Cardenas S
- Potu R
- Pozdisek Z
- Prager R
- Prasan A
- Pretorius M
- Prokhorov O
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- Rabinowitz A
- Raczak G
- Radzeviciene-Jurgute R
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- Rahimi S
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- Rajadhyaksha G
- Rallidis L
- Ramanathan Gl
- Rammer M
- Ramos Lopez Ga
- Ramos M
- Ramstad D
- Range G
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- Rapezzi C
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- Recknor C
- Reddy J
- Reichert P
- Reichman A
- Reis G
- Remler R
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- Reschak M
- Reshotko D
- Reyes H
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- Richter D
- Rider J
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- Rigler S
- Rinke A
- Risberg K
- Rishko M
- Roberts Thomson P
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- Roseman H
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- Roubille F
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- Rowe W
- Rubenfire M
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- Rubino J
- Rudenko L
- Rudyk I
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- Rupka D
- Rutherfurd S
- Rychlewska-Hanczewska A
- Rysava D
- Römer T
- Saaiman J
- Saavedra Gajardo Va
- Sabatine Marc S.
- Sabbah E
- Sabe-Affaki G
- Sacco J
- Saetre Lihn A
- Sahin T
- Sakagami S
- Sakhrani L
- Saksena R
- Saku K
- Salamon C
- Salbach P
- Samal A
- Sampietro T
- Sanabria Hd
- Sanchez Diaz Cj
- Sanchez Vallejo G
- Sanford K
- Saravanan P
- Sarkar D
- Sarvan M
- Sato K
- Satoh Y
- Savolainen M
- Saway W
- Scheen A
- Schenkenberger I
- Schernthaner G
- Schiele F
- Schiff E
- Schlau A
- Schmedtje J
- Schmidt Eb
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- Schooley C
- Schramm E
- Schreibman D
- Schäufele T
- Scott J
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- Seaton B
- Senior R
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- Sepulveda Varela Pa
- Sever Peter S.
- Shah A
- Shah M
- Shalaev S
- Shalek M
- Shaoulian E
- Shapiro M
- Shatylo V
- Shechter M
- Shen X
- Sherenkov A
- Sherman H
- Shifrin G.
- Shimizu M
- Shin Gj
- Shinozaki T
- Shirasawa K
- Shore K
- Shotan A
- Shustov S
- Shutemova E
- Shvarts Y
- Sigurdsson A
- Silverman S
- Sime I
- Simon W
- Simons R
- Simpson R
- Singh I
- Singhal A
- Sinhal A
- Sinzinger H
- Siostrzonek P
- Siu Cw
- Siu Sc
- Skonieczny G
- Skoumas I
- Skrobakova J
- Snyder B
- Soares Goncalves S
- Soares Piegas L
- Sochor K
- Sofley Cw
- Solanki B
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- Solovev O
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- Somaratne R
- Sorokina I
- Sosovec D
- Sotomayor Herazo A
- Spaulding C
- Spencer R
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- Spinarova L
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- Spyra J
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- St Amour E
- Staneta P
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- Steiner S
- Steinsapir J
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- Strandberg Te
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- Stringam S
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- Stukena I
- Su H
- Subramaniam T
- Sugino H
- Sun Y
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- Sussex B
- Suutari A
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- Sy Ra
- Szakal I
- Szpajer M
- Szymkowiak K
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- Tahirkheli N
- Tami L
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- Tang A
- Tang Y
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- Tarleton G
- Tarnovska-Kadreva R
- Tavares Russo La
- Tay L
- Teodorescu I
- Tereshenko S
- Terje R. Fish MP
- Terront Lozano Ma
- Teterovska D
- Thoeng J
- Thom S
- Thomas H
- Thompson C
- Thompson P
- Thomson S
- Thorgeirsson G
- Tie S
- Tikkanen Mj
- Timoteo At
- Tobin T
- Tokgozoglu Sl
- Tokunaga T
- Tomcsanyi J
- Tonino W
- Toplak H
- Torres M
- Toth K
- Travill C
- Trebacz J
- Trendafilova-Lazarova D
- Trenk D
- Treshkur T
- Trevelyan J
- Troquay R
- Tsai Cf
- Tseluyko V
- Tsoukas G
- Tudoran M
- Tyagi S
- Tydén P
- Tyszecka G
- Tzekova M
- Tziakas D
- Uehara H
- Uemura O
- Ueno T
- Uhliar R
- Ulla Mr
- Urbach D
- Urgeova L
- Vaclavik J
- Vakaliuk I
- Valdes Chavarri M
- Vally T
- Valter I
- Van Beek E
- van de Borne P
- van de Wal R
- van der Walt E
- van der Zwaan C
- Van Gaal W
- Van Hessen M
- Van Zyl L
- Vanbelle E
- Vandekerckhove H
- Vasco Salgado A
- Vawda G
- Velchev V
- Venceviciene L
- Venegas Carrillo La
- Verheye S
- Vertes G
- Veze I
- Vida Gutierrez M
- Vidotti Mh
- Viigimaa M
- Vijay N
- Vikman S
- Vinanska D
- Vintila Mm
- Violante Ortiz Rm
- Vishnevsky A
- Visman A
- Vita J
- Voevoda M
- Vogel Dr
- Volkov V
- Vomacka Z
- von Hodenberg E
- Vora K
- Vorpahl M
- Wada A
- Wagner S
- Wan Ahmad Wa
- Wang D
- Wang Huei
- Wang J
- Wasserman Scott M.
- Waxman F
- Webel R
- Webster J
- Weinberg B
- Weinstein D
- Welker J
- Wermuth S
- Westendorp I
- Weyland K
- Whitney R
- Wierzbicka K
- Wilhoit G
- Wilson S
- Wise J
- Wiseman A
- Witt N
- Wittert G
- Wiviott Stephen D.
- Wnetrzak-Michalska R
- Wollaert B
- Wood Sk
- Wozakowska-Kaplon B
- Wozniak I
- Wu C
- Wyatt N
- Wöhrle J
- Xu P
- Xue L
- Yakhontova P
- Yamamoto K
- Yamashita K
- Yan J
- Yang E
- Yang P
- Yang X
- Yang Y
- Yang Z
- Yao Z
- Yasumura Y
- Yataco A
- Yeh H
- Yena L
- Yeoman G
- Yigit Z
- Yilmaz Mb
- Yokoya K
- Yoshimichi G
- Yotov Y
- Youngman D
- Younis L
- Yuge M
- Zabowka M
- Zahn L
- Zamorano Gomez Jl
- Zarich S
- Zateyshchikov D
- Zdrenghea D
- Zechowicz T
- Zeig S
- Zemanek J
- Zeng X
- Zhang L
- Zhang X
- Zhao S
- Zheng Y
- Zheng Z
- Zhou C
- Zhu Y
- Zhurba S
- Zidkova E
- Zieba B
- Ziegler O
- Zilahi Z
- Zrazhevskiy K
- Ă–stergren J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets
Biologische Grundlagen der Strahlentherapie
- Author
- A Cohen
- A Howard
- A Howes
- A Wacker
- AF Hermens
- AF Hermens
- AL Wiley
- AM Kellerer
- AM Kellerer
- AM Kellerer
- AM Rauth
- B Kapstad
- B Littbrand
- BD Michael
- BM Winston
- C Heidelberger
- C Regaud
- C Rogers
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- CD Town
- CE Olson
- CM Streffer
- D Beunigen van
- DE Thrall
- DG Hirst
- DH Bewley
- DH Hussey
- DR Goffinet
- E Harbers
- E Malaise
- E Scherer
- EH Betz
- EJ Hall
- EJ Hidvegi
- EP Malaise
- F Alper
- F Ellis
- F Ghavimi
- FA Stewart
- G Froese
- GE Adams
- GE Adams
- GG Steel
- GM Hahn
- GM Hahn
- GM Hahn
- GW Barendsen
- GW Barendsen
- GW Barendsen
- GW Barendsen
- H Braun
- H Braun
- H Brenk van den
- H Brenk van den
- H Dertinger
- H Holthusen
- H Holthusen
- H Langendorff
- H-J Eichhorn
- H-J Melching
- HB Hewitt
- HD Kogelnik
- HD Suit
- HD Suit
- HD Suit
- HD Suit
- HD Suit
- HJ Edenberg
- HM Lemon
- HR Nitze
- HR Withers
- HR Withers
- HS Kaplan
- HS Kaplan
- HS Reinhold
- J Churchill-Davidson
- J Denekamp
- J Denekamp
- J Denekamp
- J Dutreix
- J Hendry
- J Kirk
- JB Little
- JB Little
- JD Chapman
- JD Chapman
- JE Byfield
- JE Byfield
- JE Cleaver
- JE Cleaver
- JE Cleaver
- JE Till
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Howlett
- JF Tannock
- JH Kim
- JI Fabrikant
- JJ Broerse
- JJ Broerse
- JM Henk
- JP Geraci
- JP Kriss
- JR Cassady
- JS Stehlin
- JT Leith
- K-R Trott
- K-R Trott
- KG Zimmer
- KH Kärcher
- KH Kärcher
- KI Altman
- L Parker
- LF Lamerton
- LG Lajtha
- LG Lajtha
- LH Gray
- LH Thompson
- LJ Lomakina
- M Andreeff
- M Catterall
- M Catterall
- M Tubiana
- M Tubiana
- M Urano
- M Wannenmacher
- MD Wharam
- MJ Waring
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- O Hug
- O JĂĽngling
- P Bosiljanoff
- P Clifford
- PL Olive
- PW Sheldon
- PW Sheldon
- R Howard
- R Wideröe
- R Wiederöe
- RA Phillips
- RA Walters
- RB Painter
- RC Urtasun
- RF Hagemann
- RG Evans
- RH Stellwagen
- RH Thomlinson
- RH Thomlinson
- RH Thomlinson
- RH Thomlinson
- RJ Berry
- RL Erikson
- S Dische
- S Dische
- S Hornsey
- S Hornsey
- S Krönig
- S Lesher
- S Shirakawa
- S Zamenhof
- SB Field
- SB Field
- SB Field
- SB Reddy
- SC Barranco
- SS Donaldson
- T Alper
- T Hoshino
- T Terasima
- TL Phillips
- TL Phillips
- TT Puck
- TT Puck
- U Hagen
- VH Bono
- W Dittrich
- W Duncan
- W Porschen
- W Porschen
- W Szybalski
- WA Linden
- WC Mohler
- WE Powers
- WK Sinclair
- ZM Bacq
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1980
- Field of study
Biologische Grundlagen der Strahlentherapie
- Author
- A Cohen
- A Howard
- A Howes
- A Maity
- A Wacker
- A Wambersie
- AC Begg
- AC Begg
- AC Begg
- AC Begg
- AE Pearson
- AF Hermens
- AL Wiley
- AM Kellerer
- AM Kellerer
- AM Kellerer
- AM Kellerer
- AM Kellerer
- AM Rauth
- AV D’Amico
- B Barlogie
- B Kapstad
- B Littbrand
- B Tributkait
- BD Michael
- BM Winston
- BT Hill
- C Heidelberger
- C LĂĽcke-Huhle
- C Regaud
- C Rogers
- C Sonntag Von
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- C Streffer
- CD Town
- CE Olson
- CH Collis
- D Beuningen van
- D Beuningen van
- D Beuningen van
- D Leeper
- DE Thrall
- DG Hirst
- DH Bewley
- DH Hussey
- DK Bewley
- DR Goffinet
- E Ben-Hur
- E Dikomey
- E Harbers
- E Malaise
- E Scherer
- EH Betz
- EJ Hall
- EJ Hall
- EJ Hall
- EJ Hidvegi
- EK Rofstad
- EP Malaise
- F Alper
- F Ellis
- F Ghavimi
- F Monschke
- F Zölzer
- FA Stewart
- G Froerse
- G Schmitt
- GE Adams
- GE Adams
- GG Steel
- GG Steel
- GM Hahn
- GM Hahn
- GM Hahn
- GM Hahn
- GW Barendsen
- GW Barendsen
- GW Barendsen
- GW Barendsen
- H Braun
- H Braun
- H Holthusen
- H Holthusen
- H Jung
- H Jung
- H Langendorff
- H Maase Von der
- H Mönig
- HAS Brenk van den
- HAS Brenk van den
- HB Hewitt
- HD Suit
- HD Suit
- HD Suit
- HD Suit
- HD Suit
- HI Feldmann
- HJ Edenberg
- HJ Eichhorn
- HJ Melching
- HM Klouwen
- HM Lemon
- HR Nitze
- HR Withers
- HR Withers
- HR Withers
- HR Withers
- HS Kaplan
- HS Kaplan
- HS Reinhold
- HS Reinhold
- I Turesson
- IF Tannock
- IJ Lomakina
- J Bergonié
- J Churchill-Davidson
- J Denekamp
- J Denekamp
- J Denekamp
- J Denekamp
- J Dutreix
- J Hendry
- J Kiefer
- J Kirk
- J Overgaard
- J Overgaard
- J Overgaard
- JB Little
- JB Little
- JB Little
- JD Chapman
- JD Chapman
- JD Chapman
- JE Byfield
- JE Byfield
- JE Cleaver
- JE Cleaver
- JE Cleaver
- JE Till
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Fowler
- JF Howlett
- JH Kim
- JI Fabrikant
- JJ Broerse
- JJ Broerse
- JM Brown
- JM Henk
- JP Geraci
- JP Kriss
- JR Cassady
- JS Stehlin
- JT Leith
- JT Lett
- JZ Beer
- K-R Trott
- KG Zimmer
- KH Chadwick
- KH Chadwick
- KH Kärcher
- KH Kärcher
- KI Altman
- KK Fu
- KR Trott
- L Parker
- L Revesz
- LF Lamerton
- LG Lajtha
- LG Lajtha
- LH Gray
- LJ Peters
- M Andreef
- M Bamberg
- M Catterall
- M Catterall
- M Höckel
- M Molls
- M Molls
- M Stuschke
- M Tubiana
- M Tubiana
- M Tubiana
- M Urano
- M Wannenmacher
- MA Konerding
- MB Kastan
- MC Joiner
- MC Joiner
- MC Paterson
- MD Wharam
- MG Ord
- MJ Waring
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- MM Elkind
- N Zamboglou
- O Hug
- O JĂĽngling
- P Bosiljanoff
- P Vaupel
- P Vaupel
- P Vaupel
- P Vaupel
- P Vaupel
- PHC Hanawalt
- PHC Hanawalt
- PL Olive
- PL Olive
- PW Sheldon
- PW Sheldon
- PW Vaupel
- R Howard
- R Wideröe
- R Wideröe
- RA Britten
- RA Walters
- RB Painter
- RC Urtasun
- RF Hagemann
- RF Kallman
- RG Evans
- RH Stellwagen
- RH Thomlinson
- RH Thomlinson
- RH Thomlinson
- RH Thomlinson
- RH Thomlinson
- RJ Berry
- RJ Berry
- RL Erikson
- RL Morgan
- RM Sutherland
- S Dische
- S Dische
- S Hornsey
- S Hornsey
- S Krönig
- S Lesher
- S Nakatsugawa
- S Shirakawa
- S Zamenhof
- SB Curtis
- SB Field
- SB Field
- SB Field
- SB Field
- SB Field
- SB Field
- SB Reddy
- SC Barranco
- SS Donaldson
- T Alper
- T Alper
- T Hoshino
- T Jung
- T Sugahara
- T Terasima
- T Vietti
- TL Phillips
- TT Puck
- TT Puck
- U Hagen
- U Weissenborn
- U Weissenborn
- UNSCEAR
- VH Bono
- W Budach
- W Dittrich
- W Duncan
- W Porschen
- W-U MĂĽller
- WA Linden
- WC Mohler
- WE Powers
- WK Sinclair
- WM Generoso
- Y Shibamoto
- ZM Bacq
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1996
- Field of study