In the clinical arena...

In the clinical arena... Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

In the clinical arena... Abstract Text:

Carol Potera,Karen Roush,

In the clinical arena... Publishing Authors By Initials

C Potera,K Roush,

For similar abstracts research abstracts see: abstracts research

PUBMED ID PMID:

MEDLINE DATE:

In the clinical arena... Journal Published:

PUBLICATION TYPE: Journal Article

Journal: The American journal of nursing

VOLUME: 108

Page Numbers: 21

Journal Abbreviation:

ISSN: 0002-936X

DAY: 24

MONTH: Jan

YEAR: 2008

In the clinical arena... Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 372646

In the clinical arena... Keywords Mesh Terms:

KEYWORDS:

MESH TERMS:

Chemical & Substance for Abstract: In the clinical arena... Information

Substance Name:

Registry Number:

Grant and Affiliation Information for In the clinical arena...

AFFILIATION:

Country: United States

AGENCY:

GRANT:

ACRONYM:

MEDLINETA: Am J Nurs

REFSOURCE:

DATABASENAME:

ACCESSION NUMBER:

Number Hits: 0

In the clinical arena Related Publications

• A fistula clinic repairs lives in Uganda. A complication of obstructed labor shatters women's lives.
• Concerning the Selective Protection of (Z)-1,5-syn-Ene-diols and (E)-1,5-anti-Ene-diols as Allylic Triethylsilyl Ethers.
• Concerning the Synthesis of the Tedanolide C(13)-C(23) Fragment via Anti-Aldol Reaction.
• Efficient protiodesilylation of unactivated C(sp3)-SiMe2Ph bonds using tetrabutylammonium fluoride.
• Enantio- and diastereoselective synthesis of syn-beta-hydroxyallylsilanes via a chiral (Z)-gamma-silylallylboronate.
• Enantioselective synthesis of 1,5-anti- and 1,5-syn-diols using a highly diastereoselective one-pot double allylboration reaction sequence.
• Endovascular exclusion of mycotic aortic aneurysm.
• Examining pre-retirement and related services offered to service-users with an intellectual disability in Ireland.
• Experimental evidence for chair-like transition states in aldol reactions of methyl ketone lithium enolates: stereoselective synthesis and utilization of a deuterium-labeled enolate as a probe of reaction stereochemistry.
• Highly Stereoselective and Modular Syntheses of 10-Hydroxytrilobacin and Three Diastereomers via Stereodivergent [3 + 2]-Annulation Reactions.
• In the clinical arena...
• Intramolecular Diels-Alder reactions of siloxacyclopentene constrained trienes.
• Procaine hydrochloride as a monoamine oxidase inhibitor: implications for Geriatric therapy.
• Remarkable phosphine-effect on the intramolecular aldol reactions of unsaturated 1,5-diketones: highly regioselective synthesis of cross-conjugated dienones.
• Stereoselective syntheses of the c(1)-c(9) fragment of amphidinolide C.
• Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin.
• Studies on the synthesis of apoptolidin a. 1. Synthesis of the c(1)-c(11) fragment.
• Studies on the synthesis of apoptolidin a. 2. Synthesis of the disaccharide unit.
• Studies on the synthesis of durhamycin a: stereoselective synthesis of a model aglycone.
• Studies on the synthesis of quartromicins a(3) and d(3): synthesis of the vertical and horizontal bis-spirotetronate fragments.
• Synthesis of (+)-bullatacin via the highly diastereoselective [3+2] annulation reaction of a racemic aldehyde and a nonracemic allylsilane.
• Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction.
• Synthesis of precursors of the agalacto (exo) fragment of the quartromicins via an auxiliary-controlled exo-selective Diels-Alder reaction.
• Synthesis of small molecule inhibitors of the orphan nuclear receptor steroidogenic factor-1 (NR5A1) based on isoquinolinone scaffolds.
• Synthesis of the C(26)-C(42) and C(43)-C(67) Pyran-Containing Fragments of Amphidinol 3 via a Common Pyran Intermediate.
• Total synthesis of (-)-spinosyn a: examination of structural features that govern the stereoselectivity of the key transannular diels-alder reaction.
• Total synthesis of +-superstolide A.
• Total synthesis of amphidinolide E.
• Total synthesis of asimicin via highly stereoselective [3 + 2] annulation reactions of substituted allylsilanes.
• Total synthesis of biologically active natural products.