Total (106) | D2 (26) | D3 (27) | D4 (53) | |
---|---|---|---|---|
Premier | 3 (2.83 %) | 1 (3.85 %) | 1 (3.70 %) | 1 (1.89 %) |
Deuxième | 3 (2.83 %) | 3 (5.66 %) | ||
Troisième | 5 (4.72 %) | 1 (3.70 %) | 4 (7.55 %) |
Eq | Saison | Div | Tour | Match | Neg | Plc | IC | ADV |
---|---|---|---|---|---|---|---|---|
KIHb | 1991 | 3 | 8 | SIRc(73.0)-KIHb(63.0) | -106 | 12 | 5.0 | 6.0 |
KIHc | 1991 | 4 | 7 | KAKb(61.0)-KIHc(72.0) | -163 | 4 | 13.0 | 2.0 |
KIHc | 1991 | 4 | 6 | KIHc(53.0)-AMAa(83.0) | -116 | 3 | 14.0 | 2.0 |
KIHc | 1991 | 4 | 5 | FUNb(59.0)-KIHc(77.0) | -185 | 7 | 10.0 | 3.0 |
KIHc | 1991 | 4 | 2 | KIHc(72.0)-KAKb(64.0) | -143 | 2 | 15.0 | 0.0 |
KIHc | 1990 | 4 | 10 | KIHc(80.5)-SRMa(55.5) | -185 | 7 | 10.0 | 2.0 |
KIHb | 1990 | 2 | 9 | CHIa(76.5)-KIHb(59.5) | -337 | 16 | 1.0 | 8.0 |
KIHc | 1990 | 4 | 8 | CINa(77.0)-KIHc(59.0) | -154 | 11 | 6.0 | 6.0 |
KIHb | 1990 | 2 | 7 | SONa(86.5)-KIHb(49.5) | -144 | 12 | 5.0 | 7.0 |
KIHc | 1990 | 4 | 6 | AMAa(53.0)-KIHc(83.0) | -228 | 8 | 9.0 | 2.0 |
KIHc | 1990 | 4 | 5 | SRMa(56.0)-KIHc(80.0) | -309 | 13 | 4.0 | 6.0 |
KIHc | 1990 | 4 | 4 | KIHc(53.5)-ACJb(82.5) | -104 | 9 | 7.5 | 6.0 |
KIHc | 1990 | 4 | 3 | KIHc(52.0)-CINa(84.0) | -123 | 5 | 12.0 | 3.0 |
KIHc | 1990 | 4 | 1 | KIHc(87.0)-AMAa(49.0) | -154 | 12 | 5.0 | 5.0 |
KIHc | 1988 | 4 | 9 | KIHc(46.5)-HELb(89.5) | -209 | 13 | 4.0 | 8.0 |
KIHc | 1988 | 4 | 8 | SASb(73.0)-KIHc(62.0) | -252 | 12 | 5.0 | 7.0 |
KIHc | 1988 | 4 | 7 | KIHc(73.0)-CINa(63.0) | -258 | 11 | 6.0 | 4.0 |
KIHc | 1988 | 4 | 6 | HELb(75.0)-KIHc(61.0) | -238 | 14 | 3.0 | 6.0 |
KIHc | 1988 | 4 | 4 | CINa(73.0)-KIHc(63.0) | -59 | 1 | 16.0 | 0.0 |
KIHc | 1988 | 4 | 3 | KIHc(62.0)-HELb(74.0) | -117 | 5 | 12.0 | 3.0 |
KIHc | 1988 | 4 | 2 | SASb(55.0)-KIHc(81.0) | -133 | 3 | 14.0 | 0.0 |
KIHc | 1988 | 4 | 1 | KIHc(64.0)-CINa(72.0) | -333 | 16 | 1.0 | 8.0 |
KIHc | 1987 | 4 | 10 | KAKa(56.0)-KIHc(80.0) | -61 | 2 | 15.0 | 1.0 |
KIHb | 1987 | 3 | 9 | SASa(84.0)-KIHb(52.0) | -214 | 14 | 3.0 | 7.0 |
KIHc | 1987 | 4 | 8 | CHEa(96.0)-KIHc(40.0) | -195 | 5 | 12.0 | 4.0 |
KIHb | 1987 | 3 | 7 | BLOa(58.5)-KIHb(77.5) | -50 | 3 | 13.5 | 1.0 |
KIHb | 1987 | 3 | 6 | KIHb(54.0)-YODa(82.0) | -159 | 16 | 1.0 | 8.0 |
KIHc | 1987 | 4 | 5 | KIHc(66.0)-KAKa(70.0) | -179 | 9 | 7.5 | 5.0 |
KIHb | 1987 | 3 | 4 | KIHb(59.0)-SASa(77.0) | -182 | 14 | 3.0 | 8.0 |
KIHc | 1987 | 4 | 3 | KIHc(51.0)-CHEa(85.0) | -239 | 8 | 9.0 | 5.0 |
KIHb | 1987 | 3 | 2 | KIHb(67.0)-BLOa(69.0) | -94 | 10 | 7.0 | 5.0 |
KIHb | 1987 | 3 | 1 | YODa(81.0)-KIHb(55.0) | -303 | 16 | 1.0 | 8.0 |
KIHb | 1986 | 4 | 9 | KIHb(96.0)-ANGa(40.0) | -85 | 4 | 13.0 | 0.0 |
KIHb | 1986 | 4 | 8 | KAKa(38.0)-KIHb(98.0) | -129 | 6 | 11.0 | 0.0 |
KIHb | 1986 | 4 | 7 | ASSc(74.5)-KIHb(61.5) | -148 | 12 | 4.5 | 6.5 |
KIHb | 1986 | 4 | 6 | KIHb(91.0)-ANGa(45.0) | -175 | 10 | 7.0 | 2.0 |
KIHb | 1986 | 4 | 5 | KIHb(88.0)-KAKa(48.0) | -139 | 5 | 12.0 | 1.0 |
KIHb | 1986 | 4 | 4 | ASSc(61.0)-KIHb(75.0) | -304 | 16 | 1.0 | 8.0 |
KIHb | 1986 | 4 | 3 | ANGa(56.0)-KIHb(80.0) | -212 | 11 | 6.0 | 4.0 |
KIHb | 1986 | 4 | 2 | KIHb(92.0)-KAKa(44.0) | -233 | 7 | 10.0 | 2.0 |
KIHb | 1986 | 4 | 1 | KIHb(81.5)-ASSc(54.5) | -291 | 16 | 1.0 | 8.0 |
KIHb | 1985 | 4 | 10 | CINa(69.5)-KIHb(66.5) | -243 | 10 | 7.0 | 5.0 |
KIHb | 1985 | 4 | 9 | KIHb(83.0)-SRMa(53.0) | -242 | 8 | 9.0 | 3.0 |
KIHb | 1985 | 4 | 7 | KIHb(80.5)-HELb(55.5) | -43 | 4 | 13.0 | 1.0 |
KIHb | 1985 | 4 | 6 | SASa(70.0)-KIHb(66.0) | -52 | 3 | 14.0 | 1.0 |
KIHb | 1985 | 4 | 5 | KIHb(73.0)-CINa(63.0) | -232 | 10 | 7.0 | 4.0 |
KIHb | 1985 | 4 | 4 | SRMa(60.0)-KIHb(76.0) | -162 | 6 | 11.0 | 2.0 |
KIHb | 1985 | 4 | 3 | KIHb(77.0)-ACJb(59.0) | -134 | 11 | 6.0 | 5.0 |
KIHb | 1985 | 4 | 2 | HELb(62.0)-KIHb(74.0) | -128 | 10 | 7.0 | 4.0 |
KIHb | 1985 | 4 | 1 | KIHb(66.0)-SASa(70.0) | -111 | 5 | 12.0 | 2.0 |
KIHb | 1984 | 4 | 14 | ACJb(38.5)-KIHb(97.5) | -142 | 10 | 6.5 | 2.5 |
KIHb | 1984 | 4 | 13 | KIHb(91.0)-CINa(45.0) | -191 | 12 | 5.0 | 4.0 |
KIHb | 1984 | 4 | 12 | KIHb(83.0)-ACJb(53.0) | -190 | 6 | 10.5 | 2.0 |
KIHb | 1984 | 4 | 11 | KIHc(44.0)-KIHb(92.0) | -189 | 10 | 7.0 | 2.0 |
KIHb | 1984 | 4 | 10 | KIHb(97.0)-SRMa(39.0) | -116 | 2 | 15.0 | 0.0 |
KIHb | 1984 | 4 | 8 | KIHb(66.5)-SASa(69.5) | -87 | 7 | 10.0 | 4.0 |
KIHb | 1984 | 4 | 7 | KIHb(75.5)-HELb(60.5) | -233 | 9 | 8.0 | 3.0 |
KIHb | 1984 | 4 | 6 | CINa(56.0)-KIHb(80.0) | -320 | 15 | 2.0 | 7.0 |
KIHb | 1984 | 4 | 5 | SRMa(48.0)-KIHb(88.0) | -203 | 6 | 11.0 | 1.0 |
KIHb | 1984 | 4 | 3 | SASa(74.5)-KIHb(61.5) | -125 | 4 | 12.5 | 2.5 |
KIHb | 1984 | 4 | 2 | HELb(58.0)-KIHb(78.0) | -227 | 10 | 7.0 | 4.0 |
KIHb | 1984 | 4 | 1 | KIHb(96.0)-KIHc(40.0) | -208 | 3 | 14.0 | 0.0 |
KIHb | 1983 | 3 | 9 | BORa(86.0)-KIHb(49.0) | -270 | 14 | 3.0 | 8.0 |
KIHb | 1983 | 3 | 8 | KIHb(52.0)-YODa(84.0) | -251 | 12 | 5.0 | 7.0 |
KIHb | 1983 | 3 | 7 | KIHb(52.0)-REBa(84.0) | -188 | 12 | 5.0 | 7.0 |
KIHb | 1983 | 3 | 6 | GRIa(97.0)-KIHb(39.0) | -175 | 14 | 3.0 | 8.0 |
KIHb | 1983 | 3 | 5 | KIHb(69.0)-BRAa(67.0) | -81 | 6 | 11.0 | 2.0 |
KIHb | 1983 | 3 | 4 | MATb(80.0)-KIHb(55.0) | -209 | 9 | 8.0 | 5.0 |
KIHb | 1983 | 3 | 2 | RESa(55.5)-KIHb(79.5) | -209 | 8 | 9.0 | 3.0 |
KIHb | 1983 | 3 | 1 | KIHb(54.0)-VALa(82.0) | -52 | 1 | 16.0 | 0.0 |
KIHb | 1982 | 2 | 11 | MJAb(74.5)-KIHb(61.5) | -161 | 7 | 9.5 | 4.5 |
KIHb | 1982 | 2 | 10 | KIHb(55.0)-MACa(80.0) | -233 | 12 | 5.0 | 7.0 |
KIHb | 1982 | 2 | 9 | HYAa(87.0)-KIHb(49.0) | -101 | 6 | 11.0 | 4.0 |
KIHb | 1982 | 2 | 8 | KIHb(67.0)-SACa(68.0) | -230 | 8 | 9.0 | 3.0 |
KIHb | 1982 | 2 | 7 | LOUb(70.0)-KIHb(66.0) | -184 | 12 | 5.0 | 6.0 |
KIHb | 1982 | 2 | 6 | KIHb(46.0)-SIRa(90.0) | -256 | 16 | 1.0 | 8.0 |
KIHb | 1982 | 2 | 5 | SCBa(72.0)-KIHb(64.0) | -189 | 10 | 7.0 | 5.0 |
KIHb | 1982 | 2 | 4 | WATb(86.0)-KIHb(50.0) | -206 | 12 | 5.0 | 8.0 |
KIHb | 1982 | 2 | 3 | KIHb(55.0)-OUEb(81.0) | -223 | 14 | 3.0 | 7.0 |
KIHb | 1982 | 2 | 2 | KIHb(48.0)-PICa(88.0) | -100 | 9 | 8.0 | 7.0 |
KIHb | 1982 | 2 | 1 | PHEb(77.5)-KIHb(58.5) | -183 | 8 | 8.5 | 5.0 |
KIHb | 1981 | 2 | 11 | KIHb(71.0)-SCBa(65.0) | -175 | 14 | 3.0 | 6.0 |
KIHb | 1981 | 2 | 10 | KIHb(42.0)-MATa(94.0) | -177 | 15 | 2.0 | 8.0 |
KIHb | 1981 | 2 | 9 | OUEb(93.0)-KIHb(43.0) | -330 | 12 | 5.0 | 8.0 |
KIHb | 1981 | 2 | 8 | SALa(69.0)-KIHb(66.0) | -207 | 11 | 6.0 | 5.0 |
KIHb | 1981 | 2 | 7 | KIHb(50.0)-ASSa(86.0) | -273 | 15 | 2.0 | 8.0 |
KIHb | 1981 | 2 | 6 | KIHb(72.0)-MJAb(33.0) | -221 | 10 | 7.0 | 4.0 |
KIHb | 1981 | 2 | 5 | MACa(74.0)-KIHb(62.0) | -203 | 10 | 7.0 | 5.0 |
KIHb | 1981 | 2 | 4 | KIHb(70.0)-MALb(66.0) | -131 | 6 | 11.0 | 3.0 |
KIHb | 1981 | 2 | 3 | VENa(69.0)-KIHb(67.0) | -245 | 11 | 6.0 | 5.0 |
KIHb | 1981 | 2 | 2 | KIHb(75.0)-LOUb(61.0) | -57 | 1 | 16.0 | 0.0 |
KIHb | 1981 | 2 | 1 | SIRa(84.0)-KIHb(52.0) | -219 | 16 | 1.0 | 8.0 |
KIHa | 1980 | 2 | 9 | MJAb(54.0)-KIHa(82.0) | -267 | 14 | 3.0 | 6.0 |
KIHb | 1980 | 3 | 7 | SASa(56.0)-KIHb(80.0) | -250 | 16 | 1.0 | 8.0 |
KIHa | 1980 | 2 | 6 | VENa(65.0)-KIHa(71.0) | -163 | 10 | 7.0 | 4.0 |
KIHb | 1980 | 3 | 5 | KIHb(74.0)-PHEb(62.0) | -192 | 13 | 4.0 | 6.0 |
KIHb | 1980 | 3 | 4 | BLOa(58.0)-KIHb(78.0) | -150 | 5 | 12.0 | 2.0 |
KIHb | 1980 | 3 | 3 | SABc(48.0)-KIHb(88.0) | -116 | 7 | 10.0 | 2.0 |
KIHb | 1980 | 3 | 2 | KIHb(70.0)-ASSa(66.0) | -162 | 12 | 5.0 | 5.0 |
KIHb | 1980 | 3 | 1 | KIHb(85.0)-KIHc(51.0) | -111 | 4 | 13.0 | 1.0 |
KIHb | 1979 | 3 | 5 | CVLa(60.0)-KIHb(76.0) | -269 | 13 | 4.0 | 6.0 |
KIHb | 1979 | 3 | 3 | SASa(48.5)-KIHb(87.5) | -207 | 11 | 5.5 | 4.0 |
KIHb | 1978 | 3 | 10 | KIHb(70.0)-CVLa(66.0) | -355 | 7 | 10.0 | 3.0 |
KIHb | 1978 | 3 | 9 | KIHb(80.5)-REBa(54.5) | -192 | 10 | 6.5 | 4.0 |
KIHb | 1978 | 3 | 8 | MALc(66.0)-KIHb(70.0) | -172 | 5 | 12.0 | 2.0 |
KIHb | 1978 | 3 | 3 | KIHb(81.0)-CREa(55.0) | -369 | 14 | 3.0 | 6.0 |