NL8901435A - Behandeling van arthritis. - Google Patents
Behandeling van arthritis. Download PDFInfo
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- NL8901435A NL8901435A NL8901435A NL8901435A NL8901435A NL 8901435 A NL8901435 A NL 8901435A NL 8901435 A NL8901435 A NL 8901435A NL 8901435 A NL8901435 A NL 8901435A NL 8901435 A NL8901435 A NL 8901435A
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- NL
- Netherlands
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- carbon atoms
- alkyl
- hydrogen atom
- alkyl group
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- 241000700157 Rattus norvegicus Species 0.000 description 1
- 208000035415 Reinfection Diseases 0.000 description 1
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- 208000025747 Rheumatic disease Diseases 0.000 description 1
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- 102000011096 Somatostatin receptor Human genes 0.000 description 1
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- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 description 1
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- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 125000003275 alpha amino acid group Chemical group 0.000 description 1
- 230000001820 anti-cytotoxin effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000000078 anti-malarial effect Effects 0.000 description 1
- 239000003430 antimalarial agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- LMEKQMALGUDUQG-UHFFFAOYSA-N azathioprine Chemical compound CN1C=NC([N+]([O-])=O)=C1SC1=NC=NC2=C1NC=N2 LMEKQMALGUDUQG-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000004181 carboxyalkyl group Chemical group 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000011260 co-administration Methods 0.000 description 1
- 239000003636 conditioned culture medium Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 231100000599 cytotoxic agent Toxicity 0.000 description 1
- 239000002619 cytotoxin Substances 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 230000009266 disease activity Effects 0.000 description 1
- 229940052760 dopamine agonists Drugs 0.000 description 1
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- 230000029142 excretion Effects 0.000 description 1
- 201000010934 exostosis Diseases 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 210000002454 frontal bone Anatomy 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 230000027119 gastric acid secretion Effects 0.000 description 1
- 201000010231 gastrointestinal system cancer Diseases 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- MNQZXJOMYWMBOU-UHFFFAOYSA-N glyceraldehyde Chemical compound OCC(O)C=O MNQZXJOMYWMBOU-UHFFFAOYSA-N 0.000 description 1
- 229940076085 gold Drugs 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 210000002216 heart Anatomy 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000000148 hypercalcaemia Effects 0.000 description 1
- 208000030915 hypercalcemia disease Diseases 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 229940073062 imuran Drugs 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 230000003914 insulin secretion Effects 0.000 description 1
- 229940126602 investigational medicinal product Drugs 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002584 ketoses Chemical class 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 208000017169 kidney disease Diseases 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 201000002364 leukopenia Diseases 0.000 description 1
- 231100001022 leukopenia Toxicity 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 206010025135 lupus erythematosus Diseases 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 230000003211 malignant effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229960000485 methotrexate Drugs 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 210000004789 organ system Anatomy 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000008533 pain sensitivity Effects 0.000 description 1
- 230000009996 pancreatic endocrine effect Effects 0.000 description 1
- 239000000199 parathyroid hormone Substances 0.000 description 1
- 229960001319 parathyroid hormone Drugs 0.000 description 1
- 210000003455 parietal bone Anatomy 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Chemical class 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 229960004618 prednisone Drugs 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 229940097325 prolactin Drugs 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000003127 radioimmunoassay Methods 0.000 description 1
- 238000001959 radiotherapy Methods 0.000 description 1
- 208000002574 reactive arthritis Diseases 0.000 description 1
- 208000023504 respiratory system disease Diseases 0.000 description 1
- 230000000552 rheumatic effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 210000003625 skull Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 208000011117 substance-related disease Diseases 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 206010043554 thrombocytopenia Diseases 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000000430 tryptophan group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 0.000 description 1
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 230000003156 vasculitic effect Effects 0.000 description 1
- 230000009278 visceral effect Effects 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/655—Somatostatins
- C07K14/6555—Somatostatins at least 1 amino acid in D-form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/31—Somatostatins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Endocrinology (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Toxicology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB888813339A GB8813339D0 (en) | 1988-06-06 | 1988-06-06 | Improvements in/relating to organic compounds |
| GB8813339 | 1988-06-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8901435A true NL8901435A (nl) | 1990-01-02 |
Family
ID=10638146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8901435A NL8901435A (nl) | 1988-06-06 | 1989-06-06 | Behandeling van arthritis. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US5145837A (cs) |
| EP (1) | EP0351354A3 (cs) |
| JP (1) | JP2809707B2 (cs) |
| KR (1) | KR910000178A (cs) |
| AU (1) | AU631547B2 (cs) |
| BE (1) | BE1004038A4 (cs) |
| CH (1) | CH680924A5 (cs) |
| DE (1) | DE3918320A1 (cs) |
| DK (1) | DK273089A (cs) |
| FR (1) | FR2632188B1 (cs) |
| GB (2) | GB8813339D0 (cs) |
| HU (1) | HU206633B (cs) |
| IT (1) | IT1231521B (cs) |
| MY (1) | MY104129A (cs) |
| NL (1) | NL8901435A (cs) |
| PT (1) | PT90753A (cs) |
| SE (1) | SE8902042L (cs) |
| ZA (1) | ZA894280B (cs) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6001960A (en) * | 1992-09-01 | 1999-12-14 | The Trustees Of The University Of Pennsylvania | Synthetic somatostatin mimics |
| US5965694A (en) * | 1992-09-01 | 1999-10-12 | The Trustees Of The University Of Pennsylvania | Somatostatin mimics and synthetic methods therefor |
| US5700905A (en) * | 1992-09-01 | 1997-12-23 | The Trustees Of The University Of Pennsylvania | Synthetic somatostatin mimics |
| US5696128A (en) * | 1994-07-07 | 1997-12-09 | The Board Of Supervisors Of Louisiana University And Agricultural And Mechanical College | Method of regulating immune function |
| US5686418A (en) * | 1996-04-08 | 1997-11-11 | Biomeasure Incorporated | Prolonging survival of transplanted pancreatic cells |
| UA66401C2 (en) * | 1998-12-02 | 2004-05-17 | Sentor Pharmaceuticals Inc | 3,4,5-trisubstituted aryl nitrone compounds and pharmaceutical composition containing the same |
| US6730700B2 (en) | 1998-12-02 | 2004-05-04 | Renovis, Inc. | 3,4,5,-trisubstituted aryl nitrone compounds and pharmaceutical compositions containing the same |
| US6146639A (en) * | 1999-07-26 | 2000-11-14 | Merich Nick | Arthritis, muscle pain, and dry skin remedy |
| US20020161026A1 (en) * | 2000-11-07 | 2002-10-31 | Paralkar Vishwas M. | Combination therapies for the stimulation of bone growth |
| KR100743212B1 (ko) * | 2001-06-08 | 2007-07-26 | 소시에떼 더 콘세이유 더 레세르세 에 다플리까띠옹 시엔띠피끄, 에스.아.에스. | 소마토스타틴-도파민 키메라 유사체 |
| DE60327843D1 (de) | 2002-03-04 | 2009-07-16 | Ipsen Pharma | Arzneimittelformulierungen mit verzögerter freisetzung mit einem trägerpeptid |
| US7521427B2 (en) * | 2004-11-09 | 2009-04-21 | Georgia Tech Research Corporation | Peptidyl allyl sulfones |
| TWI523863B (zh) | 2012-11-01 | 2016-03-01 | 艾普森藥品公司 | 體抑素－多巴胺嵌合體類似物 |
| EP2914276A4 (en) | 2012-11-01 | 2016-07-13 | Ipsen Pharma Sas | SOMATOSTATIN ANALOGA AND DIMERE OUT |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3970571A (en) * | 1974-12-20 | 1976-07-20 | Eastman Kodak Company | Method for producing improved electrographic developer |
| DE3114824A1 (de) * | 1980-05-07 | 1982-04-08 | Gerhard Prof.Dr.med. 8500 Nürnberg Weber | "verwendung eines mittels zur behandlung der psoriasis (schuppenflechte)" |
| JPS5978364A (ja) * | 1982-10-28 | 1984-05-07 | Ricoh Co Ltd | 電気的潜像現像用トナ− |
| US4474766A (en) * | 1983-06-27 | 1984-10-02 | Merck & Co., Inc. | Anti-inflammatory/analgesic combination of cyclo-(N-methyl-Ala-Tyr-D-Trp-Lys-Val-Phe) and a selected non-steroidal anti-inflammatory drug (NSAID) |
| GB8423431D0 (en) * | 1984-09-17 | 1984-10-24 | Sandoz Ltd | Organic compounds |
| HUT42101A (en) * | 1985-01-07 | 1987-06-29 | Sandoz Ag | Process for preparing stomatostatine derivatives and pharmaceutical compositions containing such compounds |
| US4585755A (en) * | 1985-04-29 | 1986-04-29 | Merck & Co., Inc. | Cyclic and bridged cyclic somatostatin analogs useful as local anti-inflammatory agents |
| JPS61258268A (ja) * | 1985-05-13 | 1986-11-15 | Canon Inc | 静電荷像現像用電荷付与材 |
| JPS638652A (ja) * | 1986-06-27 | 1988-01-14 | Ricoh Co Ltd | 静電荷像現像用トナ− |
| HU206890B (en) * | 1986-10-13 | 1993-01-28 | Sandoz Ag | Process for producing sugar-modified somatostatin peptide derivatives and pharmaceutical compositions containing them as active components |
| IT1208760B (it) * | 1986-11-04 | 1989-07-10 | Ind Farmaceutica Serono S P A | Trattamento delle malattie infiammatorie articolari |
| CH679045A5 (cs) * | 1987-06-29 | 1991-12-13 | Sandoz Ag | |
| DE3845000C2 (de) * | 1987-07-10 | 1998-11-19 | Novartis Ag | Anwendung von Octreotid zur Behandlung von Brustkrebs |
-
1988
- 1988-06-06 GB GB888813339A patent/GB8813339D0/en active Pending
-
1989
- 1989-05-30 HU HU892735A patent/HU206633B/hu not_active IP Right Cessation
- 1989-06-02 GB GB8912724A patent/GB2219503B/en not_active Expired - Lifetime
- 1989-06-02 DK DK273089A patent/DK273089A/da not_active Application Discontinuation
- 1989-06-05 AU AU36042/89A patent/AU631547B2/en not_active Ceased
- 1989-06-05 FR FR8907510A patent/FR2632188B1/fr not_active Expired - Fee Related
- 1989-06-05 EP EP19890810418 patent/EP0351354A3/en not_active Withdrawn
- 1989-06-05 MY MYPI89000759A patent/MY104129A/en unknown
- 1989-06-05 PT PT90753A patent/PT90753A/pt not_active Application Discontinuation
- 1989-06-05 CH CH2095/89A patent/CH680924A5/de not_active IP Right Cessation
- 1989-06-05 IT IT8948041A patent/IT1231521B/it active
- 1989-06-05 BE BE8900608A patent/BE1004038A4/fr not_active IP Right Cessation
- 1989-06-05 KR KR1019890007793A patent/KR910000178A/ko not_active Withdrawn
- 1989-06-05 JP JP1143957A patent/JP2809707B2/ja not_active Expired - Lifetime
- 1989-06-05 SE SE8902042A patent/SE8902042L/xx not_active Application Discontinuation
- 1989-06-05 DE DE3918320A patent/DE3918320A1/de not_active Ceased
- 1989-06-06 NL NL8901435A patent/NL8901435A/nl not_active Application Discontinuation
- 1989-06-06 ZA ZA894280A patent/ZA894280B/xx unknown
-
1991
- 1991-06-14 US US07/715,937 patent/US5145837A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| PT90753A (pt) | 1989-12-29 |
| GB2219503A (en) | 1989-12-13 |
| GB2219503B (en) | 1992-04-29 |
| GB8813339D0 (en) | 1988-07-13 |
| MY104129A (en) | 1994-02-28 |
| FR2632188B1 (fr) | 1994-10-07 |
| FR2632188A1 (fr) | 1989-12-08 |
| BE1004038A4 (fr) | 1992-09-15 |
| EP0351354A2 (en) | 1990-01-17 |
| KR910000178A (ko) | 1991-01-29 |
| AU3604289A (en) | 1989-12-07 |
| DE3918320A1 (de) | 1989-12-14 |
| JPH0242026A (ja) | 1990-02-13 |
| HU206633B (en) | 1992-12-28 |
| AU631547B2 (en) | 1992-12-03 |
| SE8902042L (sv) | 1990-03-28 |
| IT8948041A0 (it) | 1989-06-05 |
| GB8912724D0 (en) | 1989-07-19 |
| JP2809707B2 (ja) | 1998-10-15 |
| IT1231521B (it) | 1991-12-07 |
| DK273089D0 (da) | 1989-06-02 |
| US5145837A (en) | 1992-09-08 |
| EP0351354A3 (en) | 1991-11-06 |
| CH680924A5 (cs) | 1992-12-15 |
| SE8902042D0 (sv) | 1989-06-05 |
| DK273089A (da) | 1989-12-07 |
| HUT53291A (en) | 1990-10-28 |
| ZA894280B (en) | 1991-02-27 |
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