| Total (99) | D2 (1) | D3 (9) | D4 (89) | |
|---|---|---|---|---|
| Premier | 1 (1.01 %) | 1 (1.12 %) | ||
| Deuxième | 1 (1.01 %) | 1 (1.12 %) | ||
| Troisième | 4 (4.04 %) | 2 (22.22 %) | 2 (2.25 %) |
| Eq | Saison | Div | Tour | Match | Neg | Plc | IC | ADV |
|---|---|---|---|---|---|---|---|---|
| KIHc | 1998 | 4 | 9 | KIHc(23.0)-SRMb(54.0) | -370 | 9 | 4.0 | 6.0 |
| KIHb | 1997 | 4 | 10 | YODd(23.0)-KIHb(55.0) | -125 | 6 | 7.0 | 1.0 |
| KIHc | 1997 | 4 | 9 | PHEb(52.0)-KIHc(26.0) | -167 | 10 | 4.0 | 7.0 |
| KIHb | 1997 | 4 | 8 | KAKa(41.0)-KIHb(37.0) | -203 | 9 | 4.0 | 4.0 |
| KIHb | 1997 | 4 | 4 | PHEa(56.0)-KIHb(22.0) | -211 | 16 | 0.0 | 8.0 |
| KIHc | 1997 | 4 | 3 | ASSb(54.5)-KIHc(23.5) | -337 | 12 | 3.0 | 8.0 |
| KIHc | 1997 | 4 | 1 | HAWa(56.0)-KIHc(22.0) | -290 | 10 | 4.0 | 7.0 |
| KIHc | 1991 | 4 | 10 | KIHc(89.0)-FUNb(47.0) | -117 | 5 | 12.0 | 0.0 |
| KIHc | 1991 | 4 | 8 | KIHc(49.0)-KAKa(86.0) | -315 | 13 | 4.0 | 8.0 |
| KIHc | 1991 | 4 | 7 | KAKb(61.0)-KIHc(72.0) | -256 | 11 | 6.0 | 5.0 |
| KIHc | 1991 | 4 | 6 | KIHc(53.0)-AMAa(83.0) | -215 | 10 | 7.0 | 6.0 |
| KIHc | 1991 | 4 | 5 | FUNb(59.0)-KIHc(77.0) | -153 | 3 | 14.0 | 1.0 |
| KIHc | 1991 | 4 | 3 | KAKa(84.0)-KIHc(52.0) | -108 | 5 | 12.0 | 3.0 |
| KIHc | 1991 | 4 | 2 | KIHc(72.0)-KAKb(64.0) | -261 | 6 | 11.0 | 2.0 |
| KIHc | 1991 | 4 | 1 | AMAa(68.5)-KIHc(67.5) | -112 | 5 | 12.0 | 2.0 |
| KIHc | 1990 | 4 | 10 | KIHc(80.5)-SRMa(55.5) | -279 | 14 | 3.0 | 6.0 |
| KIHc | 1990 | 4 | 9 | ACJb(82.0)-KIHc(54.0) | -289 | 11 | 6.0 | 6.0 |
| KIHc | 1990 | 4 | 8 | CINa(77.0)-KIHc(59.0) | -218 | 14 | 3.0 | 7.0 |
| KIHc | 1990 | 4 | 7 | KIHc(73.0)-BOUa(63.0) | -220 | 9 | 8.0 | 4.0 |
| KIHc | 1990 | 4 | 6 | AMAa(53.0)-KIHc(83.0) | -174 | 6 | 11.0 | 1.0 |
| KIHc | 1990 | 4 | 5 | SRMa(56.0)-KIHc(80.0) | -217 | 5 | 12.0 | 1.0 |
| KIHc | 1990 | 4 | 4 | KIHc(53.5)-ACJb(82.5) | -118 | 13 | 4.0 | 7.0 |
| KIHc | 1990 | 4 | 1 | KIHc(87.0)-AMAa(49.0) | -106 | 7 | 10.0 | 1.0 |
| KIHc | 1989 | 4 | 10 | KIHc(64.0)-ACJb(72.0) | -94 | 6 | 11.0 | 4.0 |
| KIHc | 1989 | 4 | 9 | CINa(68.0)-KIHc(68.0) | -186 | 8 | 9.0 | 4.0 |
| KIHc | 1989 | 4 | 8 | KIHc(57.0)-ACJb(79.0) | -196 | 5 | 12.0 | 3.0 |
| KIHc | 1989 | 4 | 7 | SASa(73.0)-KIHc(63.0) | -237 | 11 | 6.0 | 6.0 |
| KIHc | 1989 | 4 | 5 | ACJb(81.0)-KIHc(55.0) | -231 | 13 | 4.0 | 8.0 |
| KIHc | 1989 | 4 | 4 | KIHc(56.0)-SASa(80.0) | -301 | 16 | 1.0 | 8.0 |
| KIHc | 1989 | 4 | 3 | CINa(69.0)-KIHc(67.0) | -240 | 14 | 2.5 | 7.0 |
| KIHc | 1989 | 4 | 1 | SASa(88.0)-KIHc(48.0) | -212 | 16 | 1.0 | 8.0 |
| KIHc | 1988 | 4 | 9 | KIHc(46.5)-HELb(89.5) | -126 | 7 | 9.5 | 5.5 |
| KIHc | 1988 | 4 | 8 | SASb(73.0)-KIHc(62.0) | -199 | 9 | 8.0 | 5.0 |
| KIHc | 1988 | 4 | 7 | KIHc(73.0)-CINa(63.0) | -254 | 10 | 7.0 | 4.0 |
| KIHc | 1988 | 4 | 6 | HELb(75.0)-KIHc(61.0) | -135 | 9 | 8.0 | 6.0 |
| KIHc | 1988 | 4 | 5 | KIHc(80.0)-SASb(56.0) | -170 | 5 | 12.0 | 1.0 |
| KIHc | 1988 | 4 | 4 | CINa(73.0)-KIHc(63.0) | -185 | 9 | 8.0 | 5.0 |
| KIHc | 1988 | 4 | 3 | KIHc(62.0)-HELb(74.0) | -131 | 8 | 9.0 | 4.0 |
| KIHc | 1988 | 4 | 2 | SASb(55.0)-KIHc(81.0) | -184 | 7 | 10.0 | 3.0 |
| KIHc | 1988 | 4 | 1 | KIHc(64.0)-CINa(72.0) | -208 | 8 | 9.0 | 4.0 |
| KIHc | 1987 | 4 | 10 | KAKa(56.0)-KIHc(80.0) | -101 | 6 | 11.0 | 1.0 |
| KIHc | 1987 | 4 | 9 | KIHc(58.0)-PHEb(78.0) | -188 | 8 | 9.0 | 4.0 |
| KIHc | 1987 | 4 | 8 | CHEa(96.0)-KIHc(40.0) | -347 | 13 | 4.0 | 8.0 |
| KIHc | 1987 | 4 | 7 | KIHc(68.0)-ANGa(68.0) | -60 | 1 | 16.0 | 0.0 |
| KIHc | 1987 | 4 | 6 | ASSc(84.0)-KIHc(52.0) | -269 | 13 | 4.0 | 7.0 |
| KIHc | 1987 | 4 | 5 | KIHc(66.0)-KAKa(70.0) | -123 | 4 | 13.0 | 2.0 |
| KIHc | 1987 | 4 | 4 | PHEb(84.0)-KIHc(46.0) | -148 | 12 | 5.0 | 8.0 |
| KIHc | 1987 | 4 | 3 | KIHc(51.0)-CHEa(85.0) | -302 | 11 | 6.0 | 6.0 |
| KIHc | 1987 | 4 | 2 | ANGa(63.5)-KIHc(72.5) | -202 | 13 | 4.0 | 6.0 |
| KIHc | 1987 | 4 | 1 | KIHc(45.0)-ASSc(90.0) | -214 | 11 | 6.0 | 7.0 |
| KIHc | 1986 | 4 | 10 | KIHc(73.0)-HELb(63.0) | -153 | 10 | 7.0 | 4.0 |
| KIHc | 1986 | 4 | 9 | ACJb(91.0)-KIHc(44.0) | -100 | 5 | 11.5 | 4.0 |
| KIHc | 1986 | 4 | 7 | KIHc(67.5)-CINa(67.5) | -203 | 7 | 10.0 | 3.0 |
| KIHc | 1986 | 4 | 5 | HELb(72.0)-KIHc(64.0) | -80 | 5 | 12.0 | 3.0 |
| KIHc | 1986 | 4 | 4 | KIHc(68.0)-ACJb(68.0) | -172 | 7 | 10.0 | 3.0 |
| KIHc | 1986 | 4 | 3 | KIHc(62.0)-SASb(74.0) | -217 | 13 | 4.0 | 6.0 |
| KIHc | 1986 | 4 | 2 | CINa(83.0)-KIHc(52.0) | -171 | 6 | 11.0 | 4.0 |
| KIHc | 1985 | 4 | 10 | KIHc(77.0)-ASSd(59.0) | -124 | 5 | 12.0 | 2.0 |
| KIHc | 1985 | 4 | 8 | KIHc(59.0)-CHEb(77.0) | -315 | 12 | 5.0 | 7.0 |
| KIHc | 1985 | 4 | 7 | PHEb(83.0)-KIHc(53.0) | -174 | 11 | 6.0 | 6.0 |
| KIHb | 1985 | 4 | 6 | SASa(70.0)-KIHb(66.0) | -180 | 12 | 5.0 | 6.0 |
| KIHc | 1985 | 4 | 3 | CHEb(65.0)-KIHc(71.0) | -233 | 7 | 10.0 | 3.0 |
| KIHc | 1985 | 4 | 2 | KIHc(61.0)-PHEb(75.0) | -215 | 6 | 11.0 | 3.0 |
| KIHc | 1985 | 4 | 1 | KAKa(60.0)-KIHc(75.0) | -119 | 2 | 15.0 | 0.0 |
| KIHc | 1984 | 4 | 14 | KIHc(64.0)-HELb(72.0) | -32 | 3 | 14.0 | 2.0 |
| KIHc | 1984 | 4 | 13 | SRMa(65.0)-KIHc(71.0) | -210 | 8 | 9.0 | 3.0 |
| KIHc | 1984 | 4 | 12 | HELb(79.0)-KIHc(57.0) | -283 | 16 | 1.0 | 8.0 |
| KIHc | 1984 | 4 | 11 | KIHc(44.0)-KIHb(92.0) | -263 | 16 | 1.0 | 8.0 |
| KIHc | 1984 | 4 | 10 | SASa(88.0)-KIHc(48.0) | -332 | 12 | 5.0 | 7.0 |
| KIHc | 1984 | 4 | 9 | CINa(65.5)-KIHc(70.5) | -168 | 7 | 9.5 | 2.5 |
| KIHc | 1984 | 4 | 6 | KIHc(74.5)-SRMa(61.5) | -180 | 7 | 10.0 | 3.0 |
| KIHb | 1984 | 4 | 5 | SRMa(48.0)-KIHb(88.0) | -321 | 14 | 3.0 | 6.0 |
| KIHb | 1984 | 4 | 3 | SASa(74.5)-KIHb(61.5) | -218 | 12 | 4.5 | 6.0 |
| KIHc | 1984 | 4 | 2 | KIHc(51.0)-ACJb(85.0) | -600 | 16 | 1.0 | 8.0 |
| KIHc | 1984 | 4 | 1 | KIHb(96.0)-KIHc(40.0) | -408 | 16 | 1.0 | 8.0 |
| KIHc | 1982 | 4 | 6 | PHEc(54.0)-KIHc(82.0) | -228 | 8 | 9.0 | 2.0 |
| KIHc | 1982 | 4 | 4 | KIHc(59.5)-SABb(76.5) | -205 | 11 | 5.5 | 6.0 |
| KIHc | 1982 | 4 | 3 | KIHc(70.0)-PHEc(66.0) | -129 | 10 | 6.5 | 5.0 |
| KIHc | 1982 | 4 | 2 | ASSc(75.0)-KIHc(60.0) | -226 | 11 | 6.0 | 6.0 |
| KIHc | 1982 | 4 | 1 | SABb(82.0)-KIHc(54.0) | -178 | 9 | 7.5 | 6.0 |
| KIHc | 1981 | 4 | 9 | KIHc(87.0)-ASSc(49.0) | -139 | 5 | 12.0 | 1.0 |
| KIHc | 1981 | 4 | 8 | SASb(63.0)-KIHc(73.0) | -389 | 11 | 6.0 | 5.0 |
| KIHc | 1981 | 4 | 7 | KIHc(48.0)-YODa(87.0) | -240 | 14 | 3.0 | 8.0 |
| KIHc | 1981 | 4 | 6 | HYAb(83.0)-KIHc(53.0) | -217 | 13 | 4.0 | 8.0 |
| KIHc | 1981 | 4 | 5 | PHEc(62.0)-KIHc(74.0) | -215 | 5 | 12.0 | 2.0 |
| KIHc | 1981 | 4 | 4 | KIHc(59.0)-BLOa(77.0) | -269 | 16 | 1.0 | 8.0 |
| KIHc | 1981 | 4 | 3 | CHEa(73.5)-KIHc(62.5) | -73 | 5 | 12.0 | 3.0 |
| KIHc | 1981 | 4 | 2 | KIHc(89.0)-SRMa(47.0) | -134 | 5 | 12.0 | 1.0 |
| KIHc | 1981 | 4 | 1 | CINa(51.5)-KIHc(84.5) | -194 | 5 | 12.0 | 1.0 |
| KIHc | 1980 | 3 | 7 | KIHc(78.0)-SABc(58.0) | -137 | 3 | 14.0 | 1.0 |
| KIHc | 1980 | 3 | 6 | KIHc(64.0)-SASa(72.0) | -244 | 13 | 4.0 | 7.0 |
| KIHb | 1980 | 3 | 5 | KIHb(74.0)-PHEb(62.0) | -161 | 8 | 9.0 | 3.0 |
| KIHc | 1980 | 3 | 4 | KIHc(63.0)-CVLa(73.0) | -119 | 3 | 14.0 | 2.0 |
| KIHc | 1980 | 3 | 3 | KIHc(66.0)-BLOa(70.0) | -412 | 10 | 7.0 | 5.0 |
| KIHc | 1980 | 3 | 2 | PHEb(92.0)-KIHc(44.0) | -243 | 8 | 9.0 | 6.0 |
| KIHc | 1980 | 3 | 1 | KIHb(85.0)-KIHc(51.0) | -155 | 7 | 10.0 | 4.0 |
| KIHb | 1979 | 3 | 1 | KIHb(64.0)-PHEb(72.0) | -306 | 15 | 2.0 | 7.0 |
| KIHb | 1978 | 3 | 4 | HYAa(64.0)-KIHb(72.0) | -239 | 15 | 2.0 | 7.0 |
| KIHa | 1978 | 2 | 3 | KIHa(54.0)-HELa(82.0) | -330 | 16 | 1.0 | 8.0 |