1              Conspicuously negative were the lobus paraolfactorius, including song nucleus area X, an

2 robust expression was found in area X of the lobus parolfactorius (LPO) as well as in other song regi

3  A distinct cell type was NOS-labeled in the lobus parolfactorius (LPO) in the telencephalon, and neu

4 irst station in the AFP, and the surrounding lobus parolfactorius (LPO), are both parts of the avian

5 medial hyperstriatum ventrale (IMHV) and the lobus parolfactorius (LPO).

6 m, NLc, and the magnicellular nucleus of the lobus parolfactorius (LPOm) were confirmed.

7 nd NAo upon the magnocellular nucleus of the lobus parolfactorius (LPOm), and after LPOm onto the mag

8                             For example, the lobus parolfactorius and paleostriatum augmentatum were

9 rtion of the basal ganglia in pigeons (i.e., lobus parolfactorius and paleostriatum augmentatum).

10             The magnicellular nucleus of the lobus parolfactorius in budgerigars, like the area X in

11 he rostroventral part of what was called the lobus parolfactorius was acknowledged as comparable to t

12 s in the archistriatum, basal ganglia (i.e., lobus parolfactorius), and dorsal thalamus.

13 es: the hippocampal formation, septal areas, lobus parolfactorius, nucleus accumbens, ventral paleost

14 ties, the budgerigar dorsal striatopallidum (lobus parolfactorius, paleostriatum augmentatum, and pal

15 ol circuit, the magnicellular nucleus of the lobus parolfactorius, stain heavily for iron.

16 tekeeper role, as lesions of the tonsil, the lobus semilunaris inferior, and parts of the vermal pyra

17    We recorded PC activity in the vermis and lobus simplex of head-fixed mice while monitoring lickin