A systematic experimental study on the internal, optical and structural properties of charged pNIPAM (poly-N-isopropylacrylamide) nanogels as a function of temperature, salt concentration and number concentration is presented in this Ph.D. thesis. Three types of charged pNIPAM nanogels were synthesized by emulsion polymerization with diferent proportions of initiator, surfactant and crosslinker. The internal structural properties, the form factor and the size were obtained by light scattering as a function of temperature and ionic strength, and the optical properties were measured by refractometry. Subsequently, using a very simple model to describe the radial profile of the refraction index of nanogels, and using the internal properties obtained by light scattering, it has been possible to determine the nanogel core refraction index. This result is one of the most important contributions of this Ph. D. thesis, and can be very useful in the design of core-shell particles for certain optical applications, such as refractive index-matching of particles. By other side, the spatial configurations of two diferent types of charged nanogels were characterized by means of static light scattering as a function of temperature, salt concentration and particle concentration. In the liquid phase, the structure factor was analyzed by solving integral equations, using the hypernetted chain (HNC) closure and assuming a repulsive Yukawa potential. In our case we utilize the typical Yukawa potential used to describe interactions between charged hard colloids, with the peculiarity of interpreting the charge as a net charge, in order to take into account the presence of ions inside the nanogel. This analysis shows that correlations between particles decrease as the temperature and salt concentration increase. In particular, we have noticed that the efective net charge of the nanogels decreases as the temperature increases, due to an enhanced input of counterions when the nanogel size is reduced. This phenomenon has been observed under diferent conditions of salt concentration, number concentration and bare charge of the nanogels. Nevertheless, it has been shown that at high salt concentrations, the net charge re- mains practically constant, because the number of counterions does not vary with the size of the nanogel. In addition, the phase diagram of highly charged nanogels has been studied as a function of both temperature and particle number density, at diferent salt concentrations. For all the temperatures and salt concentrations investigated, we have observed a liquid-BCC (body centred cubic) crystal transition as the particle concentration increases at relatively low nanogel densities. By further increasing the number concentration, a BCC-FCC (face centred cubic) coexistence appears. Finally, at higher concentrations, the suspensions crystallize into a FCC lattice. These results contradict the theoretical phase diagrams proposed for charged nanogels.