Charles Bird King's Indian GalleryVIOLA H. J.Art News. 1976, Vol 75, Num 10, pp 67-70Article

ZUR ARYLIERUNG VON SCHWEFELKOHLENSTOFF - EIN NEUER ZUGANG ZU CHLORDITHIOKOHLENSAEUREARYLESTERN = SUR L'ARYLATION DE DISULFURE DE CARBONE. UNE NOUVELLE VOIE D'ACCES AUX ESTERS ARYLIQUES D'ACIDE CHLORODITHIOFORMIQUEVIOLA H; MAYER R.1979; Z. CHEM.; DDR; DA. 1979; VOL. 19; NO 8; PP. 289-290; BIBL. 7 REF.Article

EINE NEUE DARSTELLUNGSMETHODE FUER AROMATISCHE THIOCARBONSAEURECHLORIDE = UNE NOUVELLE METHODE DE PREPARATION DE CHLORURES THIOCARBOXYLIQUES AROMATIQUESVIOLA H; MAYER R.1975; Z. CHEM.; DTSCH.; DA. 1975; VOL. 15; NO 9; PP. 348; BIBL. 7 REF.Article

EINE NEUE SYNTHESE FUER CYANODITHIOAMEISENSAEUREESTER BZW. 1,2-DICYANO-1,2-DIALKYMERCAPTO-ETHEN = UNE NOUVELLE SYNTHESE DE CYANO-DITHIOFORMIATES: LE DICYANO-1,2 DIALKYLTHIO-1,2 ETHYLENEMAYER R; THIEL W; VIOLA H et al.1979; Z. CHEM.; DDR; DA. 1979; VOL. 19; NO 2; PP. 56; BIBL. 3 REF.Article

DIE ERSTE SYNTHESE VON ALPHA -OXO-DITHIOCARBONSAEUREESTERN DURCH THIOLIERUNG VON PHENACYLHALOGENIDEN MIT ELEMENTAREM SCHWEFEL. = LA PREMIERE SYNTHESE D'ESTERS ALPHA -OXO DITHIOCARBOXYLIQUES PAR THIOLATION D'HALOGENURES DE PHENACYLE AVEC LE SOUFRE ELEMENTAIREMAYER R; VIOLA H; HOPF B et al.1978; Z. CHEM.; DTSCH.; DA. 1978; VOL. 18; NO 3; PP. 90; BIBL. 7 REF.Article

SYNTHESE AROMATISCHER THIOSAEUREAMIDE AUS BENZYLTHIOAETHERN DURCH THIOLIERUNG. = SYNTHESE DE THIOAMIDES AROMATIQUES A PARTIR DE SULFURES BENZYLIQUES PAR THIOLATIONMAYER R; THIEL W; VIOLA H et al.1976; Z. CHEM.; DTSCH.; DA. 1976; VOL. 16; NO 10; PP. 395-396; BIBL. 6 REF.Article

DIE ERSTE SYNTHESE VON DIOXO-DITHIOBERNSTEINSAEUREDIAMIDEN DURCH TIEFTEMPERATUR-THIOLIERUNG VON 1,4-DIHALOGENBUTAN-2,3-DION = PREMIERE SYNTHESE DE DIAMIDES D'ACIDE DIOXO DITHIOSUCCINIQUE PAR THIOLATION A BASSE TEMPERATURE DE DIHALOGENO-1,4 BUTANEDIONES-2,3MAYER R; SCHOEBEL HJ; VIOLA H et al.1980; Z. CHEM. (LEIPZIG); ISSN 0044-2402; DDR; DA. 1980; VOL. 20; NO 12; PP. 436; BIBL. 2 REF.Article

SZUBSZTITUALT FENIL-AZO-NAFTOLOK TAUTOMERIAJANAK. ES FENYALLOSAGANAK VIZSGALATA = ETUDE DE LA TAUTOMERIE ET DE LA STABILITE A LA LUMIERE DE PHENYLAZONAPHTOLS SUBSTITUESVIOLA H; HEMPEL R; MORGENSTERN J et al.1978; KOLOR. ERTES.; HUN; DA. 1978; VOL. 20; NO 6; PP. 361-369; ABS. RUS/ENG/GER; BIBL. 13 REF.Article

A pharmacist-managed clinic for treatment of latent tuberculosis infection in health care workersTAVITIAN, Sandra M; SPALEK, Viola H; BAILEY, Raymond P et al.American journal of health-system pharmacy. 2003, Vol 60, Num 18, pp 1856-1861, issn 1079-2082, 6 p.Article

AUSBLEICHUNTERSUCHUNGEN VON PHENYLAZONAPHTHOLEN IN POLYAMID-FOLIE. = ETUDES DE LA DECOLORATION DES PHENYLAZONAPHTOLES DANS LES FILMS DE POLYAMIDEHEMPEL R; VIOLA H; MORGENSTERN J et al.1978; FASERFORSCH. U. TEXTILTECH.; DDR; DA. 1978; VOL. 29; NO 3; PP. 190-193; ABS. RUS/ENG; BIBL. 15 REF.Article

PHOTOCHROMIE UND AUSBLEICHVERHALTEN SUBSTITUIERTER 1-METHOXY-4-PHENYLAZONAPHTHALENE IN POLYAMIDFOLIE = PHOTOCHROMIE ET DECOLORATION DE METHOXY-1 PHENYLAZO-4 NAPHTALENE SUBSTITUE DANS DES FILMS DE POLYAMIDEHEMPEL R; VIOLA H; MORGENSTERN J et al.1979; Z. CHEM.; DDR; DA. 1979; VOL. 19; NO 8; PP. 298-299; BIBL. 8 REF.Article

SYNTHESE VON NITRO- UND AMINOSUBSTITUIERTEN THIOBENZAMIDEN DURCH THIOLIERUNGSREAKTIONEN MIT ELEMENTAREM SCHWEFEL UNTER MILDEN BEDINGUNGEN. = SYNTHESE DE THIOBENZAMIDES NITRO- ET AMINO-SUBSTITUES PAR THIOLATION AVEC LE SOUFRE ELEMENTAIRE DANS DES CONDITIONS DOUCESMAYER R; VIOLA H; REICHERT J et al.1978; J. PRAKT. CHEM.; DTSCH.; DA. 1978; VOL. 320; NO 2; PP. 313-323; ABS. ANGL.; BIBL. 32 REF.Article

Indicators of seabird reproductive performance demonstrate the impact of commercial fisheries on seabird populations in the North SeaCOOK, Aonghais S. C. P; DADAM, Daria; MITCHELL, Ian et al.Ecological indicators. 2014, Vol 38, pp 1-11, issn 1470-160X, 11 p.Article

The L-Type Ca²⁺ Channel as a Therapeutic Target in Heart DiseaseVIOLA, H. M; MACDONALD, W. A; TANG, H et al.Current medicinal chemistry. 2009, Vol 16, Num 26, pp 3341-3358, issn 0929-8673, 18 p.Article

Possible anxiolytic effects of Chrysin, a central benzodiazepine receptor ligand isolated from Passiflora coeruleaWOLFMAN, C; VIOLA, H; PALADINI, A et al.Pharmacology, biochemistry and behavior. 1994, Vol 47, Num 1, pp 1-4, issn 0091-3057Article

Isolation of pharmacologically active benzodiazepine receptor ligands from Tilia tomentosa (Tiliaceae)VIOLA, H; WOLFMAN, C; LEVI DE STEIN, M et al.Journal of ethnopharmacology. 1994, Vol 44, Num 1, pp 47-53, issn 0378-8741Article

Habituation and inhibitory avoidance training alter brain regional levels of benzodiazepine-like molecules and are affected by intracerebral flumazenil microinjectionWOLFMAN, C; DA CUNHA, C; JERUSALINSKY, D et al.Brain research. 1991, Vol 548, Num 1-2, pp 74-80, issn 0006-8993, 7 p.Article

Anxioselective properties of 6,3'-dinitroflavone, a high-affinity benzodiazepine receptor ligandWOLFMAN, C; VIOLA, H; MARDER, M et al.European journal of pharmacology. 1996, Vol 318, Num 1, pp 23-30, issn 0014-2999Article

Overview-flavonoids : A new family of benzodiazepine receptor ligandsMEDINA, J. H; VIOLA, H; WOLFMAN, C et al.Neurochemical research. 1997, Vol 22, Num 4, pp 419-425, issn 0364-3190Article

Bis(benzo[4,5]thieno)[3,2-c:2',3'-e][1,2]dithiin, ein Valenzisomer von Dithioxo-thioindigo = Bis(benzo[4,5]thieno)[3,2-c:2',3'-e][1,2]dithiine, a valence isomer of Dithioxo-thioindigoSCHROTH, W; HINTZSCHE, E; VIOLA, H et al.Chemische Berichte. 1994, Vol 127, Num 2, pp 401-408, issn 0009-2940Article

6-Chloro-3'-nitroflavone is a potent ligand for the benzodiazepine binding site of the GABA_A receptor devoid of intrinsic activityVIOLA, H; WOLFMAN, C; MARDER, M et al.Pharmacology, biochemistry and behavior. 2000, Vol 65, Num 2, pp 313-320, issn 0091-3057Article

Behavioral effects of the putative anxiolytic (±)-1-(2,5-dimethoxy-4-ethylthiophenyl)-2-aminopropane (ALEPH-2) in rats and miceSCORZA, M. C; REYES-PARADA, M; SILVEIRA, R et al.Pharmacology, biochemistry and behavior. 1996, Vol 54, Num 2, pp 355-362, issn 0091-3057, 7 p.Article

Pharmacological characterization of 6-bromo-3'-nitroflavone, a synthetic flavonoid with high affinity for the benzodiazepine receptorsWOLFMAN, C; VIOLA, H; MARDER, M et al.Pharmacology, biochemistry and behavior. 1998, Vol 61, Num 3, pp 239-246, issn 0091-3057Article